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Wong-Type Dermatomyositis: An Extremely Rare Disease in Childhood

机译:黄型皮肌炎:儿童时期极为罕见的疾病

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摘要

Some cutaneous manifestations can hide systemic symptoms of dermatomyositis (DM). The Wong-type dermatomyositis (W-DM) should be considered in the differential diagnosis in children with overlapping symptoms of DM and pityriasis rubra pilaris (PRP). This rare form of DM is reported in only 27 cases in the literature: 6 cases of pediatric age and only 3 with associated cutaneous features of PRP (2 females aged 1 and 18 years and a 12-year-old boy) [ ]. Our patient was the fourth case of W-DM with associated cutaneous features of PRP and the first under the age of 10 years. Punch biopsy and knowledge of rare diseases improve the diagnostic ability and therapy. Differential diagnosis includes lupus erythematosus, PRP, and psoriasis.
机译:一些皮肤表现可以掩盖皮肌炎(DM)的全身症状。在DM和糠疹糠疹的重叠症状患儿的鉴别诊断中,应考虑Wong型皮肌炎(W-DM)。在文献中仅报道了这种罕见形式的DM 27例:小儿年龄6例,仅有3例具有PRP相关皮肤特征(2名1岁和18岁的女性和12岁的男孩)[]。我们的患者是第四例W-DM,伴有PRP的皮肤特征,第一例在10岁以下。打孔活组织检查和罕见疾病知识可提高诊断能力和治疗水平。鉴别诊断包括红斑狼疮,PRP和牛皮癣。

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