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先天性处女膜闭锁合并双侧肾积水、多指畸形及喉膨出:一种罕见的新生儿表现。

Congenital imperforate hymen with bilateral hydronephrosis, polydactyly and laryngocele: A rare neonatal presentation.

作者信息

Ozturk Hulya, Yazici Burhan, Kucuk Adem, Senses Dursun Ali

机构信息

Department of Pediatric Surgery, Duzce University, Turkey.

出版信息

Fetal Pediatr Pathol. 2010 Jan;29(2):89-94. doi: 10.3109/15513811003620609.

Abstract

Imperforate hymen is a rare congenital malformation to present with symptoms in the neonatal period. We present a case of a 5-day-old neonate with a marked interlabial swelling causing urinary retention. Imaging revealed hydrometrocolpos, hydrosalpinx, and bilateral hydronephrosis. Additionally, our patient had polydactyly of both feet and hands, and laryngocele that have not been previously described in literature. Hymenectomy is the mainstay of management to prevent the development of hematocolpos, pain, and possible retrograde menstruation.

摘要

处女膜闭锁是一种罕见的先天性畸形,在新生儿期出现症状。我们报告一例5天大的新生儿,阴唇间明显肿胀导致尿潴留。影像学检查显示阴道积血积脓、输卵管积水和双侧肾积水。此外,我们的患者双手和双脚均有多指畸形以及喉膨出,这在以前的文献中未曾描述过。处女膜切开术是主要的治疗方法,以防止阴道积血、疼痛和可能的逆行月经的发生。

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