Metastatic Adrenal PEComa: Case Report and Short Review of the Literature

被引：3

作者：

Battistella, Enrico ^{[1
]}

Pomba, Luca ^{[1
]}

Mirabella, Marica ^{[1
]}

Gregianin, Michele ^{[2
]}

Scapinello, Antonio ^{[3
]}

Volante, Marco ^{[4
]}

Toniato, Antonio ^{[1
]}

机构：

[1] IOV IRCCS, Veneto Inst Oncol, Dept Surg, Endocrine Surg Unit, Via Gattamelata 64, I-35128 Padua, Italy

[2] IOV IRCCS, Veneto Inst Oncol, Dept Nucl Med, Via Gattamelata 64, I-35128 Padua, Italy

[3] IOV IRCCS, Veneto Inst Oncol, Pathol Unit, Via Gattamelata 64, I-35128 Padua, Italy

[4] Univ Turin, Dept Oncol, Via Giuseppe Verdi 8, I-10124 Turin, Italy

来源：

MEDICINA-LITHUANIA | 2023年 / 59卷 / 01期

关键词：

PEComa; adrenal incidentaloma; metastatic PEComa; EPITHELIOID CELL TUMOR; SURGERY; UTERUS;

D O I：

10.3390/medicina59010149

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

PEComa has become a widely accepted entity, and increased recognition has led to descriptions of this tumor in a wide variety of anatomic sites, including the adrenal gland. PEComa (perivascular epithelioid cell tumor) is a mesenchymal tumor composed of perivascular cells, and the most frequent sites of PEComas are the uterus and retroperitoneum. The incidence is <1 per 1,000,000 people. We report a case of adrenal metastatic PEComa in a 63-year-old man discovered by a spontaneous hematoma of the rectus abdominis. In our case, PEComa of the adrenal gland was a significant diagnostic dilemma as the morphologic and immunophenotypic features of this neoplasm may easily be confused with those of other more commonly encountered lesions.

引用

页数：6

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