1. Gallbladder paraganglioma with hemorrhage: A case report and literature review
- Author
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Hee Joon Kim, Young Hoe Hur, Yang Seok Koh, Yun Ho Lee, Eun Kyu Park, Chol Kyoon Cho, and Sang Hwa Song
- Subjects
medicine.medical_specialty ,Gallbladder Fundus ,business.industry ,medicine.medical_treatment ,Gallbladder ,Case Report ,Hemorrhage ,medicine.disease ,Gross examination ,Paraganglioma ,Hematoma ,medicine.anatomical_structure ,medicine ,Cholecystitis ,Etiology ,General Materials Science ,Cholecystectomy ,Radiology ,business - Abstract
Gallbladder paraganglioma (GP) is a rare tumor, with only 12 cases reported in the literature to date. Due to its rarity, clinical information of GP is insufficient. We present a case of GP in a 48-year-old female along with a literature review of all GP cases described to date. A 48-year-old female presented with intermittent right upper abdominal pain. Preoperative imaging revealed a hematoma in the gallbladder lumen without any definite etiology. Laparoscopic cholecystectomy was performed. Gross examination of the gallbladder revealed multiple small stones and a large hematoma as well as a 1.6-cm-sized polypoid mass at the gallbladder fundus. Microscopic study of the polypoid mass showed a zellballen appearance. Immunohistochemical analysis revealed that the mass was positive for synaptophysin, CD56, and chromogranin, suggesting GP. GP is difficult to diagnose because of non-specific clinical findings. Almost all GP cases are diagnosed based on histologic findings after cholecystectomy. Simple cholecystectomy was performed as a treatment in all reported cases of GP, including our case. There was no postoperative tumor recurrence or metastasis after surgery.
- Published
- 2021