在一个女性儿科患者的eosinophilic细胞质炎 (威尔斯综合征)
María J Aráoz1, María M Buján1, María Del V Centeno2
1Department of Dermatology; Department of Pathology; Hospital de Pediatría S.A.M.I.C. Prof. Dr. Juan P. Garrahan, City of Buenos Aires, Argentina.
Archivos argentinos de pediatria
|March 14, 2024
概括
威尔斯综合征是一种罕见的儿科炎症状况,异常呈现为无症状结节. 达普森在这种埃索诺菲尔细胞质炎病例中被证明是有效的,在皮质类固醇治疗后控制了复发.
科学领域:
- 皮肤病学 皮肤病学
- 儿科 儿科 儿科
- 病理学 病理学 病理学
背景情况:
- 威尔斯综合征 (eosinophilic cellulitis) 是一种罕见的炎症性皮肤疾病,病因不明.
- 通常呈现为红血斑,结节或水泡,在儿科患者中不常见.
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