Composite pheochromocytoma of the adrenal gland—a review of published cases
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cell Biology,Molecular Biology,General Medicine,Pathology and Forensic Medicine
Link
https://link.springer.com/content/pdf/10.1007/s00428-023-03492-y.pdf
Reference15 articles.
1. Welander J, Söderkvist P, Gimm O (2011) Genetics and clinical characteristics of hereditary pheochromocytomas and paragangliomas. Endocr-Relat Cancer 18(6):R253–R276
2. Khan AN, Solomon SS, Childress RD (2010) Composite pheochromocytoma-ganglioneuroma: a rare experiment of nature. Endocr Pract 16(2):291–299
3. Kimura N, Fukase M, Wakita A, Kimura I (2002) Loss of the neurofibromin-NF1 gene product and composite pheochromocytoma. Ann N Y Acad Sci 971(1):536–538
4. Bernini GP, Moretti A, Mannelli M, Ercolino T, Bardini M, Caramella D, ... Salvetti A (2005) Unique association of non-functioning pheochromocytoma, ganglioneuroma, adrenal cortical adenoma, hepatic and vertebral hemangiomas in a patient with a new intronic variant in the VHL gene. J Endocrinol Investig 28(2):1032–1037
5. Pozza C, Sesti F, Di Dato C, Sbardella E, Pofi R, Schiavi F, ... Giannetta E (2020) A novel MAX gene mutation variant in a patient with multiple and “composite” neuroendocrine–neuroblastic tumors. Front Endocrinol 11:234
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