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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1968 1
1970 2
1978 1
1984 1
2001 1
2003 2
2004 1
2005 1
2006 3
2007 2
2008 4
2009 4
2010 6
2011 4
2012 8
2013 6
2014 5
2015 3
2016 3
2017 5
2018 4
2019 3
2020 6
2021 4
2022 6
2023 3

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80 results

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Page 1
Paraganglioma of the Head and Neck: A Review.
Sandow L, Thawani R, Kim MS, Heinrich MC. Sandow L, et al. Endocr Pract. 2023 Feb;29(2):141-147. doi: 10.1016/j.eprac.2022.10.002. Epub 2022 Oct 15. Endocr Pract. 2023. PMID: 36252779 Free PMC article. Review.
OBJECTIVE: To review the epidemiology, presentation, diagnosis, and management of head and neck paragangliomas. METHODS: A literature review of english language papers with focus on most current literature. RESULTS: Paragangliomas (PGLs) are a group of neuroendocrin …
OBJECTIVE: To review the epidemiology, presentation, diagnosis, and management of head and neck paragangliomas. METHODS: A literature …
Overview of the 2022 WHO Classification of Paragangliomas and Pheochromocytomas.
Mete O, Asa SL, Gill AJ, Kimura N, de Krijger RR, Tischler A. Mete O, et al. Endocr Pathol. 2022 Mar;33(1):90-114. doi: 10.1007/s12022-022-09704-6. Epub 2022 Mar 13. Endocr Pathol. 2022. PMID: 35285002 Review.
This classification discusses the embryologic derivation of the cells that give rise to these lesions and the historical evolution of the terminology used to classify their tumors; paragangliomas can be sympathetic or parasympathetic and the term pheochromocytoma is …
This classification discusses the embryologic derivation of the cells that give rise to these lesions and the historical evolution of the te …
Overview of primary adult retroperitoneal tumours.
Improta L, Tzanis D, Bouhadiba T, Abdelhafidh K, Bonvalot S. Improta L, et al. Eur J Surg Oncol. 2020 Sep;46(9):1573-1579. doi: 10.1016/j.ejso.2020.04.054. Epub 2020 May 21. Eur J Surg Oncol. 2020. PMID: 32600897 Review.
According to the World Health Organization (WHO) classification of tumours, mesenchymal benign and malignant tumours (including sarcomas and, currently, neurogenic tumours), parasympathetic tumours, extragonadal germ cell tumours, and lymphoid tumours have been identified. …
According to the World Health Organization (WHO) classification of tumours, mesenchymal benign and malignant tumours (including sarcomas and …
Benign Neurogenic Tumors.
Farma JM, Porpiglia AS, Vo ET. Farma JM, et al. Surg Clin North Am. 2022 Aug;102(4):679-693. doi: 10.1016/j.suc.2022.04.007. Surg Clin North Am. 2022. PMID: 35952696 Review.
These tumors can be found anywhere along the distribution of the sympathetic and parasympathetic nervous system and are categorized based on cell of origin: ganglion cell, paraganglion cell, and nerve sheath cells. Ganglion cell-derived tumors include neuroblastomas, gangl …
These tumors can be found anywhere along the distribution of the sympathetic and parasympathetic nervous system and are categorized b …
Pheochromocytoma and Paraganglioma.
Moon JK, Mattei P. Moon JK, et al. Semin Pediatr Surg. 2020 Jun;29(3):150926. doi: 10.1016/j.sempedsurg.2020.150926. Epub 2020 May 28. Semin Pediatr Surg. 2020. PMID: 32571511 Review. No abstract available.
[Phaeochromocytoma and paraganglioma].
Cornu E, Belmihoub I, Burnichon N, Grataloup C, Zinzindohoué F, Baron S, Billaud E, Azizi M, Gimenez-Roqueplo AP, Amar L. Cornu E, et al. Rev Med Interne. 2019 Nov;40(11):733-741. doi: 10.1016/j.revmed.2019.07.008. Epub 2019 Sep 4. Rev Med Interne. 2019. PMID: 31493938 Review. French.
Phaeochromocytomas and paragangliomas (PPGL) are rare neuroendocrine tumors that arise from the adrenal medulla or sympathetic and parasympathetic ganglia. ...Therapeutic management consists mostly of surgical excision, after drug preparation, and should be done in …
Phaeochromocytomas and paragangliomas (PPGL) are rare neuroendocrine tumors that arise from the adrenal medulla or sympathetic and …
Model systems in SDHx-related pheochromocytoma/paraganglioma.
Takács-Vellai K, Farkas Z, Ősz F, Stewart GW. Takács-Vellai K, et al. Cancer Metastasis Rev. 2021 Dec;40(4):1177-1201. doi: 10.1007/s10555-021-10009-z. Epub 2021 Dec 27. Cancer Metastasis Rev. 2021. PMID: 34957538 Free PMC article. Review.
Pheochromocytoma (PHEO) and paraganglioma (PGL) (together PPGL) are tumors with poor outcomes that arise from neuroendocrine cells in the adrenal gland, and sympathetic and parasympathetic ganglia outside the adrenal gland, respectively. ...
Pheochromocytoma (PHEO) and paraganglioma (PGL) (together PPGL) are tumors with poor outcomes that arise from neuroendocrine cells in …
A current review of the etiology, diagnosis, and treatment of pediatric pheochromocytoma and paraganglioma.
Waguespack SG, Rich T, Grubbs E, Ying AK, Perrier ND, Ayala-Ramirez M, Jimenez C. Waguespack SG, et al. J Clin Endocrinol Metab. 2010 May;95(5):2023-37. doi: 10.1210/jc.2009-2830. Epub 2010 Mar 9. J Clin Endocrinol Metab. 2010. PMID: 20215394 Review.
CONTEXT: Pheochromocytomas and paragangliomas (PHEO/PGL) are neuroendocrine tumors that arise from sympathetic and parasympathetic paraganglia. ...National Library of Medicine by using the search terms pheochromocytoma and paraganglioma. Results were narrowed …
CONTEXT: Pheochromocytomas and paragangliomas (PHEO/PGL) are neuroendocrine tumors that arise from sympathetic and parasympathetic …
Sporadic paraganglioma.
Lee JA, Duh QY. Lee JA, et al. World J Surg. 2008 May;32(5):683-7. doi: 10.1007/s00268-007-9360-4. World J Surg. 2008. PMID: 18224469 Review.
Paraganglioma are rare chromaffin cell tumors that develop from the neural crest cells. ...Many are malignant. Medical management of catecholamine-secreting paraganglioma is the same as for pheochromocytoma. Favorably located abdominal paragangliomas can be s …
Paraganglioma are rare chromaffin cell tumors that develop from the neural crest cells. ...Many are malignant. Medical management of …
Autonomic nervous system and cancer.
Simó M, Navarro X, Yuste VJ, Bruna J. Simó M, et al. Clin Auton Res. 2018 Jun;28(3):301-314. doi: 10.1007/s10286-018-0523-1. Epub 2018 Mar 28. Clin Auton Res. 2018. PMID: 29594605 Review.
The first includes direct cancer-related complications, such as primary ANS tumors (pheochromocytoma, paraganglioma or neuroblastoma), as well as autonomic manifestations induced by non-primary ANS tumors (primary brain tumors and metastases). ...
The first includes direct cancer-related complications, such as primary ANS tumors (pheochromocytoma, paraganglioma or neuroblastoma) …
80 results