Combination of Psoriasis and Vitiligo in a Child with Sotos Syndrome: Clinical Case

E. Efanova, Daria G. Taskaeva
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Abstract

Background. Psoriasis and vitiligo are chronic, relatively common dermatological diseases. Meanwhile, their combination in children is rare. The combination of psoriasis and vitiligo in a child with Sotos syndrome has not been previously described. Clinical case description. The boy, 10 years old, was hospitalized with complaints (according to his mother) of rashes on the scalp, body, and limbs, with mild itching that was not related to the time of day. The pathological skin process was widespread. The patient was hyperactive, restless, emotionally labile, irritable. Complaints of rashes was mentioned firstly at the age of 7. Sotos syndrome was established at the age of 8 (variant c.6559C>T (p.Arg2187Ter) in 23 exon of the NSD1 gene (5q35.3), autosomal dominant type of inheritance (pathological allele de novo)). Psoriasis vulgaris was diagnosed with secondary vitiligo (localized form) at the age of 8.5 years. Symptomatic antipruritic and external pathogenetic therapy was performed in the hospital. Phototherapy was not prescribed due to the relative contradiction (small retrocerebral cyst) and the peculiarities of major disease (hyperactivity, restlessness) that complicated to place the child in the phototherapy booth. Positive dynamics was noted during the treatment (14 days): no itching, decrease of peeling severity, flattening and blanching of psoriatic rash elements to spots of post-inflammatory hypopigmentation. The lesion (focus of depigmentation) on the right knee joint skin remained unchanged. The patient was discharged to outpatient care. The prognosis for Sotos syndrome and skin lesions is favorable. Conclusion. The first medical observation of the child with Sotos syndrome burdened with psoriasis and vitiligo is presented. The pathogenetic correlation of these diseases is not clearly defined. Management of such cases requires the joint collaboration of dermatologists, geneticists and pediatricians.
索托斯综合征患儿的银屑病和白癜风并发症:临床病例
背景。银屑病和白癜风是相对常见的慢性皮肤病。然而,儿童同时患有这两种疾病的情况却很少见。索托斯综合征患儿同时患有银屑病和白癜风的病例以前从未报道过。临床病例描述。这名男孩 10 岁,因头皮、身体和四肢出现皮疹,伴有轻微瘙痒而住院治疗(据其母亲称),瘙痒与时间无关。皮肤病变范围很广。患者多动、烦躁不安、情绪不稳定、易怒。索托斯综合征(NSD1 基因(5q35.3)23 外显子中的变异体 c.6559C>T(p.Arg2187Ter),常染色体显性遗传(病理等位基因从头产生))在患者 8 岁时被确诊。8.5 岁时,寻常型银屑病被诊断为继发性白癜风(局部型)。在医院进行了对症止痒和外部病因治疗。由于相对矛盾(小脑后囊肿)和主要疾病的特殊性(多动、躁动不安),将患儿安置在光疗室比较复杂,因此没有进行光疗。治疗期间(14 天)出现了积极的动态变化:无瘙痒,脱皮严重程度减轻,银屑病皮疹变平、变白,形成炎症后色素减退斑。右膝关节皮肤上的皮损(色素沉着灶)没有变化。患者出院后接受了门诊治疗。索托斯综合征和皮肤病变的预后良好。结论本文首次对患有索托斯综合征并伴有银屑病和白癜风的儿童进行了医学观察。这些疾病的致病相关性尚不明确。此类病例的治疗需要皮肤科医生、遗传学家和儿科医生的共同协作。
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