Head and neck paragangliomas: 30-year experience.
retrospective_cohort · Level III
Where this comes from
- Record sourced from PubMed, PMID 32427418.
- Also identified by DOI 10.1002/hed.26277 and PMC identifier 7725473.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
We aimed to review our experience and the changing trends in the management of head and neck paragangliomas (HNPG) over the last three decades. We retrospectively reviewed 103 patients with HNPG treated at our center (1986-2017). We included patients treated with surgery, radiotherapy, and patients maintained under active surveillance. Of the surgically treated patients (n = 79), 20% (12/59) of the carotid body tumors (CBT) had a cranial nerve deficit as sequela compared to 95% (19/20) of the non-CBT. Radiotherapy controlled growth in all tumors treated with this modality (n = 10). Of the initially observed patients, 70% (14/20) remained stable and did not require additional treatment. Stratifying by decades, there was a progressive increase in patients initially attempted to be observed and a decrease in upfront surgery. No deaths attributable to the HNPG were encountered. Surgery is an effective treatment for CBT. Nonsurgical treatment should be considered for non-CBT.
Medical subject headings
- Carotid Body Tumor
- Head and Neck Neoplasms
- Paraganglioma
- Paraganglioma, Extra-Adrenal