Symptomatic Infratentorial Thrombosed Developmental Venous Anomaly: Case Report and Review of the Literature

被引:20
作者
Amuluru, Krishna [1 ]
Al-Mufti, Fawaz [1 ]
Hannaford, Stephen [1 ]
Singh, Inder Paul [1 ,2 ]
Prestigiacomo, Charles J. [1 ,2 ,3 ]
Gandhi, Chirag D. [1 ,2 ,3 ]
机构
[1] Rutgers State Univ, Sch Med, Dept Neurosurg & Neurosci, 90 Bergen St,Suite 8100, Newark, NJ USA
[2] Rutgers State Univ, Sch Med, Dept Neurol, Newark, NJ USA
[3] Rutgers State Univ, Sch Med, Dept Radiol, Newark, NJ USA
关键词
Cerebral venous thrombosis; Developmental venous anomaly; Diagnostic cerebral angiography; Magnetic resonance imaging; Venous angioma;
D O I
10.1159/000444028
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Developmental venous anomalies (DVAs) are variations of normal transmedullary veins draining white and gray matter. In the vast majority of cases, DVAs are diagnosed incidentally and should be considered as benign entities. In extremely rare circumstances, DVAs may become symptomatic due to mechanical or flow-related etiologies. Thrombosis of the collector vein of a DVA is a rare type of a flow-related complication with only 29 cases reported in the literature, the majority of which are supratentorial. Infratentorial thrombosed DVAs are thus extremely rare and the few cases reported have typically caused symptoms due to venous ischemic infarctions. Summary: We report a case of an infratentorial DVA with a thrombosed drainage vein in a patient with nonhemorrhagic, noninfarcted venous congestive edema, which was successfully treated with high-dose glucocorticoids and short-term anticoagulation. We review the pertinent venous anatomy of the posterior fossa as well as the literature of symptomatic infratentorial thrombosed DVAs. Key Message: The presented case of an infratentorial thrombosed DVA with cerebellar and pontine venous congestive edema is extremely rare. A working knowledge of posterior fossa venous anatomy and possible pathomechanisms responsible for the rarely symptomatic lesion will aid in the timely and efficacious treatment of such lesions. (C) 2016 S. Karger AG, Basel
引用
收藏
页码:130 / 137
页数:8
相关论文
共 41 条
[1]   Spontaneous thrombosis of developmental venous anomaly (DVA) with venous infarct and acute cerebellar ataxia [J].
Agarwal A. ;
Kanekar S. ;
Kalapos P. ;
Vijay K. .
Emergency Radiology, 2014, 21 (4) :427-430
[2]   Developmental venous anomaly with an arteriovenous shunt and a thrombotic complication - Case report [J].
Agazzi, S ;
Regli, L ;
Uske, A ;
Maeder, P ;
de Tribolet, N .
JOURNAL OF NEUROSURGERY, 2001, 94 (03) :533-537
[3]   Venous Congestion Associated With Developmental Venous Anomaly: Findings on Susceptibility Weighted Imaging [J].
Amemiya, Shiori ;
Aoki, Shigeki ;
Takao, Hidernasa .
JOURNAL OF MAGNETIC RESONANCE IMAGING, 2008, 28 (06) :1506-1509
[4]  
Blackmore CC, 1996, AM J NEURORADIOL, V17, P458
[5]  
BOUCHACOURT E, 1986, Journal de Radiologie (Paris), V67, P631
[6]   Thrombosis of developmental venous anomaly and consecutive venous infarction [J].
Brasse, G. ;
Stammel, O. ;
Siemens, P. ;
Toepper, R. .
NERVENARZT, 2008, 79 (06) :703-705
[7]   Are steroids useful to treat cerebral venous thrombosis? [J].
Canhao, Patricia ;
Cortesao, Ana ;
Cabral, Marta ;
Ferro, Jose M. ;
Stam, Jan ;
Bousser, Marie-Germaine ;
Barinagarrementeria, Fernando .
STROKE, 2008, 39 (01) :105-110
[8]  
FIELD LR, 1995, AM J NEURORADIOL, V16, P1885
[9]  
FLACKE S, 2006, CLIN NEURORADIOL, V16, P131
[10]   Thrombosed developmental venous anomaly associated with cerebral venous infarct [J].
Gama, Romulo L. ;
Nakayama, Mauro ;
Tavora, Daniel G. F. ;
Bomfim, Rodrigo C. ;
Carneiro, Tricia C. ;
Pimentel, Leonardo H. C. .
ARQUIVOS DE NEURO-PSIQUIATRIA, 2008, 66 (3A) :560-562