Mayer-rokitansky-kuster-hauser syndrome with a borderline ovarian serous cystadenoma: A case report
Mayer-Rokitansky-Kuster-Hauser (MRKH) sendromu, vagina ile uterusun beraberce hipoplazisi olarak bilinmektedir ve 4000-5000 dişi doğumda 1 olarak gözlenmektedir. Primer amenore, sterilite ve pelvik ağrı gibi belli başlı jinekolojik problemlere yol açan bu sendromun tanısı, cerrahi eksplorasyonla olduğu kadar, günümüzde gelişen görüntüleme teknikleri ile de mümkün olabilmektedir. Bu makalede kliniğimize üç gündür süren alt kadran ağrısı şikayeti ile başvuran ve yapılan tetkikler sonucunda MRKH ile birlikte överde borderline seröz kistadenom saptanan 43 yaşında bir olgu sunulmuştur.
Mayer-rokitansky-kuster-hauser sendromlu bir olguda izlenen overin borderline seröz kistadenomu: Olgu sunumu
The Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome comprises the combined hypoplasia of the vagina and the uterus and it occurs in 1 of 4000-5000 female births. It may cause many gynecological problems such as primary amenorrhea, sterility, pelvic pain and can be diagnosed by screening or surgical methods. We report a 43-year-old women with MRKH syndrome and an ovarian serous borderline cystadenoma. She was admitted to our clinic complaining of lower abdominal pain for three days.
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