Literature DB >> 31669060

"Hey! Whatever happened to hemangiopericytoma and fibrosarcoma?" An update on selected conceptual advances in soft tissue pathology which have occurred over the past 50 years.

Andrew L Folpe1.   

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.
Copyright © 2019 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Fibrosarcoma; Hemangiopericytoma; Immunohistochemistry; Molecular genetics; Solitary fibrous tumor

Mesh:

Substances:

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


  1 in total

1.  Plexiform fibrohistiocytic tumor: a clinicopathological and immunohistochemical study of 39 tumors, with evidence for a CSF1-producing "null cell" population.

Authors:  Judith Jebastin Thangaiah; Nooshin K Dashti; Abbas Agaimy; Karen Fritchie; Andrew L Folpe
Journal:  Virchows Arch       Date:  2022-09-07       Impact factor: 4.535

  1 in total

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