混合性嗜铬细胞瘤临床病理分析(4)
[9] Galan S R，Kann P H.Genetics and molecular pathogenesis of pheochromocytoma and paraganglioma[J].Clin Endocrinol(Oxf)，2013，78(2)：165-175.
[10] Strauchen J A.Germ-line mutations in nonsyndromicpheochromocytoma[J].N Engl J Med，2002，347(11)：854-855.
[11] Robinet G，Rioux-Leclercq N，Manunta A，et al.Composite pheochromocytoma：A rare adrenal tumor[J].Ann Pathol，2017，37(2)：158-161.
[12] Gupta S，Zhang J，Erickson L A.Composite Pheochromocytoma/Paraganglioma-Ganglioneuroma：A Clinicopathologic Study of Eight Cases with Analysis of Succinate Dehydrogenase[J].Endocr Pathol，2017，28(3)：269-275.
[13] Comstock J M，Willmore-Payne C，Holden J A，et al.Composite pheochromocytoma：a clinicopathologic and molecular comparison with ordinary pheochromocytoma and neuroblastoma[J].Am J Clin Pathol，2009，132(1)：69-73.
[14] Mahajan H，Lee D，Sharma R，et al.Composite phaeochromocytoma-ganglioneuroma，an uncommon entity：report of two cases[J].Pathology，2010，42(3)：295-298.
(收稿日期：2020-03-06) (本文編辑：郎序莹), 百拇医药(陈滔 周伟 梁津杰)
[10] Strauchen J A.Germ-line mutations in nonsyndromicpheochromocytoma[J].N Engl J Med，2002，347(11)：854-855.
[11] Robinet G，Rioux-Leclercq N，Manunta A，et al.Composite pheochromocytoma：A rare adrenal tumor[J].Ann Pathol，2017，37(2)：158-161.
[12] Gupta S，Zhang J，Erickson L A.Composite Pheochromocytoma/Paraganglioma-Ganglioneuroma：A Clinicopathologic Study of Eight Cases with Analysis of Succinate Dehydrogenase[J].Endocr Pathol，2017，28(3)：269-275.
[13] Comstock J M，Willmore-Payne C，Holden J A，et al.Composite pheochromocytoma：a clinicopathologic and molecular comparison with ordinary pheochromocytoma and neuroblastoma[J].Am J Clin Pathol，2009，132(1)：69-73.
[14] Mahajan H，Lee D，Sharma R，et al.Composite phaeochromocytoma-ganglioneuroma，an uncommon entity：report of two cases[J].Pathology，2010，42(3)：295-298.
(收稿日期：2020-03-06) (本文編辑：郎序莹), 百拇医药(陈滔 周伟 梁津杰)