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
› Author Affiliations
Further Information

Publication History

23 October 2011

15 February 2012

Publication Date:
05 November 2012 (online)

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.

 
  • References

  • 1 Bell DA, Davis WL, Osborn AG, Harnsberger HR. Bithalamic hyperintensity on T2-weighted MR: vascular causes and evaluation with MR angiography. AJNR Am J Neuroradiol 1994; 15 (5) 893-899
  • 2 Smith AB, Smirniotopoulos JG, Rushing EJ, Goldstein SJ. Bilateral thalamic lesions. AJR Am J Roentgenol 2009; 192 (2) W53-62
  • 3 Ito M, Sonokawa T, Mishina H, Sato K. Reversible dural arteriovenous malformation-induced venous ischemia as a cause of dementia: treatment by surgical occlusion of draining dural sinus: case report. Neurosurgery 1995; 37 (6) 1187-1191 , discussion 1191–1192
  • 4 Greenough GP, Mamourian A, Harbaugh RE. Venous hypertension associated with a posterior fossa dural arteriovenous fistula: another cause of bithalamic lesions on MR images. AJNR Am J Neuroradiol 1999; 20 (1) 145-147
  • 5 Matsumura A, Oda M, Hozuki T, Imai T, Shimohama S. Dural arteriovenous fistula in a case of dementia with bithalamic MR lesions. Neurology 2008; 71 (19) 1553
  • 6 Sugrue PA, Hurley MC, Bendok BR , et al. High-grade dural arteriovenous fistula simulating a bilateral thalamic neoplasm. Clin Neurol Neurosurg 2009; 111 (7) 629-632
  • 7 Yamamoto T, Watanabe M, Miura A, Hirahara T, Hirano T, Uchino M. [A case of dural arteriovenous fistula associated with bilateral thalamic lesions]. Rinsho Shinkeigaku 2010; 50 (10) 718-724
  • 8 Santillan A, Safdieh JE, Gobin YP, Patsalides A. Neurological picture. Bilateral thalamic venous hypertension caused by a tentorial dural arteriovenous fistula: endovascular treatment. J Neurol Neurosurg Psychiatry 2011; 82 (7) 749-750
  • 9 Lv X, Jiang C, Li Y, Yang X, Wu Z. Clinical outcomes of endovascular treatment for intracranial pial arteriovenous fistulas. World Neurosurg 2010; 73 (4) 385-390
  • 10 Hoh BL, Putman CM, Budzik RF, Ogilvy CS. Surgical and endovascular flow disconnection of intracranial pial single-channel arteriovenous fistulae. Neurosurgery 2001; 49 (6) 1351-1363 , discussion 1363–1364
  • 11 Hurst RW, Bagley LJ, Galetta S , et al. Dementia resulting from dural arteriovenous fistulas: the pathologic findings of venous hypertensive encephalopathy. AJNR Am J Neuroradiol 1998; 19 (7) 1267-1273
  • 12 Küker W, Schmidt F, Friese S, Block F, Weller M. Unilateral thalamic edema in internal cerebral venous thrombosis: is it mostly left?. Cerebrovasc Dis 2001; 12 (4) 341-345
  • 13 Santosh C, Teasdale E, Molyneux A. Spontaneous closure of an intracranial middle cerebral arteriovenous fistula. Neuroradiology 1991; 33 (1) 65-66
  • 14 Nelson PK, Niimi Y, Lasjaunias P , et al. Endovascular embolization of congenital intracranial pial arteriovenous fistulas. Neuroimaging Clin N Am 1992; 2 (2) 309-317
  • 15 Back AG, Vollmer D, Zeck O, Shkedy C, Shedden PM. Retrospective analysis of unstaged and staged Gamma Knife surgery with and without preceding embolization for the treatment of arteriovenous malformations. J Neurosurg 2008; 109 (Suppl) 57-64