Lanfranchi J, Sachs R N, Garnier J, Breau J L, Israel L
Ann Med Interne (Paris). 1980;131(8):510-3.
A forty year old man with malignant pheochromocytoma of Zuckerkandl's body is reported. The case history is a severe hypertension with acute episodes, tachycardia and psychiatric disorders. The tumor extra adrenal site was got by abdominal scanning and its malignant type was demonstrated by pathological study and metastasis of lymph nodes occurring 4 months after surgery. The surgical treatment was associated to antimitotic and alpha blocking therapy. Clinical and biological status is still good after a twelve months follow-up.
报告了一名40岁患有祖克坎德尔氏体恶性嗜铬细胞瘤的男性。病史为严重高血压伴急性发作、心动过速和精神障碍。通过腹部扫描确定肿瘤位于肾上腺外,病理研究证实其为恶性类型,术后4个月出现淋巴结转移。手术治疗联合抗有丝分裂和α受体阻断治疗。随访12个月后,临床和生物学状况仍然良好。