A Rare Case of Lung Hypoplasia, Cardiac Anomalies and Ovarian Tumour in a Patient with Mayer-Rokitansky-Küster-Hauser Syndrome.

Q3 Medicine
Sultan Qaboos University Medical Journal Pub Date : 2023-11-01 Epub Date: 2022-09-11 DOI:10.18295/squmj.1.2023.012
Pratap Upadhya, A Arpitha, C Sivaselvi, Dasari Papa, K Vignesh
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引用次数: 0

Abstract

Hypoplasia of the lung is an uncommon congenital abnormality of the respiratory system in contrast to pulmonary agenesis. Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is the congenital absence of the upper two-thirds of the vagina and uterus with normal secondary sexual characteristics, ovary and normal karyotype. We report a 31-year-old female patient who presented in 2022 with cough with expectoration, left-side chest pain and breathlessness for 4 years to tertiary hospital, Puducherry, India. She was evaluated for amenorrhoea and diagnosed as MRKH syndrome and the patient underwent right-side oophorectomy for right ovarian torsion with a tumour. Computed tomography pulmonary angiogram and fiberoptic endoscopy were suggestive of left lung hypoplasia and the patient was advised symptomatic treatment for lung hypoplasia and planned for vaginoplasty for which she refused.

一例罕见的MRKH综合征患者肺发育不全、心脏异常和卵巢肿瘤
肺发育不良是一种罕见的先天性呼吸系统异常,与肺发育不全相反。Mayer-Rokitansky-Küster-Hauser(MRKH)综合征是指阴道和子宫上三分之二的先天性缺失,具有正常的继发性特征、卵巢和正常核型。在这里,我们描述了一例左肺发育不全和先天性心脏畸形伴MRKH综合征和卵巢平滑肌瘤的病例。一名31岁的女性在贾瓦哈拉尔医学教育与研究所(JIPMER)接受了四年的咳嗽伴咳痰、左侧胸痛和呼吸困难的治疗。她被评估为闭经,并被诊断为MRKH综合征,患者因右侧卵巢扭转伴肿瘤而接受了右侧卵巢切除术。计算机断层扫描肺血管造影(CTPA)和纤维内窥镜提示左肺发育不全,建议患者对肺发育不完全进行症状治疗,并计划进行阴道成形术。关键词:肺发育不全,不孕,穆勒氏发育不全、先天性支气管扩张、左侧上腔静脉、卵巢平滑肌瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.00
自引率
0.00%
发文量
86
审稿时长
7 weeks
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