Multiple fibroids in a postmenopausal woman with Mayer Rokitansky Kuster Hauser syndrome.
نویسنده
چکیده
The Mayer Rokitansky Kuster Hauser (MRKH) syndrome is a congenital abnormality of the genital tract which occurs in approximately 1 in 5000 women. It is characterized by a maldevelopment of the Mullerian ducts at their lower portion, which results in congenital absence of the vagina and either the absence of uterine tissue or the presence of two uterine anlage, which are nonfunctioning myometrial tissue lying laterally on the pelvic side walls. Finally, a small redundant piece of uterine tissue may lie in the midline, but it is again nonfunctional. Leiomyomata are common occurrences in women with normal uteri but the occurrence of fibroids in MRKH syndrome is a rarely reported finding. There are only 15 reported cases in the existing medical literature. This case is unique in that it occurred in a postmenopausal woman and this has never been previously described.
منابع مشابه
Uterine Adenomyosis Which Developed from Hypoplastic Uterus in Postmenopausal Woman with Mayer-Rokitansky-Kuster-Hauser Syndrome: A Case Report
Mayer-Rokitansky-Kuster-Hauser syndrome (MRKHS) is characterized by vaginal agenesis with variable Müllerian duct abnormalities. We report here a case of uterine adenomyosis which developed from a hypoplastic uterus in a patient with MRKHS. A 55-year-old postmenopausal woman visited a university hospital for pelvic mass. She had underwent vaginoplasty via the McIndoe procedure for MRKHS at 15 y...
متن کاملP-192: The Study of Cystic Fibrosis Transmembrane Conductance Regulator Gene Mutations and Polymorphisms in Iranian Patients with Mayer Rokitansky Kuster Hauser Syndrome
Background: Mayer - Rokitansky - Kuster - Hauser (MRKH) syndrome is characterized by congenital aplasia of the uterus and the upper part of the vagina in women showing normal development of secondary sexual characteristics and a normal 46, XX karyotype. Congenital anomaly of the female genital tract, estimated to occur in approximately 1 in every 5,000 females. It is caused by a failure of deve...
متن کاملIntra-Peritoneal Leiomyoma of the Round Ligament in a Patient with Mayer- Rokitansky-Kuster-Hauser (MRKH) Syndrome
Background: The occurrence of an extra-uterine leiomyoma, arising from the intra-peritoneal portion of the round ligament in a lady with Müllerian agenesis diagnosed at the age of forty is extremely rare. We report a case of this rare combination in a Middle Eastern woman. Case: A 40 years old lady, primarily amenorrheic, presented to our clinic for an infertility consultation. The work-up show...
متن کاملIntra-peritoneal leiomyoma of the round ligament in a patient with Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome
BACKGROUND The occurrence of an extra-uterine leiomyoma, arising from the intra-peritoneal portion of the round ligament in a lady with Müllerian agenesis diagnosed at the age of forty is extremely rare. We report a case of this rare combination in a Middle Eastern woman. CASE A 40 years old lady, primarily amenorrheic, presented to our clinic for an infertility consultation. The work- up sho...
متن کاملPregnancy in a case of Mayer-Rokitansky-Küster-Hauser Syndrome Gravidez num caso de Síndrome Mayer-Rokitansky-Küster-Hauser
Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome refers to the congenital absence of the upper part (2/3) of the vagina with variable uterine development. In this disorder, infertility may be the most difficult aspect for the patient to accept. This review will describe a rare case of pregnancy in a woman with MRKH syndrome through assisted reproductive
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Journal of pediatric and adolescent gynecology
دوره 16 2 شماره
صفحات -
تاریخ انتشار 2003