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자궁내막증이 동반된 Mayer-Rokitansky-$K{\ddot{u}}ster$-Hauser 증후군의 수술적 치료경험 1례
박정열,김정훈,강천식,이지영,박소연,김성훈,채희동,강병문,Park, Jeong-Yeol,Kim, Chung-Hoon,Kang, Cheon-Sik,Lee, Ji-Young,Park, So-Youn,Kim, Sung-Hoon,Chae, Hee-Dong,Kang, Byung-Moon 대한생식의학회 2003 Clinical and Experimental Reproductive Medicine Vol.30 No.2
The Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome refers to a condition which presents as normal female secondary sex characteristics, normal external genitalia, congenital absence of the internal vagina, usually a rudimentary uterus in the form of bilateral noncanaliculated muscular buds, and normal tubes and ovaries with normal cytogenetic and endocrine evaluation, frequent association of renal, skeletal and other congenital anomalies. However, rarely, whole uterus or a segment of uterus may be present, but lacking a conduit to the introitus. If a partial endometial cavity is present in a segment of uterus, cyclic abdominal pain may be a complaint and furthermore endometiosis can be developed. Recently, we experienced a case of MRKH syndrome with the segments of uterus accompanying endometriosis in young woman. We present this case with a brief review of literatures.