一名艾森曼格综合征患者的 Swyer-James-MacLeod 综合征。

Dolunay Gürses, Merve Oğuz, Doğangün Yüksel, Furkan Ufuk, Münevver Yılmaz
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引用次数: 0

摘要

Swyer-James-MacLeod 综合征的放射学特征是单肺叶高透明,伴有血管减少、肺泡过度滞留和空气潴留,但无支气管气道阻塞。室间隔缺损是儿童时期最常见的先天性心脏缺陷,如不及时治疗,会导致不可逆的肺动脉高压和艾森曼格综合征。本病例报告介绍了一名 25 岁的 Swyer-James-MacLeod 综合征和艾森曼格综合征患者。将Swyer-James-MacLeod综合征纳入分布不典型的肺气肿和单侧高透明症患者的鉴别诊断中,对于早期诊断和及时干预至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Swyer-James-MacLeod Syndrome in a Patient with Eisenmenger Syndrome.

Swyer-James-MacLeod syndrome is characterized radiologically by hyperlucency in a single lung lobe, accompanied by reduced vascularity, alveolar hyperdistention, and air trapping, without bronchial airway obstruction. The most common congenital heart defect in childhood, ventricular septal defect, leads to irreversible pulmonary hypertension and Eisenmenger syndrome if not treated promptly. This case report presents a 25-year-old patient with Swyer-James-MacLeod syndrome and Eisenmenger syndrome. It is crucial to include Swyer-James-MacLeod syndrome in the differential diagnosis of patients with atypically distributed pulmonary emphysema and unilateral hyperlucency for early diagnosis and timely intervention.

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