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Rare circle of Willis variants associated with multiple intracranial aneurysms and subarachnoid hemorrhage: A case report.

Rare circle of Willis variants associated with multiple intracranial aneurysms and subarachnoid hemorrhage: A case report.

期刊: Medicine 日期: 2026-08-28 PMID: 42675689 DOI: 10.1097/MD.0000000000050402 浏览: 6
作者: Mosi MH, Alfarra H, Soliman N, Alshaar MK, Alshaar MK, Hamzeh G
MH, M., H, A., N, S., MK, A., MK, A., & G, H. (2026). Rare circle of Willis variants associated with multiple intracranial aneurysms and subarachnoid hemorrhage: A case report.. Medicine. https://doi.org/10.1097/MD.0000000000050402
MH M, H A, N S, MK A, MK A, G H. Rare circle of Willis variants associated with multiple intracranial aneurysms and subarachnoid hemorrhage: A case report.. Medicine. 2026; doi: 10.1097/MD.0000000000050402
MH M, H A, N S, et al. Rare circle of Willis variants associated with multiple intracranial aneurysms and subarachnoid hemorrhage: A case report.[J]. Medicine. 2026. DOI: 10.1097/MD.0000000000050402.
@article{mh2026,
  author = {Mosi MH and Alfarra H and Soliman N and Alshaar MK and Alshaar MK and Hamzeh G},
  title = {Rare circle of Willis variants associated with multiple intracranial aneurysms and subarachnoid hemorrhage: A case report.},
  journal = {Medicine},
  year = {2026},
  doi = {10.1097/MD.0000000000050402},
  note = {PMID: 42675689},
}
TY  - JOUR
AU  - Mosi MH
AU  - Alfarra H
AU  - Soliman N
AU  - Alshaar MK
AU  - Alshaar MK
AU  - Hamzeh G
TI  - Rare circle of Willis variants associated with multiple intracranial aneurysms and subarachnoid hemorrhage: A case report.
T2  - Medicine
PY  - 2026
DO  - 10.1097/MD.0000000000050402
AN  - PMID:42675689
ER  - 

摘要

RATIONALE: Subarachnoid hemorrhage from a ruptured intracranial aneurysm is a type of stroke with high rates of mortality and disability, and the prevalence of aneurysm formation increases in the presence of Circle of Willis variants. PATIENT CONCERNS: A 64-year-old man with a history of hypertension and psoriatic arthritis presented with a sudden severe headache and walking difficulties without any loss of consciousness. DIAGNOSES: Non-contrast computed tomography showed a diffuse subarachnoid hemorrhage. Computed tomography angiography demonstrated multiple intracranial aneurysms together with variants of the posterior communicating artery and posterior cerebral artery, which may have contributed to aneurysm formation. INTERVENTIONS: The patient was started on oral Nimodipine to prevent cerebral vasospasm and underwent stent-assisted coil embolization of the ruptured aneurysm. OUTCOMES: His symptoms and clinical condition improved a few days after the embolization, and he was discharged after 18 days. LESSONS: This is the first documented case report from Syria, and possibly the first ever, detailing such Circle of Willis variants associated with cerebral aneurysms. It underscores the need for further studies exploring the relationship between the type of variants and the number and size of cerebral aneurysms, which is important for a better understanding of the epidemiology of cerebral aneurysms.

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