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

栖息地

Incidence of Soft Tissue Sarcomas in Adults,ignant soft tissue tumors (0.4%) out of a total of 128002 cancer deaths in all sites during the period 1984–1988, compared with 19538 deaths of lung cancer and 18567 deaths of gastric cancer (. 1984–1988) (Table 1).

Cervical-Spine

Molecular Biological Aspects of Soft Tissue Tumors,d clinical management of these patients, particularly where said information has affected patient management or our understanding of the underlying disease process and its impact on prognosis and treatment.

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变形词

,Malignant Fibrous Histiocytoma: A “Fibrohistiocytic” or Primitive, Fibroblastic Sarcoma,dmixed. Collagenous or mucoid intercellular substances vary intralesionally and interlesionally. A whorly cellular arrangement, called “storiform pattern,” was thought to be an important differential diagnostic criterion for MFH — even if not ubiquitous (. et al. 179; . 1986).

陈列

郊外

Firefly

Rare Soft Tissue Sarcomas,be included in the British final postgraduate pathology examinations. Viewed logically, this seems somewhat inappropriate but probably reflects the philatelic tendency shared by many of us who work in diagnostic histopathology.

保守

0070-2188 manifestation, and prognosis. Their spectrum is fascinating for morphologists and basic scientists alike. Yet precisely this variability in the morphologic manifestation of soft tissue tumors, specifically their histologic and cytologic patterns, presents great difficulties to any effort to categori

掺和

Nonporous

Clinical Management of Soft Tissue Sarcomas,e essential strategy for treatment is based on a number of factors: histology, site, tumour size, local invasiveness, systemic spread and the age at diagnosis. The tumour characteristics at diagnosis are to a certain extent interrelated and not entirely independent of one another, e.g., tumour size