Leiomyoma development in Mayer-Rokitansky-Küster-Hauser syndrome: a case report and a narrative review of the literature
10.5468/ogs.2019.62.4.294
- Author:
Nikolaos BLONTZOS
1
;
Christos IAVAZZO
;
George VORGIAS
;
Nikolaos KALINOGLOU
Author Information
1. Department of Gynecology, Metaxa Memorial Cancer Hospital, Piraeus, Greece. nikolas.mplontzos@yahoo.gr
- Publication Type:Case Report
- Keywords:
Mullerian duct failure;
Rokitansky Kuster Hauser syndrome;
Leiomyoma
- MeSH:
Adult;
Diagnosis;
Humans;
Laparotomy;
Leiomyoma;
Magnetic Resonance Imaging;
Pathology;
Pelvic Pain;
Pulmonary Valve Stenosis;
Ultrasonography;
Uterus
- From:Obstetrics & Gynecology Science
2019;62(4):294-297
- CountryRepublic of Korea
- Language:English
-
Abstract:
The development of leiomyomas on the grounds of an aplastic/hypoplastic uterus in patients with Mayer-Rokitansky-Küster-Hauser syndrome (MRKHS) has been rarely described. We report the first case of development of multiple leiomyomas in a patient with MRKHS complicated with pulmonary valve stenosis, and we present a narrative review of the existing literature. A 44-year-old patient with MRKHS attended our clinic because of pelvic pain, which was attributed to a pelvic mass found on ultrasound. Magnetic resonance imaging revealed a multinodular mass, indicating either ovarian pathology or the presence of leiomyomas. Exploratory laparotomy was performed, and multiple solid masses on the grounds of two rudimentary uterine buds were observed. Histological analysis revealed multiple leiomyomas arising from parametrial or paratubal tissue. We searched medical databases for articles relevant to leiomyomas and MRKHS. We present a review of the current literature and summarize the clinical manifestation, diagnosis, management, and histopathological findings of all the cases described. We underline that it is important for gynecologists to be aware of this rare clinical entity, and symptomatic leiomyomas cannot be excluded in patients with MRKHS.
