Trigeminal autonomic cephalgia due to pituitary adenomas: scoping review of the literature
Authors' conclusion
Patients with TACs secondary to pituitary adenomas are likely to be diagnosed with SUNCT, have associated secreting adenomas, and to underwent multiple trials of medications before reaching headache relief. In the included cases, TACs secondary to prolactinomas had improvement associated with medical management with dopamine agonist therapy. Surgical resection of pituitary adenomas in patients with medically refractory TACs and growth-secreting adenomas was also associated with significant improvement in headache severity. Further work is required to understand the exact pathophysiological mechanism for this rare disease in order to better treat this rare condition moving forward.
Study context
- Population
- Published cases of trigeminal autonomic cephalalgias (TAC) associated with pituitary adenomascases included in the final review
- Participants
- 57 cases
- Outcome
- Secreting adenomas
Methodological detailsin accordance with PRISMA guidelines, Medline, Embase, Scopus, and Web of Science databases
- In accordance with PRISMA guidelines
- Medline, Embase, Scopus, and Web of Science databases
Main finding
As reported in the abstract
Patients with secreting adenomas
91%
Further findings
TAC phenotype
- SUNCT and Probable SUNCT
- 47%
- Cluster headaches/ and cluster-like headaches
- 46%
Medication trials before headache relief
- Medical intervention attempted in every patient; average trials of medications before headache relief
- 4.8
Complete resolution or improvement of headaches associated with treatment (medical or surgical)
- Patients with complete resolution or improvement
- 98%
Headache improvement or complete resolution after surgery
- Patients who underwent surgery
- 26
- Of those who underwent surgery, improvement or complete resolution
- 18 (69%)
Original publication
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