Holzer Anna, Wolf Peter, Legat Franz J, Kerl Helmut, Hofer Angelika
Department of Dermatology and Venereology, Medical University of Graz, Graz, Austria.
J Dtsch Dermatol Ges. 2006 Nov;4(11):961-4. doi: 10.1111/j.1610-0387.2006.06125.x.
Actinic prurigo is a rare, often difficult-to-treat, idiopathic photodermatosis. Actinic prurigo is divided into a hereditary form appearing in the Native American population and a sporadic form occurring in non-Native Americans. We present a 28-year-old Caucasian woman who developed typical clinical signs and symptoms of actinic prurigo, just as had her mother and grandmother. The patient and her mother were HLA-A24 and HLA-DR 4 with the subtype HLA-DRB1*0408. Based on clinical symptoms and the HLA pattern, the diagnosis of actinic prurigo was made. Treatment with thalidomide led to resolution of the disease. This case report of a Caucasian woman suffering from a hereditary form of actinic prurigo questions the established classification of actinic prurigo into a hereditary Native American form and a sporadic form occurring in the non-Native American population.
光化性痒疹是一种罕见的、常难以治疗的特发性光皮肤病。光化性痒疹分为出现在美洲原住民中的遗传性形式和发生在非美洲原住民中的散发性形式。我们报告一名28岁的白种女性,她出现了光化性痒疹的典型临床体征和症状,她的母亲和祖母也同样如此。该患者及其母亲的人类白细胞抗原(HLA)为A24和DR4,亚型为HLA-DRB1*0408。根据临床症状和HLA模式,诊断为光化性痒疹。沙利度胺治疗使疾病得到缓解。这例患有遗传性光化性痒疹的白种女性病例报告对光化性痒疹既定的分类提出了质疑,即分为美洲原住民遗传性形式和非美洲原住民散发性形式。