PEComa with metastatic pulmonary embolism upon presentation: A case report

Perivascular epithelioid cell tumors (PEComas) are rare mesenchymal neoplasms with an incidence of approximately 0.3 per million. They exhibit histological and immunohistochemical features that overlap with angiomyolipomas and clear cell tumors. PEComas predominantly affect women and are either classified as being linked to tuberous sclerosis or are classified as PEComas-Not Otherwise Specified which means that their origin is not linked to tuberous sclerosis. They often arise from the genitourinary tract. The malignant potential of these tumors is determined by factors such as size (>5 cm), mitotic activity, necrosis, and vascular invasion. Treatment involves resection and mTOR inhibitors. Standardized treatment protocols are lacking due to rarity of the pathology, so each occurrence is considered on a case-by-case basis. A 69-year-old woman with dyspnea underwent CT imaging, revealing a large renal mass, a liver lesion, lung nodules, enlarged hilar lymph nodes, and a pulmonary embolism. Subsequent FDG-PET-CT confirmed FDG-avid lesions, with uptake of the pulmonary emboli suggesting their malignant origin. A subsequent liver biopsy diagnosed a malignant PEComa. MRI demonstrated T2 hyperintensity, restricted diffusion and postcontrast enhancement. Treatment with Everolimus resulted in a partial response of all lesions on 3-month follow-up imaging. PEComas were first recognized by the World Health Organization in 2002 and often present with nonspecific symptoms. They may manifest with metastatic disease at the time of diagnosis. This case highlights metastatic pulmonary embolism as an initial presentation. PEComas pose diagnostic challenges due to their nonspecific imaging findings and varied presentations. This case underscores their potential for aggressive behavior and the role of mTOR inhibitors. Despite successful treatment, the prognosis remains variable, necessitating multidisciplinary management and long-term surveillance. Early biopsy and molecular profiling are critical for optimizing outcomes. With this case report, we hope to bring attention to the possibility of pulmonary emboli being of metastatic origin when found in the context of a pre-existent oncological disease.

Authors

Institutions

Publication Details

Journal
Radiology Case Reports
Published
2025-06-24
DOI
https://doi.org/10.1016/j.radcr.2025.06.009
Primary Topic
Tuberous Sclerosis Complex Research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

PEComa with metastatic pulmonary embolism upon presentation: A case report

Emanuele Avola, Naïk Vietti Violi, David C. Rotzinger, Thomas Saliba
Radiology Case Reports
Tuberous Sclerosis Complex Research
article

PEComa with metastatic pulmonary embolism upon presentation: A case report

Emanuele Avola, Naïk Vietti Violi, David C. Rotzinger, Thomas Saliba
article en

Abstract

Perivascular epithelioid cell tumors (PEComas) are rare mesenchymal neoplasms with an incidence of approximately 0.3 per million. They exhibit histological and immunohistochemical features that overlap with angiomyolipomas and clear cell tumors. PEComas predominantly affect women and are either classified as being linked to tuberous sclerosis or are classified as PEComas-Not Otherwise Specified which means that their origin is not linked to tuberous sclerosis. They often arise from the genitourinary tract. The malignant potential of these tumors is determined by factors such as size (>5 cm), mitotic activity, necrosis, and vascular invasion. Treatment involves resection and mTOR inhibitors. Standardized treatment protocols are lacking due to rarity of the pathology, so each occurrence is considered on a case-by-case basis. A 69-year-old woman with dyspnea underwent CT imaging, revealing a large renal mass, a liver lesion, lung nodules, enlarged hilar lymph nodes, and a pulmonary embolism. Subsequent FDG-PET-CT confirmed FDG-avid lesions, with uptake of the pulmonary emboli suggesting their malignant origin. A subsequent liver biopsy diagnosed a malignant PEComa. MRI demonstrated T2 hyperintensity, restricted diffusion and postcontrast enhancement. Treatment with Everolimus resulted in a partial response of all lesions on 3-month follow-up imaging. PEComas were first recognized by the World Health Organization in 2002 and often present with nonspecific symptoms. They may manifest with metastatic disease at the time of diagnosis. This case highlights metastatic pulmonary embolism as an initial presentation. PEComas pose diagnostic challenges due to their nonspecific imaging findings and varied presentations. This case underscores their potential for aggressive behavior and the role of mTOR inhibitors. Despite successful treatment, the prognosis remains variable, necessitating multidisciplinary management and long-term surveillance. Early biopsy and molecular profiling are critical for optimizing outcomes. With this case report, we hope to bring attention to the possibility of pulmonary emboli being of metastatic origin when found in the context of a pre-existent oncological disease.

Radiology Case ReportsVol. 20(9)
Centre Hospitalier Universitaire Vaudois (CH)
Zero hunger
Openalex Percentile: Top 80%
Tuberous Sclerosis Complex Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.