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阵发性冷性血红蛋白尿(PCH)系临床罕见之疾病,笔者曾诊治1例,报导如下: 患者,女性,30岁,教师,受寒后出现“酱油色”尿4年余,86年2月6日入院。患者从82年起,常于冬、春季室外受寒,回室内约半小时后,解“酱油色”小便,颜色先深后淡,数次后恢复正常。尿色与剧烈活动及睡眠无关。伴疲倦,头昏、畏冷、腰背胀痛。
Paroxysmal cold hemoglobinuria (PCH) is a clinical rare disease, the author had a diagnosis and treatment, reported as follows: patients, women, 30 years old, after the cold, “soy sauce” urine more than 4 years, 86 February 6, admissions. Patients from 82 years, often in winter, spring outdoor cold, back to the room about half an hour later, solution “soy sauce color ” urine, the color of the first dark after the light, back to normal after several. Urine color and vigorous activity and sleep has nothing to do. With fatigue, dizziness, cold, back pain.