Morita Chiyo, Yanase Tetsuji, Shiohara Tetsuo, Aoyama Yumi
Dermatology, Onomichi General Hospital, Onomichi, Hiroshima, Japan.
Kawasaki Medical School, Kurashiki, Okayama, Japan.
BMJ Case Rep. 2018 Oct 27;2018:bcr-2018-225528. doi: 10.1136/bcr-2018-225528.
We experienced a 6-year-old case of drug-induced hypersensitivity syndrome (DiHS)/drug reaction with eosinophilia and systemic symptoms (DRESS) with subsequent development autoimmune thyroiditis (Hashimoto's thyroiditis), type 1 diabetes with antithyroglobulin, thyroid peroxidase, insulinoma-associated antigen and anti-insulin antibodies at 4 months, alopecia at 7 months, vitiligo, uveitis due to Vogt-Koyanagi-Harada disease at 8 months after clinical resolution of the DiHS/DRESS. He was diagnosed as type III polyglandular autoimmune syndrome (PASIII) after DiHS/DRESS. Prompted by this case, we sought to determine which triggering factors were responsible for later development of PASIII in previously published cases with autoimmune sequelae. In the literature review, five patients with DIHS/DRESS were found to develop autoimmune sequelae consistent with PASIII. All cases with PASIII were much younger than those without them. Four out of the five patients were treated with intravenous immunoglobulin or pulsed prednisolone in the acute stage, although effective in short-term outcomes.
我们遇到一例6岁的药物性超敏反应综合征(DiHS)/伴嗜酸性粒细胞增多和全身症状的药物反应(DRESS)病例,随后在4个月时出现自身免疫性甲状腺炎(桥本甲状腺炎)、伴有抗甲状腺球蛋白、甲状腺过氧化物酶、胰岛素瘤相关抗原和抗胰岛素抗体的1型糖尿病,7个月时出现脱发,8个月时出现白癜风、因Vogt-小柳原田病导致的葡萄膜炎,此时DiHS/DRESS已临床缓解。他在DiHS/DRESS后被诊断为III型多腺体自身免疫综合征(PASIII)。受该病例启发,我们试图确定在先前发表的有自身免疫后遗症的病例中,哪些触发因素导致了PASIII的后期发展。在文献综述中,发现5例DiHS/DRESS患者出现了与PASIII一致的自身免疫后遗症。所有患有PASIII的病例都比未患该病的病例年轻得多。5例患者中有4例在急性期接受了静脉注射免疫球蛋白或脉冲式泼尼松龙治疗,尽管对短期预后有效。