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席汉氏综合征在临床较常见,但合并尿崩症者极罕见,我们遇到1例,现报告如下。任××,女,32岁,住院号112059。四年前生第六胎,产后大出血、休克,急送县医院输血抢救脱险。产后无乳,闭经,性欲减退,毛发脱落,纳差,消瘦,乏力,怕冷,皮肤干燥。分娩后不久曾一度多尿多饮,其后此现象渐消失。1979年春我院门诊诊断席汉氏综合征,给强的松及甲状腺片治疗。因未坚持用药,癌状重现,于1980年3月16日收住院。末次分娩前无多尿多饮、肾脏疾病、颅脑炎症及外伤史。
Sheehan’s syndrome is more common in clinical practice, but with diabetes insipidus are extremely rare, we encountered 1 case, are as follows. Any × ×, female, 32 years old, hospital number 112059. Four years ago, the sixth child, postpartum hemorrhage, shock, emergency hospital blood transfusion emergency rescue. Postpartum non-milk, amenorrhea, loss of libido, hair loss, anorexia, weight loss, fatigue, cold, dry skin. Shortly after delivery, once more polyhydric drink, then the phenomenon gradually disappear. 1979 spring outpatient diagnosis of Hennessey syndrome, to strong prednisone and thyroid tablets treatment. Because they did not adhere to medication, recurrence of cancer, on March 16, 1980 admitted to hospital. No polyuria before the last delivery, kidney disease, brain inflammation and trauma history.