Darden W A, Fulenwider J T, Smith R B, Sewell C W
Surgery. 1984 Sep;96(3):567-73.
Congenital abdominal aortic aneurysms are medical curiosities because of their rare occurrence even in groups with hereditary derangements of connective tissue metabolism (e.g., Marfan's syndrome and Ehlers- Danlos syndrome). We present the case of a 2 1/2-year-old boy with a congenital aneurysm of the aortoiliac bifurcation managed by excision and graft replacement. No associated disorder of connective tissue or other pathogenetic mechanism was discovered in this patient. The authors have summarized the existing literature regarding these rare but potentially lethal aneurysms.
先天性腹主动脉瘤即便在结缔组织代谢存在遗传性紊乱的人群（如马凡综合征和埃勒斯-当洛综合征）中也较为罕见，因此属于医学上的罕见病例。我们报告一例2岁半男孩，患有主髂动脉分叉处先天性动脉瘤，通过切除和移植置换进行治疗。该患者未发现结缔组织相关疾病或其他致病机制。作者总结了关于这些罕见但可能致命的动脉瘤的现有文献。
