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吴朋, 吕国士. 64排CT增强扫描结合血管成像对恶性颈动脉体瘤的诊断价值分析[J]. 中国全科医学, 2013, 16(1C): 354- 356.

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  • 标题: 颈部异位嗜铬细胞瘤一例报告 Ectopic Pheochromocytoma in Neck: A Case Report

    作者: 刘晓蕾, 王宪伟, 黄建华

    关键字: 异位嗜铬细胞瘤, 颈部 Ectopic Pheochromocytoma; Neck

    期刊名称: 《Asian Case Reports in Surgery》, Vol.2 No.3, 2013-09-24

    摘要: 颈部异位嗜铬细胞瘤十分罕见。作者报道了一例57岁的男性患者,因“发现左颈部肿块6年,头痛眩晕、胸闷胸痛9天”入院。入院时血压大幅度波动,每隔数分钟波动在200/100 mmHg~80/50 mmHg的范围。左颈部肿块进行性增大5年余。血浆17-羟皮质类固醇和17-酮类固醇正常,24小时尿VMA升高(82.7 umol/day ( Ectopic pheochromocytoma in neck is rare. We reported a 57-year-old male patient who was admitted to hospital because of a mass in left neck for 6 years with headache, dizziness, chest tightness and chest pain for 9 days. He had an alternation of fluctuation of blood pressure between 200/100 - 80/50 mmHg in every several minutes. The mass progressively enlarges for more than 5 years in his left side of neck. His plasma 17-hydroxy corticosteroid and 17-ketosteroid levels were normal. The 24 hours urine VMA level was high (82.7 umol/day (