Titlebook: Soft Tissue Tumors; D. Harms,D. Schmidt Book 1995 Springer-Verlag Berlin Heidelberg 1995 Classification.Diagnose.Diagnosis.Klassifikation.

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Molecular Biological Aspects of Soft Tissue Tumors,f the genetic basis of malignancy have focused on specific genetic lesions that are apparently etiologic or at least represent significant risk factors for the development of these tumors. Further, immunophenotypic analyses have led to the identification of tumor-specific (or at least tumor-associat

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Characteristic Chromosome Abnormalities and Karyotype Profiles in Soft Tissue Tumors,sification of soft tissue tumors. It is well known that “accurate classification of a given tumor is often not easy, so much that acknowledged international experts are still unable to pin a label on about 10% of sarcomas” (. 1990). In this context, any new tumor marker is of paramount interest. Cyt

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DNA Ploidy in Soft Tissue Tumors: An Evaluation of the Prognostic Implications in the Different Tumividual influences such as localization, age, overall personal risk factors (operability, etc.), and the chosen therapeutic procedures (. et al. 1989). The patho-anatomical determinants are tumor size, mode and grade of tumor spread at the time of primary diagnosis, histological tumor type or subtyp

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,Malignant Fibrous Histiocytoma: A “Fibrohistiocytic” or Primitive, Fibroblastic Sarcoma, of the WHO classification of soft tissue tumors (. 1993), there is increasing criticism of MFH as an entity (. et al. 1987; . 1988; . 1992). MFH of the bone was questioned as an entity already years ago (. et al. 1977). MFH as a sarcoma type became popular during 1960s among Stout and his co-worker

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Recent Advances in Tumors of Adipose Tissue,t recent practical advance in the diagnosis and management of soft tissue tumors. In my experience, fine needle aspiration cytology investigation of soft tissue tumors presently results in an unacceptably high level of false-negative results. In my opinion, it should only be performed as a research

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Spindle Cell Rhabdomyosarcoma: Histologic Variant of Embryonal Rhabdomyosarcoma with Association toMS of the skeletal muscles by . (1946), this entity was subdivided by histologic criteria into embryonal (. and . 1950), alveolar (. and . 1956), botryoid (. et al. 1955), and pleomorphic variants (. and . 1958). Later it could be shown that the botryoid RMS is a subtype of embryonal RMS. In clinica

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