Analysis of the Causes of Newborn Priapism: A Retrospective Clinical Study.

Q4 Biochemistry, Genetics and Molecular Biology
Ekrem Guner, Fatih Akkas, Osman Ozdemir, Yusuf Arikan, Kamil Gokhan Seker, Emre Sam
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Abstract

Priapism is a rare condition in the newborn. The aim of this study was to investigate the demographic, etiologic and clinical features of neonatal priapism. We retrospectively analysed the data of 11 patients diagnosed with neonatal priapism in the neonatal intensive care unit between 2000 and 2019. Priapism was defined as an erection in the neonatal period, lasting more than 4 hours. Etiological examinations revealed polycythemia in one (9.09%) patient, D-dimer elevation in three patients, and heterozygous methyltetrahydrofolate 667 gene mutations in one patient. Other patients were considered idiopathic. Detumescence was achieved in all 11 (100%) patients during the follow-up period. The median hospitalization duration was 6 (IQR [4, 8]; range, 2-9) days. The median follow-up duration was 38 (IQR [30, 42]; range, 13-94) months for patients followed-up in our hospital after discharge. Neonatal priapism is a rare condition. Successful treatment results can be achieved with conservative methods. Data acquired from our study showed that diseases with a tendency to hypercoagulation belong to the etiology by damaging penile microcirculation and make the response to conservative treatment more challenging.

新生儿阴茎勃起障碍原因分析:回顾性临床研究。
阴茎勃起在新生儿中是一种罕见的疾病。本研究的目的是探讨新生儿阴茎勃起障碍的人口学、病因学和临床特征。我们回顾性分析了2000年至2019年在新生儿重症监护病房诊断为新生儿阴茎勃起障碍的11例患者的数据。阴茎勃起定义为新生儿期勃起,持续时间超过4小时。病因学检查显示1例(9.09%)患者有红细胞增多症,3例患者d -二聚体升高,1例患者有杂合甲基四氢叶酸667基因突变。其他患者被认为是特发性的。随访期间11例(100%)患者均消肿。中位住院时间为6 (IQR [4,8];范围:2-9天。中位随访时间为38 (IQR [30,42];出院后在我院随访13 ~ 94个月。新生儿阴茎异常勃起是一种罕见的疾病。采用保守治疗方法可获得成功的治疗效果。我们的研究数据表明,具有高凝倾向的疾病属于由破坏阴茎微循环引起的病因,这使得保守治疗的反应更具挑战性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Prague medical report
Prague medical report Medicine-Medicine (all)
CiteScore
1.10
自引率
0.00%
发文量
19
审稿时长
20 weeks
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