Key result
Laparoscopic cholecystectomy for cholelithiasis incidentally reveals a rare non-secretory gallbladder paraganglioma.
Why the study?
Due to the rarity of gallbladder paraganglioma, there are diagnostic challenges and no definitive guidelines for its diagnosis and management.
Case Report (n=1)
No
Gallbladder paraganglioma is a rare incidental finding during cholecystectomy that poses diagnostic challenges due to lack of clear differentiating criteria.
Answers are grounded in this paper and cite their sources.
Heightened awareness of gallbladder paraganglioma is prudent given diagnostic pitfalls; leaves open reliable preoperative differentiating criteria.
Paraganglioma is a rare form of tumor, with secretory and non-secretory variants. Due to the rare nature of gallbladder paraganglioma (GP), there are no definitive guidelines for management. We present the case of a 35-year-old female patient who presented with intermittent right upper quadrant abdominal pain. Preoperative imaging indicated the presence of gallstones within the gallbladder lumen. Laparoscopic cholecystectomy was performed, with pathology findings consistent with a paraganglioma. The gallbladder is a rare location to find paraganglionic tissue, with its rarity posing diagnostic challenges with a lack of clear differentiating criteria between benign paraganglionic tissue (paraganglionic rests) and benign paraganglioma tumors. Given the rare nature of this condition and the lack of definitive guidelines related to its diagnosis and management, additional documentation and awareness may assist other medical professionals in recognizing and treating paraganglionic tissue found in atypical sites with more clinical confidence.
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Padumane et al. (2026) conducted a case report in Gallbladder paraganglioma (n=1). Laparoscopic cholecystectomy was evaluated. Laparoscopic cholecystectomy in a 35-year-old female with cholelithiasis incidentally revealed a rare 0.5 mm non-secretory gallbladder paraganglioma.
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