Mayer-Rokitansky-Küster-Hauser syndrome

Cut Meurah Yeni, Khairussani Khairussani, Wardatul Bararah
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Abstract

Abstrak. Mayer–Rokitansky–Küster–Hauser syndrome (MRKH) adalah suatu sindrom yang ditandai dengan aplasia uterus, serviks, dan 2/3 vagina bagian atas karena perkembangan yang tidak sempurna dari duktus Mullerian. Dilaporkan seorang perempuan berusia 26 tahun yang mengeluh belum pernah menstruasi sampai saat ini. Secara fenotip pasien tampak sebagai perempuan yang memiliki perawakan normal. Payudara dan distribusi pertumbuhan rambut aksila serta kemaluan berkembang normal, disertai pertumbuhan lemak pada bokong dan paha. Tuba fallopi, rahim, dan vagina 2/3 proksimal tidak terbentuk. Pada pemeriksaan klinis ginekologi tampak introitus vagina dengan sonde vagina sepanjang 2 cm. Pemeriksaan USG abdominal, uterus berupa garis dan kedua ovarium sulit dinilai. Pemeriksaan MRI didapatkan agenesis uterus dan agenesis adnexa. Pemeriksaan analisa hormonal, LH 9,81 mIU/mL, FSH 6,87 mIU/mL, progesteron 0,51 ng/mL, estradiol 46,4 pg/mL, testosteron 60,45 mg/dl, TSH 1,216 mIU/L, T4 11 ug/dl, serta analisa kromosom 46XX. Pasien direncanakan untuk dilakukan vaginoplasti.Kata kunci : sindrom MRKH, anomali duktus Mulleri, vaginoplastiAbstract. Mayer–Rokitansky–Küster–Hauser syndrome (MRKH) is a syndrome characterized by uterine, cervix, and the two third of upper vagina aplasia which is the cause of incomplete development of the Müllerian duct. Reported a case of woman 26 years old, patient has not menstruated until now. The phenotype of the patient appears to be female, and with normal stature. Breast, axilla dan pubic hair distribution, fatty in buttocks and thigh developed normally. Fallopian tubes, uterine and 2/3 upper part of vagina were not formed. On gynecological clinical examination, found vaginal introitus with a vaginal sonde was 2 cm. On abdominal ultrasound examination, the uterus was seen as a line and both ovaries were difficult to assess. MRI examination obtained theresults as uterine and adnexa agenesis. Hormonal analysis showing LH 9.81 mIU/mL, FSH 6.87 mIU/mL, progesteron 0.51 ng/mL, estradiol 46.4 pg/mL, testosterone 60.45 mg/dl, TSH 1.216 mIU/L, T4 11 ug/dl, and chromosome examination is 46 XX. Patient are planned for vaginoplasty. Key words: MRKH syndrome, mullerian duct anomalies, vaginoplasty
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Mayer-Rokitansky-Kuster-Hauser综合症
抽象。Mayer——Rokitansky——Kuster——Hauser syndrome (MRKH)是一种综合症,其特征是子宫失序、宫颈颈和上三分之二的阴道,因为其进展并不完美。据报道,一名26岁的女性抱怨直到今天还没有月经。患者被认为是一个正常身材的女性。乳房和性腺生长的分布正常,臀部和大腿的脂肪生长。输卵管、子宫和阴道2/3的近端尚未形成。在妇科临床检查中,阴道与2厘米长的sonde阴道看起来很内向。腹部超声波检查,子宫是直线,两个卵巢很难评估。MRI检查了子宫增生和子宫增生。分析检查激素LH 9。81 mIU / mL, FSH - 6.87 mIU / mL,黄体酮0,51 ng / mL,雌二醇46.4 pg / mL,睾丸激素60.45 mg / dl, TSH 1,216 mIU / L, T4 11 ug / dl,以及染色体分析46XX。计划要做vaginoplasti病人。关键词:MRKH综合症,管道异常Mulleri, vaginoplastiAbstract。Mayer——Rokitansky——Kuster——Hauser is a characterized by uterine, cervix,和上阴道失活症报告了一个26岁的女人的案子,病人直到现在才发现。病人的外貌需要是女性,处于正常状态。乳房、axilla和pubic毛分布、buttocks和thigh发育正常。输卵管、uterine和上三分之二的阴道都没有被清除。在gynecocological clinical examination,发现一个阴道sonde的阴道内省是2厘米。子宫进行超声波检查时,两个卵巢都很难评估。核磁共振检查美国子宫和附录agenesis的热硫化物研究。荷尔蒙分析显示LH 9。81 mIU / mL, FSH 6 . 87 mIU / mL,黄体酮0。51 ng / mL,雌二醇46 4 pg / mL,睾丸激素60。45 mg / dl, TSH 1.216 mIU / L, T4 11 ug / dl, 46和来晚号染色体是XX。病人计划做阴道整形手术。MRKH综合症,mullerian duct反常物,阴道成形术
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