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1病例报告患者男,44岁。6年前因发作性高血压诊断为嗜铬细胞瘤,行双侧肾上腺瘤体摘除术,术后血压恢复正常,未再复查。父兄均有嗜铬细胞瘤手术病史。1个月前无明显诱因出现双侧腰痛伴双下肢疼痛、麻木、无力,右侧为著,活动后加重,不能行走。入院查体:血压130/80mmHg(未用药),心率88/min,体重指数(BMI)21.3。神清,肤色偏黑,甲状腺未及结节。背部可见陈旧性手术瘢痕。脊柱轻度左侧弯,腰部活动可,各椎体棘突及椎旁
A case report Male patient, 44 years old. Six years ago due to episodes of hypertension diagnosed as pheochromocytoma, bilateral adrenalectomy, postoperative blood pressure returned to normal, no further review. Both father and brother have a history of pheochromocytoma surgery. 1 month ago, no obvious incentive to appear bilateral low back pain with lower extremity pain, numbness, weakness, on the right, aggravating after activities, can not walk. Admission examination: blood pressure 130 / 80mmHg (no medication), heart rate 88 / min, body mass index (BMI) 21.3. Clear, dark color, thyroid nodules and not yet. Back visible old surgical scars. Spine mild left bend, waist activity can be, the vertebral spinous process and paravertebral