S3921 A Case of Primary Colonic Poorly Differentiated Neuroendocrine Carcinoma With Small Cell Features

Introduction: Colonic neuroendocrine carcinoma (NEC) is a rare, aggressive malignancy that usually presents in advanced stages, featuring rapid growth, local invasion, and distant metastasis. Median overall survival is typically less than 9 months. We report a case of poorly differentiated primary colonic NEC with small cell features. Case Description/Methods: A 49-year-old man with history of tobacco use presented after 3 days of worsening, diffuse abdominal pain and constipation. In the emergency department, vitals were stable, but white blood cell was 23.3K U/L. Computed tomography (CT) abdomen/pelvis with intravenous (IV) contrast revealed a large left upper quadrant mass (23.7 × 14.4 × 11.3 cm) with central necrosis, ill-defined hepatic lesions, a left lung base mass (4.3 × 1.7 × 3 cm), and significant lymphadenopathy. Endoscopic evaluation via esophagogastroduodenoscopy demonstrated severe esophagitis and gastritis. Colonoscopy identified a 7 cm fungating, infiltrative mass at the splenic flexure causing partial luminal obstruction and oozing. Biopsies of both colonic and hepatic lesions confirmed high-grade, poorly differentiated NEC. Immunohistochemistry was positive for synaptophysin and CD56 with a Ki-67 index >95%, but negative for chromogranin, CDX2, and CK20. Clinical course was complicated by sepsis and intra-abdominal abscess with colonic fistulization, requiring percutaneous drain placement. Repeat CT showed expansion of the mass to 32 × 18 × 21 cm. Despite broad-spectrum IV antibiotics and plans for carboplatin/etoposide chemotherapy, the extent of metastatic disease precluded surgical intervention, prompting early goals-of care discussions and transition to hospice. Discussion: Colonic NECs account for <1% of colorectal cancers. Due to their aggressive growth pattern and proclivity for both infiltration as well as metastasis, multiple peritoneal structures may become involved concomitantly. This often necessitates advanced endoscopic techniques for visualization and mitigation of intestinal complications such as obstruction. The massive tumor size at diagnosis (>30 cm) alongside metastatic disease and rare complications of both fistula and abscess formation highlight this report as an exceptionally severe case. Although platinum-based chemotherapy offers modest response rates (∼40%–50%), outcomes remain poor, with median survival under 12 months. This case highlights the challenges in addressing advanced colonic NEC and the paramountcy of early, multidisciplinary intervention to improve management strategies.

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Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001143144.01159.ae
Primary Topic
Neuroendocrine Tumor Research Advances
Type
article
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article

S3921 A Case of Primary Colonic Poorly Differentiated Neuroendocrine Carcinoma With Small Cell Features

Fahad Sarvari, Mohammed Zaman, Luqman Baloch, Sultan Ahmed et al.
The American Journal of Gastroenterology
Neuroendocrine Tumor Research Advances
article

S3921 A Case of Primary Colonic Poorly Differentiated Neuroendocrine Carcinoma With Small Cell Features

Fahad Sarvari, Mohammed Zaman, Luqman Baloch, Sultan Ahmed, Saad Rashid, Altaf Dawood
article en

Abstract

Introduction: Colonic neuroendocrine carcinoma (NEC) is a rare, aggressive malignancy that usually presents in advanced stages, featuring rapid growth, local invasion, and distant metastasis. Median overall survival is typically less than 9 months. We report a case of poorly differentiated primary colonic NEC with small cell features. Case Description/Methods: A 49-year-old man with history of tobacco use presented after 3 days of worsening, diffuse abdominal pain and constipation. In the emergency department, vitals were stable, but white blood cell was 23.3K U/L. Computed tomography (CT) abdomen/pelvis with intravenous (IV) contrast revealed a large left upper quadrant mass (23.7 × 14.4 × 11.3 cm) with central necrosis, ill-defined hepatic lesions, a left lung base mass (4.3 × 1.7 × 3 cm), and significant lymphadenopathy. Endoscopic evaluation via esophagogastroduodenoscopy demonstrated severe esophagitis and gastritis. Colonoscopy identified a 7 cm fungating, infiltrative mass at the splenic flexure causing partial luminal obstruction and oozing. Biopsies of both colonic and hepatic lesions confirmed high-grade, poorly differentiated NEC. Immunohistochemistry was positive for synaptophysin and CD56 with a Ki-67 index >95%, but negative for chromogranin, CDX2, and CK20. Clinical course was complicated by sepsis and intra-abdominal abscess with colonic fistulization, requiring percutaneous drain placement. Repeat CT showed expansion of the mass to 32 × 18 × 21 cm. Despite broad-spectrum IV antibiotics and plans for carboplatin/etoposide chemotherapy, the extent of metastatic disease precluded surgical intervention, prompting early goals-of care discussions and transition to hospice. Discussion: Colonic NECs account for <1% of colorectal cancers. Due to their aggressive growth pattern and proclivity for both infiltration as well as metastasis, multiple peritoneal structures may become involved concomitantly. This often necessitates advanced endoscopic techniques for visualization and mitigation of intestinal complications such as obstruction. The massive tumor size at diagnosis (>30 cm) alongside metastatic disease and rare complications of both fistula and abscess formation highlight this report as an exceptionally severe case. Although platinum-based chemotherapy offers modest response rates (∼40%–50%), outcomes remain poor, with median survival under 12 months. This case highlights the challenges in addressing advanced colonic NEC and the paramountcy of early, multidisciplinary intervention to improve management strategies.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 56%
Neuroendocrine Tumor Research Advances
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