MALT Lymphoma of Caecum Presenting as Acute Intestinal Obstruction: A Case Report

Vinod Jain1, Samir Misra1, Faraz Ahmad1

  • 1Department of Surgery, C. S. M. Medical University, B-41, Mahanagar Extension, Lucknow, UP India 226006.

Insights

This report details the first Indian case of cecal mucosa-associated lymphoid tissue (MALT) lymphoma, a rare condition. The MALT lymphoma presented as acute intestinal obstruction, highlighting its unusual presentation and location.

Area of Science:

  • Gastroenterology
  • Oncology
  • Pathology

Background:

  • Mucosa-associated lymphoid tissue (MALT) lymphomas are recognized lymphoid malignancies.
  • MALT lymphomas originating in the colon are exceptionally rare, with limited documented cases.
  • Colonic MALT lymphomas pose diagnostic challenges due to their rarity and varied presentations.

Purpose of the Study:

  • To report the first documented case of cecal MALT lymphoma in India.
  • To describe the clinical, radiological, and pathological features of this rare entity.
  • To emphasize the importance of considering MALT lymphoma in the differential diagnosis of colonic masses.

Main Methods:

  • Case presentation of a patient with acute intestinal obstruction.
  • Diagnostic workup including CECT scan and video colonoscopy with biopsies.
  • Surgical resection (right hemicolectomy) and histopathological examination with immunohistochemistry.

Main Results:

  • A 35-year-old male presented with symptoms of acute intestinal obstruction.
  • CECT revealed a mass in the right iliac fossa with diffuse thickening and lumen obliteration of the ascending colon and cecum.
  • Video colonoscopy showed circumferential ulcerated growth at the cecum; histopathology confirmed low-grade B-cell MALT lymphoma invading the muscular layer.

Conclusions:

  • Cecal MALT lymphoma is an extremely rare malignancy that can present as acute intestinal obstruction.
  • Multimodality imaging and endoscopic evaluation are crucial for diagnosis.
  • Histopathology and immunohistochemistry are essential for definitive diagnosis and classification of MALT lymphoma.

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