甲状腺机能亢进症(简称甲亢)并原发性血小板减少性紫癜(简称 ITP)临床上较为少见,国内迄今仅见报告10余例。本院在12年中见到3例,现简要报告如下,并复习有关文献,对其发病情况,病理基础,诊断及治疗进行粗略的讨论。病例报告例1,叶××,女性,27岁,因食欲亢进,性急,怕热,多汗2年,反复鼻血,皮肤紫癜,齿龈出血与面色苍白2个月;11天来症状加重,鼻血不止,于1977年7月13日入院。查体:T:37.6℃ P136/分。呈急性重病容,消瘦与贫血外观。全身皮肤大量散在 Hyperthyroidism (referred to as hyperthyroidism) and idiopathic thrombocytopenic purpura (referred to as ITP) clinically rare, so far only see the domestic report of more than 10 cases. The hospital in 12 years to see 3 cases, are now briefly reported as follows, and review the literature, its incidence, pathology, diagnosis and treatment of a rough discussion. Case report 1, Ye × ×, female, 27 years old, due to loss of appetite, impatience, fear of heat, sweating 2 years, repeated nosebleed, purpura, bleeding gums and pale 2 months; 11 days to aggravate the symptoms, nosebleed More than that, admitted to hospital on July 13, 1977. Physical examination: T: 37.6 ℃ P136 / min. Acute serious illness, weight loss and anemia appearance. A lot of scattered body skin