A diagnostic journey started with yellow nail syndrome (YNS) ended with the Kartagener's syndrome: a rare case report of coexistence of YNS and Kartagener's syndrome.

IF 1.7 Q2 MEDICINE, GENERAL & INTERNAL
Annals of Medicine and Surgery Pub Date : 2025-04-02 eCollection Date: 2025-05-01 DOI:10.1097/MS9.0000000000002878
Mishaim Khan, Noor Ul Ain Saleem, Waseem Sajjad, Javed Iqbal
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Abstract

Introduction and importance: Yellow nail syndrome (YNS) is a rare disorder diagnosed by a triad of yellowish-green discoloration of the nails, respiratory manifestations, and lymphedema. Kartagener's syndrome (KS) is an autosomal recessive syndrome characterized by chronic sinusitis, bronchiectasis, infertility, and situs inversus. In this case we report the rare coexistence of these solitary occurring disorders.

Case presentation: This report details an interesting case wherein the clinical manifestation of YNS in a 54-year-old male patient not only led to its diagnosis but also revealed the coexistence of another distinctive underlying genetic disorder - KS.

Clinical discussion: KS is an autosomal recessive syndrome characterized by chronic sinusitis, bronchiectasis, infertility, and situs inversus. While KS and YNS are two discernibly unique syndromes, the simultaneous clinical manifestation of their pathologies within a single patient, as presented in our patient, is notably infrequent and rare.

Conclusion: While there is significant documented evidence of YNS co-occurring with only bronchiectasis, we present this case due to the rarity of the amalgamation of YNS with the complete spectrum of pathologies associated with KS. This may help in early diagnosis of either disorder via investigation on the basis of their coexistence as presented in this case and may result in better health outcomes in clinical practice.

诊断旅程从黄指甲综合征(YNS)开始,以Kartagener综合征结束:一个罕见的YNS和Kartagener综合征共存的病例报告。
简介及重要性:黄指甲综合征(YNS)是一种罕见的疾病,诊断为黄绿色的指甲变色,呼吸症状,和淋巴水肿。Kartagener综合征(KS)是一种常染色体隐性综合征,以慢性鼻窦炎、支气管扩张、不孕症和倒位为特征。在这种情况下,我们报告罕见的共存这些孤立发生的疾病。病例介绍:本报告详细介绍了一个有趣的病例,其中54岁男性患者的YNS的临床表现不仅导致了其诊断,而且揭示了另一种独特的潜在遗传疾病- KS的共存。临床讨论:KS是一种常染色体隐性综合征,以慢性鼻窦炎、支气管扩张、不孕症和倒位为特征。虽然KS和YNS是两种明显独特的综合征,但在单个患者中同时出现其病理的临床表现,如本例患者所示,是罕见的。结论:虽然有重要的文献证据表明,YNS仅与支气管扩张共存,但由于罕见的YNS合并与KS相关的完整病理谱系,我们提出了这个病例。这可能有助于通过对这两种疾病共存的调查来早期诊断,并可能在临床实践中产生更好的健康结果。
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来源期刊
Annals of Medicine and Surgery
Annals of Medicine and Surgery MEDICINE, GENERAL & INTERNAL-
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5.90%
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