A case of adrenocortical carcinoma accompanying secondary acute adrenal hypofunction postoperation
Author:
Publisher
Springer Science and Business Media LLC
Subject
Oncology,Surgery
Link
http://link.springer.com/content/pdf/10.1186/s12957-018-1326-5.pdf
Reference17 articles.
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2. Ye J, Qi Y, Wang W, Sun F, Wei Q, Su T, et al. Lower expression of ATM and gene deletion is more frequent in adrenocortical carcinomas than adrenocortical adenomas. Endocrine. 2012;41(3):479–86. https://doi.org/10.1007/s12020-012-9593-3 .
3. Patel VV, Shah DS, Raychaudhari CR, Patel KB. Giant non-functioning adrenocortical carcinoma: a rare childhood tumor. Indian J Med Paediatr Oncol. 2010;31(2):65–8. https://doi.org/10.4103/0971-5851.71659 .
4. Sakoda A, Mushtaq I, Levitt G, Sebire NJ. Clinical and histopathological features of adrenocortical neoplasms in children: retrospective review from a single specialist center. J Pediatr Surg. 2014;49(3):410–5. https://doi.org/10.1016/j.jpedsurg.2013.09.008 .
5. Weissferdt A, Phan A, Suster S, Moran CA. Adrenocortical carcinoma: a comprehensive immunohistochemical study of 40 cases. Appl Immunohistochem Mol Morphol. 2014;22(1):24–30. https://doi.org/10.1097/PAI.0b013e31828a96cf .
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