نتایج جستجو برای: hematocolpos
تعداد نتایج: 79 فیلتر نتایج به سال:
Obstructed hemivagina and ipsilateral renal anomaly (OHVIRA) syndrome is a characterised by obstructed hemivagina, agenesis uterine didelphys. It rare congenital results from defective fusion of the Müllerian ducts during development female reproductive system. also known as Herlyn-Werner-Wunderlich syndrome. Aim study was to project case developmental Mullerian OHVIRA anomaly. The most common ...
Hematometrocolpos is accumulation of blood in the vagina and uterine cavity due to intra-uterine hemorrhage. A 20-year-old female presented to our clinic with massive menorrhagia at menarche after progestin usage. Hematometrocolpos was detected by transabdominal ultrasonography. She was pale because of heavy bleeding for 5 days and hemoglobin level was measured as 5.1 g/dl. Initial treatment wa...
Bicornuate uterus has two symmetric uterine cavities that are fused caudally and have some degree of communication between two cavities, usually at the uterine isthmus. A complete bicornuate uterus has a seperatory cleft of tissue that is extended to the internal OS. Lesser degree of septation of the two uterine horns has constitution, a partial bicornuate uterus. Bicornuate uterus is a class o...
Uterus didelphys with obstructed hemivagina and ipsilateral renal agenesis is a rare congenital anomaly. Excision of the obstructed vaginal septum is the treatment of choice for symptom relief and the preservation of reproductive capability. A 14-yr-old girl complained of persistent vaginal spotting following each menstruation. Pelvic magnetic resonance imaging revealed a uterus didelphys with ...
سابقه و هدف: پرده بکارت بدون سوراخ، نوعی ناهنجاری مادرزادی نادر ناشی از نقص در روند دژنرسانس سلولهای مرکزی پرده بکارت است. این تشخیص معمولا تا دوران بلوغ و نوجوانی نادیده گرفته میشود. پس از بلوغ، تجمع خون در واژن (hematocolpos) بهعلت انسداد مجرای خروجی سبب ایجاد علائم بالینی میشود. این گزارش با توجه به نادر بودن این ناهنجاری ارائه میشود. معرفی بیمار: مورد گزارش شده دختر خانم 14 سالهای است...
Correspondence To the Editor: We have read with interest the article entitled " New classification of Herlyn–Werner–Wunderlich syndrome (HWWS) " by Zhu et al. and we want to clarify a few points. Such syndrome, although often reported as such in the literature, does not exist. Herlyn–Werner syndrome in their original description is a unilateral renal aplasia, with double uterus and blind vagina...
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