| Literature DB >> 19664493 |
Paola Collini1, Poul H B Sorensen, Shreyaskumar Patel, Jean-Yves Blay, Rolf D Issels, Robert G Maki, Mikael Eriksson, Xavier Garcia del Muro.
Abstract
In the days before the term "high-grade undifferentiated pleomorphic sarcoma" came into use, one of the most common sarcoma diagnoses was "malignant fibrous histiocytoma," and before that, in an era before immunohistochemistry, "fibrosarcoma" was used to describe most sarcomas. "Spindle cell" is a descriptive phrase that denotes the cellular shape of many of the sarcomas encountered in the adult population. As a result, they are usually treated differently from small round cell sarcomas, and have different biological characteristics than those tumors and sarcomas with epithelioid morphology. As a very broad generalization, sarcomas with a spindle cell microscopic morphology occur in adults and are treated primarily with surgery and often adjuvant or neoadjuvant radiation as primary therapy. In comparison to small round cell sarcomas such as Ewing sarcoma, the use of adjuvant chemotherapy remains controversial, and the sensitivity of these tumors to chemotherapy in the metastatic setting is highly variable. In this article, we describe some of the clinical and biological characteristics of this group of sarcomas.Entities:
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Year: 2009 PMID: 19664493 DOI: 10.1053/j.seminoncol.2009.06.007
Source DB: PubMed Journal: Semin Oncol ISSN: 0093-7754 Impact factor: 4.929