Abdominal wall inflammatory myofibroblastic tumor initially misdiagnosed as leiomyoma: a rare case report

Read full text
Authors: Youssef T. Youssef, Mohamed Ibrahem Baklola, Mohamed Abdelhai Mahmoud, Mohammed R Arrabyee, Eslam Ashraf Mustafa Ibrahim, Tamer Youssef
Cited by: 0
References: 11

Abstract

Inflammatory myofibroblastic tumor is a rare mesenchymal neoplasm that most commonly arises in the lung and intra-abdominal soft tissues. Involvement of the anterior abdominal wall is exceptionally uncommon and can lead to diagnostic difficulty. We report a case of a 34-year-old male who presented with a painless, enlarging supraumbilical mass. Imaging demonstrated a heterogeneously enhancing lesion with intra-abdominal extension and close proximity to bowel loops. Core needle biopsy suggested a benign spindle cell tumor consistent with leiomyoma. Due to diagnostic uncertainty, complete surgical excision was performed. Final histopathology confirmed inflammatory myofibroblastic tumor with clear margins. The postoperative course was uneventful, and follow-up was arranged because of the risk of recurrence. This case highlights the diagnostic challenges of abdominal wall inflammatory myofibroblastic tumors and emphasizes the role of surgery in achieving definitive diagnosis and treatment.

Fields of Study & Subjects

IgG4-Related and Inflammatory Diseases Soft tissue tumor case studies Gastrointestinal Tumor Research and Treatment

Publication details

Journal / source
Journal of Surgical Case Reports
Volume
2026
Issue
2
Pages
rjag065–rjag065
Publication date
31 January 2026
Language
EN