A rare case of small cell neuroendocrine carcinoma of gallbladder origin.
Uğur Can DülgerŞahin ErdemEmine Sena CünükFatih AltıntoprakPublished in: Journal of surgical case reports (2024)
Neuroendocrine carcinomas (NECs) of the gallbladder are very rare and aggressive tumors with poor prognosis. Most of them are poorly differentiated and belong to the small cell type. We report a case of a 59-year-old woman who presented with abdominal pain and distension. Contrast-enhanced computed tomography revealed a large heterogeneous mass in the liver, adjacent to the gallbladder, and omental nodules. CA 19-9 level was elevated and ascitic fluid cytology was suspicious for malignancy. Percutaneous biopsy of the liver mass confirmed the diagnosis of small cell NEC of the gallbladder. The patient was considered inoperable and planned for chemotherapy, but she died 20 days after admission. This case illustrates the diagnostic challenges and the dismal outcome of small cell NEC of the gallbladder. Early detection and multimodal treatment are essential for improving the survival of these patients.
Keyphrases
- computed tomography
- poor prognosis
- single cell
- contrast enhanced
- magnetic resonance imaging
- rare case
- cell therapy
- magnetic resonance
- long non coding rna
- abdominal pain
- end stage renal disease
- high grade
- emergency department
- newly diagnosed
- positron emission tomography
- case report
- peritoneal dialysis
- locally advanced
- patient reported outcomes
- bone marrow
- pet ct
- protein kinase
- smoking cessation
- replacement therapy