Malignant perivascular epithelioid cell tumor arising in the mesentery: A case report

Yinghong Shi1, Junzu Geng2, Haizhu Xie2

  • 1Department of Radiology, Shandong Medical Imaging Research Institution, Shandong University, Jinan, Shandong 250021, P.R. China ; Department of Radiology, Yuhuangding Hospital, Yantai, Shandong 264000, P.R. China.

Oncology Letters
|July 3, 2015
PubMed

Insights

This study details a rare mesenteric perivascular epithelioid cell tumor (PEComa). Imaging revealed a large, heterogeneous mass, highlighting the diagnostic challenges of PEComas in the mesentery.

Area of Science:

  • Oncology
  • Radiology
  • Gastroenterology

Background:

  • Primary perivascular epithelioid cell tumors (PEComas) of the mesentery are exceptionally rare.
  • Limited data exists on the clinical and imaging characteristics of these rare mesenteric tumors.

Purpose of the Study:

  • To report a case of a primary mesenteric PEComa.
  • To describe the computed tomography (CT) findings associated with this rare tumor.

Main Methods:

  • A case report of a 48-year-old female patient with a mesenteric PEComa.
  • Detailed analysis of abdominal plain and contrast-enhanced CT imaging features.

Main Results:

  • A large (12.5×8.5 cm), heterogeneous, partially ill-defined mesenteric mass was identified.
  • Contrast-enhanced CT showed nonhomogeneous enhancement with hypodense areas and multiple tumor vessels during the arterial phase.

Conclusions:

  • Perivascular epithelioid cell tumors (PEComas) should be included in the differential diagnosis for mesenteric lesions.
  • Distinguishing PEComas from other mesenteric masses based solely on imaging criteria can be challenging.