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产后出现的法洛四联症未矫正合并鼻皮样囊肿及正中唇裂的罕见病例。

A unique case of uncorrected Fallot's tetralogy with nasal dermoid cyst and median cleft lip presenting during postpartum.

作者信息

Chatterjee Subhankar, Ojha Umesh K, Chavan Suraj H, Singh Diksha, Kumari Priyanshu, Kumar Kunal, Shafi Ramsha, Baskey Surendra, Dasgupta Rituparna, Benito-León Julián, Ghosh Ritwik

机构信息

Department of General Medicine, Patliputra Medical College and Hospital, Dhanbad, India.

Department of Cardiology, Asarfi Hospital, Dhanbad, Jharkhand, India.

出版信息

J Family Med Prim Care. 2022 Jan;11(1):353-356. doi: 10.4103/jfmpc.jfmpc_1036_21. Epub 2022 Jan 31.

Abstract

While tetralogy of Fallot (TOF) is the most common cyanotic congenital heart disease among children, its first presentation in the third decade of life just after successful pregnancy outcome is extremely rare. In fact, survival of both child and mother having uncorrected TOF after noninstitutional delivery is unheard of. Herein, authors report a case of previously undiagnosed TOF associated with other midline congenital abnormalities, that is, nasal dermoid cyst and cleft palate, who presented for the first time with postpartum hemorrhage after an unsupervised home birth. To the best of our knowledge, this unique association has never been described before.

摘要

虽然法洛四联症(TOF)是儿童中最常见的青紫型先天性心脏病,但其在成功妊娠分娩后第三个十年首次出现极为罕见。事实上,未经矫正的TOF患儿及其母亲在非医疗机构分娩后存活的情况闻所未闻。在此,作者报告一例先前未被诊断出的TOF病例,该病例伴有其他中线先天性异常,即鼻皮样囊肿和腭裂,患者在无人监管的家中分娩后首次出现产后出血。据我们所知,这种独特的关联以前从未被描述过。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbee/8930167/a1348bd3564a/JFMPC-11-353-g001.jpg

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