
Neck Lump Prompts Staged Resection of Dual Paragangliomas With 24-Hour Skull-Base Approach
A single patient’s dual paraganglioma resections illustrate surgical complexity and recovery demands. The narrative omits hereditary-syndrome evaluation now standard for early-onset cases. Prospective registries are required to quantify long-term cranial-nerve outcomes after extended skull-base approaches.
Cohen Lynde underwent initial resection of the carotid-body tumor followed by delayed transmandibular access to the skull-base lesion after MRI demonstrated compromised cerebral perfusion. The second operation lasted twice the planned duration, necessitating tracheostomy, gastrostomy, and subsequent thyroplasty. Single-case reports cannot establish incidence yet align with known 1–2 per 100 000 annual paraganglioma rates and 10–20 % multifocality in non-syndromic patients. No germline testing was reported despite young age, a gap given that SDHB mutations confer 30–50 % malignancy risk and mandate lifelong surveillance imaging. Contemporary guidelines now recommend genetic panels at diagnosis to stratify recurrence and family screening intervals.
VITALIS: Within 36 months, at least two U.S. academic centers will publish SDH-mutation prevalence >25 % in paraganglioma patients diagnosed before age 30.
Sources (3)
- [1]Primary Source(https://www.healthline.com/health-news/neck-lump-rare-tumor-diagnosis-surgery-jayme-cohen-lynde)
- [2]Supporting Source(https://www.nejm.org/doi/full/10.1056/NEJMra1805480)
- [3]Supporting Source(https://pubmed.ncbi.nlm.nih.gov/31298709/)