Perforated hemorrhagic cholecystitis in a patient with Bernard-Soulier syndrome.
Serkan KaraıslıSalih Can CelikIbrahim KokuluHizir Taner CoskunMehmet HaciyanliPublished in: Clinical journal of gastroenterology (2022)
Bernard-Soulier syndrome is an inherited coagulopathy, with an incidence of one per million. Hemorrhagic cholecystitis is a rare and life-threatening complication of acute cholecystitis. Less than 50 patients have been reported in the previous literature. Bleeding diathesis and anticoagulant treatment are well-known predisposing factors for hemorrhagic cholecystitis. We present a 57-year-old male patient who was referred to our department with a complaint of right upper quadrant abdominal pain. Contrast-enhanced computed tomography revealed a high-density mass associated with the gallbladder lumen, and blood clot in the gallbladder lumen and hemoperitoneum which were compatible for hemorrhagic cholecystitis and gallbladder perforation. The patient underwent urgent cholecystectomy. Hemorrhagic cholecystitis often manifests as typical acute cholecystitis presentation; but several clinical findings such as fever, lower gastrointestinal bleeding or severe intraabdominal bleeding-related hypovolemic shock may also occur. Most of the described cases in prior literature have been reported to use anticoagulant medications. This report describes the second hemorrhagic cholecystitis patient with inherited bleeding diathesis and the first case with Bernard-Soulier syndrome.
Keyphrases
- case report
- computed tomography
- atrial fibrillation
- contrast enhanced
- magnetic resonance imaging
- high density
- abdominal pain
- systematic review
- end stage renal disease
- magnetic resonance
- drug induced
- venous thromboembolism
- newly diagnosed
- risk factors
- chronic kidney disease
- positron emission tomography
- respiratory failure
- intensive care unit
- early onset
- extracorporeal membrane oxygenation
- hepatitis b virus
- replacement therapy