Clinically silent chromaffin-cell tumors: Tumor characteristics and long-term prognosis in patients with incidentally discovered pheochromocytomas-Reference-Cited by-同舟云学术

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Clinically silent chromaffin-cell tumors: Tumor characteristics and long-term prognosis in patients with incidentally discovered pheochromocytomas

Published:2010-05-17 Issue:10 Volume:33 Page:739-744
ISSN:0391-4097
Container-title:Journal of Endocrinological Investigation
language:en
Short-container-title:J Endocrinol Invest

Author:

Grozinsky-Glasberg S.,Szalat A.,Benbassat C. A.,Gorshtein A.,Weinstein R.,Hirsch D.,Shraga-Slutzky I.,Tsvetov G.,Gross D. J.,Shimon I.

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

http://link.springer.com/content/pdf/10.1007/BF03346680.pdf

Reference26 articles.

1. Grumbach MM, Biller BM, Braunstein GD, et al. Management of the clinically inapparent adrenal mass (“incidentaloma”). Ann Intern Med 2003, 138: 424–9.

2. O’Riordain DS, Young WF Jr, Grant CS, Carney JA, van Heerden JA. Clinical spectrum and outcome of functional extraadrenal paraganglioma. World J Surg 1996, 20: 916–21.

3. Maher ER, Eng C. The pressure rises: update on the genetics of phaeochromocytoma. Hum Mol Genet 2002, 11: 2347–54.

4. Astuti D, Morris M, Krona C, et al. Investigation of the role of SD-HB inactivation in sporadic phaeochromocytoma and neuroblastoma. Br J Cancer 2004, 91: 1835–41.

5. Eisenhofer G, Bornstein SR, Brouwers FM, et al. Malignant pheochromocytoma: current status and initiatives for future progress. Endocr Relat Cancer 2004, 11: 423–36.

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3. Silent pheochromocytoma and paraganglioma: Systematic review and proposed definitions for standardized terminology;Frontiers in Endocrinology;2022-10-17

4. Retroperitoneal Paraganglioma often Atypical: Short Case Series and Review of the Literature;World Journal of Endocrine Surgery;2022-07-16

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