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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.
Abstract:
Mucosa-associated lymphoid tissue lymphomas (MALT lymphoma) are well known, but colonic MALT lymphomas are extremely rare. We report the first case of mucosa-associated lymphoid tissue (MALT) lymphoma in the cecum from India presenting as acute intestinal obstruction with mass in right iliac fossa showing diffuse thickening of ascending colon and caecum with obliterated lumen along with nodular mass on CECT scan of abdomen. On video colonoscopy, circumferential ulcerated growth was seen at cecum, and the rest of the colon was normal. Multiple biopsies from growth suggested malignancy. Right hemicolectomy was performed. The histopathology of resected specimen demonstrated low-grade B-cell MALT lymphoma of the cecum, and the depth of invasion was up to the muscular layer. This was confirmed by immunohistochemistry.
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