复发性荨麻疹:一种罕见的低温素相关周期性综合征-粘液-井综合征。

IF 0.9 Q4 DERMATOLOGY
Case Reports in Dermatology Pub Date : 2025-02-25 eCollection Date: 2025-01-01 DOI:10.1159/000544705
Richa, Siddhi Gawhale
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引用次数: 0

摘要

简介:Muckle-Wells综合征(MWS)是一种罕见的cryopyrin相关周期性综合征(CAPS),是一种由NLRP3基因NACHT结构域功能缺失突变引起的自身炎症性疾病。crypyrin活性的丧失最终导致炎症失调和促炎细胞因子白细胞介素(IL)-1 β的释放增加。它具有常染色体显性遗传。病例介绍:我们在此报告一名8岁女孩,反复发烧,反复荨麻疹,感音神经性听力丧失,炎症标志物和血清淀粉样蛋白水平升高,抗组胺药物无效,被误诊为肺结核,经进一步遗传评估诊断为MWS。结论:尽管MWS不常见,但鉴于其特殊的临床表现,临床医生应将其纳入治疗考虑。通过适当的药物治疗,可以预防未来的并发症,预后也较好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recurrent Urticaria: A Rare Cryopyrin-Associated Periodic Syndrome - Muckle-Wells Syndrome.

Introduction: Muckle-Wells syndrome (MWS) is a rare cryopyrin-associated periodic syndrome (CAPS), an autoinflammatory disorder due to a loss of function mutation in the NACHT domain of the NLRP3 gene. The loss of cryopyrin activity brought on by this deficiency eventually causes dysregulated inflammation and increased release of the proinflammatory cytokine interleukin (IL)-1 beta. It has an autosomal dominant inheritance.

Case presentation: We present here an 8-year-old girl with recurrent fever, recurrent urticarial rash, sensorineural hearing loss, raised inflammatory markers and serum amyloid levels, which did not respond to the anti-histaminic drugs, was wrongly diagnosed as tuberculosis, which on further genetic evaluation was diagnosed as MWS.

Conclusion: Despite being uncommon, treating clinicians should take MWS into consideration given the specific clinical presentation. With the availability of appropriate medications, future complications can be prevented, and the prognosis is better.

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来源期刊
CiteScore
1.60
自引率
0.00%
发文量
57
审稿时长
9 weeks
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