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伴有非交通性功能性子宫角和单角子宫的VATER/VACTERL综合征(脊柱/肛门/心脏/气管/食管/桡骨/肾脏/肢体异常):病例报告

VATER/VACTERL syndrome (vertebra/anus/cardiac/trachea/esophogus/radius/renal/limb anomalies) with a noncommunicating functioning uterine horn and a unicornuate uterus: a case report.

作者信息

Nunes Natalie, Karandikar Sharad, Cooper Sarah, Jaganathan Ramasamy, Irani Shirin

机构信息

Department of Obstetrics and Gynecology, Birmingham Heartlands Hospital, Heart of England Foundation Trust, Birmingham, United Kingdom.

出版信息

Fertil Steril. 2009 May;91(5):1957.e11-2. doi: 10.1016/j.fertnstert.2008.12.140. Epub 2009 Mar 17.

Abstract

OBJECTIVE

To describe the presentation and outcome of a patient with an unusual association of VATER/VACTERL syndrome (vertebra/anus/cardiac/trachea/esophogus/radius/renal/limb) and noncommunicating functioning uterine horn and a unicornuate uterus.

DESIGN

Descriptive case report.

SETTING

A foundation trust in the United Kingdom. MATERIALS AND METHOD(S): A patient known to have VATER/VACTERL syndrome was diagnosed with a hematometra of a noncommunicating uterine horn and hematosalpinx. She underwent multidisciplinary surgery to remove the functioning uterine horn, after which she had a full recovery.

CONCLUSION(S): This case documents the association of VATER/VACTERL syndrome with a unicornuate uterus and noncommunicating horn.

摘要

目的

描述一名患有VATER/VACTERL综合征(椎体/肛门/心脏/气管/食管/桡骨/肾脏/肢体)、非交通性功能性子宫角和单角子宫的不寻常关联患者的临床表现及预后。

设计

描述性病例报告。

地点

英国一家基础信托医院。

材料与方法

一名已知患有VATER/VACTERL综合征的患者被诊断为非交通性子宫角积血和输卵管积血。她接受了多学科手术以切除功能性子宫角,术后完全康复。

结论

本病例记录了VATER/VACTERL综合征与单角子宫及非交通性子宫角的关联。

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