1Arbay O, Ciftci F, Tanyel C, et al. Pheochromocytoma in children[J]. J Pediatr Surg, 2001, 36(5): 447.
2Inabnet W B, Carag liano P, Pertsem lid is D. Pheochromocy- toma inherited associations, bilaterality, and cortex preserva- tion[J]. Surgery, 2000, 128(6): 1007.
8Pacak K, Linehan W M, Eisenhofer G, et al. Recen advances ingenetics, diagnosis, localization, and treatment of pheochro- mocytoma[J]. Anna Int Med, 2001, 134(4): 315.
4Arbay O, Ciftci F, Tanyel C, et al. Pheochromocytoma in children. J Pediatr Surg, 2001,36:447~452.
5Ross JH. Pheochromocytoma Special considerations in children.Urol Clin North Am,2000,27(3):393~402.
6Perel Y, Schlumberger M, Marguerite G, et al. Pheochromocytoma and praganglioma in children: a report of 24 cases of the French Society of Pediatric Oncology. Pediatr Hematol Oncol,1997,14: 413~422.
7Pacak K, Linehan WM, Eisenhofer G, et al. Recent advances in genetics, diagnosis, localization, and treatment of pheochromocytoma. Anna Int Med, 2001,134 (4): 315 ~ 329.
8Inabnet WB, Caragliano P,Pertsemlidis D. Pheochromocytoma:inherited associations, bilaterality, and cortex preservation. Surgery,2000, 128(6): 1007~1011.
9Walther MM, Keise HR, Lineha WM. Pheochromocytoma: Evaluation, diagnosis, and treatment. World J Urol, 1999, 17:35~39.
10Goldstein RE, Oneill JA, Holcomb GW, et al. Clinical experience over 48 years with pheochromocytoma. AnnSurg, 1999,229(6) : 755~764.