Endoscopic resection of an intraventricular cavernoma: a case report.

cerebral cavernous malformation endoscopic resection

Journal

International medical case reports journal
ISSN: 1179-142X
Titre abrégé: Int Med Case Rep J
Pays: New Zealand
ID NLM: 101566269

Informations de publication

Date de publication:
2019
Historique:
received: 08 05 2019
accepted: 09 07 2019
entrez: 10 9 2019
pubmed: 10 9 2019
medline: 10 9 2019
Statut: epublish

Résumé

Cerebral cavernous malformations occur in 0.5% of the population. They consist of thin-walled vessels and can be found as congenital or sporadic lesions. Most of them are asymptomatic, however, due to their anatomical features blood leakage into the surrounding tissue can cause severe neurological symptoms. Although risk of bleeding is low, symptomatic lesions should be treated, with microsurgical resection being the therapy of choice for surgically accessible cavernomas. Intraventricular cavernous malformations are a rare subtype, and due to their anatomical localization, they are eligible for endoscopic surgery. However, there are only a few reports on endoscopic resection of intraventricular cavernomas to be found in the literature. We report the case of a 48-year-old woman who suffers from multiple cerebral cavernous malformations. Since the first diagnosis, several of these cavernomas had been removed in open microsurgical interventions. Most recently, a new lesion arose intraventricularly, adjacent to the ependymal wall of the right lateral ventricle. In follow-up, cranial MR imaging microbleeding and an increasing size were detected. Eventually, the lesion was endoscopically removed. Presurgery the patient suffered from right-sided sensibility loss and gait disturbances as a consequence of prior surgeries. Postsurgery, no new neurological symptoms could be found. We here present MR images and intraoperative pictures as well as a short video of the resection itself. In our opinion, endoscopic resection of intraventricular cavernomas should be considered in selected cases.

Identifiants

pubmed: 31496833
doi: 10.2147/IMCRJ.S214917
pii: 214917
pmc: PMC6689546
doi:

Types de publication

Journal Article

Langues

eng

Pagination

249-252

Déclaration de conflit d'intérêts

The authors report no conflicts of interest in this work.

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Auteurs

M K Fehrenbach (MK)

Department of Neurosurgery, University Clinic of Leipzig, Leipzig 04103, Germany.

P Kuzman (P)

Department of Neuropathology, University Clinic of Leipzig, Leipzig 04103, Germany.

U Quaeschling (U)

Department of Neuroradiology, University Clinic of Leipzig, Leipzig 04103, Germany.

J Meixensberger (J)

Department of Neurosurgery, University Clinic of Leipzig, Leipzig 04103, Germany.

U Nestler (U)

Department of Neurosurgery, University Clinic of Leipzig, Leipzig 04103, Germany.

Classifications MeSH