Incidentally Detected Pancreatic Tail Neuroendocrine Tumor Coexisting with a Right Adrenal Interaortocaval Pheochromocytoma in the Absence of Familial Syndrome-Reference-Cited by-同舟云学术

Incidentally Detected Pancreatic Tail Neuroendocrine Tumor Coexisting with a Right Adrenal Interaortocaval Pheochromocytoma in the Absence of Familial Syndrome

Published:2023-06-10 Issue: Volume: Page:
ISSN:0972-2068
Container-title:Indian Journal of Surgery
language:en
Short-container-title:Indian J Surg

Author:

Kushwaha Naveen Kumar^ORCID,Singh Vijay Pratap,Gupta Prashant^ORCID,Mishra Niharika

Publisher

Springer Science and Business Media LLC

Subject

Surgery

Link

https://link.springer.com/content/pdf/10.1007/s12262-023-03843-8.pdf

Reference6 articles.

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2. Das S, Dasari A (2021) Epidemiology, incidence, and prevalence of neuroendocrine neoplasms: are there global differences? Curr Oncol Rep 23(4):43

3. Sarkadi B, Saskoi E, Butz H, Patocs A (2022) Genetics of pheochromocytomas and paragangliomas determine the therapeutical approach. Int J Mol Sci 23:3

4. Thompson LD (2002 May) Pheochromocytoma of the adrenal gland scaled score (PASS) to separate benign from malignant neoplasms: a clinicopathologic and immunophenotypic study of 100 cases. Am J Surg Pathol 26(5):551–566. https://doi.org/10.1097/00000478-200205000-00002

5. Kulkarni MM, Khandeparkar SG, Deshmukh SD, Karekar RR, Gaopande VL, Joshi AR, Kesari MV, Shelke RR (2016) Risk stratification in paragangliomas with PASS (pheochromocytoma of the adrenal gland scaled score) and immunohistochemical markers. J Clin Diagn Res 10(9):EC01–EC04