Sandoval Karina Romero, Machado Maria Cecília Rivitti, Oliveira Zilda Najjar Prado de, Nico Marcello Menta Simonsen
Department of Dermatology, Hospital das Clínica, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brazil.
Division of Dermatology, Ambulatório de Dermatologia Pediátrica, Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brazil.
An Bras Dermatol. 2019 Jul 26;94(3):341-343. doi: 10.1590/abd1806-4841.20198789.
CHILD syndrome (Congenital Hemidysplasia, Ichthyosiform erythroderma, Limb Defects) is a rare X-linked dominant disease. The authors report a 2-month-old patient presenting with typical features of CHILD syndrome that was treated with a topical solution containing cholesterol and lovastatin, with complete clearance of her CHILD nevus. The changes in skin lipid metabolism that explain the CHILD ichthyosiform nevus and their correction through topical application of cholesterol and lovastatin are discussed.
儿童综合征(先天性半侧发育不全、鱼鳞病样红皮病、肢体缺陷)是一种罕见的X连锁显性疾病。作者报告了一名2个月大的患有儿童综合征典型特征的患者,该患者接受了含有胆固醇和洛伐他汀的外用溶液治疗,其儿童痣完全消退。本文讨论了解释儿童鱼鳞病样痣的皮肤脂质代谢变化以及通过局部应用胆固醇和洛伐他汀对其进行的纠正。