# Abdominal Wall Perivascular Epithelioid Cell Tumor Mimicking an Intra-Abdominal Tumor: A Case Report

**Authors:** Saki Kubota, Yoshiaki Fujimoto, Takuya Honboh, Kosuke Hirose, Taichi Nagano, Huanlin Wang, Fumihiko Hirai, Noboru Harada, Seiya Kato, Noriaki Sadanaga, Tomoharu Yoshizumi

PMC · DOI: 10.70352/scrj.cr.25-0826 · Surgical Case Reports · 2026-03-19

## TL;DR

A rare abdominal wall tumor was mistaken for an intra-abdominal tumor, but a laparoscopic approach helped confirm its origin and guide successful surgery.

## Contribution

Highlights the diagnostic challenge of abdominal wall PEComas and advocates for a laparoscopic first-look approach in surgical planning.

## Key findings

- Abdominal wall PEComas are rare and can mimic intra-abdominal tumors on imaging.
- A laparoscopic first-look approach clarified the tumor's origin and enabled safe resection.
- The tumor showed malignant potential but had no recurrence during follow-up.

## Abstract

Perivascular epithelioid cell tumors (PEComas) are rare mesenchymal neoplasms; those arising from the abdominal wall are exceptionally uncommon. Because imaging findings are nonspecific, an abdominal wall PEComa may be mistaken for an intra-abdominal tumor, leading to diagnostic uncertainty and challenges in surgical planning.

A 25-year-old woman was referred to our hospital after a screening of the upper gastrointestinal series revealed extrinsic compression of the stomach. Cross-sectional imaging demonstrated a well-circumscribed midline mass with early enhancement and calcifications, which was initially suspected to be intra-abdominal in origin. Because the precise anatomical origin of the lesion remained unclear and malignancy could not be excluded, a laparoscopic first-look approach was employed. Intraoperative inspection confirmed that the tumor originated from the subperitoneal abdominal wall, without intraperitoneal involvement. The lesion was resected en bloc with negative margins through a limited incision. The histopathological and immunohistochemical findings were consistent with those of a PEComa with malignant potential. The postoperative course was uneventful, and no recurrence was observed during follow-up.

Abdominal wall PEComa is an extremely rare entity that can closely mimic an intra-abdominal tumor on imaging studies. When the anatomical origin of a midline mass cannot be clearly determined preoperatively, a laparoscopic first-look approach is a useful strategy for clarifying the tumor’s origin and guiding safe surgical management. Long-term follow-up is warranted because of the malignant potential of PEComas.

## Linked entities

- **Diseases:** PEComa (MONDO:0006359)

## Full-text entities

- **Diseases:** Intra-Abdominal Tumor (MESH:D000082122), PEComa (MESH:D054973), Tumor (MESH:D009369), midline (MESH:C538667), extrinsic compression (MESH:D020920)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

4 references — full list in the complete paper: https://tomesphere.com/paper/PMC13006143/full.md

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Source: https://tomesphere.com/paper/PMC13006143