Mina RE, Álvarez DS, Valencia ACA, Murúa MOA, Piña RLE, Gómez PMG

Language: Spanish
References: 3
Page: 353-355
PDF size: 196.79 Kb.

ABSTRACT

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.

REFERENCES

1. Herlin MK, Petersen MB, Brannstrom M. Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: a comprehensive update. Orphanet J Rare Dis. 2020; 15: 214.

2. Medina SC, Aguirre FJ, Montecinos GJ, Schiappacasse FG. Revisión pictográfica de las anomalías de los conductos de Müller por resonancia magnética. Rev Chil Obstet Ginecol. 2015; 80 (2): 181-190.

3. Rojas GPZ, Mera LFA, López LMR, Samper LVR. Síndrome de Mayer Von Rokitansky Küster Hauser, más que una actualización clínica, diagnóstica y tratamiento quirúrgico asociada a complicaciones anestésicas en el paciente pediátrico. Sci Educ Med J. 2021; 2 (1): 227-241.