Kartagener's syndrome presenting with secondary spontaneous pneumothorax: A rare case report

N. Prabhakar, R. Anand, Preetha Ramesh
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引用次数: 1

Abstract

Kartagener's syndrome (KS) is a part of a larger family of diseases classified as primary ciliary dyskinesia (PCD). The triad of KS consists of bronchiectasis, chronic sinusitis, and situs inversus, which is likely underdiagnosed, as a limited amount of centers have resources to provide an accurate diagnosis. Symptoms are more prevalent in children that too in the first decade of life. Pneumothorax might be one of the rare complications of the PCD. A review of literature revealed that few patients are diagnosed with PCD complicated with secondary spontaneous pneumothorax. In this case report, we describe a PCD patient with spontaneous pneumothorax and how we treated him in our institution.
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以继发性自发性气胸为表现的Kartagener综合征:一例罕见病例报告
Kartagener综合征(KS)是一个更大的疾病家族的一部分,被归类为原发性纤毛运动障碍(PCD)。KS的三联征包括支气管扩张、慢性鼻窦炎和倒位,由于有限的中心有资源提供准确的诊断,这可能未被充分诊断。症状在儿童中更为普遍,在生命的头十年也是如此。气胸可能是PCD的罕见并发症之一。回顾文献发现,很少有患者被诊断为PCD并发继发性自发性气胸。在这个病例报告中,我们描述了一个PCD患者自发性气胸和我们如何治疗他在我们的机构。
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