scholarly journals Not just another thunderclap headache: a case of isolated cortical vein thrombosis and subarachnoid haemorrhage

2015 ◽  
Vol 2015 (nov12 1) ◽  
pp. bcr2015212273-bcr2015212273
Author(s):  
E. Vassallo ◽  
C. Azzopardi ◽  
R. Grech
2007 ◽  
Vol 34 (S 2) ◽  
Author(s):  
J Linn ◽  
T Pfefferkorn ◽  
S Michl ◽  
M Wiesmann ◽  
S Hartz ◽  
...  

BMC Neurology ◽  
2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Hongfeng Wen ◽  
Di Jin ◽  
Yu Chen ◽  
Bin Cui ◽  
Tianyi Xiao

Abstract Background Cerebral venous thrombosis (CVT) occurs rarely in the general population and is frequently associated with confused clinical findings and delayed diagnosis. Isolated cerebellar cortical vein thrombosis is a very rare phenomenon. Case presentation This report describes a case with CVT, which is manifested as space-occupying lesions of the cerebellar hemisphere and mimics a cerebellar tumor at the beginning. The diagnosis of CVT was finalized given the laboratory and brain biopsy findings. The etiology may be related to polycythemia vera with Janus Kinase 2 V617F mutation. Conclusion Isolated cerebellar vein thrombosis should be considered when swelling and enhancing cerebellar lesions are detected. Polycythemia vera, especially with a positive JAK2 V617F mutation, may be a rare risk factor for CVT.


2013 ◽  
Vol 61 (2) ◽  
pp. 173 ◽  
Author(s):  
PedroTadao Hamamoto Filho ◽  
RobertoColichio Gabarra ◽  
GabrielPereira Braga ◽  
LucileneSilva Ruiz e Resende ◽  
Rodrigo Bazan ◽  
...  

BMC Neurology ◽  
2016 ◽  
Vol 16 (1) ◽  
Author(s):  
Nobuhiko Arai ◽  
Masanao Tabuse ◽  
Akiyoshi Nakamura ◽  
Hiromichi Miyazaki

1987 ◽  
Vol 7 (2) ◽  
pp. 54
Author(s):  
D. Younker ◽  
M. M. Jones ◽  
J. Adenwala ◽  
A. Citrin ◽  
T. H. Joyce

2010 ◽  
Vol 120 (6) ◽  
pp. 447-450 ◽  
Author(s):  
Ozlem Kayim Yildiz ◽  
Hatice Balaban ◽  
Gulsum Cil ◽  
Ibrahim Oztoprak ◽  
Ertugrul Bolayir ◽  
...  

1987 ◽  
Vol 42 (5) ◽  
pp. 300-301
Author(s):  
DIRK YOUNKER ◽  
MONICA M. JONES ◽  
JAYSHREE ADENWALA ◽  
ALAN CITRIN ◽  
THOMAS H. JOYCE

Cephalalgia ◽  
2007 ◽  
Vol 27 (12) ◽  
pp. 1413-1417 ◽  
Author(s):  
Y-F Wang ◽  
J-L Fuh ◽  
J-F Lirng ◽  
F-C Chang ◽  
S-J Wang

Spontaneous intracranial hypotension (SIH) associated with subarachnoid haemorrhage (SAH) has never been reported. Here, we report on a case of a 33-year-old woman with SIH, who developed simple partial sensory seizures 3 weeks later. Neuroimaging studies, including brain computed tomography and angiography, were initially normal, but revealed an isolated cortical venous thrombosis at 3 weeks. One week later, brain magnetic resonance imaging showed SAH around the thrombosed cortical vein. We postulate that the decline in the venous blood flow velocity due to SIH may have resulted in cortical venous thrombosis, which in turn led to rupture of the vessel wall and SAH in this patient.


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