Work

Mesenteric Inflammatory Myofibroblastic Tumor in an Infant: A Case Report and Literature Review

Year: 2025

Type: article

Abstract: Inflammatory myofibroblastic tumor (IMT) is a rare mesenchymal neoplasm predominantly affecting children and young adults. Here, we present a case of IMT incidentally discovered in the mesentery of a six-month-old infant, managed through radical surgery. The patient initially presented with decreased oral intake and post-feeding vomiting, leading to the discovery of a large pelvic mass. Following comprehensive evaluation and multidisciplinary management, including surgical excision, the patient experienced a favorable clinical outcome. Histopathological examination confirmed the diagnosis of IMT, highlighting the importance of accurate diagnosis and appropriate management strategies for this rare entity.

Source: Cureus

DOI: 10.7759/cureus.83700

Authors: Rola Abu Alwafa, Amna Akkawi, Qutaiba Mahmoud, Jehad I Zuhd, Samer Bustame

Institution: An-Najah National University

Language: English