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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 4
2024 0

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81 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 …
Diagnosis and Management of Pheochromocytomas and Paragangliomas: A Guide for the Clinician.
Sharma S, Fishbein L. Sharma S, et al. Endocr Pract. 2023 Dec;29(12):999-1006. doi: 10.1016/j.eprac.2023.07.027. Epub 2023 Aug 15. Endocr Pract. 2023. PMID: 37586639 Review.
OBJECTIVE: The aim of this review was to provide a practical approach for clinicians regarding the diagnosis and management of pheochromocytomas and paragangliomas (PPGLs). METHODS: A literature search of PubMed was carried out using key words, including pheochromocytoma, …
OBJECTIVE: The aim of this review was to provide a practical approach for clinicians regarding the diagnosis and management of pheochromocyt …
Multimodality imaging appearance of intrapericardial paragangliomas.
Palacio D, Jo N, Del Pilar Gutierrez M, Shponka V, Betancourt S. Palacio D, et al. Clin Radiol. 2022 Dec;77(12):952-959. doi: 10.1016/j.crad.2022.08.131. Epub 2022 Sep 26. Clin Radiol. 2022. PMID: 36175258 Review.
Paragangliomas are neuroendocrine tumours of the sympathetic and parasympathetic nervous systems originating from neural crest cells. Less than 1% of paragangliomas in the heart originate from intrinsic cardiac ganglia cells in the posterior wall of the atria
Paragangliomas are neuroendocrine tumours of the sympathetic and parasympathetic nervous systems originating from neural crest
Pheochromocytoma and abdominal paraganglioma.
Renard J, Clerici T, Licker M, Triponez F. Renard J, et al. J Visc Surg. 2011 Dec;148(6):e409-16. doi: 10.1016/j.jviscsurg.2011.07.003. Epub 2011 Sep 8. J Visc Surg. 2011. PMID: 21862435 Free article. Review.
Pheochromocytomas (PHEO) and paragangliomas (PGL) are tumors derived from the sympathetic and parasympathetic nervous system. The parasympathetic-associated paragangliomas arising in the neck are usually non-functioning and are rarely encountered by ge …
Pheochromocytomas (PHEO) and paragangliomas (PGL) are tumors derived from the sympathetic and parasympathetic nervous system. …
81 results