Do Jee Eun, Harvey Kathryn, Rana Abdul, Swalling Adam, Bruening Martin
Department of Surgery, The Queen Elizabeth Hospital, Adelaide, AUS.
Department of General Surgery, Lyell McEwin Hospital, Adelaide, AUS.
Cureus. 2023 Feb 22;15(2):e35327. doi: 10.7759/cureus.35327. eCollection 2023 Feb.
Gallbladder paragangliomas are extremely rare with only a handful of cases reported so far. There are no definitive guidelines for the management of gallbladder paragangliomas due to their rarity. We present a case of a 53-year-old male who was found to have gallbladder paraganglioma post-laparoscopic cholecystectomy, performed for right upper abdominal pain. On review of the literature, all previously reported cases had been nonsecretory and benign. For patients who have no symptoms of secretory paragangliomas and no family history of endocrine syndromes, cholecystectomy and clinical follow-up may be a sufficient initial management following an incidental finding of gallbladder paraganglioma.
胆囊副神经节瘤极为罕见,迄今为止仅有少数病例报道。由于其罕见性,目前尚无胆囊副神经节瘤的明确管理指南。我们报告一例53岁男性,因右上腹疼痛接受腹腔镜胆囊切除术后被发现患有胆囊副神经节瘤。经文献检索,所有既往报道的病例均为无分泌功能的良性肿瘤。对于无分泌性副神经节瘤症状且无内分泌综合征家族史的患者,偶然发现胆囊副神经节瘤后,胆囊切除术及临床随访可能是充分的初始治疗方法。