Diminished prostacyclin formation in forearm venous tissue of patients with peripheral occlusive arteriopathy

1980 ◽  
Vol 18 (4) ◽  
pp. 254-255
Author(s):  
H. Sinzinger ◽  
J. Kaliman ◽  
K. Silberbauer ◽  
R. Oppolzer
ASAIO Journal ◽  
1993 ◽  
Vol 39 (3) ◽  
pp. M746-M749 ◽  
Author(s):  
YASUHARU NOISHIKI ◽  
YOSHIHISA YAMANE ◽  
YASUKO TOMIZAWA ◽  
TAKAFUMI OKOSHI ◽  
SLNICHI SATOH ◽  
...  

1978 ◽  
Vol 49 (1) ◽  
pp. 22-35 ◽  
Author(s):  
Koreaki Mori ◽  
Fuji Takeuchi ◽  
Masatsune Ishikawa ◽  
Hajime Handa ◽  
Mitsuo Toyama ◽  
...  

✓ Four cases with the association of occlusive arteriopathy and brain tumor are presented. A clinical analysis of these cases and cases reported in the literature revealed that occlusive arteriopathy at the base of the brain was often associated with a slowly growing basal tumor in children. Possible causes of occlusive arteriopathy in these cases were compression of the circle of Willis by a slowly growing basal tumor, secondary arterial occlusive changes by radiation therapy for a basal tumor, or vasculopathy associated with neurocutaneous syndrome. Symptoms of sudden onset or episodic nature suggest the presence of occlusive arteriopathy rather than the mass effect of a tumor. Cerebral angiography is mandatory whenever computerized tomography (CT), performed to rule out recurrence of a basal tumor, shows an ischemic lesion with low-density areas without any evidence of mass effect of the tumor. Cerebral angiography is also necessary when a basal tumor is suspected in children, particularly in cases associated with neurocutaneous syndrome and a basal tumor. Care should be taken not to scarify the abnormal vascular network at the base of the brain at the time of operation, because it is considered to be functioning as collateral circulation. The potential hazards of radiotherapy to radiation-induced occlusive changes of the circle of Willis must be considered in treating a benign basal brain tumor in children. Even in adults, repeated large doses of irradiation could cause occlusive arteriopathy.


1970 ◽  
Vol 12 (2) ◽  
pp. 207-210
Author(s):  
T. Kheim ◽  
J.E. Kirk

1992 ◽  
Vol 104 (3) ◽  
pp. 770-778 ◽  
Author(s):  
Yasuharu Noishiki ◽  
Yoshihisa Yamane ◽  
Yasuko Tomizawa ◽  
Takafumi Okoshi ◽  
Shinichi Satoh ◽  
...  

2011 ◽  
Vol 25 (12) ◽  
pp. 4150-4161 ◽  
Author(s):  
Jamie K. Harrington ◽  
Halima Chahboune ◽  
Jason M. Criscione ◽  
Alice Y. Li ◽  
Narutoshi Hibino ◽  
...  

2011 ◽  
Vol 15 (11) ◽  
pp. 2326-2334 ◽  
Author(s):  
Vu Thao-Vi Dao ◽  
Melanie Floeren ◽  
Stephanie Kumpf ◽  
Charlotte Both ◽  
Bärbel Peter ◽  
...  

2015 ◽  
Vol 11 (02) ◽  
pp. 89
Author(s):  
Priyank Khandelwal ◽  
Nirav Shah ◽  
Tannvi Prakash ◽  
Gustavo Ortiz ◽  
◽  
...  

Background:The comorbidity of intracranial occlusive arteriopathy and Graves’ disease (GD) is increasingly being reported.Methods:We describe two patients (mother and daughter) with GD, intracranial occlusive arteriopathy, and ischemic strokes.Results:Both patients were thyrotoxic at the time of the ischemic event, and the intracranial arterial stenosis was progressive while in thyrotoxic state. In one of the cases, there was no further progression of the disease after 1 year of follow up, once hyperthyroidism was well controlled.Conclusion:To the best of our knowledge, this is the first report of familial presentation of moyamoya-like vasculopathy in patients with GD in Latin population.


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