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早产儿先天性胃窦蹼。

Congenital antral web in premature baby.

作者信息

Nam So-Hyun, Koo Soo Hyun, Chung Mi Lim, Jung Yu Jin, Lim Yun-Jung

机构信息

Department of Pediatric Surgery, Inje University Haeundae Paik Hospital, Busan, Korea.

出版信息

Pediatr Gastroenterol Hepatol Nutr. 2013 Mar;16(1):49-52. doi: 10.5223/pghn.2013.16.1.49. Epub 2013 Mar 31.

Abstract

Antral web is a rare cause of gastric outlet obstruction in neonate. It is a 2-4 mm thin mucous membrane that can be found anywhere from 1 to 7 cm proximal to the pylorus. The baby was born at gestational age of 32(+1) weeks with 1,880 g as 2nd baby of dizygotic twin. After birth, the baby had constant non-bilious vomiting without feeding while he didn't show abdominal distension or discoloration. The infantogram showed distended stomach with distal small bowel gas. Upper gastrointestinal series revealed that the antrum was abruptly narrowed at 1 cm proximal to pylorus. We performed laparotomy at the 10th day after birth and excised the 2 mm-thick web circumferentially. He began milk feeding after 6 days and discharged uneventfully at postoperative 35 days with corrected age of 38(+4) weeks with body weight 2,420 g. The antral web should be considered in the case of non-bilious vomiting in neonate.

摘要

胃窦蹼是新生儿胃出口梗阻的罕见原因。它是一层2至4毫米厚的薄黏膜,可在幽门近端1至7厘米的任何位置发现。该婴儿为孕32(+1)周出生的双卵双胎中的第二个,体重1880克。出生后,婴儿持续出现非胆汁性呕吐,进食时即吐,且无腹胀或皮肤变色。腹平片显示胃扩张,远端小肠有气体。上消化道造影显示胃窦在幽门近端1厘米处突然变窄。我们在婴儿出生后第10天进行了剖腹手术,环形切除了2毫米厚的蹼。术后6天开始喂奶,术后35天顺利出院,矫正年龄为38(+4)周,体重2420克。对于新生儿非胆汁性呕吐的病例,应考虑胃窦蹼的可能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6e7/3746043/cc180ab1deca/pghn-16-49-g001.jpg

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