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 sixmonth-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.

العنوان

cureus

الناشر

springer nature

بلد الناشر

الولايات المتحدة الأمريكية

نوع المنشور

Both (Printed and Online)

المجلد

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السنة

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الصفحات

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