一名患有迈耶-罗基坦斯基-库斯特-豪泽综合征患者的直肠阴道瘘。
Rectovaginal fistula in a patient with Mayer-Rokitansky-Kuster-Hauser syndrome.
作者信息
Sandeep Puvvada, Shanthakumar S, Chalumuru Venkata Mahesh, Ramesh D, Javali Tarun Dilip
机构信息
M S Ramaiah Medical College Hospital, New BEL Rd, M S Ramaiah Nagar, MSRIT Post, Bengaluru, Karnataka, 560054, India.
出版信息
Urol Case Rep. 2025 May 21;61:103075. doi: 10.1016/j.eucr.2025.103075. eCollection 2025 Jul.
MRKH syndrome is defined by the congenital absence of the uterus and the upper two-thirds of the vagina in females, who otherwise exhibit normal secondary sexual characteristics and possess a typical 46, XX karyotype. Here we report a case of 23 year old female diagnosed with Mayer-Rokitansky-Kuster-Hauser syndrome when presenting with features of rectovaginal fistula.
先天性无阴道综合征的定义是女性先天性子宫及阴道上三分之二缺如，而其他方面表现为正常的第二性征且具有典型的46, XX核型。在此，我们报告一例23岁女性，该患者因直肠阴道瘘症状就诊时被诊断为梅耶-罗基坦斯基-库斯特-豪泽综合征。
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