Zusammenfassung
Die klassische Pathologie unterteilt Erkrankungen in sieben Gruppen:
-
Hamartome
-
Malformationen
-
Hyperplasien
-
Entzündungen
-
gut- und bösartige Neoplasien
-
Zysten und
-
Ablagerungserkrankungen.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
Literatur
Literatur zu Abschn. 36.2 bis 36.10
Blatt J, Jaffe R, Deutsch M, Adkins JC (1986) Neurofibromatosis and childhood tumors. Cancer 57: 1225–1229
Cieslak AK, Stout AP (1946) Traumatic and amputation neuromas. Arch Surg 53: 646–651
Dehner LP (1993) Primitive neuroectodermal tumor and Ewing’s sarcoma. Am J Surg Pathol 17: 1–13
Fletcher CDM (1994) Malignant peripheral nerve sheath tumours. In: Harms D, Schmidt D (eds) Current topics in pathology: Soft tissue tumours, vol 89. Springer, Berlin Heidelberg New York Tokyo, pp 333–354
Fletcher CDM, Carpenter G, McKee PH (1986) Nasal glioma–a rarity. Am J Dermatopathol 8: 341–346
Gorlin RJ, Sedano HO, Vickers RA, Cervenka J (1968) Multiple mucosal neuromas, pheochromocytoma and medullary carcinoma of the thyroid. A syndrome. Cancer 22: 293–299
Hirose T, Sumimoto M, Kudo E et al. (1989) Malignant peripheral nerve sheath tumor ( MPNST) showing perineurial cell differentiation. Am J Surg Pathol 13: 613–620
Khansur T, Balducci, Tavassoli M (1987) Granular cell tumor. Clinical spectrum of the benign and malignant entity. Cancer 6o: 220–222
King P, Cooper PN, Malcolm AJ (1993) Soft tissue ependymo- ma: A report of three cases. Histopathology 22: 394–396
Lazarus SS, Trombetta LD (1978) Ultrastructural identification of a benign perineurial cell tumor. Cancer 41: 1823–1829
Markel SF, Enzinger FM (1982) Neuromuscular hamartoma–a benign „triton tumor“ composed of mature neural and striated muscle elements. Cancer 49: 140–144
Requena L, Sangüeza OP 1995 Benign neoplasms with neural differentiation. A review. Am J Dermatopathol 17: 75–96
Suster S, Rosai J (1990) Hamartoma of the scalp with ectopic meningothelial elements. A distinctive benign soft tissue lesion that may simulate angiosarcoma. Am J Surg Pathol 14: 1–11
Literatur zu Abschn. 36.11 bis 36.14
Fitzpatrick JE, Mellette JR, Hwang RJ, Golitz LE, Zaim T, Clemons D (199o) Cutaneous angiolipoleiomyoma. J Am Acad Dermatol 23: 1093–1098
Granter SR, Nucci MR, Fletcher CDM (1997) Aggressive angiomyxoma: Reappraisal of its relationship to angiomyofibroblastoma in a series of 16 cases. Histopathology 3o: 3–10
Hachisuga T, Hashimoto H, Enjoji M (1984) Angioleiomyoma. A clinicopathologic reappraisal of 562 cases. Cancer 54: 126–130
Kaddu S, Beham A, Cerroni L, Humer-Fuchs U, Salmhofer W, Kerl H, Soyer HP (1997) Cutaneous leiomyosarcoma. Am J Surg Pathol 21: 979–987
Mentzel T, Calonje E, Fletcher CDM (1994) Leiomyosarcoma with prominent osteoclast-like giant cells. Analysis of eight cases mimicking the so-called giant cell variant of malignant fibrous histiocytoma. Am J Surg Pathol 18: 258–265
Newman PL, Fletcher CDM (1991) Smooth muscle tumours of the external genitalia: Clinicopathological analysis of a series. Histopathology 18: 523–529
Salm R, Evans DJ (1985) Myxoid leiomyosarcoma. Histopathology 9: 159–169
Suster S (1994) Epithelioid leiomyosarcoma of the skin and subcutaneous tissue. Clinicopathologic, immunohistochemical and ultrastructural study of five cases. Am J Surg Pathol 18: 232–240
Suster S, Rosen LB, Sanchez JL (1988) Granular cell leiomyosarcoma of the skin. Am J Dermatopathol 1o: 234239
Van Dorpe J, Sciot R, De Vos R, Uyttebroeck A, Stas M, Van Damme B (1997) Neuromuscular hamartoma (choristoma) with smooth and striated muscle component. Am J Surg Pathol 21: 1090–1095
Literatur zu Abschn. 36.15 bis 36.17
Agamanolis DP, Dasu S, Krill CE (1986) Tumors of skeletal muscle. Hum Pathol 17: 778–795
Cavazzana AO, Schmidt D, Ninfo V et al. (1992) Spindle cell rhabdomyosarcoma. A prognostically favorable variant of rhabdomyosarcoma. Am J Surg Pathol 16: 229–235
Enzinger FM, Shiraki M (1969) Alveolar rhabdomyosarcoma. An analysis of no cases. Cancer 24: 18–31
Farris PE, Manning S, Vuitch F (1994) Rhabdomyomatous mesenchymal hamartoma. Am J Dermatopathol 16: 73–74
Fletcher CDM (1995) Skeletal muscle tumors. In: Fletcher CDM (ed) Diagnostic histopathology of tumors, vol 2. Churchill Livingstone, New York, pp 1076–1081
Foschini MP, Eusebi V (1994) Alveolar soft part sarcoma: A new type of rhabdomyosarcoma? Semin Diagn Pathol 11: 58–68
Gaffney EF, Dervan PA, Fletcher CDM (1993) Pleomorphic rhabdomyosarcoma in adulthood. Analysis of 11 cases with definition of diagnostic criteria. Am J Surg Pathol 17: 601–609
Hollowood K, Fletcher CDM (1994) Rhabdomyosarcoma in adults. Semin Diagn Pathol 47–57
Tsokos M (1994) The diagnosis and classification of childhood rhabdomyosarcoma. Semin Diagn Pathol 26–38
Willis J, Abdul-Karim FW, Di Sant’ Agnese PA (1994) Extra- cardiac rhabdomyomas. Semin Diagn Pathol u: 15–25
Literatur zu Abschn. 36.18 bis 36.24
Allan CJ, Soule EH (1971) Osteogenic sarcoma of the somatic soft tissues. Clinicopathologic study of 26 cases and review of the literature. Cancer 27: 1121–1133
Chung EB, Enzinger FM (1978) Chondroma of soft parts. Cancer 41: 1414–1424
Chung EB, Enzinger FM (1987) Extraskeletal osteosarcoma. Cancer 6o: 1132–1143
Enzinger FM, Shiraki M (1972) Extraskeletal myxoid chondrosarcoma. An analysis of 34 cases. Hum Pathol 3: 421–435
Landon GC, Johnson KA, Dahlin DC (1979) Subungual exostoses. J Bone Joint Surg (Am) 61: 256–259
Peterson WC, Mandel SL (1963) Primary osteomas of the skin. Arch Dermatol 87: 132–138
Saleh G, Evans HL, Ro JY, Ayala AG (1992) Extraskeletal myxoid chondrosarcoma. A clinicopathologic study of ten patients with long-term follow-up. Cancer 7o: 2827–2830
Literatur zu Abschn. 36.25 bis 36.32
Beham A, Schmid Ch, Hödl St, Fletcher CDM (1989) Spindle cell and pleomorphic lipoma: An immunohistochemical study and histogenetic analysis. J Pathol 158: 219–222
Dei Tos A, Mentzel T, Fletcher CDM (1998) Primary liposarcoma of the skin: A rare neoplasm with unusual high grade features. Am J Surg Pathol 22: 332–338
Dei Tos AP, Mentzel T, Newman PL, Fletcher CDM (1994) Spindle cell liposarcoma: A hitherto unrecognized variant of liposarcoma: Analysis of six cases. Am J Surg Pathol 18: 913–921
Enzi G (1984) Multiple symmetric lipomatosis: Updated clinical report. Medicine 63: 56–64
Evans HL (1979) Liposarcoma. A study of 55 cases with reassessment of its classification. Am J Surg Pathol 3: 507–523
Hawley IC, Krausz T, Evans DJ, Fletcher CDM (1994) Spindle cell lipoma–a pseudoangiomatous variant. Histopathology 24: 565–569
Howard WR, Helwig EB (1960) Angiolipoma. Arch Dermatol 82: 924–931
Kindblom LG,Angervall L, Stener B,Wickbom I (1974) Intermuscular and intramuscular lipomas and hibernomas. A clinical, roentgenologic, histologic, and prognostic study of 46 cases. Cancer 33: 754–762
Meis JM, Enzinger FM (1993) Chondroid lipoma. A unique tumor simulating liposarcoma and myxoid chondrosarcoma. Am J Surg Pathol 17: 1103–1112
Mentzel T, Calonje E, Fletcher CDM (1993) Lipoblastoma and lipoblastomatosis: A clinicopathological study of 14 cases. Histopathology 23: 527–533
Nascimento AG, Kurtin PJ, Guillou L, Fletcher CDM (1998) Dedifferentiated liposarcoma. A report of nine cases with peculiar neurallike whorling pattern associated with metaplastic bone formation. Am J Surg Pathol 22: 945955
Novy FG, Wilson JW (1956) Hibernomas, brown fat tumors. Arch Dermatol 73: 149–157
Silverman TA, Enzinger FM (1985) Fibrolipomatous hamartoma of nerve. A clinicopathologic analysis of 26 cases. Am J Surg Pathol 9: 7–14
Wilson Jones E, Marks R, Pongeshirun D (1975) Naevus lipomatosus superficialis. A clinicopathological report of twenty cases. Br J Dermatol 93: 121–133
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2003 Springer-Verlag Berlin Heidelberg
About this chapter
Cite this chapter
Zelger, B. (2003). Nerven-, Muskel-, Knorpel-, Knochen- und Fettgewebetumoren der Haut. In: Kerl, H., Garbe, C., Cerroni, L., Wolff, H.H. (eds) Histopathologie der Haut. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-07784-9_36
Download citation
DOI: https://doi.org/10.1007/978-3-662-07784-9_36
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-662-07785-6
Online ISBN: 978-3-662-07784-9
eBook Packages: Springer Book Archive