论文部分内容阅读
嗜铬细胞瘤约占高血压病因的0.5%,临床表现极为复杂多样,非典型者占60%。嗜铬细胞瘤可伪似肾病综合征,贻误诊断,本文报告一例,并指出处理中注意事项。 病人,女,19岁,主因持续性头痛、视力听力减退,心前区针刺样痛,恶心、纳差、口渴、衰弱、发热于1980年10月30日就医。一月前诊断为急性呼吸道感染,门诊治疗无好转,三周后血压升高达200/130mmHg,急诊入院。既往患过流感,咽峡炎,猩红热,双耳聋。其母亦罹双耳聋。
Pheochromocytoma accounts for about 0.5% of the cause of hypertension, the clinical manifestations are extremely complex and diverse, with atypia accounting for 60%. Pheochromocytoma can be pseudo-nephrotic syndrome, delaying the diagnosis, the paper reports a case, and pointed out the precautions in the treatment. The patient, female, 19 years old, was hospitalized on October 30, 1980 due to persistent headache, decreased visual acuity, acupuncture-like pain in the precord area, nausea, anorexia, thirst, weakness and fever. A month ago, the diagnosis of acute respiratory infections, outpatient treatment without improvement, three weeks after the blood pressure up to 200 / 130mmHg, emergency admission. Previously had a flu, angina, scarlet fever, deafness. His mother also suffered deafness.