混合型肺闭塞症、囊性肺腺瘤样畸形和右心室缺血:三重打击

Pub Date : 2024-01-01 Epub Date: 2024-02-20 DOI:10.4103/ijabmr.ijabmr_376_23
Jyoti Bajpai, Shreya Verma, Surya Kant, Ajay Kumar Verma, Darshan Bajaj, Akshyaya Pradhan, Shalini Bhalla
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引用次数: 0

摘要

肺动脉闭塞症和囊性肺腺瘤样畸形是罕见的先天性肺囊性疾病。因此,在同一个人身上同时出现这两种疾病的情况非常罕见。肺封闭是一种无功能的肺组织肿块,其血液供应来自肺循环以外的全身血液供应。先天性囊性肺腺瘤样畸形是一种由异常支气管气室和功能性肺泡缺乏组成的肿块。本病例报告了一名 9 岁女孩的病例,她在过去 15 天里出现间歇性发热、左侧胸痛和咳嗽,并且自孩提时代起就反复咳嗽,这提示她患有混合性肺动脉栓塞、先天性肺囊样腺瘤畸形和右心室突出症。
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Hybrid Pulmonary Sequestration, Cystic Pulmonary Adenomatoid Malformation, and Dextrocardia: A Triple Whammy.

Pulmonary sequestration and cystic pulmonary adenomatoid malformation are rare congenital cystic disorders of the lungs. The presence of both the diseases in the same individual is therefore very uncommon. Pulmonary sequestration is a nonfunctional pulmonary tissue mass that derives its blood supply from systemic blood supply other than pulmonary circulation. Congenital cystic pulmonary adenomatoid malformation represents a mass consisting of abnormal bronchiolar air spaces and a deficiency of functional alveoli. This is the case report of a 9-year-old girl with intermittent fever, left-sided chest pain, and cough for the past 15 days along with recurrent coughs since childhood suggestive of hybrid pulmonary sequestration, congenital cystic adenomatoid malformation, and dextrocardia.

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