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Case report: A case of giant accessory hepatic lobe torsion combined with left hepatic vein branch thrombosis in a child
Frontiers in Pediatrics ( IF 2.6 ) Pub Date : 2022-09-26 , DOI: 10.3389/fped.2022.970876
Xiangang Xiong 1, 2 , Yonghua Lou 3 , Teng Zhou 1, 2 , Zebing Zheng 1, 2 , Yuanmei Liu 1, 2 , Rui Liu 1, 2 , Kaizhi Zhang 1, 2 , Yuan Gong 1, 2 , Chengyan Tang 1, 2 , Zhu Jin 1, 2
Affiliation  

The accessory hepatic lobe (AHL) is a rare congenital malformation of the hepatic tissue, among which the giant AHL is the rarest in children. Patients without complications are usually asymptomatic, and most auxiliary examinations cannot provide a definitive preoperative diagnosis. Surgical procedure is the only recommended management for patients who suffered from the complications of AHL. We report the case of a rare pediatric giant AHL torsion combined with left hepatic vein branch thrombosis which was successfully treated by laparoscopic lobectomy followed by excision of AHL.



中文翻译:

病例报告:小儿巨大副肝叶扭转合并肝左静脉分支血栓形成

副肝叶(AHL)是一种少见的先天性肝组织畸形,其中巨大型AHL以儿童最为罕见。无并发症的患者通常无症状,大多数辅助检查不能提供明确的术前诊断。对于患有 AHL 并发症的患者,手术是唯一推荐的治疗方法。我们报告了一例罕见的小儿巨大 AHL 扭转合并左肝静脉分支血栓形成的病例,该病例通过腹腔镜肺叶切除术后 AHL 切除术成功治疗。

更新日期:2022-09-26
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