Recalcitrant tinea capitis in WHIM syndrome.

Q3 Medicine
Skin health and disease Pub Date : 2025-01-22 eCollection Date: 2025-02-01 DOI:10.1093/skinhd/vzae002
Jasmine C Meltzer, Jennifer Strong, Sophia Martinez, Abigail Salancy, Rutha Adhanom, Edward W Cowen, Leslie Castelo-Soccio, Philip M Murphy, David H McDermott, Isaac Brownell
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引用次数: 0

Abstract

WHIM syndrome is a rare primary immunodeficiency typically caused by autosomal dominant activating mutations in the CXCR4 gene. WHIM refers to warts, hypogammaglobulinaemia, infections and myelokathexis, which are the primary phenotypes of the syndrome. Here we describe a case of tinea capitis in a patient with WHIM syndrome that was unresponsive to multiple systemic antifungal treatments for over 10 years. The patient's recalcitrant tinea infection was ultimately cured after treatment with posaconazole. These findings suggest that the CXCR4 defects in WHIM syndrome may confer susceptibility to dermatophyte infections.

WHIM综合征中的顽固性头癣。
WHIM综合征是一种罕见的原发性免疫缺陷,通常由CXCR4基因的常染色体显性激活突变引起。WHIM是指疣、低γ -球蛋白血症、感染和骨髓增生,这是该综合征的主要表型。在这里,我们描述了一例头癣患者的突发奇想综合征,是无反应的多个系统抗真菌治疗超过10年。患者顽固性癣感染经泊沙康唑治疗后最终治愈。这些发现表明,WHIM综合征中的CXCR4缺陷可能与皮肤真菌感染的易感性有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.70
自引率
0.00%
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审稿时长
10 weeks
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