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Article Name - Genetic Variations in Multiple Head and Neck Paragangliomas Patients: A Management Dilemma

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  • Introduction Paragangliomas are rare neuroendocrine tumors that arise from paraganglia, which are clusters of neuroendocrine cells associated with the autonomic nervous system. These tumors can occur throu ... 2024-07-12
  • Description Patients with multiple head and neck paragangliomas often present with symptoms related to the mass effect of the tumors, such as dysphagia, hoarseness, hearing loss, and cranial nerve palsies ... 2024-07-12
  • Conclusion The management of multiple head and neck paragangliomas presents a complex clinical dilemma, driven by the intricate anatomy of the region and the genetic heterogeneity of the disease. Advance ... 2024-07-12
  • Acknowledgement None. ... 2024-07-12
  • Conflict of Interest None. ... 2024-07-12
  • References King, Kathryn S. and Karel Pacak. "Familial pheochromocytomas and paragangliomas." Mol Cell Endocrinol 386 (2014): 92-100. Google Scholar, Crossref, Indexed at Gimenez-Roqu ... 2024-07-12