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一种罕见病例:新生儿特发性阴茎异常勃起及文献综述

A rare entity: idiopathic priapism in a newborn and review of the literature.

作者信息

Karakaya Ali Erdal, Koklu Esad, Ozturk Şenol

机构信息

a Department of Pediatric Surgery, Medical Faculty , Kahramanmaras Sutcuimam University , Kahramanmaras , Turkey and.

b Division of Neonatology , Megapark Hospital , Kahramanmaraş , Turkey.

出版信息

J Matern Fetal Neonatal Med. 2016;29(3):440-2. doi: 10.3109/14767058.2014.1003538. Epub 2015 Jan 23.

DOI:10.3109/14767058.2014.1003538
PMID:25612466
Abstract

Priapism is a pathological condition of a penile erection that persists beyond or is unrelated to sexual stimulation. Priapism is an important medical condition, which requires evaluation and may require emergency management. This condition occurs very infrequently in paediatrics outside of the sickle-cell population and is exceedingly rare in newborns. The evaluation and management of neonatal priapism can be challenging for paediatricians, neonatologists and paediatric urologists alike given the lack of experience with this condition, its poorly understood pathophysiology and the absence of well-established guidelines. We present a case of idiopathic neonatal priapism because of its rarity and review of the literature.

摘要

阴茎异常勃起是一种阴茎勃起的病理状态,其持续时间超过性刺激或与性刺激无关。阴茎异常勃起是一种重要的医学病症,需要进行评估,可能还需要紧急处理。这种情况在镰状细胞病患者群体之外的儿科中非常罕见,在新生儿中极为罕见。鉴于缺乏对这种病症的经验、对其病理生理学了解不足以及缺乏成熟的指南,对于儿科医生、新生儿科医生和儿科泌尿科医生来说,新生儿阴茎异常勃起的评估和处理都具有挑战性。由于其罕见性,我们呈现一例特发性新生儿阴茎异常勃起病例并对文献进行综述。

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Idiopathic high-flow priapism in a 4-month-old infant: A case report and review of literature.一名4个月大婴儿的特发性高流量型阴茎异常勃起:病例报告及文献综述
Clin Case Rep. 2023 Sep 27;11(10):e7985. doi: 10.1002/ccr3.7985. eCollection 2023 Oct.
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Priapism in the newborn: Management of a case.新生儿阴茎异常勃起:1例病例的处理
Urol Case Rep. 2021 Sep 9;39:101845. doi: 10.1016/j.eucr.2021.101845. eCollection 2021 Nov.
3
The first case of neonatal priapism during hypothermia for hypoxic-ischemic encephalopathy and a literature review.
新生儿缺氧缺血性脑病低温治疗中发生阴茎异常勃起 1 例并文献复习
Ital J Pediatr. 2018 Jul 27;44(1):85. doi: 10.1186/s13052-018-0514-9.