论文部分内容阅读
巴特氏综合征是1960年 Bartter 等首先报告,该病的临床特点为肾小球旁器增生,低血钾、硷中毒、血浆血管紧张素Ⅱ浓度增高及高醛固酮血症,但血压是正常的一组征候群。今就我院所见一例报道如下:病例介绍患者女、62岁,病历号84～2629。因全身色素沉着,伴有消瘦乏力2年,近8个月来发烧、纳差,于1984年4月16日疑肾上腺皮质功能低下入院。自幼有多饮、多尿、乏力,但仍能正常工作和操持家务。近两年常感发烧(未测体温),全身出现皮疹,痒,曾以湿诊疣状苔癣等症治疗,皮疹消失后留色素沉着;逐日消瘦乏力纳差加重。近三月发烧,体温波动在38°～39℃,
Bartter syndrome was first reported in 1960 by Bartter et al. The clinical features of this disease were glomerular hyperplasia, hypokalemia, alkalosis, elevated plasma angiotensin II concentration and hyperdistrophinia, but blood pressure was normal A group of syndromes. This hospital to see a case of this report is as follows: Case Description Female patient, aged 62, medical record number 84 to 2629. Due to systemic pigmentation, accompanied by weight-loss 2 years, nearly 8 months to fever, anorexia, on April 16, 1984 suspected adrenocortical dysfunction admitted to hospital. Since childhood, drink more, more urine, fatigue, but still able to work and housework. The past two years often feel fever (not measured body temperature), the whole body rash, itch, had wet treatment of verruca lichen planus embolism, rash disappeared after leaving pigmentation; daily weight loss aggravate anorexia. Nearly three months of fever, body temperature fluctuations in 38 ° ~ 39 ℃,