Abstract
Histiocytosis is a general term used to indicate several pathological disorders of the reticuloendothelial system. Cells of this system have been classified as the mononuclear phagocytic system because of their common origin and function. These cells all originate from the pro-monocyte in the bone marrow and give rise to two different cell lineages. One cell line (the antigen-processing) includes the peripheral monocyte which, in turn, gives rise to the tissue macrophage (histiocyte). The other cell line (the antigen-presenting) is referred to as the dendritic cell population and is generally not phagocytic. These antigen-presenting cells are divided into three well-defined, although not fully characterized, subsets: dendritic reticulum cells, interdigitating reticulum cells and Langerhans’ cells [1]. Table 1 summarizes characteristics of the Langerhans cell and other cell systems of the mononuclear phagocytic system. The dendritic cell line is intimately involved with the thymus-dependent regions of the body. These cells are powerful stimulators of mixed lymphocyte response. Each disorder in the histiocytosis syndromes is viewed as resulting from a reactive or neoplastic proliferation of cells similar, if not identical, to one of these cell types. The cells of the mononuclear phagocytic system constitute an important defence system in the body against infections and foreign particulate matter, as well as being an important cellular component of the afferent limb of the immune response.
This research was supported by PHS grant CA-07306 and the Children’s Cancer Research Fund of the University of Minnesota, Minneapolis, Minnesota, USA. R.M.E. is supported by the Ter Meulen Fonds, Royal Academy of Arts and Sciences, Amsterdam, The Netherlands.
Preview
Unable to display preview. Download preview PDF.
References
Gonzalez CL, Jaffe ES (1990) The histiocytosis: clinical presentation and differential diagnosis. Oncology 4: 47–60
Lichtenstein L, Jaffe HL (1940) Eosinophilic granuloma of bone. Am J Pathol 16: 595–604
Hand A (1921) Defects of membranous bones, exophthalmos and polyuria in childhood: is it dyspituitarism? Am J Med Sci 162: 509–515
Siwe S (1933) Die Reticuloendotheliose — ein neues Krankheitsbild unter den Hepatosplenomegalien. Z Kinderheilk 55: 212–247
Lichtenstein L (1953) Integration of eosinophilic granuloma of bone, “Letterer-Siwe Disease” and “Schüller-Christian Disease” as related manifestations of a single nosologic entity. Arch Pathol 56: 84–102
Nezelof C, Basset F, Rousseau MF (1973) Histiocytosis X; histogenetic arguments of a Langerhans cell origin. Biomed 18: 365–371
Writing Group of the Histiocyte Society (1987) Histiocytosis syndromes in children. Lancet I: 208–209
van Heerde P, Egeler RM (1991) Cytology of Langerhans cell histiocytosis (histiocytosis X). Cytopathology 2: 149–158
Birbeck MS, Breathnach AJ, Everall JD (1951) An electron microscopic study of basal melanocytes and high-level clear cells ( Langerhans’) cells in vitiligo. J Invest Dermatol 37: 51–64
Favara BE (1991) Langerhans’ cell histiocytosis pathobiology and pathogenesis. Semin Oncol 18: 3–7
Arenzana-Seisdedos F, Barbey S, Virelizier JL, Kornprobst M, Nezelof C (1986) Histiocytosis X purified (T6+) cells from bone granuloma pro- duce interleukin 1 and prostaglandin E2 in culture. J Clin Invest 77: 326–329
Barbey S, Gane P, Le Pelletier O, Nezelof C (1987) Histiocytosis X Langerhans cells react with antiinterleukin-2 receptor monoclonal anti body. Pediatr Pathol 7: 569–574
Luger TA (1989) Epidermal cytokines. Acta Derm Venereol (Stockh) 69: 61–76
Lahey ME (1962) Prognosis in reticulo endotheliosis in children. J Pediatr 60: 664–671
Clinical Writing Group of the Histiocyte Society (Broadbent V, Gadner H, Komp DM, Ladisch S) (1989) Histiocytosis syndromes in children. II. Approach to the clinical and laboratory evaluation of children with Langerhans cell histio cytosis. Med Pediatr Oncol 17: 492–495
Lahey ME (1975) Histiocytosis X: an analysis of prognostic factors. J Pediatr 87: 184–189
Komp DM (1987) Langerhans cell histiocytosis.N Engl J Med 316: 747–748
Cohen M, Zornoza J, Cangir A, Murray JA,Wallace S (1980) Direct injection of methyl-sodium succinate in the treatment of solitary eosinophilic granuloma of bone. Radiology 136: 289–293
Smith DG, Nesbit ME, D’Angio GJ, Levitt SH(1973) Histiocytosis X. Role of radiation therapy in management with special reference to dose levels employed. Radiology 106: 419–422
Helbock H, Krivit W, Nesbit M (1971) Patterns of antidiuretic function in diabetes insipidus caused by histiocytosis X. J Clin Lab Med 78: 194–202
McClain K, Ramsay NKC, Robison L, Sundberg RD, Nesbit ME (1983) Bone marrow involve ment in histiocytosis X. Med Pediatr Oncol 11:167–171
Hamoudi AB, Newton WA Jr, Mancer K, Penn Karolinska Hospital, Stockholm GM (1982) Thymic Changes in Histiocytosis. Am J Clin Pathol 84: 169–173
Starling KA, Donaldson MH, Haggaad ME,Vietti T, Sutow WW (1972) Therapy of histiocytosis with vincristine, vinblastine, and cyclo-phosphamide. Am J Dis Child 123: 105–110
Jones B, Kung F, Chevalier L (1974) Chemo therapy of reticuloendotheliosis, comparison of methotrexate plus prednisone vs. vincristine plus prednisone. Cancer 34: 1011–1017
Lahey ME (1975) Histiocytosis X — comparison of three treatment regimens. J Pediatr 87: 193–197
Starling KA (1981) Chemotherapy of histio- cytosis. Am J Pediatr Hematol Oncol 3: 157–163
Ceci A, de Terlizzi M, Collela R, Balducci D,Toma MG, Zurlo MG, Macchia P, Mancini A,Indolfi P, Locurto M, Calculli G, Cristiani M,Castello M (1988) Etoposide in recurrent child-hood Langerhans cell histiocytosis: an Italian cooperative study. Cancer 62: 2528–2531
Gadner H (on behalf of the Study Group) (1990) Langerhans cell histiocytosis treatment protocol of the International Study. Langerhans Cell Histiocytosis Symposium, 6th annual meeting of the Histiocyte Society, Rome
Jakobson AM, Kreuger A, Hagberg H, Sundstrom C (1987) Treatment of Langerhans cell histiocytosis with alpha-interferon. Lancet II: 1520–1521
Mahmoud HH, Wang WC, Murphy SB (1991) Cyclosporine therapy for advanced Langerhans cell histiocytosis. Blood 77: 721–725
Foucar E, Rosai J, Dorfman RF (1990) Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease): review of the entity. Semin Diagn Pathol 7: 19–73
Komp DM (1990) The treatment of sinus histio-cytosis with massive lymphadenopathy (Rosai-H Dorfman disease). Semin Diagn Pathol 7: 83–86
Risdall RJ, McKenna RW, Nesbit ME, Krivit W, Balfour HH Jr, Simmons RL, Brunning RD (1979) Virus-associated hemophagocytic syn-s drome; a benign histiocytic proliferation dis-tinct from malignant histiocytosis. Cancer 44: 993–1002
Henter JI (1990) Familial hemophagocytic lymphohistiocytosis. A clinical, metabolic and immunological study of a lymphohistiocytic inflammatory disorder. Thesis, Karolinska Institute, St. Göran’s Children’s Hospital and Karolinska Hospitsl,stockholm
Nezelof C, Frileux-Herbet F, Cronier-Sachot J (1979) Disseminated histiocytosis X: analysis of prognostic factors bases on a retrospective study of 50 cases. Cancer 44: 1824–1838
Raney RB, D’Angio GJ (1989) Langerhans’ cell histiocytosis (histiocytosis X): experience at the Children’s Hospital of Philadelphia, 1970–1984.Med Pediatr Oncol 17: 20–28
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1992 Springer-Verlag Berlin Heidelberg
About this chapter
Cite this chapter
Egeler, R.M., Nesbit, M.E. (1992). Current Concepts and Treatment of Langerhans’ Cell Histiocytosis. In: Voûte, P.A., Barrett, A., Lemerle, J. (eds) Cancer in Children. UICC International Union Against Cancer. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-84722-6_15
Download citation
DOI: https://doi.org/10.1007/978-3-642-84722-6_15
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-642-84724-0
Online ISBN: 978-3-642-84722-6
eBook Packages: Springer Book Archive