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Unusual Presentation of a Rectovestibular Fistula as Gastrointestinal Hemorrhage in a Postmenopausal Woman

机译:绝经后女性胃肠道出血的前庭瘘异常表现。

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摘要

Background. Anorectal malformations (ARMs) are extremely rare and are usually identified neonatally. It is unusual for these cases to present in the postmenopausal period. This case report describes a postmenopausal patient with ARM and rectovaginal hemorrhage. Case. An 86-year-old, gravida 11, para 9, presented to the emergency department complaining of profuse postmenopausal vaginal bleeding. Her gynecologic history was significant only for an unclear history of an anal abnormality that was noted at birth. Speculum examination revealed profuse rectal bleeding from a rectovestibular fistula exterior to her hymenal ring. Colonoscopic examination revealed severe diverticular disease. Conclusion. This patient was born with an imperforate anus which resolved as rectovestibular fistula and ectopic anus. This case presents a rare clinical circumstance which integrates the fields of obstetrics, gynecology, gastroenterology, and embryology alike.
机译:背景。肛肠畸形(ARMs)极为罕见,通常在新生儿时就可以发现。这些情况通常在绝经后出现。该病例报告描述了绝经后患有ARM和直肠阴道出血的患者。案件。一名86岁的孕妇,重力11,第9段,出现在急诊科,抱怨绝经后阴道大量出血。她的妇科病史仅对出生时肛门异常的不清楚病史有意义。窥镜检查发现,处女膜环外侧的直肠前庭瘘引起大量直肠出血。结肠镜检查发现严重的憩室病。结论。该患者出生时肛门无孔,可分解为前庭前庭瘘和异位肛门。该病例表现出罕见的临床情况,将产科,妇科,肠胃病和胚胎学等领域融合在一起。

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