Tato A, Orte L, Diz P, Quereda C, Ortuno J
Department of Nephrology, Hospital Ramon y Cajal, Universidad de Alcala de Henares, Madrid, Spain.
Am J Hypertens. 1997 Apr;10(4 Pt 1):479-81. doi: 10.1016/s0895-7061(97)00064-2.
For cases of malignant pheochromocytoma the prognosis is poor and experience with its treatment remains limited. We present a case of a hypertensive 16 year old woman with malignant pheochromocytoma and a good treatment response. Bone metastases appeared 6 months after the first resection. Local excision of the thoracic vertebrae metastases and palliative radiation therapy were performed, after which she received twelve cycles of cyclophosphamide, vincristine, and dacarbazine. Sixteen months later the patient remains asymptomatic without biochemical catecholamine activity.
对于恶性嗜铬细胞瘤病例,预后较差,且其治疗经验仍然有限。我们报告一例16岁患有恶性嗜铬细胞瘤的高血压女性患者,其治疗反应良好。首次切除术后6个月出现骨转移。对胸椎转移灶进行了局部切除和姑息性放射治疗,之后她接受了12个周期的环磷酰胺、长春新碱和达卡巴嗪治疗。16个月后,患者无症状,且无生化儿茶酚胺活性。