Choroid plexus AVM with anomalous origin of the capsulothalamic artery: A case report

Author:

Yamauchi Shigeru12,Kawakami Taichiro3,Murata Keiji2,Ishiguro Tomoya4,Ikeda Hidetoshi14,Nishio Akimasa1

Affiliation:

1. Department of Neurosurgery, Hokuto Social Medical Corporation Hokuto Hospital, Obihiro, Japan

2. Department of Neurosurgery, Shimada Municipal Hospital, Shimada, Japan

3. Department of Neurosurgery, Osaka City University Graduate School of Medicine, Osaka, Japan

4. Department of Neurosurgery, Osaka City General Hospital, Osaka, Japan

Abstract

Background and importance Traditionally, it has been believed that the plexal segment of the anterior choroidal artery (AChoA) can be sacrificed safely. Here, we present a case of choroid plexus arteriovenous malformation (AVM) in which the capsulothalamic artery originated from distal plexal segment of the AChoA. Clinical presentation A 45-year-old man was diagnosed with arteriovenous malformation involving the left inferior horn in screening MRI. Preceding stereotactic radiosurgery, transarterial target embolization was performed. In this procedure, 20% n-butyl-2-cyanoacrylate (NBCA) was successfully injected from the lateral plexal branch of the AChoA. After embolization, right homonymous hemianopsia developed due to cerebral infarction on the left optic radiation. This infarction was considered to be within the territory of the capsulothalamic artery. Conclusion This anomalous capsulothalamic artery might be formed by hemodynamic compromise of the brain surrounding AVM in early gestation. We must be aware of this unusual anatomical variation to avoid ischemic complication in embolization of the AChoA.

Publisher

SAGE Publications

Subject

Immunology

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