Internal Medicine Section, Universidad de Antioquia, Medellín, Colombia.
Rheumatology Section, Universidad de Antioquia, Medellín, Colombia.
Clin Rheumatol. 2022 Nov;41(11):3565-3572. doi: 10.1007/s10067-022-06338-1. Epub 2022 Aug 20.
Vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic syndrome (VEXAS syndrome) is a recently described genetic disorder that gathers autoinflammatory symptoms and myeloid dysplasia. The first description was reported in 2020, and subsequently, a growing number of cases have been described worldwide. Herein, we describe a case of a 72-year-old male patient with VEXAS syndrome with p.Met41Val mutation of the UBA1 gene, prominent supraglottic larynx involvement, and costochondritis. To our knowledge, this is the first report of VEXAS syndrome in Colombia and South America. This disease could present features of relapsing polychondritis, polyarteritis nodosa, giant cell arteritis, and Sweet syndrome, associated with hematologic involvement, including cytopenias, myelodysplastic syndrome, or thromboembolic disease. Supraglottic larynx chondritis and costochondritis are atypical manifestations. These features were proposed previously to differentiate relapsing polychondritis from VEXAS syndrome but are not entirely reliable like in the case described. A diagnosis of VEXAS should be considered in male patients with incomplete or complete features of the previously described conditions, refractory to treatment, requiring high-dose glucocorticoids, and associated progressive hematologic abnormalities. Key Points • VEXAS syndrome is a recently described genetic (somatic mutations in UBA1 gene) disorder that gathers autoinflammatory and hematologic manifestations. • VEXAS syndrome should be considered in male patients with incomplete or complete features of relapsing polychondritis, polyarteritis nodosa, giant cell arteritis, and Sweet syndrome, refractory to treatment, associated with hematologic involvement, including cytopenias, myelodysplastic syndrome, or thromboembolic disease. • Glucocorticoids ameliorate symptoms effectively. However, other treatment options are limited due to a lack of evidence. Traditional immunosuppressants and biological therapy have been used empirically with limited efficacy and a transient effect. Bone marrow transplant offers a curative approach, but it has high morbidity and mortality.
空泡性、E1 酶、X 连锁、自身炎症、体细胞综合征(VEXAS 综合征)是一种最近描述的遗传疾病,它汇集了自身炎症症状和骨髓增生异常。首次描述是在 2020 年报告的,此后,全世界越来越多的病例被描述。在此,我们描述了一例 72 岁男性患者,患有 VEXAS 综合征,携带 UBA1 基因的 p.Met41Val 突变,明显的声门上喉受累和肋软骨炎。据我们所知,这是哥伦比亚和南美洲首例 VEXAS 综合征报告。这种疾病可能表现为复发性多软骨炎、结节性多动脉炎、巨细胞动脉炎和 Sweet 综合征,伴有血液学受累,包括血细胞减少、骨髓增生异常或血栓栓塞性疾病。声门上喉软骨炎和肋软骨炎是非典型表现。这些特征之前被提出用于区分复发性多软骨炎和 VEXAS 综合征,但在描述的病例中并不完全可靠。对于不完全或完全符合先前描述的条件、对治疗有抗性、需要大剂量糖皮质激素且伴有进行性血液学异常的男性患者,应考虑 VEXAS 诊断。关键点 • VEXAS 综合征是一种最近描述的遗传(UBA1 基因突变)疾病,它汇集了自身炎症和血液学表现。 • 对于不完全或完全符合复发性多软骨炎、结节性多动脉炎、巨细胞动脉炎和 Sweet 综合征特征、对治疗有抗性、伴有血液学受累(包括血细胞减少、骨髓增生异常或血栓栓塞性疾病)的男性患者,应考虑 VEXAS 诊断。 • 糖皮质激素可有效改善症状。然而,由于缺乏证据,其他治疗选择有限。传统的免疫抑制剂和生物疗法已被经验性地用于治疗,但疗效有限且效果短暂。骨髓移植提供了一种治愈方法,但它具有高发病率和死亡率。