Suppr超能文献

先天性长直肠阴囊瘘:一种罕见的变异型。

A congenital long rectoscrotal fistula: A rare variant.

作者信息

Shripati Aihole Jayalaxmi

机构信息

Department of Paediatric Surgery, IGICH, Bangalore, Karnataka, India.

出版信息

Radiol Case Rep. 2022 Jul 27;17(10):3511-3514. doi: 10.1016/j.radcr.2022.07.005. eCollection 2022 Oct.

Abstract

Congenital rectoscrotal fistula is a rare variant of anorectal malformations (ARM) as per pena classification. Its nomenclature as well as the management, obviously has not been discussed in literature so far. One such rare case and its management in a male neonate have been discussed here. Non or occasionally deflating congenital recto scrotal fistula has to be managed like an intermediate ARM.

摘要

根据佩纳分类法,先天性直肠阴囊瘘是一种罕见的肛门直肠畸形(ARM)变体。到目前为止,其命名以及治疗方法在文献中显然尚未被讨论过。本文讨论了一名男性新生儿的此类罕见病例及其治疗方法。无或偶尔不排气的先天性直肠阴囊瘘必须像治疗中度肛门直肠畸形一样进行处理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c9d/9334912/ac4dc5fa066b/gr1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验