ehers - danlos综合征的盆腔器官脱垂。

Azadeh Nazemi, Katherine Shapiro, Shavy Nagpal, Nirit Rosenblum, Benjamin M Brucker
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引用次数: 0

摘要

ehers - danlos综合征(EDS)是一种遗传性组织和胶原合成障碍,可使患者易患妇科和产科并发症。女性患者经常患有麻烦的盆底疾病,但由于EDS的医学复杂性,需要特别注意盆腔器官脱垂和相关的尿失禁的治疗。在本文中,我们报告了三个独特的盆腔器官脱垂(POP)患者,并深入探讨了涉及泌尿妇科、风湿病学、物理学、胃肠病学和麻醉学的多学科方法,以适当地处理这种情况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Pelvic Organ Prolapse in Ehlers-Danlos Syndrome.

Pelvic Organ Prolapse in Ehlers-Danlos Syndrome.

Pelvic Organ Prolapse in Ehlers-Danlos Syndrome.

Pelvic Organ Prolapse in Ehlers-Danlos Syndrome.

Ehlers-Danlos syndrome (EDS) is a hereditary tissue and collagen synthesis disorder that can predispose patients to gynecologic and obstetric complications. Female patients often suffer from bothersome pelvic floor disorders, but due to the medical complexity of EDS, special considerations are needed for the treatment of pelvic organ prolapse and associated incontinence. In this paper, we present three unique cases of pelvic organ prolapse (POP) in EDS patients and delve deeper into the multidisciplinary approach involving urogynecology, rheumatology, physiatry, gastroenterology, and anesthesiology required to appropriately manage this condition.

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