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Published on: May 26, 2023
Laryngeal Paraganglioma - A Rare Entity
S B Ghimire1, A K Kc1, S Karmacharya1
1Department of Otorhinolaryngology-Head and Neck Surgery, Dhulikhel Hospital, Kathmandu University Hospital, Kathmandu University School of Medical Sciences, Dhulikhel, Kavre, Nepal.
Chemotherapy may offer effective management for laryngeal paragangliomas, a rare neuroendocrine tumor. Further research is needed to confirm its role in treating these laryngeal tumors.
Area of Science:
- Neuroendocrinology
- Oncology
- Head and Neck Surgery
Background:
- Laryngeal paragangliomas are rare, neural crest-derived neuroendocrine tumors originating from laryngeal paraganglia.
- These tumors most commonly occur in the supraglottis, with a mean age of onset at 44 years, and are more prevalent in females.
Observation:
- A case involved a 39-year-old female initially diagnosed with squamous cell carcinoma after tumor debulking and excision.
- The patient received one cycle of chemotherapy, leading to apparent complete resolution of the mass, confirmed by follow-up.
- Subsequent immunohistochemistry re-diagnosed the tumor as a laryngeal paraganglioma.
Findings:
- The initial histopathology suggested squamous cell carcinoma, but immunohistochemistry confirmed laryngeal paraganglioma.
- Chemotherapy appeared effective in resolving the laryngeal mass in this specific case.
Implications:
- This case raises questions about the efficacy of chemotherapy in managing laryngeal paragangliomas.
- Further investigation is warranted to determine the role and effectiveness of chemotherapy in the treatment protocols for laryngeal paragangliomas.
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