Suppr超能文献

先天性肠旋转不良并发多胎妊娠所致肠梗阻:一例罕见病例报告

Intestinal obstruction due to congenital malrotation complicating a multiple pregnancy: A rare case report.

作者信息

Yin Yuzhu, Li Chuo, Xu Chengfang, Wu Lingling, Deng Ni, Hou Hongying, Wu Bin

机构信息

Department of Obstetrics and Gynecology, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou, Guangdong Province, China.

Department of Gastroenterology, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou, Guangdong Province, China.

出版信息

J Pak Med Assoc. 2017 Feb;67(2):308-310.

Abstract

Intestinal obstruction due to congenital intestinal malrotation is usually diagnosed in neonates but may, in rare cases, occur during pregnancy. The absence of specific symptoms in combination with its low incidence makes timely detection of intestinal malrotation-related obstruction difficult in expectant mothers. We present a rare case of a 23-year-old woman with a twin pregnancy following in vitro fertilization-embryo transfer (IVF-ET) who presented with symptoms of intestinal obstruction at 22+4 weeks of gestation. This diagnosis was not confirmed by imaging and the patient was managed conservatively. Following caesarean section, she gave birth to two healthy full-term infants. During the operation, malposition of the bowel and the typical Ladd's band confirmed intestinal malrotation. This is the first report of a congential malrotation complicating a multiple pregnancy, and highlights that malrotation without volvulus can be managed conservatively.

摘要

先天性肠旋转不良所致肠梗阻通常在新生儿期被诊断,但在极少数情况下可能发生于孕期。由于缺乏特异性症状且发病率低,期待中的母亲很难及时发现与肠旋转不良相关的肠梗阻。我们报告一例罕见病例,一名23岁体外受精 - 胚胎移植(IVF - ET)后的双胎妊娠女性,在妊娠22 + 4周时出现肠梗阻症状。影像学检查未确诊,患者接受保守治疗。剖宫产术后,她产下两名健康的足月婴儿。手术中,肠管位置异常及典型的Ladd束证实了肠旋转不良。这是先天性肠旋转不良并发多胎妊娠的首例报告,并强调无肠扭转的肠旋转不良可保守治疗。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验