Gawhale Siddhi
Department of Pediatrics, Dr. D.Y. Patil Medical College, Hospital and Research Centre, Pune, India.
Case Rep Dermatol. 2025 Feb 25;17(1):86-90. doi: 10.1159/000544705. eCollection 2025 Jan-Dec.
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.
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.
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.
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。
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。
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。