Spörkmann K H, Eickhoff R, Dominick H C
Kinderklinik des St.-Marien- und St.-Annastifts-Krankenhauses, Ludwigshafen.
Monatsschr Kinderheilkd. 1990 Sep;138(9):619-22.
A 10.6 year old Turkish girl developed + the signs of a polyglandular autoimmune syndrome (PGA) type I since her first year of age. Apart from the endocrine and non-endocrine symptoms of PGA, she suffered from an acute state of illness with therapy-resistant fever and multiform exanthemas in the early course of disease. All included the criteria of Wissler-Fanconi syndrome became clear which has not yet been reported in association with PGA. Although this syndrome generally is considered an equivalent of Still's syndrome, rheumatoid symptoms could not be ascertained during the following 9-year-course of PGA.
一名10.6岁的土耳其女孩自1岁起就出现了Ⅰ型多腺体自身免疫综合征(PGA)的症状。除了PGA的内分泌和非内分泌症状外,在疾病早期她还出现了病情急性发作,伴有治疗抵抗性发热和多形性皮疹。所有符合威斯勒-范科尼综合征的标准都很明确,此前尚未有与PGA相关的报道。尽管该综合征通常被认为等同于斯蒂尔病,但在随后9年的PGA病程中未发现类风湿症状。