Sonkodi S, Jarmay K, Korom I, Kemeny E, Szabo E, Abraham G, Sonkodi I, Ribari O, Mohacsi G
Nephron. 1987;47(1):32-5. doi: 10.1159/000184453.
A 24-year-old female developed a painless swelling adjacent to the left ear. This was shown to be eosinophilic angiolymphoid hyperplasia (ALH). Three months later she developed a nephrotic syndrome. Renal biopsy revealed membranous nephropathy. This is the first non-Japanese case of dermal eosinophilic ALH and nephrotic syndrome; steroid treatment followed by surgical removal of the tumour resulted in complete remission in the renal lesion.
一名24岁女性左耳旁出现无痛性肿胀,经诊断为嗜酸性血管淋巴样增生症(ALH)。三个月后,她发展为肾病综合征。肾活检显示为膜性肾病。这是首例非日本籍患者出现皮肤嗜酸性ALH合并肾病综合征的病例;采用类固醇治疗并随后手术切除肿瘤后,肾脏病变完全缓解。