Angiomatoid fibrous histiocytoma in a 25-year-old male
Open Access
- 1 June 2010
- journal article
- Published by SAGE Publications in Rare Tumors
- Vol. 2 (2) , 54-56
Abstract
Angiomatoid fibrous histiocytoma (AFH) is a rare disease that is often misdiagnosed initially. Patients can present with a clinical picture concerning for other diseases, and pathologic review is not always revealing. Molecular diagnostics are increasingly being utilized to detect gene fusions characteristic for AFH. Surgery remains the mainstay of management, and can effectively control local recurrences and metastases. Herein we describe a case report of a 25-year-old gentleman whose presentation was concerning for lymphoma. Subsequently we review of the relevant literature.Keywords
This publication has 17 references indexed in Scilit:
- Pleomorphic angiomatoid fibrous histiocytoma: a case confirmed by fluorescence in situ hybridization analysis for EWSR1 rearrangementJournal of Cutaneous Pathology, 2008
- EWSR1-CREB1 and EWSR1-ATF1 Fusion Genes in Angiomatoid Fibrous HistiocytomaClinical Cancer Research, 2007
- EWSR1‐CREB1 is the predominant gene fusion in angiomatoid fibrous histiocytomaGenes, Chromosomes and Cancer, 2007
- Fusion genes in angiomatoid fibrous histiocytomaCancer Letters, 2007
- Fusion of theEWSR1andATF1genes without expression of theMITF‐Mtranscript in angiomatoid fibrous histiocytomaGenes, Chromosomes and Cancer, 2005
- Late radiation morbidity following randomization to preoperative versus postoperative radiotherapy in extremity soft tissue sarcomaRadiotherapy and Oncology, 2005
- Malignant fibrous histiocytoma and other fibrohistiocytic tumors in pediatric patientsCancer, 2003
- Molecular genetic characterization of the EWS/ATF1 fusion gene in clear cell sarcoma of tendons and aponeurosesInternational Journal of Cancer, 2002
- Angiomatoid Fibrous HistiocytomaAnnals of Plastic Surgery, 1996
- Angiomatoid Malignant Fibrous HistiocytomaAmerican Journal of Surgical Pathology, 1990