泛滥成灾的双重打击导致VEXAS综合征的新诊断。

Journal of medical cases Pub Date : 2023-10-01 Epub Date: 2023-10-13 DOI:10.14740/jmc4127
Helen Pozdniakova, Apurva Vedire, Anand Kadakia, Steven Imburgio, Ravneet Bajwa, Varsha Gupta, Ruchi Bhatt, Mohammad A Hossain
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引用次数: 0

摘要

VEXAS(液泡、E1酶、X连锁、自身炎症、体细胞)综合征是一种新定义的疾病,连接了血液学、肿瘤学和风湿病。其病理生理学起源于UBA1基因的突变,该突变导致泛素化缺陷,从而导致严重的全身炎症综合征。它与显著的发病率和死亡率有关;然而,由于文献中描述的案例有限,数据很少。在这里,我们描述了一个60多岁的男性病例,他因进行性呼吸困难、口腔摄入不足和体重减轻而被转诊到血液肿瘤学。2年前,他被诊断为复发性多软骨炎;然而,尽管接受了治疗,他的症状并没有改善。他最终被诊断为VEXAS综合征,UBA1(泛素样修饰物激活酶1)发生突变,同时发生SQSTM1突变。此外,到目前为止,还没有报道在同一患者中泛素化途径中存在两个突变。将该患者和治疗过程与已有文献进行比较,以提高对VEXAS综合征的认识并改善其医疗管理。
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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A Double Hit to Ubiquitination Leading to a New Diagnosis of VEXAS Syndrome.

VEXAS (vacuoles, E1 enzyme, X-linked, auto-inflammatory, somatic) syndrome is a newly defined illness that bridges hematology, oncology, and rheumatology. Its pathophysiology originates in a mutation in the UBA1 gene that leads to a defect in ubiquitination resulting in a severe systemic inflammatory syndrome. It is associated with significant morbidity and mortality; however, data are scarce due to limited cases described in the literature. Here we describe a case of a male in his 60s who was referred to hematology-oncology due to progressive dyspnea, poor oral intake, and weight loss. He was diagnosed with relapsing polychondritis 2 years prior; however, his symptoms did not improve despite treatment. He was ultimately diagnosed with VEXAS syndrome with a mutation in UBA1 (ubiquitin-like modifier activating enzyme 1) and a concurrent SQSTM1 mutation. In addition, the coexistence of two mutations in the ubiquitination pathway in the same patient has not been reported to date. This patient and the treatment course were compared to pre-existing literature to increase awareness and improve the medical management of VEXAS syndrome.

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