# Rare presentation of ileal mucosa-associated lymphoid tissue lymphoma: a case of obstructive syndrome in a Moroccan patient

## TL;DR

A rare case of ileal MALT lymphoma in a Moroccan patient presented with an obstructive syndrome, highlighting the challenges in diagnosing this uncommon condition.

## Contribution

This paper presents a rare case of ileal MALT lymphoma with an unusual obstructive syndrome presentation in a Moroccan patient.

## Key findings

- Ileal MALT lymphoma is uncommon compared to gastric MALT lymphoma.
- Clinical and radiological assessments alone are insufficient for differentiating ileal MALT lymphoma from other tumors.
- Histopathological examination is essential for accurate diagnosis and identifying underlying disease.

## Abstract

The majority of extranodal lymphomas of the gastrointestinal tract involve the stomach and are often associated with Helicobacter pylori (H. pylori) infection. When lymphomas occur in the small intestine, diffuse large B-cell lymphomas are most common; however, mucosa-associated lymphoid tissue (MALT) lymphomas account for approximately one-third of small intestinal lymphomas. We report the case of an ileal MALT lymphoma in a 58-year-old Moroccan patient, characterized by its rare ileal localization and unusual presentation with an obstructive syndrome. Ileal MALT lymphoma is relatively uncommon compared to other gastrointestinal MALT lymphomas, such as gastric MALT lymphoma. Differentiating ileal MALT lymphoma from other tumors at this site based solely on clinical and radiological assessments can be challenging. Histopathological examination is pivotal for definitive diagnosis and for identifying underlying disease. Effective management relies on close collaboration among gastroenterologists, radiologists, surgeons, pathologists, and hematologists.