S3906 Rare Colonic Diffuse Large B-Cell Lymphoma With Aggressive Progression

Introduction: Primary gastrointestinal lymphomas comprise 1–4% of all gastrointestinal malignancies, most commonly involving the stomach or small intestine. Primary colonic lymphoma is rare, accounting for only 0.2–1% of colorectal cancers. We present a case of diffuse large B-cell lymphoma (DLBCL) of the ascending colon presenting as an obstructing mass with atypical and aggressive progression. Case Description/Methods: A 71-year-old man with type 2 diabetes mellitus presented with 1 week of right lower quadrant abdominal pain and decreased bowel movements, following 6 months of intermittent constipation. He denied weight loss, gastrointestinal bleeding, or family history of malignancy, and had never undergone colonoscopy. Laboratory studies revealed microcytic anemia (hemoglobin 11.4 g/dL). Computed tomography (CT) imaging of the abdomen and pelvis showed an 8.9 × 7.7 cm cecal mass and a 4.8 × 3.9 cm mesenteric nodal mass. Colonoscopy revealed a large, friable, obstructing mass in the ascending colon. Biopsies confirmed DLBCL with a Ki-67 proliferation index >90%. Staging CT identified an additional mass in the pancreatic body and tail, concerning for metastatic disease. The patient was discharged with plans for outpatient chemotherapy and multidisciplinary follow-up. Four weeks later, positron emission tomography/CT demonstrated widespread hypermetabolic disease involving the colon (including the rectosigmoid region), pancreas (with interval enlargement), peritoneum, and multiple lymph node basins. Discussion: Primary colonic DLBCL is a rare malignancy that can mimic colorectal adenocarcinoma. Nonspecific symptoms such as abdominal pain and altered bowel habits often delay diagnosis. The cecum is a common site due to its abundant lymphoid tissue. Diagnosis requires endoscopic biopsy, with a high Ki-67 index indicating aggressive disease behavior. While lymphatic spread is typical, pancreatic involvement is rarely reported and suggests advanced disease. Management generally involves CHOP-based chemotherapy, with surgery or radiotherapy considered in select cases. This case underscores the importance of including lymphoma in the differential diagnosis of colonic masses, particularly in older adults presenting without classic B symptoms.

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Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001143084.55694.83
Primary Topic
Lymphoma Diagnosis and Treatment
Type
article
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article

S3906 Rare Colonic Diffuse Large B-Cell Lymphoma With Aggressive Progression

Kovil Ramasamy, George Koutras, Taofeek Kolade
The American Journal of Gastroenterology
Lymphoma Diagnosis and Treatment
article

S3906 Rare Colonic Diffuse Large B-Cell Lymphoma With Aggressive Progression

Kovil Ramasamy, George Koutras, Taofeek Kolade
article en

Abstract

Introduction: Primary gastrointestinal lymphomas comprise 1–4% of all gastrointestinal malignancies, most commonly involving the stomach or small intestine. Primary colonic lymphoma is rare, accounting for only 0.2–1% of colorectal cancers. We present a case of diffuse large B-cell lymphoma (DLBCL) of the ascending colon presenting as an obstructing mass with atypical and aggressive progression. Case Description/Methods: A 71-year-old man with type 2 diabetes mellitus presented with 1 week of right lower quadrant abdominal pain and decreased bowel movements, following 6 months of intermittent constipation. He denied weight loss, gastrointestinal bleeding, or family history of malignancy, and had never undergone colonoscopy. Laboratory studies revealed microcytic anemia (hemoglobin 11.4 g/dL). Computed tomography (CT) imaging of the abdomen and pelvis showed an 8.9 × 7.7 cm cecal mass and a 4.8 × 3.9 cm mesenteric nodal mass. Colonoscopy revealed a large, friable, obstructing mass in the ascending colon. Biopsies confirmed DLBCL with a Ki-67 proliferation index >90%. Staging CT identified an additional mass in the pancreatic body and tail, concerning for metastatic disease. The patient was discharged with plans for outpatient chemotherapy and multidisciplinary follow-up. Four weeks later, positron emission tomography/CT demonstrated widespread hypermetabolic disease involving the colon (including the rectosigmoid region), pancreas (with interval enlargement), peritoneum, and multiple lymph node basins. Discussion: Primary colonic DLBCL is a rare malignancy that can mimic colorectal adenocarcinoma. Nonspecific symptoms such as abdominal pain and altered bowel habits often delay diagnosis. The cecum is a common site due to its abundant lymphoid tissue. Diagnosis requires endoscopic biopsy, with a high Ki-67 index indicating aggressive disease behavior. While lymphatic spread is typical, pancreatic involvement is rarely reported and suggests advanced disease. Management generally involves CHOP-based chemotherapy, with surgery or radiotherapy considered in select cases. This case underscores the importance of including lymphoma in the differential diagnosis of colonic masses, particularly in older adults presenting without classic B symptoms.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 54%
Lymphoma Diagnosis and Treatment
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S3906 Rare Colonic Diffuse Large B-Cell Lymphoma With Aggressive Progression — Kovil Ramasamy, George Koutras, et al. · The American Journal of Gastroenterology (2025) | TGRS Research Map | TGRS