Clinical characteristics and outcomes of SDHB-related pheochromocytoma and paraganglioma in children and adolescents
Author:
Funder
National Institute of Child Health and Human Development
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Oncology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s00432-020-03138-5.pdf
Reference48 articles.
1. Amar L, Bertherat J, Baudin E et al (2005) Genetic testing in pheochromocytoma or functional paraganglioma. J Clin Oncol 23:8812–8818. https://doi.org/10.1200/JCO.2005.03.1484
2. Amar L, Baudin E, Burnichon N et al (2007) Succinate dehydrogenase B gene mutations predict survival in patients with malignant pheochromocytomas or paragangliomas. J Clin Endocrinol Metab 92:3822–3828. https://doi.org/10.1210/jc.2007-0709
3. Armstrong R, Sridhar M, Greenhalgh KL et al (2008) Phaeochromocytoma in children. Arch Dis Child 93:899–904. https://doi.org/10.1136/adc.2008.139121
4. Assadipour Y, Sadowski SM, Alimchandani M et al (2017) SDHB mutation status and tumor size but not tumor grade are important predictors of clinical outcome in pheochromocytoma and abdominal paraganglioma. Surgery 161:230–239. https://doi.org/10.1016/j.surg.2016.05.050
5. Babic B, Patel D, Aufforth R et al (2017) Pediatric patients with pheochromocytoma and paraganglioma should have routine preoperative genetic testing for common susceptibility genes in addition to imaging to detect extra-adrenal and metastatic tumors. Surgery 161:220–227. https://doi.org/10.1016/j.surg.2016.05.059
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