先天性幽门闭锁伴大疱性表皮松解一例

Q4 Medicine Journal of Neonatal Surgery Pub Date : 2022-11-06 DOI:10.47338/jns.v11.1071
Shishir Kumar, V. Manchanda, Parveen Kumar, R. Bhandari
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引用次数: 0

摘要

背景:Carmi综合征是指先天性幽门闭锁和大疱性表皮松解症。它的死亡率很高。病例系列:我们报告了3名新生儿,其特征是多个皮肤水泡,并有一张单一水泡外观的经典X光照片。其中2人接受了手术,1人在术前死于败血症。一个婴儿的死亡率较低,另一个婴儿在随访中表现良好。结论:Carmi综合征应作为皮肤水泡和喂养不耐受新生儿的鉴别诊断。早期识别并及时进行医疗和外科治疗可能有助于取得成功。
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Congenital pyloric atresia with epidermolysis bullosa: A case series
Background: Carmi syndrome is the name given to the association of congenital pyloric atresia and epidermolysis bullosa. It has a high mortality. Case series: We report 3 neonates with features of multiple skin blisters and a classical X-ray picture of a single bubble appearance. Two of them underwent surgery while 1 succumbed to sepsis in the pre-operative period. One baby had delayed mortality and the other is doing well in follow-up. Conclusions: Carmi syndrome should be kept as a differential diagnosis in neonates with skin blisters and feed intolerance. Early recognition with prompt medical and surgical management may contribute to a successful outcome.
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来源期刊
Journal of Neonatal Surgery
Journal of Neonatal Surgery Medicine-Surgery
CiteScore
0.30
自引率
0.00%
发文量
29
审稿时长
6 weeks
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