Duhra P, Charles-Holmes R
South Warwickshire Hospital, Warwick, U.K.
Br J Dermatol. 1991 Aug;125(2):172-4. doi: 10.1111/j.1365-2133.1991.tb06066.x.
A case of haemorrhagic pompholyx occurring in a 29-year-old man with linear IgA disease is described. There were several features in our patient that are usually seen in chronic bullous disease of childhood. Treatment with dapsone cleared the eruption but induced a progressive yet reversible neutropenia.
本文描述了一例发生在一名患有线状IgA疾病的29岁男性身上的出血性汗疱疹。我们的患者有几个通常在儿童慢性大疱性疾病中出现的特征。使用氨苯砜治疗使皮疹消退,但诱发了进行性但可逆的中性粒细胞减少症。