期刊文献+

嗜铬细胞瘤/副神经节瘤遗传基因研究进展 被引量:4

原文传递
导出
摘要 嗜铬细胞瘤(PHEO)/副神经节瘤(PGL)源于有神经嵴交感和副交感链嗜铬组织分布的部位,PHEO在肾上腺髓质;PGL位于自颅底至骨盆的肾上腺外交感或副交感神经的副神经节,最常见于头颈部、腹部肾血管附近或Zuckerkandl 体,后者位于肠系膜下动脉起始部,是肾上腺外最大的嗜铬组织[1-2].
出处 《中华医学杂志》 CAS CSCD 北大核心 2015年第15期1193-1195,共3页 National Medical Journal of China
  • 相关文献

参考文献31

  • 1Lenders JW, Eisenhofer G, Mannelli M, et al. Phaeochromoeytoma [ J ]. Lancet, 2005, 366 ( 9486 ) :665-675.
  • 2Kahraman D, Goretzki PE, Szangolies M, et al. Extra-adrenal pheochromoeytoma in the organ of Zuckerkandl: diagnosis and treatment strategies [ J ]. Exp Clin Endoerinol Diabetes, 2011, 119 (7) :436-439.
  • 3Wyszyfiska T, Ciehocka E, Wieteska-Klimezak A, et al. A single pediatric center experience with 1025 children with hypertension [ J ]. Aeta Paediatr, 1992, 81 (3) :244-246.
  • 4Amar L, Bertherat J, Baudin E, et al. Genetic testing in pheochromoeytoma or functional paraganglioma[ J ]. J Clin Oncol, 2005, 23(34) :8812-8818.
  • 5Ladroue C, Carcenac R, Leporrier M, et al. PHD2 mutation and congenital erythrocytosis with paraganglioma [ J ]. N Engl J Med, 2008, 359(25) :2685-2692.
  • 6Sehlisio S, Kenchappa RS, Vredeveld LC, et al. The kinesin KIF1 Bbeta acts downstream from EglN3 to induce apoptosis and is a potential 1 p36 tumor suppressor [ J ]. Genes Dev, 2008, 22 (7) : 884-893.
  • 7Hao HX, Khalimonchuk O, Schraders M, et al. SDH5, a gene required for flavination of sueeinate dehydrogenase, is mutated in paraganglioma [ J ]. Science, 2009, 325 (5944) : 1139-1142.
  • 8Gaal J, Bumiehon N, Korpershoek E, et al. Isoeitrate dehydrogenase mutations are rare in pheoehromocytomas and paragangliomas [ J ]. J Clin Endocrinol Metab, 2010, 95 ( 3 ) : 1274-1278.
  • 9Qin Y, Yao L, King EE, et al. Germline mutations in TMEM127 confer susceptibility to pheochmmocytoma [ J ]. Nat Genet, 2010, 42(3 ) :229-233.
  • 10Bumichon N, Briere j J, Lib6 R, et al. SDHA is a tumor suppressor gene causing paraganglioma [ J ]. Hum Mol Genet, 2010, 19( 15 ) :3011-3020.

二级参考文献15

  • 1周瑜琳,赵咏桔,成昌友,赵铁耘,殷志强,洪洁,张翼飞,顾丽群,汤正义,崔斌,宁光.五个多发性内分泌肿瘤2B家系的临床分析和RET原癌基因突变研究[J].中华内分泌代谢杂志,2006,22(6):549-553. 被引量:14
  • 2Raue F,Frank-Raue K. Update multiple endocrine neoplasia type 2[J].Familial Cancer,2010.449-457.
  • 3Vasen HF,van der Feltz M,Raue F. The natural course of multiple endocrine neoplasia type Ⅱ b.A study of 18 cases[J].Archives of Internal Medicine,1992.1250-1252.
  • 4Hofstra RM,Landsvater RM,Ceccherini I. A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sproadic medullary throid carcinoma[J].Nature,1994.375-376.
  • 5Taccaliti A,Silvetti F,Palmonella G. Genetic alterations in medullary thyroid cancer:diagnostic and prognostic markers[J].Current Genomics,2011.618-625.
  • 6Brauckhoff M,Gimm O,Weiss CL. Multiple endocrine neoplasia 2B syndrom due to codon 918 mutation:clinical manifestation and course in early and late onset disease[J].World Journal of Surgery,2004.1305-1311.
  • 7Erdogan MF,Gulec B,Gursoy A. Multiple endocrine neoplasia 2B presenting with pseudo-Hirschsprung's disease[J].Journal of the National Medical Association,2006.783-786.
  • 8Raue F,Frank-Raue K. Genotype-phenotype correlation in multiple endocrine neoplasia type 2[J].Clinics(Sao Paulo brazil),2012.69-75.
  • 9Wohllk N,Schweizer H,Erlic Z. Multiple endocrine neoplasia type 2[J].Best Practice and Research:Clinical Endocrinology and Metabolism,2010.371-387.
  • 10Cohen R,Campos JM,Salaun C. Preoperative calcitonin levels are predictive of tumor size and postoperative calcitonin normalization in medullary thyroid carcinoma[J].Journal of Clinical Endocrinology and Metabolism,2000.905-918.

共引文献4

同被引文献28

引证文献4

二级引证文献18

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部