Fusiform aneurysms of the vertebrobasilar complex: a single-center series.


Journal

Acta neurochirurgica
ISSN: 0942-0940
Titre abrégé: Acta Neurochir (Wien)
Pays: Austria
ID NLM: 0151000

Informations de publication

Date de publication:
06 2020
Historique:
received: 10 02 2020
accepted: 19 03 2020
pubmed: 6 4 2020
medline: 29 12 2020
entrez: 6 4 2020
Statut: ppublish

Résumé

Fusiform vertebrobasilar aneurysms (FVBAs) may exhibit a disastrous clinical course. Due to their rare occurrence, evidence concerning optimal management is lackluster. To describe the epidemiology, clinical features and treatment outcomes of a consecutive series of patients admitted to our institution. We retrospectively evaluated patient charts with respect to clinical presentation, treatment procedures, and the outcomes of all patients diagnosed with an FVBA, which were seen at our institution between March 2006 and February 2017. Forty-five consecutive patients were analyzed. Follow-up was available for 39 patients (86.7%) with a median duration of 28.8 months. Seventeen patients (37.7%) were asymptomatic, 14 patients (31.1%) presented with brainstem ischemia, 8 patients (17.8%) with supratentorial ischemia, and 3 (6.7%) patients with brain stem compression. Aneurysm rupture occurred in 3 patients upon presentation (6.7%). Initially, 19 patients (42.2%) were significantly disabled with Modified Rankin Scale (mRS) scores ≥ 3. Twelve patients (26.7%) underwent invasive treatment: endovascular therapy in 9 cases and surgical treatment in 3 cases. Thirty-three patients received conservative treatment. During follow-up, 6 events (66.7%) of severe disability or death (mRS 4-6) occurred in the endovascular group versus 1 event (33%) in the surgical group versus 19 events (63.3%) among conservatively treated aneurysms. Deterioration was significantly more frequent in patients with symptomatic aneurysms (p = 0.030). Patients harboring an FVBA frequently present with disabling symptoms caused by various pathomechanisms. The natural history is aggressive, mostly for initially symptomatic aneurysms, and periprocedural morbidity of surgical or endovascular treatment remains substantial.

Sections du résumé

BACKGROUND
Fusiform vertebrobasilar aneurysms (FVBAs) may exhibit a disastrous clinical course. Due to their rare occurrence, evidence concerning optimal management is lackluster.
OBJECTIVE
To describe the epidemiology, clinical features and treatment outcomes of a consecutive series of patients admitted to our institution.
METHODS
We retrospectively evaluated patient charts with respect to clinical presentation, treatment procedures, and the outcomes of all patients diagnosed with an FVBA, which were seen at our institution between March 2006 and February 2017.
RESULTS
Forty-five consecutive patients were analyzed. Follow-up was available for 39 patients (86.7%) with a median duration of 28.8 months. Seventeen patients (37.7%) were asymptomatic, 14 patients (31.1%) presented with brainstem ischemia, 8 patients (17.8%) with supratentorial ischemia, and 3 (6.7%) patients with brain stem compression. Aneurysm rupture occurred in 3 patients upon presentation (6.7%). Initially, 19 patients (42.2%) were significantly disabled with Modified Rankin Scale (mRS) scores ≥ 3. Twelve patients (26.7%) underwent invasive treatment: endovascular therapy in 9 cases and surgical treatment in 3 cases. Thirty-three patients received conservative treatment. During follow-up, 6 events (66.7%) of severe disability or death (mRS 4-6) occurred in the endovascular group versus 1 event (33%) in the surgical group versus 19 events (63.3%) among conservatively treated aneurysms. Deterioration was significantly more frequent in patients with symptomatic aneurysms (p = 0.030).
CONCLUSION
Patients harboring an FVBA frequently present with disabling symptoms caused by various pathomechanisms. The natural history is aggressive, mostly for initially symptomatic aneurysms, and periprocedural morbidity of surgical or endovascular treatment remains substantial.

Identifiants

pubmed: 32248295
doi: 10.1007/s00701-020-04304-x
pii: 10.1007/s00701-020-04304-x
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1343-1351

Auteurs

Arthur Wagner (A)

Department of Neurosurgery, Klinikum rechts der Isar, Technical University Munich School of Medicine, Munich, Germany. arthur.wagner@tum.de.

Sascha Prothmann (S)

Department of Diagnostic and Interventional Neuroradiology, Helios Klinikum München West, Munich, Germany.

Dennis Hedderich (D)

Department of Diagnostic and Interventional Neuroradiology, Klinikum rechts der Isar, Technical University Munich School of Medicine, Munich, Germany.

Silke Wunderlich (S)

Department of Neurology, Klinikum rechts der Isar, Technical University Munich School of Medicine, Munich, Germany.

Bernhard Meyer (B)

Department of Neurosurgery, Klinikum rechts der Isar, Technical University Munich School of Medicine, Munich, Germany.

Jens Lehmberg (J)

Department of Neurosurgery, Klinikum rechts der Isar, Technical University Munich School of Medicine, Munich, Germany.
Department of Neurosurgery, München Klinik Bogenhausen, Munich, Germany.

Maria Wostrack (M)

Department of Neurosurgery, Klinikum rechts der Isar, Technical University Munich School of Medicine, Munich, Germany.

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Classifications MeSH