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法洛四联症合并肛门直肠畸形:1 例报告。

Pentalogy of Fallot with Anorectal Malformation: A Case Report.

机构信息

Neonatology Division, Department of Pediatrics, Kathmandu Medical College and Teaching Hospital, Kathmandu, Nepal.

Department of Radiology0, Kathmandu Medical College and Teaching Hospital, Kathmandu, Nepal.

出版信息

JNMA J Nepal Med Assoc. 2024 Jul 31;62(276):542-544. doi: 10.31729/jnma.8705.

Abstract

Pentalogy of Fallot is a rare form of congenital cyanotic heart disease with a prevalence of 3/10,000 live births characterized by an association of Tetralogy of Fallot with Atrial Septal Defect. Pentalogy of Fallot with anorectal malformation is also a rare combination. Here we describe one of the rare case reports of a full-term, 38 weeks, female baby diagnosed with pentalogy of Fallot with imperforate anus and rectovaginal fistula at a tertiary care hospital. Pentalogy of Fallot combined with an imperforate anus and rectovaginal fistula is an exceptionally rare and complex congenital condition. The co- existence of these anomalies emphasizes the need for thorough prenatal and postnatal evaluation for early detection and management.

摘要

法洛五联症是一种罕见的先天性发绀性心脏病,发病率为每 10,000 例活产儿中有 3 例,其特征是法洛四联症与房间隔缺损相关。法洛五联症伴直肠肛门畸形也是一种罕见的组合。在这里,我们描述了在一家三级保健医院诊断为法洛五联症伴肛门闭锁和直肠阴道瘘的一例足月 38 周女性婴儿的罕见病例报告之一。法洛五联症伴肛门闭锁和直肠阴道瘘是一种极其罕见和复杂的先天性疾病。这些异常的并存强调了需要进行彻底的产前和产后评估,以便早期发现和管理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e11/11455648/e4d803ebe7b3/JNMA-62-276-542-g1.jpg

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