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子宫动静脉畸形的综合征型和孤立型:两例病例报告。

A syndromal and an isolated form of uterine arteriovenous malformations: two case-reports.

作者信息

Geerinckx I, Willemsen W, Hanselaar T

机构信息

Department of Obstetrics and Gynecology, UMC St Radboud, N. Engelschmanlaan 16, 6532 CS Nijmegen, The Netherlands.

出版信息

Eur J Obstet Gynecol Reprod Biol. 2001 Dec 10;100(1):87-91. doi: 10.1016/s0301-2115(01)00462-6.

Abstract

Uterine arteriovenous malformations are rare lesions with a considerable risk potential. Clinical presentation varies from no signs over various degrees of menorrhagia to massive life threatening vaginal bleeding. This is the first report of congenital uterine arteriovenous malformations in two patients with primary infertility. In one case, the uterine lesions were found in conjunction with other congenital malformations suggesting the diagnosis of hemihyperplasia/lipomatosis syndrome. Etiology, symptoms, diagnostic and therapeutic work-up are discussed; pathological findings are illustrated.

摘要

子宫动静脉畸形是罕见的病变,具有相当大的潜在风险。临床表现从无体征到不同程度的月经过多,再到危及生命的大量阴道出血不等。这是关于两名原发性不孕症患者先天性子宫动静脉畸形的首例报告。在其中一例中,子宫病变与其他先天性畸形同时发现,提示诊断为偏身肥大/脂肪瘤综合征。文中讨论了病因、症状、诊断和治疗过程,并展示了病理结果。

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