Elmqaddem Ouiam, Koulali Hajar, Zazour Abdelkrim, Nasiri Meryem, Ismaili Moulay Zahi, Kharrasse Ghizlane
Digestive Disease Research Laboratory, Medical School, Mohammed First University, Faculty of Medicine and Pharmacy Oujda, Morocco.
Department of Hepato-gastroenterology, Mohammed VI University Hospital, Oujda, Morocco.
Radiol Case Rep. 2024 Jun 19;19(9):3810-3813. doi: 10.1016/j.radcr.2024.04.033. eCollection 2024 Sep.
Osler-Weber-Rendu disease (OWRD), also known as hereditary haemorrhagic telangiectasia (HHT), is an autosomal dominant genetic disorder characterised by arteriovenous malformations in several organs. Ischemic cholangitis is a rare life-threatening complication of OWRD, with only a few documented cases in the literature. A liver transplant is the main curative treatment. In this paper, we report a case of a 33-year-old woman with a history of recurrent epistaxis, admitted with abdominal pain and fever, physical examination found multiple cutaneous and mucosal telangiectasias and the biological workup showed cholestasis, abdominal imaging identified arterio-venous shunts and multiple cystic hepatic lesions, one of them seemed to communicate with an intrahepatic biliary duct, finally the diagnosis of ischemic cholangitis due to OWRD was retained and antibiotic treatment has been initiated. We review the various therapeutic options available to improve the management of this fatal complication.
奥斯勒-韦伯-伦杜病(OWRD),也称为遗传性出血性毛细血管扩张症(HHT),是一种常染色体显性遗传病,其特征是多个器官出现动静脉畸形。缺血性胆管炎是OWRD一种罕见的危及生命的并发症,文献中仅有少数病例记载。肝移植是主要的治疗方法。本文报告了一例33岁有反复鼻出血病史的女性,因腹痛和发热入院,体格检查发现多处皮肤和黏膜毛细血管扩张,实验室检查显示胆汁淤积,腹部影像学检查发现动静脉分流和多个肝脏囊性病变,其中一个似乎与肝内胆管相通,最终确诊为OWRD所致的缺血性胆管炎并开始抗生素治疗。我们回顾了可用于改善这种致命并发症治疗的各种治疗选择。