Keywords
To read this article in full you will need to make a payment
Purchase one-time access:
Academic & Personal: 24 hour online accessCorporate R&D Professionals: 24 hour online accessOne-time access price info
- For academic or personal research use, select 'Academic and Personal'
- For corporate R&D use, select 'Corporate R&D Professionals'
Subscribers receive full online access to your subscription and archive of back issues up to and including 2002.
Content published before 2002 is available via pay-per-view purchase only.
Subscribe:
Subscribe to Surgical Oncology ClinicsAlready a print subscriber? Claim online access
Already an online subscriber? Sign in
Register: Create an account
Institutional Access: Sign in to ScienceDirect
References
- The Human Genome Project: big science transforms biology and medicine.Genome Med. 2013; 5: 79
- Key principles and clinical applications of “next-generation” DNA sequencing.Cancer Prev Res Phila Pa. 2012; 5: 887-900
- Pheochromocytoma and Paraganglioma: Genetics, Diagnosis, and Treatment.Hematol Oncol Clin North Am. 2016; 30: 135-150
- Update of Pheochromocytoma Syndromes: Genetics, Biochemical Evaluation, and Imaging.Front Endocrinol. 2018; 9: 515
- Update on Pheochromocytoma and Paraganglioma from the SSO Endocrine/Head and Neck Disease-Site Work Group. Part 1 of 2: Advances in Pathogenesis and Diagnosis of Pheochromocytoma and Paraganglioma.Ann Surg Oncol. 2020; 27: 1329-1337
- Clinical and Biochemical Features of Pheochromocytoma Characteristic of Von Hippel-Lindau Syndrome.World J Surg. 2020; 44: 570-577
- Pheochromocytoma and paraganglioma in patients with neurofibromatosis type 1.Clin Endocrinol (Oxf). 2017; 86: 141-149
- Pheochromocytoma and paraganglioma syndromes: genetics and management update.Curr Oncol Tor Ont. 2014; 21: e8-e17
- Succinate dehydrogenase (SDH) deficiency, Carney triad and the epigenome.Mol Cell Endocrinol. 2018; 469: 107-111
- European Society of Endocrinology Clinical Practice Guideline for long-term follow-up of patients operated on for a phaeochromocytoma or a paraganglioma.Eur J Endocrinol. 2016; 174: G1-G10
- Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline.J Clin Endocrinol Metab. 2014; 99: 1915-1942
- Characteristics of germline mutations in Korean patients with pheochromocytoma/paraganglioma.J Med Genet. 2022; 59: 56-64
- Preoperative genetic testing in pheochromocytomas and paragangliomas influences the surgical approach and the extent of adrenal surgery.Surgery. 2018; 163: 191-196
- Update on Pheochromocytoma and Paraganglioma from the SSO Endocrine and Head and Neck Disease Site Working Group, Part 2 of 2: Perioperative Management and Outcomes of Pheochromocytoma and Paraganglioma.Ann Surg Oncol. 2020; 27: 1338-1347
- The evolution of primary aldosteronism: 1954-1967.Harvey Lect. 1966; 62: 257-291
- The Management of Primary Aldosteronism: Case Detection, Diagnosis, and Treatment: An Endocrine Society Clinical Practice Guideline.J Clin Endocrinol Metab. 2016; 101: 1889-1916
- Prevalence and characteristics of familial hyperaldosteronism: the PATOGEN study (Primary Aldosteronism in TOrino-GENetic forms).Hypertens Dallas Tex 1979. 2011; 58: 797-803
- Familial hyperaldosteronism type II is linked to the chromosome 7p22 region but also shows predicted heterogeneity.J Hypertens. 2005; 23: 1477-1484
- A gain-of-function mutation in the CLCN2 chloride channel gene causes primary aldosteronism.Nat Genet. 2018; 50: 355-361
- K+ channel mutations in adrenal aldosterone-producing adenomas and hereditary hypertension.Science. 2011; 331: 768-772
Melmed S, Polonsky K, Larsen P, Kronenberg H. (2016) Williams Textbook of Endcrinology. 13th edition. Elsevier.
- NIH - GTR: Genetic Testing Registry.(Available at:) (Accessed July 7, 2022)
- A novel form of human mendelian hypertension featuring nonglucocorticoid-remediable aldosteronism.J Clin Endocrinol Metab. 2008; 93: 3117-3123
- Constitutive activation of PKA catalytic subunit in adrenal Cushing’s syndrome.N Engl J Med. 2014; 370: 1019-1028
- Carney complex and McCune Albright syndrome: an overview of clinical manifestations and human molecular genetics.Mol Cell Endocrinol. 2014; 386: 85-91
- Familial Cushing’s syndrome due to primary pigmented nodular adrenocortical disease. Reinvestigation 50 years later.N Engl J Med. 1989; 321: 1659-1664
- Genetics of micronodular adrenal hyperplasia and Carney complex.Presse Medicale Paris Fr 1983. 2018; 47: e127-e137
- Mutations of the gene encoding the protein kinase A type I-alpha regulatory subunit in patients with the Carney complex.Nat Genet. 2000; 26: 89-92
- Aberrant expression of hormone receptors in adrenal Cushing’s syndrome.Pituitary. 2004; 7: 225-235
- ARMC5 mutations in macronodular adrenal hyperplasia with Cushing’s syndrome.N Engl J Med. 2013; 369: 2105-2114
- An Overview of the Heterogeneous Causes of Cushing Syndrome Resulting From Primary Macronodular Adrenal Hyperplasia (PMAH).J Endocr Soc. 2022; 6: bvac041
- Update on primary bilateral macronodular adrenal hyperplasia (PBMAH).Endocrine. 2021; 71: 595-603
- Adrenocortical carcinoma (ACC): When and why should we consider germline testing?.Presse Medicale Paris Fr 1983. 2018; 47: e119-e125
- Association of adrenocortical carcinoma with familial cancer susceptibility syndromes.Mol Cell Endocrinol. 2012; 351: 66-70
- Biology, clinical characteristics, and management of adrenocortical tumors in children.Pediatr Blood Cancer. 2005; 45: 265-273
- Adrenal involvement in MEN1. Analysis of 715 cases from the Groupe d’etude des Tumeurs Endocrines database.Eur J Endocrinol. 2012; 166: 269-279
- Natural course of small adrenal lesions in multiple endocrine neoplasia type 1: an endoscopic ultrasound imaging study.Eur J Endocrinol. 2008; 158: 699-704
- Adrenal masses are associated with familial adenomatous polyposis.Dis Colon Rectum. 2000; 43: 1739-1742
- Adrenocortical carcinoma is a lynch syndrome-associated cancer.J Clin Oncol Off J Am Soc Clin Oncol. 2013; 31: 3012-3018
- TP53 germline mutation testing in 180 families suspected of Li-Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes.J Med Genet. 2010; 47: 421-428
- Ionizing radiation, inflammation, and their interactions in colon carcinogenesis in Mlh1-deficient mice.Cancer Sci. 2015; 106: 217-226
Article info
Identification
Copyright
© 2022 Elsevier Inc. All rights reserved.