J Neurol Surg A Cent Eur Neurosurg 2013; 74(S 01): e18-e24
DOI: 10.1055/s-0032-1315793
Case Report
Georg Thieme Verlag KG Stuttgart · New York

Pial Arteriovenous Fistula as a Cause of Bilateral Thalamic Hyperintensities—an Unusual Case Report and Review of the Literature

Rahul Gupta
1   Department of Neurosurgery, Nagoya University Graduate School of Medicine, Nagoya, Japan
2   Department of Neurosurgery, Maulana Azad Medical College, G B Pant Hospital, University of Delhi, New Delhi, India
,
Shigeru Miyachi
1   Department of Neurosurgery, Nagoya University Graduate School of Medicine, Nagoya, Japan
,
Noriaki Matsubara
1   Department of Neurosurgery, Nagoya University Graduate School of Medicine, Nagoya, Japan
,
Takashi Izumi
1   Department of Neurosurgery, Nagoya University Graduate School of Medicine, Nagoya, Japan
,
Takehiro Naito
1   Department of Neurosurgery, Nagoya University Graduate School of Medicine, Nagoya, Japan
,
Ken-ichi Haraguchi
1   Department of Neurosurgery, Nagoya University Graduate School of Medicine, Nagoya, Japan
,
Toshihiko Wakabayashi
1   Department of Neurosurgery, Nagoya University Graduate School of Medicine, Nagoya, Japan
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Publikationsverlauf

23. Oktober 2011

15. Februar 2012

Publikationsdatum:
05. November 2012 (online)

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Abstract

Introduction Isolated bilateral thalamic congestion due to an arteriovenous malformation (AVM) is a rare entity. Few case reports of dural arteriovenous fistula associated with it have been reported in the literature. The association of pial arteriovenous fistula (pial AVF) with thalamic hyperintensities has never been described before. The pial AVF is a recently recognized lesion in which the multiple pial arterial feeders drain into a single venous channel without a nidus like in conventional AVM. In spite of being congenital in origin, these lesions may have expression in adulthood due to abrupt change in the venous drainage system. Successful management of pial AVF associated with bilateral thalamic hyperintensities is described here with review of the literature.

Case Presentation A 60-year-old man presented with rapidly progressive gait disturbance and cognitive decline. Magnetic resonance imaging (MRI) showed hyperintensities in the thalami on T2-weighted and fluid attenuated inversion recovery image. Digital subtraction angiography revealed a pial AVF near the splenium of corpus callosum. It had feeders from posterior choroidal arteries and drained into the vein of Galen through an abnormal mesencephalic vein. The stagnation and increase of pressure in the deep venous system led to congestion in the thalami. He was treated by partial transarterial embolization of the feeders followed by gamma knife therapy (GKT). The clinical symptoms and MRI improved rapidly after embolization and further reduction in shunt flow was observed after GKT.

Conclusion Strong suspicion of vascular malformation as a cause of bilateral thalamic hyperintensities helps in early detection. Such lesions like pial AVF presented here require active intervention by surgery or endovascular therapy. GKT is an important adjuvant in lesions refractory to either of them.