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小儿嗜铬细胞瘤比较少见,我组于1973年10月经治1例右肾上腺嗜铬细胞瘤,报告于后: 江×,男,10岁,1973年10月31日因双眼视力模糊1月余入院。患儿3月前因高热、昏迷,诊断为“金葡败血症”,在县医院治疗40余日痊愈出院,当时发现血压维持140～130/110～90毫米汞柱。月余前因穿线不见针孔而发现视力模糊。门诊眼底检查示高血压乳突视网膜病变,尿常规蛋白(±),入院诊断:肾性高血压。检查:体温37.5℃,脉搏108次/分,血压:右上肢150/120、右下肢170/130、左上肢148/112、左下肢166/130毫米汞柱。
Pediatric pheochromocytoma is rare, and my group treated one case of right adrenal pheochromocytoma in October 1973. It was reported later: Jiang X, male, 10 years old, October 31, 1973, due to blurred vision for more than one month in October Admitted to hospital. The patient had been diagnosed as “septicemia of gold and silver” due to high fever and coma 3 months ago. He was discharged from the county hospital after treatment for more than 40 days. He was found to maintain blood pressure at 140-130/110-90 mm Hg. More than a month ago, blurred vision was found due to not seeing the pinhole. Out-patient fundus examination showed hypertensive papillary retinopathy, urine routine protein (±), admission diagnosis: renal hypertension. Check: Body temperature 37.5°C, pulse 108 beats/minute, blood pressure: 150/120 right upper limb, 170/130 right lower limb, 148/112 left upper limb, 166/130 mm Hg left lower limb.