Zusammenfassung
Die granulopoetischen Zellen leiten sich von einer als pluripotent bezeichneten Stammzelle ab. Tierexperimentell erweist sich deren Pluripotenz insofern, als die Transplantation solcher Stammzellen auf letal bestrahlte Empfänger in der Milz zur Bildung von Kolonien führt („Cell Forming Unit-Spleen“ = CFU-S), die gemischt aus megakaryozytären, erythroblastischen und granulopoetischen Zellelementen aufgebaut sind und jeweils von einzelnen Stammzellen ausgehen. Solche pluripotenten Stammzellen sind einerseits zur Autoreproduktion fähig, andererseits können sie sich zu determinierten Stammzellen („committed stem cells“) entwickeln, welche gezielt in eine erythropoetische, megakaryozytäre, monozytopoetische oder granulo-zytopoetische Zellentwicklung übergehen.
This is a preview of subscription content, log in via an institution.
Buying options
Tax calculation will be finalised at checkout
Purchases are for personal use only
Learn about institutional subscriptionsPreview
Unable to display preview. Download preview PDF.
Literatur
Weiterführende Literatur
Begemann H, Rastetter J (1978) Atlas der klinischen Hämatologie. Springer, Berlin Heidelberg New York
Bessis M (1973) Living Blood Cells and their Ultrastructure. Springer, Berlin Heidelberg New York
Queißer W (ed) (1978) Das Knochenmark. Morphologie, Funktion, Diagnostik. Thieme, Stuttgart
Schmalzl F, Huhn D, Schaefer HE (1981) Disorders of the Monocyte Macrophage System. Haemat Blood Transf, Vol 27. Springer, Berlin Heidelberg New York
Williams WJ, Beutler E, Erslev AJ, Rundles RW (1977) Hematology, 2nd edn. McGraw-Hill Book Co, New York
Wintrobe MM, Lee GR, Boggs DR, Bithell TC, Athens JW, Foerster J (1974) Clinical Hematology, 7th edn. Lea & Febiger, Philadelphia
Literatur
Abernathy MR (1966) Döhle bodies associated with uncomplicated pregnancy. Blood 27: 380
Alder A (1939) Über konstitutionell bedingte Granulationsveränderungen der Leukozyten. Dtsch Arch klin Med 183: 372
Alonso K, Dew JM, Starke WR (1972) Thymic alymphoplasia and congenital aleukocytosis (reticular dysgenesia). Arch Path 94: 179
Alper CA, Colten HR, Rosen FS, Rabson AR, Macnab GM, Gear JSS (1972) Homozygous deficiency of C3 in a patient with repeated infections. Lancet II: 1179
AMA (1964, 1965, 1967) Adverse reactions, registry on, tabulations of reports. Panel on Hematoloy. Council on Drugs, AMA, Chicago
Ament ME, Ochs HD (1973) Gastrointestinal manifestations of chronic granulomatous disease of childhood. New Engl J Med 288:382
Athens JW, Raab SO, Haab OP, Mauer AM, Ashenbrucker H, Cartwright GE, Wintrobe MM (1961) Leukokinetic studies. III The distribution of granulocytes in the blood of normal subjects. J clin Invest 40:159
Athens JW, Haab OP, Raab SO, Mauer AM, Ashenbrucker H, Cartwright GE, Wintrobe MM (1961) Leukokinetic studies. III The total blood, circulating and marginal granulocyte pools and the granulocyte turnover rate in normal subjects. J clin Invest 40: 989
Aznar J, Vaya A (1981) Homozygous form of the Pelger-Huët leukocyte anomaly in man. Acta haemat 66: 59
Babior BM, Crowley CH (1983) Chronic granulomatous disease and other disorders of oxidative killing by phagocytes. In: Stanbury JB, Wyngaarden JB, Fredrickson DS, Goldstein JL, Brown MS (eds) The metabolic basis of inherited disease, 5th edn. Mc Graw-Hill, New York, p 1956
Baehner RL, Nathan DG (1968) Quantitative nitroblue tetrazolium test in chronic granulomatous disease. New Engl J Med 278:971
Barth RF, Khurana SK, Vergara GG, Lowman JT, Beckwith JB (1972) Rapidly fatal familial histiocytosis associated with eosinophilia and primary immunological deficiency. Lancet II: 503
Basten A, Beason PB (1970) Mechanism of eosinophilia. II. Role of the lymphocytes. J exp Med 131:1288
Baumann T (1951) Konstitutionelle Panmyelophthise mit multipler Abartung (Fanconi-Syndrome). Ann Paediatr 177: 65
Bedoya V, Grimley PM, Duque O (1969) Chédiak-Higashi Syndrome. Arch Path 88: 340
Begemann WH, van Campagne AL (1952) Homozygous form of Pelger-Huët’s anomaly in man. Acta haemat (Basel) 7:295
Bell TG, Meyers KM, Prieur DJ, Fauci AS, Wolff SM, Padgett GA (1976) Decreased nucleotide and serotonin storage associated with defective function in Chédiak-Higashi syndrome cattle and human platelets. Blood 48:175
Bennett JM, Blume RS, Wolff SM (1969) Characterization and significance of abnormal leukocyte granules in the beige mouse: a possible homologue for Chediak-Higashi aleutian trait. J lab clin Med 73: 235
Berendes H, Bridges RA, Good RA (1957) A fatal granulomatosis of childhood: The clinical study of a new syndrome. Minn Med 40: 309
Bessis M, Bernard J, Seligmann M (1961) Etude cytologique d’un cas de maladie de Chédiak. Nouv Rev franc Hemat 1: 422
Bishop CR, Athens JW, Boggs DR, Warner HR, Cartwright GE, Wintrobe MM (1968) Leukokinetic studies. XIII. A non-steady-state kinetic evaluation of the mechanism of cortisone-induced granulocytosis. J clin Invest 47: 249
Bishop CR, Rothstein G, Ashenbrucker H, Athens JW (1971) Leukokinetic studies. XIV. Blood neutrophil kinetics in chronic, steady-state neutropenia. J clin Invest 50:1678
Bodian M, Sheldon W, Lightwood R (1964) Congenital hypoplasia of the exocrine pancreas. Acta paediatr 53: 282
Boll J (1978) Erkrankungen des granulozytären Systems. In: Queißer W (ed) Das Knochenmark. Thieme, Stuttgart, S 501
Boll J, Koeppen K-M (1978) Die hereditären und konstitutionellen Granulozytopenien. In: Queißer W (ed) Das Knochenmark. Thieme, Stuttgart, S 504
Boseila AWA (1963) Hormonal influence on blood and tissue basophilic granulocytes. Ann NY Acad Sei 103: 394
Boxer LA, Hedley-Whyte ET, Stossel TP (1974) Neutrophil actin dysfunction and abnormal neutrophil behavior. New Engl J Med 291:1093
Breton-Gorius J, Mason DY, Buriot D, Vilde JL, Griscelli C (1980) Lactoferrin deficiency as a consequence of a lack of specific granules in neutrophils from a patient with recurrent infections: detection by immunoperoxidase staining of lactoferrin and cytochemical electron microscopy. Amer J Path 99: 413
Brown PK, Ophuls W (1902) A fatal case of acute primary infectious pharyngitis with extreme leukopenia. Amer Med 3:649
Bryan HG, Nixon RK (1965) Dyskeratosis congenita and familial pancytopenia. J Amer Med Assoc 192: 203
Burke V, Colebatch JH, Anderson CM, Simons MJ (1967) Association of pancreatic insufficiency and chronic neutropenia in childhood. Arch Dis Child 42:147
Burchardt K, Zawilska K (1972) Benign familial neutropenia with deficiency of alkaline phosphatase in granulocytes. Pol Arch Med Wewn 49: 486
Carper HA, Hoffman PL (1966) The intravascular survival of transfused canine Pelger-Huet neurophils and eosinophils. Blood 27:739
Cartwright GE, Hui-Lan Chung, An Chang (1948) Studies on the pancytopenia of kala-azar. Blood 3: 249
Chédiak M (1952) Nouvelle anomalie leucocytaire de caractére constitutionel et familial. Rev Hémat 7: 362
Clark RA, Kimball HR (1971) Defective granulocyte chemotaxis in the Chédiak-Higashi syndrome. J clin Invest 50: 2645
Clark RA, Root RK, Kimball HR, Kirkpatrick CH (1973) Defective neutrophil chemotaxis and cellular immunity in a child with recurrent infections. Ann intern Med 78: 515
Cline MJ (1977) Cellular kinetics of monocytes and macrophages. In: Williams WJ, Beutler E, Erslev AJ, Rundles RW (eds) Hematology. McGraw-Hill, New York, p 869
Copeland GD, von Capeller D, Stem TN (1958) Systemic lupus erythematosus: A clinical report of 47 cases with pathological findings. Amer J Med Sei 236: 318
Cronkite EP, Fliedner TM (1964) Granulocytopoiesis. New Engl J Med 270:1347
Cyr WL, Johnson H, Balfour J (1973) Granulomatous cystitis as a manifestation of chronic granulomatous disease of childhood. J Urol 110: 357
Dale DC, Graw RG (1974) Transplantation of allogeneic bone marrow in canine cyclic neutropenia. Science 183: 83
Dameshek W (1931) The appearance of histiocytes in the peripheral blood. Arch intern Med 47: 968
Danaraj TJ (1958) The treatment of eosinophilic lung (tropical eosinophilia) with diethylcarbamazine. Quart J Med 27: 243
Dannenberg AM, Suga M, Garcia-Gonzales JE (1981) Macrophage in granulomas: Histochemical evidence suggesting local control of heterogeneous functions. In: Schmalzl F, Huhn D, Schaefer H-E (eds) Disorders of the monocyte macrophage system. Springer, Berlin Heidelberg New York, p 109
Darling RC, Parker F, Jackson H (1936) The pathological changes in the bone marrow in agranulocytosis. Amer J Path 12:1
Davidson WM, Smith DR (1954) A morphological sex difference in polymorphonuclear neutrophil leucocytes. Brit Med J IV: 4878
Davidson WM, Milner RDG, Lawler SD (1960) Giant neutrophil leukocytes: an inherited anomaly. Brit J Haemat 6: 399
Davis SD, SchallerJ, Wedgwood RJ (1966) Job’s syndrome: Recurrent „cold” staphylococcal abszesses. Lancet I:1013
Döhle H (1911) Leukozyteneinschlüsse bei Scharlach. Zbl Bakteriol 61:63
Donohugh DL (1963) Tropical eosinophilia: An etiologic inquiry. New Engl J Med 269:1357
Edwin E (1967) The segmentation of polymorphonuclear neutrophils. Acta med scand 182:1
Edwin E (1969) The segmentation of polymorphonuclear neutrophils in rheumatoid arthritis and ankylosing spondylitis. Acta rheum scand 15:121
Engle RL, Koprowska J (1959) The appearance of histiocytes in the blood in subacute bacterial endocarditis. Amer J Med 26: 965
Fanconi G (1941) Benigne chronische Agranulozytopenie beim Säugling. Ann paediat (Basel) 157: 317
Farquhar JW, Mac Gregor A, Richmond J (1958) Familial hemophagocytic reticulosis. Brit Med J 2:1561
Finch SC (1977) Granulocytopenia. In: Williams WJ, Beutler E, Erslev AJ, Rundles RW (eds) Hematology, 2nd edn. Mac Graw-Hill, New York, p 717
Finch SC (1977) Granulocytosis. In: Williams WJ, Beutler E, Ersles AJ, Rundles RW (eds) Hematology, 2nd edn. Mac Graw-Hill, New York, p 746
Fischer R, Schaefer HE (1971) Zur pathologischen Anatomie der Panmyelopathie und des Hypersplenismus. Internist 12: 151
Fontan G, Lorente F, Garcia Rodriguez MC, Ojeda JA (1976) Defective neutrophil chemotaxis and hyperimmunglobulinemia E-a reversible defect? Acta paediatr Scand 65: 509
Fraumeni JF (1967) Bone marrow depression induced by chloramphenicol or phenylbutazone: Leukemia and other sequelae. J Amer Med Assoc 201: 828
Gänsslen M (1941) Konstitutionelle familiäre Leukopenie (Neutropenie). Klin Wschr 20: 922
Gasser C (1952) Die Pathogenese der essentiellen chronischen Granulocytopenie im Kindesalter aufgrund der Knochenmarksbefunde. Helv paediatr Acta 7: 426
Gilman PA, Jackson DP, Guild KG (1969) Congenital agranulocytosis: Prolonged survival and terminal acute leukemia. Blood 34:827
Glass DN, Fearon DT, Austen KF (1983) Inherited abnormalities of the complement system. In: Stanbury JB, Wyngaard-en JB, Fredrickson DS, Goldstein JL, Brown MS (eds) The metabolic basis of inherited disease, 5th edn. Mac Graw-Hill, New York, p 1934
Golde DW (1975) Disorders of mononuclear phagocyte proliferation, maturation, and function. Clin Haematol 4: 705
Golde DW, Cline MJ (1977) Production, distribution, and fate of granulocytes. In: Williams WJ, Beutler E, Erslev AJ, Rundles RW (eds) Hematology. Mac Graw-Hill, New York, p 698
Good RA, Zack SJ (1956) Disturbances in gamma globulin synthesis as „experiments of nature”. Pediatrics 18:109
Gordin R (1952) Toxic granulation in leukocytes. Acta Med scand Suppl 270
Goudsmit R, v Leeuwen AM, James J (1971) Döhle bodies and acute leukaemia in one family: a new familial disorder? Brit J Haemat 20: 557
Grić VZ, KalafaticZ (1958) Drei Fälle von inkompletter Alder-Anomalie. Schweiz Med Wschr 88: 994
Grignaschi VJ, Sperperato AM, Etcheverry MJ (1963) Un nuevo cadro citoquimico: negatividad espontanea de las reacciones de peroxidasas, oxidasas y lipido en la neutrofila y en los monocitos de dos hermanos. Rev Assoc Med Argent 77: 218
Groover RV, Burke EC, Gordon H, Berdon WE (1972) The genetic mucopolysaccharidoses. Semin Hemat 9: 371
Hall JW, Kozak M, Spink WW (1964) Pulmonary infiltrates, pericorditis and eosinophilia. Amer J Med 36: 135
Hahneman BM, Alt HL (1958) Cyclic neutropenia in a father and daughter. J Amer Med Assoc 168: 270
Hansson H, Linell F, Nilsson LR, Söderhjelm L, Undritz E (1959) Die Chédiak-Steinbrinck-Anomalie resp. erblich konstitutionelle Riesengranulation (Granulagiganten) der Leukozyten in Nordschweden. Folia haemat., Neue Folge 3:152
Hardy WR, Anderson RE (1968) Hypereosinophilic syndromes. Ann intern Med 68:1220
Hargraves MM, Richmond H, Morton R (1948) Presentation of two bone marrow elements: the „Tart” cell and the „LE” cell. Proc Staff Meet Mayo Clin 23: 25
Hargraves MM (1969) The discovery of the L. E. cell and its morphology. Mayo Clin Proc 44: 579
Harm H (1952) Beiträge zur Morphologie und Genetik der Pelger-Anomalie bei Mensch und Kaninchen. Z menschl Vereb Konstitutionslehre 30: 501
Hartl W (1965) Drug allergic agranulocytosis (Schultz’s disease). Semin Hemat 2: 313
Hegglin R, Gross R, LöhrGW (1964) Anomalie Hegglin-May (polyphyle Reifungsstörung). Schweiz Med Wschr 94:1357
Hegglin R (1945) Gleichzeitige konstitutionelle Veränderungen an Neutrophilen und Thrombozyten. Helv Med Acta 12:439
Heinivaara O, Kaipainen WJ (1961) Pelger-Huët anomaly in lymphocytic leukaemia. Acta haemat 25: 375
Heller P, Zimmermann HJ (1956) Nucleophagocytosis: studies on three hundred thirty-six patients: review of incidence of L. E. phenomenon and allied conditions. Arch intern Med 97: 403
Herring WB, Smith LG, Walker RJ, Herion JC (1974) Hereditary neutrophilia. Amer J Med 56: 729
Higashi O (1954) Congenital gigantism of peroxidase granules. Tohoku J exper Med 59: 315
Hill HR, Quie PG (1974) Raised serum IgE levels and defective neutrophil chemotaxis in three children with eczema and recurrent bacterial infections. Lancet I: 183
Hill HR, Ochs HD, Quie PG, Clark RA, Pabst HF, Klebanoff SJ, Wedgwood RJ (1974) Defect in neutrophil granulocyte chemotaxis in Job’s syndrome of recurrent “cold” staphylococcal abszesses. Lancet II: 617
Hill RW, Bayrd ED (1960) Phagocytic reticuloendothelial cells in subacute bacterial endocarditis with negative cultures. Ann intern Med 52: 310
Hittmair A, Leibetseder F (1958) Fälle von Pelger-Huëtscher Kemanomalie in Tirol. Schweiz Med Wschr 88:1004
Hitzig WH (1959) Familiäre Neutropenie mit dominantem Erbgang und Hypergammaglobulinämie. Helv Med Acta 26:779
Hofmann C, Braun-Falco O, Petzoldt D (1976) Akute febrile neutrophile Dermatose (Sweet-Syndrom). Dtsch Med Wschr 101:1113
Hong R, Schubert WK, Perrin EV, West CD (1962) Antibody deficiency syndrome associated with beta-2-macroglobulinemia. J Pediatr 61: 831
Huber H (1939) Stammbaumuntersuchungen bei Panmyelophthisekranken. Klin Wschr 18:1145
Huët GJ (1932) Über eine bisher unbekannte familiäre Anomalie der Leukozyten. Klin Wschr 11:1264
Ingraham LM, Bums CP, Boxer LA, Baehner RL, Haak RA (1981) Fluidity properties and lipid composition of erythrocyte membranes in Chediak-Higashi syndrome. J Cell Biol 89: 510
Isaacson NH, Rapoport P (1946) Eosinophilia in malignant tumors: Its significance. Ann intern Med 25: 893
Itoga T, Laszlo J (1962) Döhle bodies and other granulocytic alterations with cyclophosphamide. Blood 20: 668
Ishizaka K, Ishizaka T (1970) The significance of immunoglobulin E in reagenic hypersensitivity. Ann Allergy 28:189
Jeunet F, Good RA (1968) Thymoma, immunologic deficiencies, and hematological abnormalities. In: Good RA, Bergsma D (eds) Immunologic deficiency diseases in man, Vol 4. National Foundation Press, New York, p 192
Jewis EH, Takenchi A, Dillon DE, Ruymann FB, Rivken S (1971) The May-Hegglin anomaly: ultrastructure of the granulocyte inclusion. Amer J clin Path 55:187
Jones JB, Lange RD, Yang TJ, Vodopick H, Jones ES (1975) Canine cyclic neutropenia: Erythropoietin and platelet cycles after bone marrow transplantation. Blood 45: 213
Jordans GHW (1947) Hereditary granulation anomaly of the leucocytes (Alder). Acta Med Scand 129: 348
Jordan SE, Larsen WE (1965) Ultrastructure studies of the May-Hegglin anomaly. Blood 25: 921
Juhlin L (1963) Basophil and eosinophil leukocytes in various disorders. Acta Med Scand 174: 249
Kaplan JM, Barrett O (1967) Reversible pseudo-Pelger anomaly related to sulfisoxazole therapy. New Engl J Med 277: 421
Kaplow LS (1975) Cytochemical heterogeneity of human circulating monocytes. Acta Cytologica 19: 358
Kauer GL, Engle RL (1964) Eosinophilic leukaemia with Ph1-positive cells. Lancet II: 1340
Kay AB (1974) The eosinophil in infectious diseases. J infect Dis 129: 606
Knicker WT, Panos TC (1957) Idiopathic infantile agranulocytosis with hypergammaglobulinaemia. Amer J Dis Child 94: 549
Killman SA (1957) Leukocyte agglutinins in collagen disease. Acta rheum scand 3: 209
Klebanoff SJ (1968) Myeloperoxidase-halide-hydrogen peroxide antibacterial system. J Bacteriol 95: 2131
Klebanoff SJ, Clem WH, Luebke RG (1966) The peroxide-thio-cyanate-hydrogen peroxide antimicrobial system. Biochim bio-phys Acta 117: 63
Kostmann R (1956) Infantile genetic agranulocytosis. Acta paediat 45, Suppl 105: 1
Koszewski BJ, Vahabzedeh H, Willrodt BS (1967) Hemosiderin content of leukocytes in animals and in man and its significance in the physiology of granulocytes. Amer J clin Path 48: 474
Kracke RR (1931) Recurrent agranulocytosis. Amer J clin Path 1:385
Krill CE, Smith HD, Mauer AM (1964) Chronic idiopathic granulocytopenia. New Engl J Med 270: 973
Lalezari P, Murphy GB, Allen FH (1971) NB1, a new neutrophil-specific antigen involved in the pathogenesis of neonatal neutropenia. J clin Invest 50:1108
Lalezari P, Radel H (1974) Neutrophil specific antigens: Immunology and clinical significance. Semin Hemat 11: 281
Landing BH, Shirkey HS (1957) Syndrome of recurrent infection and infiltration of viscera by pigmented lipid histiocytes. Pediatrics 20: 431
Leader RW, Padgett GA, Gorham JR (1963) Studies of abnormal leukocyte bodies in the mink. Blood 22: 477
Leale M (1910) Recurrent furunculosis in an infant showing an unusual blood picture. J Amer Med Assoc 54:1854
Leder LD (1971) Zytochemische Untersuchungen an Blutleukozyten beim Chediak-Higashi-Syndrom. Verhandl Dtsch Ges Path 55: 793
Levin DC (1967) The „P.I.E.” syndrome - pulmonary infiltrates with eosinophilia; a report of 3 cases with lung biopsy. Radiology 84: 461
Levine S (1959) Chronic familial neutropenia with marked periodontal lesions. Oral Surg 12: 310
Lin YK (1973) Leukopenia in alcoholics. Amer J Med 54: 605
Litt M (1964) Eosinophils and antigen-antibody reactions. Ann NY Acad Sei 116: 964
Lockie LM, Norcross BM, George CW (1947) Treatment of two reactions due to gold: Response of thrombocytopenic purpura and granulocytopenia to BAL therapy. J Amer Med Assoc 133:754
Löffler W (1936) Endocarditis parietalis fibroplastica mit Bluteosinophilie. Ein eigenartiges Krankheitsbild. Schweiz Med Wschr 66:817
Löffler W (1936) Die flüchtigen Lungeninfiltrate mit Eosinophilie. Schweiz Med Wschr 66: 1069
Lonsdale D, DeodharSD, Mercer RD (1967) Familial granulocytopenia and associated immunglobulin abnormality: Report of three cases in young brothers. J Pediatr 71: 790
Louie JS, Pearson CM (1971) Felty’s syndrome. Semin Hematol 8:216
Lübbers P, Koch E (1949) Leukocytäre Abbauformen im Blut bei entzündlichen Erkrankungen. Klin Wschr 25/26: 442
Lüers T (1956) Ein morphologisches Geschlechtsmerkmal in Leukocytenkemen. Berl Med 7:120
Lüers VT (1960) Das numerische Verhalten der geschlechtsspezifischen Kemanhänge bei der erblich-konstitutionellen Hochsegmentierung der Neutrophilenkeme Undritz. Schweiz Med Wschr 90: 246
Luhby AL, Slobody L (1956) Transient neonatal agranulocytosis in two siblings: Transplacental isoimmunization to a leukocyte factor. Amer J Dis Child 92: 496
Lutzner MA, Lowrie ChT, Jordan HW (1967) Giant granules in leukocytes of the beige mouse. J Heredity 58: 299
Lux Se, Johnston RB, August CS, Say B, Penchaszadeh VB, Rosen FS, McKusick VA (1970) Neutropenia and abnormal cellular immunity in cartilage-hair hypoplasia. New Engl J Med 282:234
Major RH, Leger LH (1939) Marked eosinophilia in Hodgkin’s disease. J Amer Med Asso 112: 2601
Maldonado JE, Hanlon DG (1965) Monocytosis: a current appraisal. Mayo Clin Proc 40: 248
Marsh JC, Boggs DR, Cartwright Ge, Wintrobe MM (1967) Neutrophil kinetics in acute infection. J clin Invest 46: 1943
Masina N (1932) Das Blutbild bei Leberzirrhose mit besonderer Berücksichtigung der Monozytengranulation. Folia haematol 46:335
Matsaniotis N, Kiossoglou KA, Karpuzas J, Anastasea-Vlachou K (1966) Chromosomes in Kostmann’s disease. Lancet II: 104
May R (1909) Leukozyten-Einschlüsse. Arch klin Med 96:1
McCall CE, Katayamal, Cotran RS, Finland M (1969) Lysosomal and ultrastructural changes in human „toxic” neutrophils during bacterial infection. J exper Med 129: 267
McCall CE, Caves J, Cooper R, DeChatelet L (1971) Functional characteristics of human toxic neutrophils. J infect Dis 124: 68
McCall CE, DeChatelet LR, Cooper MR, Shannon C (1973) Human toxic neutrophils. III. Metabolic characteristics. J infect Dis 127: 26
McKusick V (1983) Mendelian inheritance in man. The John Hopkins University Press, 6th edt. Baltimore
Meuret G, FliednerTM (1970) Zellkinetik der Granulopoese und des Neutrophilensystems bei einem Fall von zyklischer Neutropenie. Acta haemat (Basel) 53: 48
Miale JB (1982) Laboratory Medicine Hematology. Mosby, 6th edt. St. Louis
Miller ME, Oski FA, Harris MB (1971) Lazy-leukocyte syndrome. A new disorder of neutrophil function. Lancet I: 665
Miller ME, Norman ME, Koblenzer PJ, SchonauerT (1973) A new familial defect of neutrophil movement. J lab clin Med 82: 1
Miller ME (1975) Pathology of chemotaxis and random mobility. Semin Hematol 12: 59
Moeschlin S, Wagner K (1952) Agranulocytosis due to the occurrence of leukocyte-agglutinins (Pyramidon and cold agglutinins). Acta haemat 8: 29
Moran TJ, Estevez JM (1969) Chediak-Higashi disease. Morphologic studies of a patient and her family. Arch Path 88: 329
Morley AA, Carew JP, Baikie AG (1967) Familial cyclical neutropenia. Brit J Haemat 13: 719
Musser JH (1921) The leukocytes after hemorrhages. Amer J med Sei 162:40
Nachtsheimer H (1950) The Pelger-anomaly in man and rabbit; mendelian character of the nuclei of the leucocytes. J Hered 41: 131
Naiman JL, Oski FA, Allen FH, Diamond LK (1964) Hereditary eosinophilia: Report of a family and review of the literature. Amer J human Genet 16: 195
Nichols BA, Bainton DF, Farquhar MG (1971) Differentiation of monocytes. Origin, nature and fate of their azurophil granules. J Cell Biol 50: 498
Ochs HD, Davis SD, Mickelson E, Lemer KG, Wedgewood RJ (1974) Combined immundeficiency and reticuloendotheliosis with eosinophilia. J Pediatr 85: 463
Oliver MJ, Krawiec JA, Berlin RD (1976) Carbamylcholine prevents giant granule formation in cultured fibroblasts from beige (Chediak-Higashi) mice. J Cell Biol 69: 205
Padgett GA, Leader RW, Gorham JR, O’Mary CC (1964) The familial occurrence of the Chediak-Higashi syndrome in the mink and cattle. Genetics 49: 505
Payne R (1962) The development and persistence of leukoag-glutinins in parous women. Blood 19: 411
Pearson HA, Lorincz AE (1964) A characteristic bone marrow finding in Horber syndrome. Pediatrics 34: 281
Pelger K (1928) Demonstratie van den paar zeldzaam voorkom-mende typen van vloedlichchaampges en bespreking der patienten. Ned T Geneesk 72: 1178
Pinkerton PH, Robinson JB, Senn JS (1978) Lazy leucocyte syndrome-disorder of the granulocyte membrane? J clin Pathol 31: 300
Pisciotta AV, Ebbe SN, Lennon ES, Metzger GO, Madison FW (1958) Agranulocytosis following administration of phenothiazine derivates. Amer J Med 15: 210
Pisciotta AV (1969) Agranulocytosis induced by certain phenothiazine derivates. J Amer Med Assoc 208:1862
Plum P (1937) Clinical and experimental investigations in agranulocytosis. HK Lewis & Co Ltd, London
Presentey BZ (1968) A new anomaly of eosinophilic granulocytes. Amer J clin Path 49: 887
Redies H, Quenzer K, Tolksdorf M, Saile ML, Wiedemann HR (1958) Über die Häufigkeit der Pelger-Anomalie. Schweiz Med Wschr 88:1002
Reed RJ, Terazaki N (1972) Subcutaneous angioblastic lymphoid hyperplasia with eosinophilia (Kimura’s disease). Cancer 29:489
Reilly WA (1941) The granules in the leukocytes in gargoylism. Amer J Dis Child 62: 489
Rodin AE, Haggord ME, Nichols MM, Gustaussen LP (1973) Infantile genetic agranulocytosis: Two cases occurring in siblings and one in a distant relative. Amer J Dis Child 126: 818
Rohr K (1939) Der heutige Stand der Agranulozytoseforschung. Helv Med Acta 6: 611
Rosenthal N, Abel HA (1936) The significance of the monocytes in agranulocytosis (leukopenic infectious monocytosis). Amer J clin Path 6: 205
Ruscetti R, Cypress R, Chorvenick P (1975) Specific release of neutrophil and eosinophil stimulating factors from sensitized lymphocytes. Clin Res 23: 406 A
Salomon SE, Cline MJ, Schultz J, Lehrer RL (1970) Myeoloper-oxidase deficiency. Immunologic study of a genetic leukocyte defect. New Engl J Med 282: 250
Savilahti M (1956) Mehr als 100 Vergiftungsfälle durch Benzol in einer Schuhfabrik. Arch Gewerbepath Gewerbehyg 15: 147
Schaefer HE, Weller P, Lansch D (1983) Erworbene und ererbte Defektformen der granulozytären Peroxidase (POX). Acta histochem, Suppl XXVIII: 219
Schäli H (1964) Die erblich-konstitutionelle Hochsegmentierung der Kerne der neutrophilen Leukozyten im Rahmen der humanen und der vergleichenden Haematologie. Inaug Diss, Basel
Schilling V (1951) Periodisch-rezidivierende Neutropenie mit Monocytose. II Haematologie der periodischen Neutropenie; ihre Bedeutung für die Monocytogenese und den Trialismus der Monocyten. Folia haemat 70: 1
Schneiderman LY, Sampson WJ, Schoene WC, Haydon GB (1969) Genetic studies of a family with two unusual autosomal dominant conditions: muscular dystrophy and Pelger-Huet anomaly. Clinical, pathologic and linkage considerations. Amer J Med 46:380
Schultz W (1922) Über eigenartige Halserkrankungen. Dtsch Med Wschr 48: 1495
Schwachman H, Diamond LK, Oski FA, Khaw KT (1964) The syndrome of pancreatic insufficiency and bone marrow dysfunction. J Pediatr 65: 645
Sears WG (1932) The blood in Hodgkin’s disease, with special reference to eosinophilia. Guy’s Hosp. Rep 82: 40
Shanbrom E, Tanaka KR (1962) Acquired Pelger-Huet granulocytes in severe myxedema. Acta haemat 27: 289
Shelley WB, Pames HM (1965) The absolute basophile count: Technique and significance. J Amer Med Assoc 192: 368
Steinbrinck W (1948) Über eine neue Granulationsanomalie der Leukozyten. Dtsch Arch klin Med 193: 577
Stobbe H, Jorke D (1965) Befunde an homozygoten Pelger-Merkmalsträgem. Schweiz Med Wschr 95: 1529
Stone GE, Redmond AJ (1963) Leukopenie infectious monocytosis. Amer J Med 34: 541
Stossel TP, Boxer LA (1977) Qualitative abnormalities of granulocytes. In: Williams WJ, Beutler E, Erslev AJ, Rundles RW (eds). McGraw-Hill, New York, p 756
Straus DJ (1973) Hematologic aspects of alcoholism. Semin Hematol 10:183
Strauss RG, Bove KE, Jones JF, Mauer AM, Fulginiti NA (1974) An anomaly of neutrophil morphology with impaired function. New Engl J Med 290:478
Sty JR, Chusid MJ, Babbitt DP, Werlin SL (1979) Involvement of the colon in chronic granulomatous disease of childhood. Radiology 132:618
Sullivan AL, Grimley PM, Metzger H (1971) Electron microscopic localization of immunoglobulin E on the surface membrane of human basophils. J exp Med 134:1403
Sweet RD (1964) An acute febrile neutrophilic dermatosis. Brit J Dermatol 76:394
Taylor RE, Farrell RK (1973) Light and electron microscopy of peripheral blood neutrophiles in a killer whale affected with Chediak-Higashi-Syndrome. Fed Proc 32:822
Trentham DE, Masi AT, Bale GF (1976) Arthritis with an inflammatory dermatosis resembling Sweet’s syndrome. Report of a unique case and review of the literature on arthritis associated with inflammatory dermatoses. Amer J Med 61:424
Türk W (1907) Septische Erkrankungen bei Verkümmerung des Granulocytensystems. Wien klin Wschr 20:157
Twomey JJ, Leavell BS (1965) Leukemoid reactions to tuberculosis. Arch intern Med 116:21
Uchida T, Kariyone S (1973) Intravascular granulocyte kinetics and spleen size in patients with chronic benign neutropenia of childhood
Undritz E, de Sepilus C (1957) Results of recent examination of a family from Wallis, in which was found 25 years ago the first Swiss case of Pelger-Huëtscher nuclear anomaly: Present states of studies on this abnormality. Schweiz Med Wschr 87: 1258
Undritz E (1958) Eine neue Sippe mit erblich-konstitutioneller Hochsegmentierung der Neutrophilenkeme. Schweiz Med Wschr 88: 1000
Undritz E, Schäli H (1964) Eine neue Sippe mit erblich-konstitutioneller Hochsegmentierung der Neutrophilenkeme und das Knochenmarkbild beim homozygoten Träger dieser Anomalie. Schweiz Med Wschr 94:1365
de Vaal OM, Seynhaeve V (1959) Reticular dysgenesia. Lancet II: 1123
Weening RS, Schooreil EP, Roos D, van Schaik MU, Voetman AA, Bot AAM, Batenburg-Plenter AM, Willems C, Zeijle-maker WP, AstaldiA (1981) Effect of ascorbate on abnormal neutrophil, platelet, and lymphocyte function in a patient with the Chediak-Higashi syndrome. Blood 57:856
Weil P (1922) Études sur les leucocytes. II. Les corpuscules basophiles des leucocytes neutrophiles. Arch d’Anat microscop 18:46
Weiner W, Topley E (1955) Döhle bodies in the leucocytes of patients with bums. J clin Path 8: 324
Weisman G (1972) Lysosomal mechanisms of tissue injury in arthritis. New Engl J Med 286:141
White JG (1973) The Chediak-Higashi syndrome. Fine structure of giant inclusions in freeze-fractured neutrophils. Amer J Path 72:503
Windhorst DB, Good RA (1971) Dermatologie manifestations of fatal granulomatous disease of childhood. Arch Dermatol 103:351
Wolfson JJ, Kane WJ, Laxdal SD, Good RA, Quie PG (1969) Bone findings in chronic granulomatous disease of childhood. J Bone Joint Surg 51:1573
Young AK, Middleton RG (1980) Urologie manifestation of chronic granulomatous disease. J Urol 123:119
Yunis AA, Bloomberg GR (1964) Chloramphenicol toxicity: Clinical features and pathogenesis. Prog Hematol 4:138
Zeni G, Nardi F, Frezza M (1964) In tema di ipereosinofilia constituzionale familiale idiopatica. Acta Med Patav 24: 589
Zieve PD, Haghshenass M, Blanks M, Krevans JR (1966) Vacuolization of the neutrophil. An aid in the diagnosis of septicemia. Arch intern Med 118: 356
Zuelzer WW, Bajoghli M (1964) Chronic granulocytopenia in childhood. Blood 23:359
Zuelzer WW (1964) „Myelokathexis” - a new form of chronic granulocytopenie. New Engl J Med 270: 699
Literatur
Bessis M (1972) Cellules du sang normal et pathologique. Masson et Cie, Paris
Queißer W (ed) (1978) Das Knochenmark. Morphologie, Funktion, Diagnostik. Thieme, Stuttgart
Rappaport H (1963) Tumors of the hematopoietic system. In: Atlas of tumor pathology, Section III-Fascicle 8. Armed Forces Institute of Pathology, Washington
Rywlin AM (1976) Histopathology of the bone marrow, 1st edn. Little Brown and Co (Inc)
Sagher F, Even-Paz Z (1967) Mastocytosis and the mast cell. Karger, Basel
Williams WJ, Beutler E, Erslev AJ, Rundles RW (1977) Hematology, 2nd edn. McGraw-Hill, New York
Wintrobe MM, Lee GR, Boggs DR, Bithell TC, Athens JW, Foerster J (1974) Clinical Hematology, 7th edn. Lea & Febiger, Philadelphia
Abe S, Sandberg AA (1979) Chromosomes and causation of human cancer and leukemia. XXXII. Unusual features of Ph1-positive acute myeloblastic leukemia (AML), including a review of literature. Cancer 43: 2352
Ackerman A, Grasso JA, Knouff RA (1960) Morphological and histochemical studies of leukemic cells from a patient with atypical myeloblastic leukemia with special reference to intracytoplasmic mucopolysaccharide vacuoles and fibrillar formation. Blood 16:1253
Ackerman GA (1964) Eosinophilic leukemia. A morphologic and histochemical study. Blood 24: 372
Albrecht M (1966) „Gaucher-Zellen” bei chronischer Myeloischer Leukämie. Blut 13:169
Albrecht M (1972) Ergebnisse von Langzeitbeobachtungen bei Patienten mit chronisch myeloischer Leukämie. In: Gross R, van de Loo J (eds) Leukämie. Springer, Berlin Heidelberg New York, S 399–404
Anderson RE, Hoshino T, Yamamoto T (1964) Myelofibrosis with myeloid metaplasia in survivors of the atomic bomb. Ann Intern Med 60:1
Aptuna E, Anteunis A, Kralik M, Astesano A, Robineaux R, Debray J (1978) Hairy cell leukemia. A clinical immunological and ultrastructural study. New data for the origin of the hairy cell. Virchows Arch B Cell Path 28:135
Arinkin MJ (1929) Intravitale Untersuchungsmethodik des Knochenmarks. Folia haematol 38: 233
Athens JW, Raab SO, Haab OP, Boggs DR, Ashenbrucker J, Catwright GE, Wintrobe MM (1965) Leukokinetic studies. X. Blood granulocyte kinetics in chronic myelocytic leukemia. J clin Invest 44: 765
Auer J (1906) Some hitherto undescribed structures in the large lymphocytes in a case of acute leukaemia. Amer J med Sei 131: 1002
Baikie AG, Court Brown WM, Buckton KE, Hamden DG, Jacobs PA, Tough IM (1960) A possible specific chromosome abnormality in human chronic myeloid leukemia. Nature 188: 1165
Bain BJ, Catovsky D, O’Brien M, Grant Prentice H, Lawlor E, Kumaran TO, McCann SR, Matutes E, Galton DAG (1981) Megakaryoblastic leukemia presenting as acute myelofibrosis. A study of four cases with a platelet-peroxidase-reaction. Blood 58:206
Bainton D, Friedländer LM, Shohet SB (1977) Abnormalities in granule formation in acute myelogenous leukemia. Blood 49: 693
Bennett JM, Catovsky D, Daniel MT, Flandrin G, Galton DAG, Gralnick HR, Sultan C (1976) Proposal for classification of acute leukaemias. Brit J Haemat 33: 451
Benett JM, Catovsky D, Daniel MT, Flandrin G, Galton DAG, Gralnick HR, Sultan C (1981) The morphological classification of acute lymphoblastic leukaemia: concordance among observers and clinical correlation. Brit J Haematol 47: 553
Bentley HP, Reardon AE, Knoedler JP, Krivit W (1961) Eosinophilic leukemia. Report of a case, with review and classification. Amer J Med 30: 310
Bernard J (1976) Preleukemic states. Blood Cells 2: 5
Bouroncle BA, Doan CA (1937) Myelofibrosis: Clinical hematologic and pathologic study of 110 patients. Amer J Med Sei 243:697
Bousser J (1957) Eosinophilie et leucemie. Sang 28:553
Bozdech MJ, Bainton DF (1981) Identification of alpha-naphthyl butyrate esterase as a plasma membrane ectoenzyme of monocytes and as a discrete intracellular membrane-bounded organelle in lymphocytes. J exper Med 153: 182
Brady RO (1978) Glucosyl ceramide lipidosis: Gaucher’s disease. In: Stanbury JB, Wyngaarden JB, Fredrickson DS (eds) The metabolic basis of inherited disease, 4th edn. McGraw-Hill, New York, p 731
Braylan RC, Jaffe ES, Triche TJ, Nanba K, Fowlkes BJ, Metzger H, Frank MM, Dolan MS, Yee CL, Green I, Berard CW (1978) Structural and functional properties of the „hairy” cells of leukemic reticuloendotheliosis. Cancer 41: 210
Breton-Gorius J, Coquin Y, Vilde JL, Dreyfus B (1976) Cytochemical and ultrastructural studies of aberrant granules in the neutrophils of two patients with myeloperoxidase deficiency during a preleukemic state. Blood Cells 2:187
Breton-Gorius J, Reyes F, Duhamel G, Najman A, Gorin NC (1978) Megakaryoblastic acute leukemia: Identification by the ultrastructural demonstration of platelet peroxidase. Blood 51: 45–60
Burke SJ, Byme GE, Rappaport H (1974) Hairy cell leukemia (leukemic reticuloendotheliosis). I. A clinical pathologic study of 21 patients. Cancer 33:1399
Burnet M (1958) Leukemia as a problem in preventive medicine. New Engl J Med 259: 423
Court Brown WM, Abbatt JD (1955) The incidence of leukemia in ankylosing spondylitis treated with x-rays: A preliminary report. Lancet I:1283
Cutler SJ, Axteil L, Heise J (1967) Ten thousand cases of leukemia. J nat Cancer Inst 39: 993
Dameshek W (1951) Some speculations on the myeloproliferative disorders. Blood 6: 372
Dameshek W, Gunz F (1964) Leukemia, 2nd edn. Grune & Stratton, New York
Daniel MT, Flandrin G (1974) Fine structure of abnormal cells in hairy cell (tricholeukocytic) leukemia, with special reference to their in vitro phagocytic capacity. Lab Invest 30:1
Darte JM, Dacie JV, McSorley JGA (1954) Pelger-like leucocytes in chronic myeloid leukemia. Acta haemat 12: 117
Davidson WM, Knight LA (1973) Acquired trisomy 9. Lancet I: 1510
Delbeke MJ, Dacremont G (1972) Gaucher cells in chronic myelogenous leukemia. Acta paediatr belg 26: 70
Didisheim P, Trombold JS, Vandervoot RLE, Songin MR (1964) Acute promyelocytic leukemia with fibrinogen and factor V deficiencies. Blood 23: 717
Dietrich M, Rasche H, Kubanek B (1975) Coagulation disorder in acute leukemia as a prognostic factor. Adv Biosci 14: 175
Dittrich H (1952) Zur Frage der eosinophilen Leukämie. Acta haemat 7: 230
Doan CA, Reinhardt HL (1941) The basophil granulocyte, basophilocytosis and myeloid leukemia, basophil and „mixed granule” types; an experimental, clinical and pathologic study with the report of a new syndrome. Amer J clin Pathol 11:1
Dosik H, Rosner F, Sawitzky A (1972) Acquired lipidosis: Gaucher-like cells and „blue cells” in chronic granulocytic leukemia. Sem Hemat 9: 309
Downey H (1934) Diseases of the Blood. In: Bell ET (ed) A Text-Book of Pathology, 2nd edn. Lea & Febiger, Philadelphia
Drings P (1978) Die chronische myeloische Leukämie. In: Queißer W (ed) Das Knochenmark. Morphologie-Funktion-Dia-gnostik. Thieme, Stuttgart, S 297
Düllmann J, Wulfhekel U, Großschupff G, Kühl M, Bartelt D, Hausmann K (1983) Die Haarzell-Leukämie. Zweiter Bericht zur Klinik, Morphologie und Therapie bei nunmehr 27 Patienten. Dtsch Med Wschr 108: 46
Duhamel G (1971) Lymphoid myelofibrosis. About 10 further observations. Acta haemat 45: 85
Eagan JW, Baughman KL, Miller S, Conley CL, Eggleston JC (1977) Systemic mastocytosis in a patient with polycythemia vera treated with radioactive phosphorus. Blood 49: 563
Ebstein W (1889) Über die akute Leukämie und Pseudoleukämie. Dtsch Arch klin Med 44: 343
Efrati P, Klajman A, Spitz H (1957) Mast cell leukemia? - Malignant mastocytosis with leukemia-like manifestations. Blood 12:869
Ellis JM (1949) Urticaria pigmentosa. A report of a case with autopsy. Arch Pathol 48: 426
Emile-Weil P (1933) La leucémie myélogéne à polynucléaires neutrophiles. Sang 7: 445
Epstein E, Goedel A (1934) Hämorrhagische Thrombocythämie bei vasculärer Schrumpfmilz. Virchows Arch 292: 233
Fialkow PJ (1980) Clonal and stem cell origin of blood cell neoplasms. In: LoBue J (ed) Contemporary Hematology and Oncology, Vol 1. Plenum Press, New York, pp 1–46
Fischer R, Schmalzl F (1964) Über die Hemmbarkeit der Esteraseaktivität in Blutmonozyten durch Natriumfluorid. Klin Wschr 42:751
Fischer R, Hennekeuser HH, Schaefer HE (1970) Extramedulläre Blutbildung in der Milz, insbesondere bei Knochenmetastasierung. In: Lennert K, Harms D (eds) Die Milz. Springer, Berlin Heidelberg New York, S 81–92
Fischer R, Schaefer HE (1972) Die pathologische Anatomie der Leukosen. In: Gross R, van de Loo J (eds) Leukämie. Springer, Berlin Heidelberg New York, S 1 –24
Fischer R, Schaefer HE (1976) Pathologisch-anatomische Befunde bei Leukämien und anderen myeloproliferativen Erkran-kungen. In: Stacher A, Höcker P (eds) Erkrankungen der Myelopoese. Urban und Schwarzenberg, München, S 42–46
Fischer R, Schaefer HE (1979) Präleukämien. Verhandl Dtsch Ges Path 63: 154
Fohlmeister I, Hellriegel KP, Schaefer HE, Fischer R (1978) Klinische und morphologische Beobachtungen bei einer partiell peroxydasedefekten, Ph1-positiven chronischen myelomonozytären Leukämie. Blut 37: 168
Fohlmeister I, Schaefer HE, Mödder B, Hellriegel KP, Fischer R (1981) Chronische lymphoproliferative Erkrankung unter dem Bilde einer Haarzell-Leukämie. Blut 42: 367
Fohlmeister I, Schaefer HE, Fischer R (1982) On the pathogenesis of preleukemic myelodysplastic syndromes. Development of a dysplastic hemopoietic proliferation in the rat after a single pulse dose of dimethylbenz(a)-anthracene (DMBA). J Cancer Res clin Oncol 104: 249
Frame B, Nixon RK (1968) Bone-marrow mast cells in osteoporosis of aging. New England J Med 279: 626
Freeman AI, Journey LJ (1971) Ultrastructural studies on monocytic leukaemia. Brit J Haematol 20: 225
Freeman HE, Koletsky S (1939) Cutaneous lesions in monocytic leukemia. Report of two cases, with pathologic study. Arch Dermatol Syphilis 40: 218
Freireich EJ, Thomas LB, Frei E, Fritz RD, Forkner CE (1960) A distinctive type of intracerebral hemorrhage associated with „blastic crisis” in patients with leukemia. Cancer 13: 146
Friedreich N (1857) Ein neuer Fall von Leukämie. Virchows Arch Path Anat 12: 37
Galton DAG (1969) Chronic granulocytic leukemia. Semin Hemat 6: 323
Garson OM, Milligan WJ (1972) The 45, XO, Ph1 subgroup of chronic granulocytic leukemia. Scand J Haematol 9:186
Geary CG, Catovsky D, Wiltshaw E, Milner GR, Scholes MC, van Noorden S, Wadsworth LD, Muldal S, Maclver JE, Galton DAG (1975) Chronic myelomonocytic leukaemia. Brit J Haemat 30:289
Georgii A, Vykoupil KF, Thiele J (1980) Chronic megakaryo-cytic granulocytic myelosis - CMGM. A subtype of chronic myeloid leukemia. Virchows Arch A Path Anat and Histol 389: 253
Golding PL, Green AE (1976) Blast-cell transformation chronic granulocytic leukaemia. Lancet II: 854
Golomb HM, Braylan R, Pollack A (1975) Hairy cell leukaemia (leukaemic reticuloendotheliosis): a scanning microscopic study of eight cases. Brit J Haemat 29: 455
Gooi JHC, Bums GF, Cawley JC (1979) Hairy-cell leukaemia: an immunoperoxidase study of paraffin embedded tissues. J Clin Path 32:1244
Graham DC (1960) Leukemic following x-ray therapy for ankylosing spondylitis. Arch intern Med 105: 51
Gralnick HR, Marchesi S, Givelber H (1972) Intravascular coagulation in acute leukemia: Clinical and subclinical abnormalities. Blood 40: 709
Gross R, Hellweg G, Lambers K (1955) Zur Frage der eosinophilen Leukämie. Z Kinderheilkunde 77: 208
Grouls V (1983) Die Haarzellen-Leukämie. Dtsch Ärzteblatt 47:31
Grieshammer W (1937) Beitrag zur sog. „Osteosklerotischen Anämie”. Verhandl Dtsch Ges Path 30: 381
di Guglielmo G (1917) Un caso di eritroleucemia. Folia Med 13: 386
Gunz FW (1977) Myelofibrosis. In: Williams WJ, Beutler E, Erslev AJ, Rundles RW (eds) Hematology, 2nd edn. McGraw-Hill, New York, p 797
Haas OA, Gadner H, Nacheva E, Fischer P, Schmidmeier W (1982) The Significance of Chromosomal Findings in Myeloid Leukemia of Childhood. Blut: 45: 207
Hauswaldt Ch, Raju S, Bianchi L, Hunstein W (1967) Kasuistischer Beitrag zum Krankheitsbild der akuten Eosinophilen-Leukämie. Acta haemat 37: 143
Heinivara O, Kaipainen WJ (1962) Pseudo-Pelger leukocytic anomaly in haematologie disorders. Acta Pathol Microbiol Scand 54: 269
Heller A (1973) Formvariabilitäten von sog. Auerstäbchen bei akuten Leukosen. Med Welt 24: 733
Hellriegel KP (1976) Zytogenetische Befunde bei chronischer myeloischer Leukämie. In: Stacher A, Höcker P (eds) Erkrankungen der Myelopoese. Leukämien, myeloproliferatives Syndrom, Polyzythämie. Urban und Schwarzenberg, München, S 82–86
Hennekeuser HH, Fischer R, Talke H, Mainzer K (1956) Pseu-do-Pelger-Zellen vom homozygoten Typ bei unreifzelliger myeloischer Leukämie. Dtsch Med Wschr 94: 2284
Herrmann R, Ho AD, Dörken B, Möller P (1981) Zwei Fälle von TdT-positiver akuter myeloischer Leukämie. Onkologie 4: 276
Heuck G (1879) Zwei Fälle von Leukämie mit eigenthümlichem Blutresp. Knochenmarksbefund. Virchows Arch path Anat 78:475
von Heyden HW, Waller HD, Pape GR, Benöhr HC, Braun HJ, Wilms K, Rieber EP, Riethmüller G (1976) Haarzell-Leukämie.I. Klinik, Zytochemie, Phagozytosefähigkeit von Haarzellen, Etablierung permanent wachsender Zellinien. Dtsch Med Wschr 101:3
von Heyden HW (1979) Haarzell-Leukämie. II. Diagnostik und Verläufe bei 12 Patienten. Dtsch Med Wschr 104: 467
Heyssel R, Brill AM, Woodbury LA, Nishimura ET, Ghose T, Hoshino T, Yamasaki M (1960) Leukemia in Hiroshima atomic bomb survivors. Blood 15: 313
Hittmaier A, Rittmann R (1926) Über azuro-eosinophile Leukozyteneinlagerungen. Ein Beitrag zur Kenntnis der akuten Myelosen mit Zelleinschlüssen. Haematologica 7: 149
Ho AD, Hunstein W, Uhl N, Storch HH (1981) Bedeutung der terminalen Desoxynucleotidyltransferase bei akuten Leukämien und bei malignen Lymphomen. Dtsch Med Wschr 106: 643
Homy HP, Parwaresch MR, Lennert K (1983) Basophilenleuk- ämie und generalisierte Mastozytose. Verhandl Dtsch Ges Path 67:192
Hubler WR, Netherton EW (1947) Cutaneous manifestations of monocytic leukemia. Arch Dermatol Syphilis 56: 70
Jaffe ES, Shevach EM, Frank MM, Green J (1974) Leukemic reticuloendotheliosis: presence of a receptor for cytophilic antibody. Amer J Med 57:108
Jaffé RH (1935) Histologic studies on the spleen in cases of leukemia. Arch Path 19: 647
Kass L (1977) Nonspecific esterase activity in „hairy cells”. Acta haemat 58:103
Katayama I, Li CY, Yam LT (1972) Ultrastructural characteristics of the „hairy cells” of leukemic reticuloendotheliosis. Amer J Path 67:361
Katayama J, Finkel H (1974) Leukemic reticuloendotheliosis. A clinicopathologic study with review of the literature. Amer J Med 57:115
Kautz D, Schaefer HE, Fischer R (1980) Das Verhalten der Osteoklasten bei Osteomyelofibrose unter Berücksichtigung histochemischer und morphometrischer Befunde. Verhandl Dtsch Ges Path 64: 569
Kautz D (1981) Histomorphometrische Untersuchungen der Beckenkammspongiosa bei Osteomyelofibrose unter Berücksichtigung der sauren Osteoklastenphosphatase
Kirchen ME, Marshall GJ (1976) Marrow storage cells: Un ultrastructural study. J Reticuloendothelial Soc 19: 109
Kung PC, Long JC, McCafrey RP, Ratliff RL, Harrison TA, Baltimore D (1978) Terminal deoxynucleotidyl transferase in the diagnosis of leukemia and malignant lymphoma. Amer J Med 64:788
Lagerlöf B (1972) Cytophotometric study of megakaryocyte ploidy in polycythemia vera and chronic granulocytic leukemia. Acta cytol 16: 240
Leder LD (1970) Akute myelo-monocytäre Leukämie mit atypischen Naphthol-AS-D-Chloroacetat-Esterase-positiven Eosinophilen. Acta haemat 44: 52
Lee KS, Tobin MS, Chen KTK, Ahmed F, Gomez-Leon G (1982) Acquired Gaucher’s cells in Hodgkin’s disease. Amer J Med 73:290
Lee RE, Ellis LD (1971) The storage cells of chronic myelogenous leukemia. Lab Invest 24: 261
Lennert K (1962) Zur Pathologischen Anatomie der Urticaria pigmentosa und Mastzellreticulose. Klin Wschr 40: 61
Lennert K, Parwaresch MR (1979) Mast cells and mast cell neoplasia: a review. Histopathology 3: 349
Lindner HJ, Linker H, Schaefer HE (1981) Zytochemisch und ultrastrukturell nachweisbare ringförmige Einschlüsse bei akuter myeloischer Leukämie. Blut 43: 14
Löffler H, Lück R, Syed Ali S (1975) Eosinophilenleukämie mit Chloracetat-Esterase-positiven Granula bei einem Kinde. Dtsch Med Wschr 100: 2092
Löffler H (1978) Die akuten (unreifzelligen) Leukämien. In: Queißer W (ed) Das Knochenmark, Morphologie - Funktion - Diagnostik. Thieme, Stuttgart, S 273–294
Löffler W (1936) Endocarditis parietalis fibroplastica mit Bluteosinophilie. Schweiz Med Wschr 66: 817
Löffler W, Essellier AF, Macado ME (1948) Zur Pathogenese und Ätiologie der flüchtigen Lungeninfiltrate mit Bluteosinophilie (Löfflersches Syndrom). Helvetica Med Acta 15: 223
Lorbacher P, Yam L, Quaynor E (1968) Cytochemischer Nachweis von ß-Glucuronidase in normalen und leukämischen Blut-lymphocyten. Klin Wschr 46:1046
McKee C, Collins RD (1974) Intracerebral leukocyte thrombi and aggregates as a cause of morbidity and mortality in leukemia. Medicine 53:463
Maldonado JE, Pintado T, Pierre RV (1974) Dysplastic platelets and circulating megakaryocytes in chronic myeloproliferative diseases. I. The platelets: Ultrastructure and peroxidase reaction. Blood 43: 797
Maldonado JE (1974) Dysplastic platelets and circulating megakaryocytes in chronic myeloproliferative diseases. II. Ultrastructure of circulating megakaryocytes. Blood 43: 811
Mason JE, de Vita VT, Canello GP (1974) Thrombocytosis in chronic granulocytic leukemia: Incidence and clinical significance. Blood 44: 483
Mertelsmann R, Thaler HT, To L, Gee TS, McKenzie S, Schauer P, Friedman A, Arlin Z, Cirrincione C, Clarkson B (1980) Morphologic classification, response to therapy, and survival in 263 adult patients with acute nonlymphoblastic leukemia. Blood 56:773
Minot GR, Buckman TE (1925) The blood platelets in the leukemias. Amer J Med Sei 169: 477
Möbius W (1970) Liquorzelldiagnostik mit der Sedimentkammermethode. Med Welt (NF) 21: 846
Moloney WC (1955) Leukemia in survivors of atomic bombing. New Engl J Med 253:88
Moore EW, Thomas LB, Shaw RK, Freireich EJ (1960) The central nervous system in acute leukemia. Arch intern Med 105: 451
Morley AA, Baikie AG, Galton DAG (1967) Cyclic leucocytosis as evidence for retention of normal haemostatic control in chronic granulocytic leukemia. Lancet II: 1320
Naegeli O (1900) Ueber rothes Knochenmark und Myeloblasten. Dtsch Med Wschr 26: 287
Naegeli O (1931) Blutkrankheiten und Blutdiagnostik. Springer, Berlin
Negri-Gualdi C (1967) Emile Weil’s chronic myeloid leukemia with polynucleated neutrophils. Minerva Med 58: 3850
Neumann E (1870) Ein Fall von Leukämie mit Erkrankung des Knochenmarkes. Arch Heilk 11:1
Neumann E (1878) Über myelogene Leukämie. Berlin klin Wschr 15: 69
Niederle N, Hellriegel KP, Schaefer HE (1976) Zur Problematik „gaucherartiger Zellen” bei der chronischen myeloischen Leukämie. In: Stacher A, Höcker P (eds) Erkrankungen der Myelopoese. Urban und Schwarzenberg, München, S 313–315
Niederle N, Hellriegel KP (1978) Primärer Blastenschub bei chronischer myeloischer Leukämie. Verhandl Dtsch Ges innere Med 84:173
Nies BA, Thomas LB, Freireich E (1965) Meningeal leukemia. Cancer 18: 546
Ninni M, Belloni F (1953) Sulla transformazione della leucemia mieloide cronica in leucemia basofila subacuta. Haematologica 37: 1455
Nowell PC, Hungerford DA (1960) A minute chromosome in human chronic granulocytic leukemia. Science 132:1497
O’Riordan ML, Robinson JA, Buckton KE, Evans HJ (1971) Distinguishing between the chromosomes involved in Down’s syndrome (trisomy 21) and chronic myeloid leukemia (Ph1) by fluorescence. Nature 230:167
Osler W (1903) Chronic cyanosis, with polycythaemia and enlarged spleen: A new clinical entity. Amer J Med Sei 126:187
den Ottolander GJ, te Velde J, Brederoo P, Geraedts JPM, Slee PHT, Wellemze SR, Zwaan FE, Haak HL, Muller HP, Beiger R (1979) Megakaryoblastic leukemia (acute myelofibrosis): a report of three cases. Brit J Haematol 42: 9
Paietta E, Schwarzmeier JD (1982) Terminal Deoxynucleotidyl Transferase (TDT): Its Significance in the Classification of Hematological Diseases. Blut 45:205
Palakovongs P, Teichberg S, Vinciguerra V, Degnan TJ, Sinlaratana P (1977) Ultrastructural cytochemical analysis of blastic transformation of chronic myelocytic leukemia. Blood 49:535
Plenderleith IH (1970) Hairy cell leukemia. Canad Med Ass J 102:1056
Rawson R, Parker F, Jackson H (1941) Industrial solvents as possible etiologic agents in myeloid metaplasia. Science 93:541
Reschad H, Schilling-Torgau V (1913) Über eine Leukämie durch echte Übergangsformen (Splenozytenleukämie) und ihre Bedeutung für die Selbständigkeit dieser Zellen. Münch Med Wschr 60: 1981
Rieber EP, v Heyden HW, Linke RP, Saal JG, Riethmüller G, Waller HD (1976) Haarzell-Leukämie. Charakterisierung der leukämischen Zelle: Oberflächen-Immunglobuline, Fc-Rezeptoren und Stimulation durch Mitogene. Klin Wschr 54:1011
Rodermund O-E, Hauser W, Burkhardt R, Grips KH, Stein G (1978) Veränderungen am Knochenmark bei Mastozytose. Dermatol Monatsschr 164: 493
Rosenthal S, Canellos GP, DeVita VT, Gralnick HR (1977) Characteristics of blast crisis in chronic granulocytic leukemia. Blood 49:705
Ross R, Vogel R (1980) The platelet derived growth factor. Cell 14: 203
Rowley JE (1973) The Ph1 chromosome: evidence for a specific chromosomal translocation. J clin Invest 52: 71a
Rowley JD (1976) The role of cytogenetics in hematology. Blood 48: 1
Rubin H (1966) Chronic neutrophilic leukemia. Ann intern Med 65:93
Rundles WR (1973) Chronic granulocytic leukemia. In: Williams WJ, Beutler E, Erslev AJ, Rundles WR (eds) Hematology. McGraw-Hill, New York, pp 680–695
Rundles WR (1977) Chronic granulocytic leukemia. In: Williams WJ, Beutler E, Erslev AJ, Rundles WR (eds) Hematology, 2nd edn. McGraw-Hill, New York, pp 777–796
Ruzicka F, Pawlowsky J, Erber A, Nowotny H (1976) Drei Fälle von Eosinophilenleukämie mit atypischer Granulation in Eosinophilen und Neutrophilen. Blut 32: 337
Sagher F, Even-Paz Z (1967) Mastocytosis and mast cell. Karger, Basel
Sayk J (1960) Cytologie der Cerebrospinalflüssigkeit. Fischer, Jena
Schaefer HE, Hellriegel KP, Hennekeuser HH, Hübner G, Zach J, Fischer R, Gross R (1973) Eosinophilenleukämie, eine unreifzellige Myelose mit Chloracetatesterase-positiver Eosinophilie. Blut 26:7
Schaefer HE, Hellriegel KP, Fischer R (1977) Der cytochemische Nachweis der Eosinophilen-Peroxidase unter besonderer Berücksichtigung des isolierten Peroxydasedefektes in Eosinophilen. Acta histochem Suppl XVIII 195
Schaefer HE, Schmalzl F, Fischer R (1978) Stammen eosinophile und neutrophile Granulozyten von einer gemeinsamen promyelozytären Vorstufe ab? Untersuchungen an der normalen, peroxydasedefekten und leukämischen Granulopoiese. Verhandl Dtsch Ges Path 62: 343
Schaefer HE, Weller P, Lansch D (1983) Erworbene und ererbte Defektformen der granulozytären Peroxidase (POX). Acta histochem Suppl XXVIII 219
Schaefer HE (1983) Zur Zytologie und Histologie des normalen menschlichen Knochenmarkes. Verhandl Dtsch Ges Path 67:80
Schmahl M (1983) Pseudogaucherzellen und Megakaryozyten bei der chronischen myeloischen Leukämie. - Häufigkeit, wechselseitige Beziehung und prognostische Bedeutung - Inauguraldissertation, Köln
Schmalzl F, Braunsteiner H (1968) Zur Cytochemie der Monocytenleukämie. Klin Wschr 46: 1185
Schmalzl F, Huhn D, Asamer H, Rindler R, Braunsteiner H (1973) Cytochemistry and ultrastructure of pathologic granulation in myelogenous leukemia. Blut 27:243
Sézary A (1952) Les réticuloses cutanées. Bull Soc franc Derm Ann Derm Syph 79:378
Shaw MT (1974) „Pure” monocytic leukemia: A revised concept. Proc Amer Soc Clin Oncol 15:162
Silverstein MN, Gomes MR, ReMine WH, Elveback LR (1967) Agnogenic myeloid metaplasia. Arch intern Med 120:546
van Slyck EJ, Weiss L, Dully M (1970) Chromosomal evidence for the secondary role of fibroblastic proliferation in acute myelofibrosis. Blood 36: 729
Spiers ASD (1974) Chronic granulocytic leukaemia and chronic lymphocytic leukaemia. Brit Med J: 4: 460
Srodes CH, Hyde EH, Boggs DR (1973) Autonomous erythroid megaloblastosis occurring during blastic transformation of chronic myelocytic leukemia. J clin Invest 52:512
Stacher A, Höcker P (eds) Erkrankungen der Myelopoese. Leukämien, myeloproliferatives Syndrom, Polycythämie. Urban und Schwarzenberg, München
Stass SA, Veach S, Pasquale SM, Schumacher HR, Keneklis TP, Bollum FJ (1978) Terminal-deoxynucleotidyl-transferase positive acute lymphoblastic leukaemia with Auer rods. Lancet I: 1042
Terheggen HG, Haug H, Hellriegel KP, Schaefer HE (1975) Der sogenannte infantile Typ der chronischen myeloischen Leukämie. Zschr Kinderheilk 119:123
Thiele J, Vykoupil KF, Georgii A (1979) Chronic myelomonocytic leukemia: Light and electron microscopy of the bone marrow. Blut 39:177
Thiele J, Holgado S, Choritz A, Georgii A (1982) Abnormalities of megakaryocytes in myelitis and chronic myeloproliferative diseases. Virchows Arch (Cell Pathol) 41:67
Thomas LB (1965) Pathology of leukemia in the brain and meninges: Postmortem studies of patients with acute leukemia and of mice given inoculations of L 1210 leukemia. Cancer Res 25: 1555
Tjio JH, Carbone PP, Whang J, Frei E (1966) The Philadelphia chromosome in chronic myelogenous leukemia. J nat Cancer Inst 36:567
Tough IM, Court Brown WM (1965) Chromosome aberrations and exposure to ambient benzene. Lancet I: 684
Tough IM (1965) Cytogenetic studies in cases of myeloid leukemia with a previous history of radiation. In: Hayhoe FGJ (ed) Current Research in Leukemia. Cambridge University Press, London, p 47
Tulliez M, Vemant JP, Breton-Gorius J, Imbert M, Sultan C (1979) Pseudo-Chediak-Higashi anomaly in a case of acute myeloid leukemia: electron microscopic studies. Blood 54:863
Undritz E (1969) Die Differentialdiagnose der malignen Hämoblastosen. In: Stacher A (ed) Chemo- und Immunotherapie der Leukosen und malignen Lymphome. Bohmann, Wien, S 101
Vanivich S, Marks SM, Rosenthal DS, Moloney WC, Schlossman SF (1979) Cell-surface characteristics of hairy cell leukemia in seven patients. Cancer 43: 2348
Vaquez MH (1892) Sur une forme speciale de cyanose s’accom-pagnant d’hyperglobulie excessive et persistante. Compt rend Soc Biol 44: 384
Vaughn JM (1936) Leuco-erythroblastic anaemia. J Pathol 42: 541
te Velde J, Vismans FJEF, Leenheers-Binnendijk L, Vos CJ, Sneenk D, Bijvoet OLM (1978) The eosinophilic fibrohistiocytic lesion of the bone marrow. A mastocellular lesion in bone disease. Virchows Arch A 377: 277
Vigliani EC, Saita G (1964) Benzene and leukemia. New Engl J Med 271:872
Virchow R (1845) Weißes Blut. Froriep’s Notizen 36:151
Wasastjema C, Vuorinen E, Lehtinen M, Ikkala E, Huhtala E (1975) The cytochemical ß-glucuronidase reaction in the differential diagnosis of acute leukaemias. Acta Haematologica 53: 277
Werner W, Krause AP (1965) Die Gewebsmastzellen im menschlichen Knochenmark. Frankf Zschr Path 74: 651
Wheldon TE, Kirk J, Finlay HM (1974) Cyclic granulopoiesis in chronic granulocytic leukemia: A simulation study. Blood 43:379
Wiener L (1965) A family with a high incidence of leukemia and unique Ph1 chromosome findings. Blood 26: 871
Woessner S, Lafuente R, Pardo P, Rosseil R, Rozman C, Sans-Sabrafen J (1977) Systemic mastocytosis: a case report. Cytological, cytochemical and ultrastructural considerations. Acta haemat 58: 321
Wolk RN, Masse SR, Conklin R, Freireich EJ (1974) Incidence of central nervous system leukemia in adults. Cancer 33: 863
Zaino EC, Rossi MB, Pham TD, Azar HA (1971) Gaucher’s cells in thalassemia. Blood 38: 457
Zittoun R, Bemadou A, Bilski-Pasquier G, Bousser J (1972) Les leucémies myélo-monocytaires subaigues. Etudes de 27 cas et revue de la littérature. Sem Höpit (Paris) 48:1943
Zittoun R (1976) Subacute and chronic myelomonocytic leukaemia: A distinct haematological entity. Brit J Haematol 32: 1
Literatur
Barka T (1960) A simple azo-dye method for histochemical demonstration of acid phosphatase. Nature 187: 248–249
Bartl R Weichert HC, Schmitt G, Firusian N, Wetter O (1978) Rationelle Beckenkamm-Biopsie. Langsteilung der Proben zur Anwendung von mehreren Präparationsverfahren ohne Materialverlust. Klin Wschr. 56: 545–550
Bauer-Sić P (1966) Signifikante Veranderung des alkalischen Leukozytenphosphatase-Index während des menstruellen Zyklus. Acta endocrin 52: 130–148
Beckstead JH, Halverson PS, Ries CA, Bainton DF (1981) Enzyme histochemistry and immunohistochemistry on biopsy specimens of patholic human bone marrow. Blood 57: 1088–1098
Beisel WR, Benjamin N, Austen KF (1953) Absence of leukocyte alkaline phosphatase activity in hypophosphatasia. Blood 14: 975–977
Beisel WR (1967) Neutrophile alkaline phosphatase changes in tularemia, sandfly fever, Q-fever and oninfectious fevers. Blood 29: 257–268
Beutler E, Ohno S, Goldenburg EW, Yettra M (1964) Chromosome-21 and paroxysmal natumal hemoglobinuria. Blood 24: 160–163
Burkhardt R (1956) Die Myelotomie, eine neue Methode zur kombinierten cytologisch-histologischen Knochenmarksbiopsie. Blut 2: 267
Burkhardt R (1966) Ein neues Verfahren zur histologischen Präparation von Biopsien aus Knochenmark und Knochen. Blut 14: 30
Curran RC, Gregory J (1980) Effects of fixation and processing on immunohistochemical demonstration of immunoglobulin in paraffin sections of tonsil and bone marrow. J clin Pathol 338: 1047–1057
Davis BJ, Omstein L (1959) High resolution enzyme localization with a new diazo reagent, „hexazonium pararosaniline”. J Histochem Cytochem 7:297
Dempsey SI, Crockard AD, Brigges JM (1980) An estimation of β-Glucuronidase and N-Acetyl-β-D-Glucosaminidase activity in normal and chronic lymphocytic leukaemia lymphocytes
Goldenberg AF, Barka T (1962) Acid phosphatase activity in human blood cells. Nature 195:297
Gomori G (1953) Chloracylesters as histochemical substrates. J Histochem Cytochem 1: 469–470
Hautzer NW, Wittkuhn JF, McCaughey WTE (1980) Trypsin digestion in immunoperoxidase staining. J Histochem Cytochem 28:52–53
Hayashi M, Nakajima Y, Fishman WH (1964) The cytologic demonstration of β -glucuronidase employing naphthol-AS-BI glucuronide and hexazonium pararosanilin; a preliminary report. J Histochem Cytochem 12: 293–297
Horwitz DA, Allison AC, Ward P, Kight N (1977) Identification of human mononuclear leucocyte populations by esterase staining. Clin exper Immunol 30: 289–298
Hsu SM, Raine L (1982) Versatility of biotin-labeled lectins and avidin-biotin-peroxidase complex for localization of carbohydrate in tissue sections. J Histochem Cytochem 30:157–161
Kaplow LS (1955) A histochemical procedure for localizing and evaluating leukocyte alkaline phosphatase activity in smears of blood and marrow. Blood 10: 1023–1029
Kaplow LS (1963) Cytochemistry of leukocyte alkaline phosphatase. Use of complex naphthol-AS-phosphate in azo dye-coupling technics. Am J clin Pathol 39: 439–449
Laskowski M (1971) Venom exonuclease. In: Boyer PD (ed) The enzymes, Vol IV, 3. ed. Academic Press, New York, pp 313–328
Leder LD (1964) Über die selektive fermentcytochemische Darstellung von neutrophilen myeloischen Zellen und Gewebsmastzellen im Paraffinschnitt. Klin Wschr 42: 553–555
Lewis SM, Dacie JO (1965) Neutrophil (leucocyte) alkaline phosphatase in paroxysmal nocturnal haemoglobinuria. Brit J Haemat 11: 549–556
Lorbacher P (1969) Der zytochemische β -Glucuronidasenachweis; ein Beitrag zur Differenzierung lymphatischer Leukosen. In: Stacher A (ed) Chemo- und Immunotherapie der Leukosen und malignen Lymphome. Bohmann, Wien, p 160
Moloney WC, Me Pherson L, Fliegelman L (1960) Esterase activity in leucocytes demonstrated by the use of Naphthol AS-D chloroazetate substrate. J Histochem Cytochem 8: 200–207
Müller D (1967) Zur Frage der endokrinen Beeinflussung der alkalischen Leukozytenphosphatase. Blut 14: 273–276
Mueller J, del Brun R, Buerki H, Keller HU, Hess MW, Cottier H (1975) Nonspecific acid esterase activity: a criterion for differentiation of T and B lymphocytes in mouse lymph nodes. Europ J Immunol 5: 270–274
Peris M (1867) Nachweis von Eisenoxyd in gewissen Pigmenten. Virchows Arch pathol Anat 39: 42–48
Pralle H, Löffler H (1979) Erythrocytosis with alkaline phosphatase in the membrane of the erythrocytes. Intern Soc Haematol Europ African Div 5th Meeting, Abstracts IV, 32
Quigley HJ, Dawson EA, Hyun BH, Custer RP (1960) The activity of alkaline phosphatase in granular leukocytes during pregnancy and the puerperium: A preliminary report. Amer J clin Path 33:109–114
Schaefer HE, Hellriegel KP, Fischer R (1977) Vorkommen von tartratresistenter saurer Phosphatase in verschiedenen Zelltypen des lymphoretikulären und hämatopoetischen Zellsystems. Blut 34:393–397
Schaefer HE (1980) Ein atypisches Verteilungsmuster der tartratresistenten sauren Phosphatase in Osteoklasten bei Ostitits deformans Paget - zur pathogenetischen und diagnostischen Bedeutung. Verhandl Dtsch Ges Path 64: 569
Schaefer HE (1983) Zur Zytologie und Histologie des normalen menschlichen Knochenmarkes. Verhandl Dtsch Ges Path 67: 80–100
Schaefer HE (1983) Neuere histochemische Aspekte zur Differenzierung und Funktion normaler und pathologischer Blutzellen. Eine Einführung zur Thematik. Acta histochem, Suppl XXVIII 129–133
Schaefer HE, Assmann G (1983) Das Verhalten lymphozytärer Lysosomen bei der Cholesterinester-Speicherkrankheit (CESK). Acta histochem, Suppl XXVI 135–148
Schaefer HE, Weller P, Lansch D (1983) Erworbene und ererbte Defektformen der granulozytären Peroxidase (POX). Acta histochem, Suppl XXVIII 219–234
Seifert G, Denk H, Klein JH, Stein H, Otto HF (1984) Die Anwendung der Immunzytochemie in der praktischen Diagnostik des Pathologen. Pathologe 5:187–199
Shugar D, Sierakowska H (1967) Mammalian nucleolytic enzymes and their localization. Progr Nucleic Acid Res 7: 396–429
Sierakowska H, Shugar D (1963) Cytochemical localization of phosphodiesterase by the azo dye simultaneous coupling method. Biochem Biophys Res Comm 11: 70–75
Trubowitz S, Moschides E, Feldman D (1961) Alkaline phosphatase activity of the polymorphonuclear leukocyte in rapidly induced leukopenia and leukocytosis. J lab clin Med 57: 747–754
Undritz E (1965) Zur Aktivität der alkalischen Phosphatase bei der chronisch myeloischen Leukämie. Schweiz Med Wschr 95: 1515–1519
Valentine WN, Follette JH, Hardin EB, Beck WS Lawrence JS (1954) Studies on leucocyte alkaline phosphatase activity: relation to „stress” and pituitary-adrenal activity. J lab clin Med 44: 219–228
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1984 Springer-Verlag Berlin Heidelberg
About this chapter
Cite this chapter
Schaefer, H.E. (1984). Leukopoese und myeloproliferative Erkrankungen. In: Remmele, W. (eds) Pathologie. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-97874-6_6
Download citation
DOI: https://doi.org/10.1007/978-3-642-97874-6_6
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-642-97875-3
Online ISBN: 978-3-642-97874-6
eBook Packages: Springer Book Archive