Small Cell Neuroendocrine Carcinoma of the Gallbladder: Natural History and Therapeutic Challenges

Small cell neuroendocrine carcinoma (SNEC) of the gallbladder is an extremely rare and aggressive primary gallbladder malignancy with poor prognosis. A 65-year-old woman presented with constipation followed by jaundice and right upper quadrant pain one month later. Imaging revealed a porta hepatis mass with hepatic and duodenal involvement. Fine needle aspiration confirmed metastatic small cell carcinoma positive for synaptophysin, chromogranin, and CDX2 with Ki-67 >70%. Despite planned platinum-etoposide chemotherapy, rapid disease progression with inferior vena cava invasion precluded treatment. The patient died 13 weeks after symptom onset. This case demonstrates the aggressive natural history of gallbladder SNEC. Early tissue diagnosis and prompt platinum-etoposide chemotherapy initiation while performance status permits remain critical for meaningful survival benefit.

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Publication Details

Journal
Cureus
Published
2025-09-27
DOI
https://doi.org/10.7759/cureus.93358
Primary Topic
Neuroendocrine Tumor Research Advances
Type
article
Field-Weighted Citation Impact
0.00
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article

Small Cell Neuroendocrine Carcinoma of the Gallbladder: Natural History and Therapeutic Challenges

Niket Shah, Mukta Sharma, Alicia Edwards, Nasreen Al-Qadi et al.
Cureus
Neuroendocrine Tumor Research Advances
article

Small Cell Neuroendocrine Carcinoma of the Gallbladder: Natural History and Therapeutic Challenges

Niket Shah, Mukta Sharma, Alicia Edwards, Nasreen Al-Qadi, Jason Law
article en

Abstract

Small cell neuroendocrine carcinoma (SNEC) of the gallbladder is an extremely rare and aggressive primary gallbladder malignancy with poor prognosis. A 65-year-old woman presented with constipation followed by jaundice and right upper quadrant pain one month later. Imaging revealed a porta hepatis mass with hepatic and duodenal involvement. Fine needle aspiration confirmed metastatic small cell carcinoma positive for synaptophysin, chromogranin, and CDX2 with Ki-67 >70%. Despite planned platinum-etoposide chemotherapy, rapid disease progression with inferior vena cava invasion precluded treatment. The patient died 13 weeks after symptom onset. This case demonstrates the aggressive natural history of gallbladder SNEC. Early tissue diagnosis and prompt platinum-etoposide chemotherapy initiation while performance status permits remain critical for meaningful survival benefit.

CureusVol. 17(9)
Michigan State University (US)
Openalex Percentile: Top 64%
Neuroendocrine Tumor Research Advances
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