| Literature DB >> 31669060 |
Abstract
Hemangiopericytoma and fibrosarcoma represented at one time two of the most common diagnoses in soft tissue pathology. Both terms are now largely extinct. This article will review the clinicopathologic, immunohistochemical and molecular genetic advances that have led to these changes, and review the pathologic features of a select group of soft tissue tumors previously classified as hemangiopericytoma or fibrosarcoma.Entities:
Keywords: Fibrosarcoma; Hemangiopericytoma; Immunohistochemistry; Molecular genetics; Solitary fibrous tumor
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Year: 2019 PMID: 31669060 DOI: 10.1016/j.humpath.2019.10.001
Source DB: PubMed Journal: Hum Pathol ISSN: 0046-8177 Impact factor: 3.466