S3749 Beyond Adenocarcinoma: A Case of Primary Colonic Diffuse Large B-Cell Lymphoma

Introduction: Primary gastrointestinal lymphomas are rare, with the colon representing an uncommon site of involvement. Adenocarcinoma is the most common colorectal malignancy with diffuse large B-cell lymphoma (DLBCL) of the colon accounting for less than 1% of cases. DLBCL requires prompt recognition due to its distinct clinical behavior and management. Case Description/Methods: A 50-year-old previously healthy man presented with 5 days of worsening right-sided abdominal cramping, bloating, and non-bloody emesis. He denied hematochezia, changes in bowel habits, or prior gastrointestinal history. However, he reported mild unintentional weight loss and night sweats over several months. Computed tomography (CT) of the abdomen and pelvis revealed a 12.4 cm centrally necrotic soft tissue mass involving the ascending colon and hepatic flexure with mildly enlarged retroperitoneal and pericolic lymph nodes. No bowel obstruction or metastatic disease was noted. Magnetic resonance imaging (MRI) demonstrated aneurysmal dilation without upstream obstruction—features concerning for lymphoma. Colonoscopy revealed a friable, ulcerated, and traversable mass extending from the cecum to the mid-ascending colon. Biopsies confirmed primary colonic DLBCL, non–germinal center subtype. Immunohistochemistry (IHC) was positive for CD20 and BCL6 and negative for CD3 and CD10, with a high Ki-67 proliferation index of 70–80%. Fluorescence in situ hybridization (FISH) analysis showed no MYC, BCL2, or BCL6 rearrangements. The patient was referred to hematology-oncology and initiated on systemic chemotherapy (R-CHOP). Discussion: Primary colonic DLBCL is an exceptionally rare malignancy that may initially resemble colorectal adenocarcinoma. However, key distinguishing features—such as systemic B symptoms, aneurysmal dilation with luminal preservation, absence of hematochezia, and a friable yet traversable mass on endoscopy—should raise suspicion for lymphoma. Histologic confirmation is essential, as treatment with systemic chemotherapy differs substantially from the surgical resection typically employed for colorectal adenocarcinoma. This case underscores the importance of maintaining a broad differential diagnosis when evaluating colonic masses to ensure timely recognition, appropriate oncologic management, and optimal patient outcomes.

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Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001142456.09203.1f
Primary Topic
Lymphoma Diagnosis and Treatment
Type
article
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0.00
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article

S3749 Beyond Adenocarcinoma: A Case of Primary Colonic Diffuse Large B-Cell Lymphoma

Tanima Jana, Ruth Bell, Aastha Bharwad, Varun Vemulapalli et al.
The American Journal of Gastroenterology
Lymphoma Diagnosis and Treatment
article

S3749 Beyond Adenocarcinoma: A Case of Primary Colonic Diffuse Large B-Cell Lymphoma

Tanima Jana, Ruth Bell, Aastha Bharwad, Varun Vemulapalli, Cristina Natha, Alexander Banerjee
article en

Abstract

Introduction: Primary gastrointestinal lymphomas are rare, with the colon representing an uncommon site of involvement. Adenocarcinoma is the most common colorectal malignancy with diffuse large B-cell lymphoma (DLBCL) of the colon accounting for less than 1% of cases. DLBCL requires prompt recognition due to its distinct clinical behavior and management. Case Description/Methods: A 50-year-old previously healthy man presented with 5 days of worsening right-sided abdominal cramping, bloating, and non-bloody emesis. He denied hematochezia, changes in bowel habits, or prior gastrointestinal history. However, he reported mild unintentional weight loss and night sweats over several months. Computed tomography (CT) of the abdomen and pelvis revealed a 12.4 cm centrally necrotic soft tissue mass involving the ascending colon and hepatic flexure with mildly enlarged retroperitoneal and pericolic lymph nodes. No bowel obstruction or metastatic disease was noted. Magnetic resonance imaging (MRI) demonstrated aneurysmal dilation without upstream obstruction—features concerning for lymphoma. Colonoscopy revealed a friable, ulcerated, and traversable mass extending from the cecum to the mid-ascending colon. Biopsies confirmed primary colonic DLBCL, non–germinal center subtype. Immunohistochemistry (IHC) was positive for CD20 and BCL6 and negative for CD3 and CD10, with a high Ki-67 proliferation index of 70–80%. Fluorescence in situ hybridization (FISH) analysis showed no MYC, BCL2, or BCL6 rearrangements. The patient was referred to hematology-oncology and initiated on systemic chemotherapy (R-CHOP). Discussion: Primary colonic DLBCL is an exceptionally rare malignancy that may initially resemble colorectal adenocarcinoma. However, key distinguishing features—such as systemic B symptoms, aneurysmal dilation with luminal preservation, absence of hematochezia, and a friable yet traversable mass on endoscopy—should raise suspicion for lymphoma. Histologic confirmation is essential, as treatment with systemic chemotherapy differs substantially from the surgical resection typically employed for colorectal adenocarcinoma. This case underscores the importance of maintaining a broad differential diagnosis when evaluating colonic masses to ensure timely recognition, appropriate oncologic management, and optimal patient outcomes.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 57%
Lymphoma Diagnosis and Treatment
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