Refractory Acrodermatitis Continua of Hallopeau in a Pediatric Patient: Unveiling Underlying Mixed Connective Tissue Disorder.

Q2 Medicine
Nadine A Del Rosario, Shayla H U Nguyen, Ethan Q H Nguyen
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引用次数: 0

Abstract

Acrodermatitis continua of Hallopeau (ACH) is a rare pustular psoriasis variant that presents as sterile pustules on the hands and feet with a relapsing course. This condition is not easily treated, but literature shows some cases are successfully controlled with biologics such as etanercept, adalimumab, secukinumab, and ustekinumab. Mixed connective tissue disease (MCTD) is a type of autoimmune disease and is rarely seen in the pediatric population. It is characterized by overlapping features of various autoimmune disorders, often involving scleroderma, systemic lupus erythematosus, polymyositis, and other organ dysfunction. MCTD is typically diagnosed with lab testing to indicate the presence of specific autoantibodies to a nuclear matrix protein, such as ribonucleoprotein. This communication emphasizes the importance of revisiting diagnoses in patients with persistent, refractory skin conditions and highlights the need for comprehensive evaluation in the presence of evolving or atypical presentations, especially when autoimmune diseases are suspected. Steps for diagnostic workup and treatment may provide clinical benefits to patients and serve as a reference for other clinicians. The course of treatment for ACH and MCTD in the pediatric and adolescent population is discussed.

顽固性持续肢端皮炎在儿科患者:揭示潜在的混合结缔组织疾病。
持续性埃洛珀肢端皮炎(ACH)是一种罕见的脓疱型牛皮癣变种,表现为手部和足部的无菌脓疱,并伴有复发过程。这种情况不容易治疗,但文献显示,一些病例可以通过依那西普、阿达木单抗、secukinumab和ustekinumab等生物制剂成功控制。混合性结缔组织病(MCTD)是一种自身免疫性疾病,在儿科人群中很少见。它的特点是多种自身免疫性疾病的重叠特征,常涉及硬皮病、系统性红斑狼疮、多发性肌炎和其他器官功能障碍。MCTD通常通过实验室检测来诊断,以表明存在针对核基质蛋白(如核糖核蛋白)的特异性自身抗体。本报告强调了对持续性、难治性皮肤病患者重新诊断的重要性,并强调了在出现演变或非典型症状时,特别是当怀疑存在自身免疫性疾病时,需要进行全面评估。诊断检查和治疗的步骤可以为患者提供临床益处,并作为其他临床医生的参考。讨论了ACH和MCTD在儿科和青少年人群中的治疗过程。
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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来源期刊
CiteScore
2.60
自引率
0.00%
发文量
104
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