Of them 5 cases were confirmed as malignant pheochromocytoma.
病理及随访证实5例为恶性嗜铬细胞瘤。
Methods 12 cases of malignant pheochromocytoma surgically treated were reviewed.
方法总结12例恶性嗜铬细胞瘤患者临床资料。
CONCLUSIONS Surgical excision of malignant pheochromocytoma can achieve long term remission of symptoms.
结论恶性嗜铬细胞瘤经手术切除后，症状可以长期缓解。
Remember 10% when you think of a pheochromocytoma: 10% are bilateral, 10% are in children, 10% are malignant.
一想到嗜铬细胞瘤一定要记得10%这个数值：10%的肿瘤是双侧的，10%发生于儿童，10%的肿瘤是恶性的。
Pheochromocytoma is an important cause of secondary hypertension, whose pathogenesis is yet to be clarified. It is still difficult to identify malignant cases at early stage.
嗜铬细胞瘤是引起继发性高血压的重要原因，其发病机制目前还不完全清楚，临床上早期鉴别良恶性肿瘤尚有困难。
Pheochromocytoma is an important cause of secondary hypertension, whose pathogenesis is yet to be clarified. It is still difficult to identify malignant cases at early stage.
嗜铬细胞瘤是引起继发性高血压的重要原因，其发病机制目前还不完全清楚，临床上早期鉴别良恶性肿瘤尚有困难。
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