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Gaceta mexicana de oncología
versión On-line ISSN 2565-005Xversión impresa ISSN 1665-9201
Resumen
PADRON-RIVERA, Luis Héctor; BARRERA-FRANCO, José Luis; LOPEZ-ZAVALA, Carlos y DOLORES-VELAZQUEZ, Rigoberto. Adnexal tumor in Mayer-Rokitansky-Küster-Hauser syndrome. Presentation of a clinical case and review of the literatura. Gac. mex. oncol. [online]. 2019, vol.18, suppl.1, pp.60-63. Epub 17-Oct-2022. ISSN 2565-005X. https://doi.org/10.24875/j.gamo.19000096.
Introduction:
The Mayer-Rokitansky-Küster-Hauser (MRKH), defined as congenital hypoplasia of the structures derived from the müllerian ducts, occurs in female patients, usually with proper development and karyotype 46XX, with an incidence of 1/5,000, and is the second cause of consultation by secondary amenorrhea. It is classically divided into type I, or isolated, and type II, associated with other malformations. There have been described isolated cases of MRKH associated with the presence of adnexal tumors.
Clinical case:
A case of a female patient with a diagnosis of type II MRKH with the presence of adnexal tumor is presented, which according to Jacobs presents risk of malignancy; she was treated at our institution according to international clinical practice guidelines.
Palabras llave : MRKH; Adnexal tumor; International Clinical Practice Guidelines.
