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一名成年女性卡塔格内综合征的迟发性诊断

Late Diagnosis of Kartagener Syndrome in an Adult Female.

作者信息

Tsetsou Ilianna, Balomenos Vasileios, Koreas Panagiotis, Biliara Irini Elissavet, Tavernaraki Kyriaki

机构信息

Department of Imaging and Interventional Radiology, "Sotiria" General and Chest Diseases Hospital of Athens, Athens, GRC.

出版信息

Cureus. 2024 Apr 22;16(4):e58747. doi: 10.7759/cureus.58747. eCollection 2024 Apr.

DOI:10.7759/cureus.58747
PMID:38779262
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11110918/
Abstract

Kartagener syndrome (KS), also known as primary ciliary dyskinesia, is a rare genetic disorder commonly diagnosed early in childhood. It is characterized by a triad of findings, namely, situs inversus, chronic sinusitis, and bronchiectasis. Here, we present the case of a 73-year-old female who incidentally presented the KS triad during her imaging tests in the emergency department of our institution for COVID-19 symptoms.

摘要

卡塔格内综合征（KS），也称为原发性纤毛运动障碍，是一种罕见的遗传性疾病，通常在儿童早期被诊断出来。它的特征是有一组三联征表现，即内脏转位、慢性鼻窦炎和支气管扩张。在此，我们报告一例73岁女性病例，该患者在我院急诊科因新冠病毒疾病症状进行影像检查时偶然发现了卡塔格内综合征三联征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aac9/11110918/99a5fc94f834/cureus-0016-00000058747-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aac9/11110918/5627b2c7b73d/cureus-0016-00000058747-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aac9/11110918/396d4b0cc184/cureus-0016-00000058747-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aac9/11110918/99a5fc94f834/cureus-0016-00000058747-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aac9/11110918/5627b2c7b73d/cureus-0016-00000058747-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aac9/11110918/396d4b0cc184/cureus-0016-00000058747-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aac9/11110918/99a5fc94f834/cureus-0016-00000058747-i03.jpg

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引用本文的文献

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Cureus. 2025 Jul 20;17(7):e88375. doi: 10.7759/cureus.88375. eCollection 2025 Jul.

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