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1986年1月至1987年3月,我科收治席汉氏病5例,均因误诊,末能得到及时、正确治疗,而使患者长期丧失工作能力,现报告如下:临床资料本组年龄28—59岁,病史4—32年。均有产后大出血史.共同表现为怕冷、无乳、闭经、纳差、乏力、懒言、表情淡漠、腋毛和阴毛完全脱落,贫血及血压偏低。心悸3例,多次意识丧失3例,精神失常1例,粘液性水肿2例,乳房萎缩2例,肌肉松弛2例,肌张力增强1例,阴唇和阴道粘膜萎缩2例,子宫体缩小2例,心音低钝3例,心电图异常改变3例,脑电图异常改变1例。血糖正常5例,低血钾1例。3例查T3、T_4、17—羟、17—酮,
From January 1986 to March 1987, 5 cases of Henrietchy’s disease were admitted and treated in our department. All of them were misdiagnosed and could not be treated promptly and correctly. As a result, patients were incapacitated for a long time. The report is as follows: Clinical data The age of this group 28 -59 years old, history of 4 - 32 years. Have a history of postpartum hemorrhage. Common manifestations of cold, no milk, amenorrhea, anorexia, fatigue, laziness, indifference, armpit hair and pubic hair completely off, anemia and low blood pressure. Palpitations in 3 cases, multiple loss of consciousness in 3 cases, 1 case of mental disorders, 2 cases of mucinous edema, breast atrophy in 2 cases, muscle relaxation in 2 cases, muscle tension increased in 1 case, labia and vaginal mucosa atrophy in 2 cases, uterine body reduced 2 Cases, low blunted heart sound in 3 cases, abnormal ECG changes in 3 cases, 1 case of abnormal changes in EEG. 5 cases of normal blood sugar, hypokalemia in 1 case. 3 cases investigated T3, T_4, 17-hydroxy, 17-keto,