S3926 Not All Colon Masses Are Adenocarcinoma: An Unusual Case of Mantle Cell Lymphoma

Introduction: While adenocarcinoma accounts for the overwhelming majority of colorectal malignancies, it is crucial to consider alternative and less common pathologies when evaluating colonic masses. These include lymphomas, carcinoid tumors, neuroendocrine tumors, and squamous cell carcinoma—each with distinct pathophysiology, clinical progression, and treatment strategies. Failure to consider these differential diagnoses can delay appropriate therapy and impact patient outcomes. We present a rare case of mantle cell lymphoma (MCL), an uncommon gastrointestinal lymphoma, presenting as an isolated cecal mass that was initially suspected to be adenocarcinoma based on endoscopic appearance. Case Description/Methods: A 70-year-old man with a history of coronary artery disease and longstanding iron deficiency anemia was referred for evaluation of abdominal pain, worsening anemia, and unintentional weight loss. As part of his workup, both esophagogastroduodenoscopy (EGD) and colonoscopy were performed. The EGD was grossly unremarkable. However, colonoscopy revealed a large, fungating, and partially obstructing mass within the cecum extending into the ileocecal valve. Biopsies of the lesion confirmed the unexpected diagnosis of mantle cell lymphoma. Further staging with positron emission tomography-computed tomography revealed intussusception at the ileocecal junction and mesenteric lymphadenopathy, but no evidence of distant metastatic disease. Given the lack of obstructive symptoms, surgical intervention was deferred. The patient was managed with rituximab, lenalidomide, and localized cecal radiation and showed favorable clinical response. Discussion: MCL is a rare subtype of B-cell non-Hodgkin lymphoma. While it typically presents generalized lymphadenopathy, gastrointestinal involvement can occur in up to one-third of patients. GI involvement often presents as multiple lymphomatous polyps but can also appear as isolated mass lesions. This case highlights the importance of maintaining a broad differential when evaluating colonic lesions. Early tissue diagnosis is essential, as the management of lymphomas differs significantly from adenocarcinomas and relies primarily on systemic rather than surgical therapy.

Authors

Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001143164.42385.52
Primary Topic
Lymphoma Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
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article

S3926 Not All Colon Masses Are Adenocarcinoma: An Unusual Case of Mantle Cell Lymphoma

John Erikson Yap, Benjamin Gow-Lee, Jessica Schmitt
The American Journal of Gastroenterology
Lymphoma Diagnosis and Treatment
article

S3926 Not All Colon Masses Are Adenocarcinoma: An Unusual Case of Mantle Cell Lymphoma

John Erikson Yap, Benjamin Gow-Lee, Jessica Schmitt
article en

Abstract

Introduction: While adenocarcinoma accounts for the overwhelming majority of colorectal malignancies, it is crucial to consider alternative and less common pathologies when evaluating colonic masses. These include lymphomas, carcinoid tumors, neuroendocrine tumors, and squamous cell carcinoma—each with distinct pathophysiology, clinical progression, and treatment strategies. Failure to consider these differential diagnoses can delay appropriate therapy and impact patient outcomes. We present a rare case of mantle cell lymphoma (MCL), an uncommon gastrointestinal lymphoma, presenting as an isolated cecal mass that was initially suspected to be adenocarcinoma based on endoscopic appearance. Case Description/Methods: A 70-year-old man with a history of coronary artery disease and longstanding iron deficiency anemia was referred for evaluation of abdominal pain, worsening anemia, and unintentional weight loss. As part of his workup, both esophagogastroduodenoscopy (EGD) and colonoscopy were performed. The EGD was grossly unremarkable. However, colonoscopy revealed a large, fungating, and partially obstructing mass within the cecum extending into the ileocecal valve. Biopsies of the lesion confirmed the unexpected diagnosis of mantle cell lymphoma. Further staging with positron emission tomography-computed tomography revealed intussusception at the ileocecal junction and mesenteric lymphadenopathy, but no evidence of distant metastatic disease. Given the lack of obstructive symptoms, surgical intervention was deferred. The patient was managed with rituximab, lenalidomide, and localized cecal radiation and showed favorable clinical response. Discussion: MCL is a rare subtype of B-cell non-Hodgkin lymphoma. While it typically presents generalized lymphadenopathy, gastrointestinal involvement can occur in up to one-third of patients. GI involvement often presents as multiple lymphomatous polyps but can also appear as isolated mass lesions. This case highlights the importance of maintaining a broad differential when evaluating colonic lesions. Early tissue diagnosis is essential, as the management of lymphomas differs significantly from adenocarcinomas and relies primarily on systemic rather than surgical therapy.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 54%
Lymphoma Diagnosis and Treatment
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