A Rare Case of Serous Cystadenofibroma in a Patient with Mayer-Rokitansky-Kuster-Hauser Syndrome
Philippine Journal of Reproductive Endocrinology and Infertility
; : 35-38, 2020.
Article
em En
| WPRIM
| ID: wpr-960184
Biblioteca responsável:
WPRO
ABSTRACT
@#<p>Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is characterized by failure of embryologic growth of the mullerian ducts resulting to agenesis or hypoplasia of the uterus and upper part of the vagina while both ovaries and fallopian tubes are normal. Various associated malformation with MRKH syndrome are noted in literature, with a renal system anomaly as the most common. However, adnexal tumors in MRKH syndome are rare. To date there have been no reported cases of fallopian tube tumors in patients diagnosed with MRKH. This paper presents a case of an 18 year old nulligravida who presented with primary amenorrhea secondary to MRKH sydnrome, with an associated Papiliary Serous Cystadenofibroma of the right fallopian tube Management of the case as well as review of related literature are presented. </p>
Palavras-chave
Buscar no Google
Base de dados:
WPRIM
Assunto principal:
Cistoadenofibroma
Idioma:
En
Revista:
Philippine Journal of Reproductive Endocrinology and Infertility
Ano de publicação:
2020
Tipo de documento:
Article