Bani-Hani Kamal E
Department of Surgery, King Abdullah University Hospital, Faculty of Medicine, Jordan University of Science and Technology, Irbid, Jordan.
J Gastroenterol Hepatol. 2005 May;20(5):671-5. doi: 10.1111/j.1440-1746.2005.03740.x.
Gallbladder agenesis is a rare congenital biliary anomaly that may be associated with other biliary and extrabiliary congenital anomalies. Awareness of this entity by clinicians and radiologists is essential because many of these patients present with biliary symptoms and have unnecessary operations. In the present article, the relative epidemiological, etiological (embryology and development), pathophysiological, diagnostic tools and pitfalls and management aspects of this rare anatomic anomaly are briefly discussed through review of the literature. Particular reference to the difficulty in preoperative diagnosis is highlighted. The importance of the possibility of preoperative diagnosis to avoid unnecessary surgery is stressed.
胆囊缺如是一种罕见的先天性胆道异常,可能与其他胆道及非胆道先天性异常相关。临床医生和放射科医生认识这一病症至关重要,因为许多此类患者表现出胆道症状并接受了不必要的手术。在本文中,通过文献回顾简要讨论了这种罕见解剖异常的相对流行病学、病因学(胚胎学与发育)、病理生理学、诊断工具及陷阱以及管理方面。特别强调了术前诊断的困难。强调了术前诊断以避免不必要手术的可能性的重要性。