Nuclear cerebral angiography. Usefulness in the differential diagnosis of cerebrovascular disease and tumor

1973 ◽  
Vol 131 (2) ◽  
pp. 211-216 ◽  
Author(s):  
H. W. Strauss
2018 ◽  
Vol 2018 ◽  
pp. 1-3
Author(s):  
Durga Shankar Meena ◽  
Gopal Krishana Bohra ◽  
Mahadev Meena ◽  
Bharat Kumar Maheshwari

Moyamoya disease is a chronic progressive cerebrovascular disease characterized by bilateral occlusion or stenosis of arteries around circle of Willis. We report a case of 18-year-old female presented with recurrent episodes of headache and vertigo. On cerebral angiography, the patient was diagnosed to have moyamoya disease. On further evaluation, thrombophilia profile showed increased homocysteine level. The patient was treated conservatively with cobalamin and aspirin and advised for revascularization. According to the literature, there are few case reports of moyamoya disease with thrombotic disorders. Hence, we are reporting this interesting and rare case.


1980 ◽  
Vol 52 (4) ◽  
pp. 525-528 ◽  
Author(s):  
Jerry Bauer ◽  
Jose Luis Salazar ◽  
Oscar Sugar ◽  
Ronald P. Pawl

✓ A retrospective analysis of 1171 consecutive percutaneous retrograde brachial and carotid cerebral angiograms was performed on 635 patients, 50.7% of whom were in the sixth decade or older. Symptoms and signs of cerebrovascular disease were the most frequently investigated and diagnosed, accounting for 46.7% of all the angiograms. Despite this relatively high-risk population, we have found direct percutaneous cerebral angiography to have a very low risk. The pros and cons of direct percutaneous versus transfemoral cerebral angiography are discussed. The literature of the previous 10 years is reviewed, and the complication rate of these two techniques is compared.


2009 ◽  
Vol 4 (3) ◽  
pp. 266-269 ◽  
Author(s):  
Arjun V. Pendharkar ◽  
Raphael Guzman ◽  
Robert Dodd ◽  
David Cornfield ◽  
Michael S. B. Edwards

The authors describe the case of a 13-year-old boy who presented with an intraventricular hemorrhage caused by a left trigonal arteriovenous malformation. After an initial recovery, the patient experienced complete right-sided paresis on posthemorrhage Day 6. Severe cerebral vasospasm was found on MR angiography and confirmed on conventional cerebral angiography. Intraarterial nicardipine injection and balloon angioplasty were successfully performed with improved vasospasm and subsequent neurological recovery. Cerebral vasospasm should be considered in the differential diagnosis for neurological deterioration following an arteriovenous malformation hemorrhage, and aggressive treatment can be administered to prevent ischemia and further neurological deficits.


Radiology ◽  
1947 ◽  
Vol 48 (5) ◽  
pp. 493-508 ◽  
Author(s):  
Carl F. List ◽  
Fred J. Hodges

1999 ◽  
Vol 57 (2B) ◽  
pp. 371-376 ◽  
Author(s):  
CLÉLIA MARIA RIBEIRO FRANCO ◽  
MARCIA MAIUMI FUKUJIMA ◽  
ROBERTO DE MAGALHÃES CARNEIRO DE OLIVEIRA ◽  
ALBERTO ALAIN GABBAI

Moyamoya disease (MMD) is a chronic occlusive cerebrovascular disease of unknown etiology reported mainly in the Japanese. Most cases occur in children. The disease is rare in non-Oriental adults manifesting itself mostly as intracerebral hemorrhages. We describe MMD in 2 non-Oriental young adults and one adolescent that developed cerebral infarctions. The adults were medicated with aspirin and no medication was given to the adolescent. All patients did not deteriorate in a follow-up period from 1 to 4 years. Although rare, MMD is an important cause of stroke in young individuals and may well be underreported: only 18 patients have been reported till 1997 in Brazil. Neurologists should include MMD in differential diagnosis of ischemic and hemorrhagic strokes in young adults.


Nosotchu ◽  
1994 ◽  
Vol 16 (2) ◽  
pp. 95-101
Author(s):  
Shinya Yoshinaga ◽  
Akira Tanaka ◽  
Masato Kimura ◽  
Masamichi Tomonaga

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