中国麻风皮肤病杂志 ›› 2023, Vol. 39 ›› Issue (6): 420-422.doi: 10.12144/zgmfskin202306420

• 临床研究 • 上一篇    下一篇

经免疫学检查确诊的氨苯砜综合征一例

杨宝琦,于长平,孙乐乐,张福仁   

  1. 山东第一医科大学附属皮肤病医院(山东省皮肤病医院),山东省皮肤病性病防治研究所,山东济南,250022
  • 出版日期:2023-06-15 发布日期:2023-05-18

Dapsone hypersensitivity syndrome confirmed by immunological examination

YANG Baoqi, YU Changping, SUN Lele, ZHANG Furen   

  1. Shandong Provincial Hospital for Skin Diseases & Shandong Provincial Institute of Dermatology and Venereology, Shandong First Medical University & Shandong Academy of Medical Sciences, Jinan 250022, China
  • Online:2023-06-15 Published:2023-05-18

摘要: 患者,男,28岁。因发热4周全身皮肤潮红、脱屑3周于2004年8月入院。患者入院9周前因寻常型银屑病给予雷公藤、氨苯砜、罗红霉素、复方甘草酸铵等药物治疗。4周前出现发热。3周前躯干四肢皮肤红斑、淋巴结肿大、肝功异常。外院给予糖皮质激素、抗菌素治疗,皮疹逐渐加重。入院时查体:T 37.7℃,颈、腋、腹股沟数个淋巴结肿大,全身皮肤弥漫性潮红、脱屑。实验室检查示:丙氨酸氨基转移酶(ALT)384 U/L、门冬氨酸氨基转移酶(AST)152 U/L、血白蛋白(ALB)31.2 g/L、总胆红素140.2 μmol/L、直接胆红素107.7 μmol/L。诊断为红皮病型药疹、药物性肝炎。停用氨苯砜等可疑药物后,给予糖皮质激素、营养支持以及对症治疗47天后痊愈出院。出院13年后随访,检测患者HLA-B*13:01基因阳性,采用氨苯砜体外刺激外周血单一核细胞IL-5酶联免疫斑点实验阳性。最终确诊为氨苯砜综合征。

关键词: 氨苯砜, HLA-B*13:01等位基因, 药物超敏综合征

Abstract: A 28-year-old man was admitted to our hospital due to fever for four weeks and erythema and scales on all his skin for three weeks in August, 2004. The patient developed psoriasis vulgaris nine weeks ago and was treated with tripterygium wilfordii, dapsone, roxithromycin and compound ammonium glycyrrhizinate. He began fever four weeks ago and had erythema on trunk and extremities, elevated transaminase and lymphadenopathy three weeks ago. He was given glucocorticoid and antibiotic therapy by other hospitals. But his lesions gradually became severe. Physical examination revealed his temperature was 37.7℃ and several lymph nodes in his neck, axillary and groin were found with skin erythema and scales all around his body. Laboratory tests showed increased alanine aminotransferase (ALT,384 U/L), aspartate aminotransferase (AST,152 U/L), total bilirubin (TBIL, 140.2 μmol/L), direct bilirubin (DBIL, 107.7 μmol/L) and decreased albumin albumin (ALB,31.2 g/L). The patient was diagnosed with erythrodermic drug eruption and drug induced hepatitis. Then dapsone and other agents were ceased. After 47 days of treatment with glucocorticoid and extra-nutrition, the patient was cured and discharged. His was found carrying HLA-B*13:01 allele 13 years later during follow up. The IL-5 enzyme-linked immunospot assay on his peripheral blood mononuclear cells stimulated by dapsone in vitro was positive. Finally, the diagnosis of dapsone hypersensitivity syndrome was made.

Key words: dapsone, HLA-B*13:01 allele, drug hypersensitivity syndrome