PEComa: Another Member of the MiT Tumor Family?

Author:

Righi Alberto1,Dimosthenous Kypros2,Rosai Juan2

Affiliation:

1. Centro Diagnostico Italiano (CDI), Milan, Anatomic Pathology, University of Bologna, Bellaria Hospital, Bologna Italy,

2. Centro Diagnostico Italiano (CDI), Milan

Abstract

We report 2 cases of PEComa, one occurring in the colon of an 11-year-old boy and the other in the bone (fibula) of a 92-year-old woman. Both tumors consisted of nests of large epithelioid cells surrounded by a fibrovascular stroma. The nuclei were large and vesicular, with prominent centrally located nucleoli. The cytoplasm was eosinophilic, with a fine to coarse granularity. Mitoses and individual cell necrosis were infrequent. Immunohistochemically, both tumors showed strong cytoplasmic expression of HMB-45 and intense nuclear positivity for TFE3. To our knowledge, nuclear positivity for TFE3 has been previously reported in only 5 cases of PEComa. Reactivity to this marker suggests that PEComa should be added to the growing list of human tumors of the so-called MiT family gene.

Publisher

SAGE Publications

Subject

Pathology and Forensic Medicine,Surgery,Anatomy

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