Florou Evangelia, Ubaid Shirin, Seager Matthew, Heneghan Michael, Prachalias Andreas, Patel Ameet G
Hepato-Pancreato-Biliary Surgery, King's College Hospital, London, GBR.
Hepato-Pancreato-Biliary Interventional Radiology, King's College Hospital, London, GBR.
Cureus. 2025 Apr 16;17(4):e82352. doi: 10.7759/cureus.82352. eCollection 2025 Apr.
Haemorrhagic gallbladder (HG) is a very rare complication of acute cholecystitis. Cases are not frequently described in the literature, but frail elderly patients on anticoagulants are the primary group of patients affected. Semi-elective or emergency laparoscopic cholecystectomy is the treatment of choice, while haemorrhagic shock requiring emergency laparotomy is an extremely rare event. Primary sclerosing cholangitis (PSC) is an autoimmune liver disease (AiLD), and its association with bleeding complications remains a clinical observation that lacks robust scientific evidence and comprehensive understanding. Here, we present a case of gallbladder rupture causing haemorrhagic shock in a young patient with a background of cirrhotic PSC. A 29-year-old female with PSC and a history of splenic artery aneurysm previously treated with embolization presented to the emergency department complaining of abdominal pain. A striking feature in the biochemistry results was the high bilirubin level without clinical detection of jaundice. Computed tomography (CT) showed a ruptured gallbladder with active bleeding and haemoperitoneum. Emergency laparotomy was mandated as the patient was becoming progressively haemodynamically unstable. The necrosed gallbladder was resected, and blood was evacuated from the abdominal cavity. The patient recovered well with no postoperative complications observed. HG causing haemodynamic shock is quite a rare complication of acute cholecystitis. This is the first case reported in the literature of internal haemorrhage due to HG in a patient with a background of PSC. This case alerts clinicians dealing with PSC patients who may be susceptible to rare complications of common pathologies. AiLD and their relationship with bleeding events remains unclear and subject of future studies.
出血性胆囊炎(HG)是急性胆囊炎一种非常罕见的并发症。文献中对此类病例的描述并不常见,但正在接受抗凝治疗的体弱老年患者是主要的受影响患者群体。半择期或急诊腹腔镜胆囊切除术是首选治疗方法,而需要急诊剖腹手术的出血性休克极为罕见。原发性硬化性胆管炎(PSC)是一种自身免疫性肝病(AiLD),其与出血并发症的关联仍是一项缺乏有力科学证据和全面理解的临床观察结果。在此,我们报告一例在患有肝硬化性PSC的年轻患者中,胆囊破裂导致出血性休克的病例。一名29岁患有PSC且有脾动脉瘤病史(此前已接受栓塞治疗)的女性因腹痛就诊于急诊科。生化检查结果中的一个显著特征是胆红素水平升高,但临床上未检测到黄疸。计算机断层扫描(CT)显示胆囊破裂伴活动性出血和腹腔积血。由于患者血流动力学逐渐不稳定,因此必须进行急诊剖腹手术。切除坏死的胆囊,并将腹腔内的血液排空。患者恢复良好,未观察到术后并发症。HG导致血流动力学休克是急性胆囊炎一种相当罕见的并发症。这是文献中报道的首例背景为PSC的患者因HG导致内出血的病例。该病例提醒临床医生,在处理可能易患常见疾病罕见并发症的PSC患者时需加以注意。AiLD及其与出血事件的关系仍不明确,有待未来研究。