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先天性腹主动脉瘤:一例报告及文献综述

Congenital Abdominal Aortic Aneurysm: A Case Report and Literature Review.

作者信息

Zhou Zhibin, Yue Yongqiang, Ma Ke, Hua Zhaohui, Li Zhen

机构信息

Department of Endovascular Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.

出版信息

Front Pediatr. 2022 Mar 1;10:853517. doi: 10.3389/fped.2022.853517. eCollection 2022.

Abstract

Congenital abdominal aortic aneurysm is a rare disease with unknown etiology, and the common symptoms are abdominal pulsatile mass and pain caused by aneurysm rupture. The disease has a high mortality rate and fewer reports of surgical treatment. Here, we present a case of an idiopathic congenital abdominal aortic aneurysm. A 4-year-old boy had an abdominal pulsatile mass, and computed tomography angiography revealed an isolated infrarenal abdominal aortic aneurysm. To prevent rupture of the aneurysm, we repaired the aneurysm with artificial graft transplantation. No genetic mutation of the known congenital aneurysmal diseases was found in the whole-exome sequencing of the patient and his parents. There was no graft obstruction, and the patient grew well 40 months after surgery. Open surgery is the best treatment for idiopathic congenital abdominal aortic aneurysms. Surgical details such as timing and graft selection need to be further explored.

摘要

先天性腹主动脉瘤是一种病因不明的罕见疾病,常见症状为腹部搏动性肿块和动脉瘤破裂引起的疼痛。该疾病死亡率高,手术治疗的报道较少。在此,我们报告一例特发性先天性腹主动脉瘤病例。一名4岁男孩有腹部搏动性肿块,计算机断层血管造影显示为孤立性肾下腹主动脉瘤。为防止动脉瘤破裂,我们采用人工血管移植修复了动脉瘤。对患者及其父母进行的全外显子组测序未发现已知先天性动脉瘤疾病的基因突变。术后未出现移植物阻塞,患者术后40个月生长良好。开放手术是治疗特发性先天性腹主动脉瘤的最佳方法。手术时机和移植物选择等手术细节有待进一步探索。

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