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Acta médica Grupo Ángeles
versão impressa ISSN 1870-7203
Resumo
MINA ROMERO, Elizabeth et al. Mayer-Rokitansky-Küster-Hauser syndrome. Acta méd. Grupo Ángeles [online]. 2022, vol.20, n.4, pp.353-355. Epub 26-Maio-2023. ISSN 1870-7203. https://doi.org/10.35366/107122.
Introduction:
Mayer-Rokitansky-Küster-Hauser syndrome (also known as müllerian aplasia) is a rare congenital anomaly of the tract genital, of unknown etiology, characterized by the congenital absence of the uterus, cervix and upper portion of the vagina.
Clinical case:
A 16-year-old female patient with primary amenorrhea, normal hormonal profile, adequate sexual development Tanner 5, 46 XX karyotype. A magnetic sound is performed where the absence of the uterus and the proximal two-thirds of the vagina are detected.
Conclusion:
Magnetic resonance is a diagnostic test that provides great anatomical detail of the uterus and vagina, allowing to correctly characterize and classify Müllerian anomalies.
Palavras-chave : Rokitansky syndrome; magnetic resonance imaging; uterine malformations; müllerian malformations.