- 【Updated on May 12, 2025】 Integration of CiNii Dissertations and CiNii Books into CiNii Research
- Trial version of CiNii Research Automatic Translation feature is available on CiNii Labs
- Suspension and deletion of data provided by Nikkei BP
- Regarding the recording of “Research Data” and “Evidence Data”
Perivascular Epithelioid Cell Tumor
-
- Henry B. Armah
- From the Department of Pathology, University of Pittsburgh Medical Center, Pittsburgh, Pa
-
- Anil V. Parwani
- From the Department of Pathology, University of Pittsburgh Medical Center, Pittsburgh, Pa
Description
<jats:title>Abstract</jats:title> <jats:p>Perivascular epithelioid cell tumors are mesenchymal neoplasms defined by the presence of histologically and immunohistochemically distinctive perivascular epithelioid cells. The perivascular epithelioid cell has no known normal tissue counterpart and coexpresses myoid and melanocytic markers. This tumor family shows marked female predominance and includes angiomyolipoma, clear cell sugar tumor, lymphangioleiomyomatosis, and a group of rare, morphologically and immunophenotypically similar tumors arising at a variety of visceral and soft tissue sites. This latter subset has been collectively termed perivascular epithelioid cell tumors–not otherwise specified. They are usually composed of epithelioid, but occasionally spindled, cells with clear to granular eosinophilic cytoplasm and focal perivascular accentuation. The mainstay of treatment is wide excision. Although most cases are benign, a subset behaves in a malignant fashion. Since few malignant cases have been reported, firm criteria for malignancy have yet to be established. This review focuses on the perivascular epithelioid cell tumors–not otherwise specified subset.</jats:p>
Journal
-
- Archives of Pathology & Laboratory Medicine
-
Archives of Pathology & Laboratory Medicine 133 (4), 648-654, 2009-04-01
Archives of Pathology and Laboratory Medicine
- Tweet
Details 詳細情報について
-
- CRID
- 1360294647897126272
-
- ISSN
- 15432165
- 00039985
-
- Data Source
-
- Crossref