Incidence of Soft Tissue Sarcomas in Adults --;Clinical Management of Soft Tissue Sarcomas --;Soft Tissue Sarcomas in the Kiel Pediatric Tumor Registry --;Molecular Biological Aspects of Soft Tissue Tumors --;Characteristic Chromosome Abnormalities and Karyotype Profiles in Soft Tissue Tumors --;DNA Ploidy in Soft Tissue Tumors: An Evaluation of the Prognostic Implications in the Different Tumor Types --;Heterogeneity in Malignant Soft Tissue Tumors --;Grading of Soft Tissue Sarcomas: Proposal for a Reproducible, Albeit Limited Scheme --;Fibrous Tumors and Tumor-like Lesions of Childhood: Diagnosis, Differential Diagnosis, and Prognosis --;Malignant Fibrous Histiocytoma: 'A Fibrohistiocytic' or Primitive, Fibroblastic Sarcoma --;Recent Advances in Tumors of Adipose Tissue --;Classification of Rhabdomyosarcoma --;Spindle Cell Rhabdomyosarcoma: Histologic Variant of Embryonal Rhabdomyosarcoma with Association to Favorable Prognosis --;Alveolar Rhabdomyosarcoma: A Prognostically Unfavorable Rhabdomyosarcoma Type and Its Necessary Distinction from Embryonal Rhabdomyosarcoma --;Malignant Peripheral Neuroectodermal Tumor --;Leiomyosarcoma --;Malignant Peripheral Nerve Sheath Tumors --;Rare Soft Tissue Sarcomas.
SUMMARY OR ABSTRACT
Text of Note
Soft tissue tumors are a very heterogeneous group of tumors in terms of histogenesis, morphology, cytogenetics, molecular biology, clinical manifestation, and prognosis.