Intramammary Angiomatoid Fibrous Histiocytoma, a Rare
Journal
Case reports in pathology
ISSN: 2090-6781
Titre abrégé: Case Rep Pathol
Pays: United States
ID NLM: 101576609
Informations de publication
Date de publication:
2019
2019
Historique:
received:
04
03
2019
revised:
19
04
2019
accepted:
07
05
2019
entrez:
26
6
2019
pubmed:
27
6
2019
medline:
27
6
2019
Statut:
epublish
Résumé
Angiomatoid fibrous histiocytoma (AFH) is a rare soft tissue tumor that is most commonly reported to arise in the subcutaneous tissues of the upper extremities in adolescents and young adults. At present, the WHO classifies this neoplasm as a tumor of uncertain differentiation. AFH is most often clinically regarded as a tumor of intermediate risk due to low reported rates of recurrence and only rare occurrences of metastases. Its histomorphological hallmarks are a prominent lymphoid cuff surrounding a spindle cell neoplasm with syncytial-appearing cytoplasm. Several variant morphologies have been described. Genetically, the tumor is characterized by translocations involving the
Identifiants
pubmed: 31236300
doi: 10.1155/2019/9012878
pmc: PMC6545754
doi:
Types de publication
Case Reports
Langues
eng
Pagination
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