Published online May 16, 2021. doi: 10.12998/wjcc.v9.i14.3294
Peer-review started: September 19, 2020
First decision: January 7, 2021
Revised: January 21, 2021
Accepted: March 24, 2021
Article in press: March 24, 2021
Published online: May 16, 2021
Processing time: 221 Days and 20.4 Hours
Among the primary headaches, cluster headache (CH) presents very particular features allowing a relatively easy diagnosis based on criteria listed in Chapter 3 of the International Classification of Headache Disorders. However, as in all primary headaches, possible underlying causal conditions must be excluded to rule out a secondary cluster-like headache (CLH).
The review aims to contribute to the knowledge on CLH caused by structural lesions and to provide better guides in the distinguishing process.
We analysed the published cases of symptomatic CH and CLH in PubMed and Google Scholar databases.
We conducted a systematic review of published cases of symptomatic CH and CLH and analysed the features of the patients.
Structural pathologies associated with CH were vascular (37.7%), tumoural (32.5%) and inflammatory (27.2%). Patients with atypical clinical features require careful evaluation for structural origins. CLH patients may be responsive to typical CH treatments; the treatment response is not specific. CLH can be triggered by contralateral structural pathologies. CLH-associated sinusitis and cerebral venous thrombosis are worth paying attention to.
Secondary headaches could perfectly mimick primary CH, hence neuroimaging should be conducted in patients in whom primary and secondary headaches are suspected. Cerebral magnetic resonance imaging scans are the diagnostic management of choice, and further examinations include vessel imaging with contrast agents and dedicated scans focusing on specific cerebral areas (sinuses, ocular and sellar regions). Neuroimaging is as necessary at follow-up visits as at the first observation.
We investigated the clinical features of CLH patients in published cases and tried to summarize their distinctive characteristics by comparing to patients with primary CH.