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Muckle-Wells syndrome: clinical perspectives.穆克-韦尔斯综合征:临床视角
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Diagnostic criteria for cryopyrin-associated periodic syndrome (CAPS).Cryopyrin 相关周期性综合征(CAPS)的诊断标准。
Ann Rheum Dis. 2017 Jun;76(6):942-947. doi: 10.1136/annrheumdis-2016-209686. Epub 2016 Oct 4.
3
Current treatment recommendations and considerations for cryopyrin-associated periodic syndrome.冷吡啉相关周期性综合征的当前治疗建议与考量
Expert Rev Clin Immunol. 2015;11(10):1083-92. doi: 10.1586/1744666X.2015.1077702. Epub 2015 Aug 27.
4
Muckle-Wells syndrome in an Indian family associated with NLRP3 mutation.一个与NLRP3突变相关的印度家族中的穆克勒-韦尔斯综合征。
J Postgrad Med. 2015 Apr-Jun;61(2):120-2. doi: 10.4103/0022-3859.153107.
5
Urticarial vasculitis and urticarial autoinflammatory syndromes.荨麻疹性血管炎和荨麻疹性自身炎症综合征。
G Ital Dermatol Venereol. 2015 Feb;150(1):41-50. Epub 2015 Jan 14.
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Phenotypic and genotypic characteristics of cryopyrin-associated periodic syndrome: a series of 136 patients from the Eurofever Registry.Cryopyrin 相关周期性综合征的表型和基因型特征:来自 Eurofever 登记处的 136 例患者系列。
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Monogenic autoinflammatory diseases: concept and clinical manifestations.单基因自身炎症性疾病:概念与临床表现。
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Clinical characteristics in subjects with NLRP3 V198M diagnosed at a single UK center and a review of the literature.英国某单一中心诊断的NLRP3 V198M患者的临床特征及文献综述。
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Sustained remission of symptoms and improved health-related quality of life in patients with cryopyrin-associated periodic syndrome treated with canakinumab: results of a double-blind placebo-controlled randomized withdrawal study.康纳单抗治疗 cryopyrin 相关周期性综合征患者的症状持续缓解和改善健康相关生活质量:一项双盲安慰剂对照随机停药研究的结果。
Arthritis Res Ther. 2011;13(6):R202. doi: 10.1186/ar3535. Epub 2011 Dec 9.
10
Cryopyrin-associated periodic syndromes: otolaryngologic and audiologic manifestations.Cryopyrin 相关周期性综合征:耳鼻喉和听力表现。
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复发性荨麻疹:一种罕见的冷吡啉相关周期性综合征——穆克-韦尔斯综合征。

Recurrent Urticaria: A Rare Cryopyrin-Associated Periodic Syndrome - Muckle-Wells Syndrome.

作者信息

Gawhale Siddhi

机构信息

Department of Pediatrics, Dr. D.Y. Patil Medical College, Hospital and Research Centre, Pune, India.

出版信息

Case Rep Dermatol. 2025 Feb 25;17(1):86-90. doi: 10.1159/000544705. eCollection 2025 Jan-Dec.

DOI:10.1159/000544705
PMID:40171048
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11961156/
Abstract

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.

摘要

引言

穆克-韦尔斯综合征(MWS)是一种罕见的冷吡啉相关周期性综合征(CAPS),是一种由于NLRP3基因NACHT结构域功能丧失突变导致的自身炎症性疾病。这种缺陷导致的冷吡啉活性丧失最终会引起炎症调节失调以及促炎细胞因子白细胞介素(IL)-1β释放增加。它具有常染色体显性遗传。

病例介绍

我们在此呈现一名8岁女孩,她反复发热、反复出现荨麻疹样皮疹、感音神经性听力损失、炎症标志物和血清淀粉样蛋白水平升高,对抗组胺药物无反应,曾被误诊为结核病,经进一步基因评估后被诊断为MWS。

结论

尽管并不常见,但鉴于其特定的临床表现,临床治疗医生应考虑到MWS。随着合适药物的出现,未来并发症可得到预防,且预后较好。