Moyamoya Disease Associated with Graves’ Disease and Down Syndrome: A Case Report and Literature Review

Author(s):  
Hikaru Nakamura ◽  
Kei Sato ◽  
Shota Yoshimura ◽  
Yukishige Hayashi ◽  
Tsuyoshi Izumo ◽  
...  
2011 ◽  
Vol 44 (4) ◽  
pp. 299-302 ◽  
Author(s):  
Catherine Amlie-Lefond ◽  
Osama O. Zaidat ◽  
Sean M. Lew

2021 ◽  
Vol 1 (5) ◽  
Author(s):  
Saeed Mohammed ◽  
Mallika Tripathi ◽  
Narine Mack ◽  
Surujpal Teelucksingh

Author(s):  
Chao Fu ◽  
Peng Jiang ◽  
Yang Zhao ◽  
Youxiang Li

Background: Clinically, the recurrent artery of Heubner (RAH) aneurysm is extremely rare, commonly presents with subarachnoid hemorrhage (SAH). Case Report: A 73-year-old man with a known moyamoya disease who presented as caudate hemorrhage attributable to an incidental flow aneurysm distal on the right RAH, which was managed conservatively after an unsuccessful endovascular attempt. Unfortunately, the patient died five weeks after  hospital discharge because of re-rupture of the aneurysm. To the best of our knowledge, the RAH aneurysm manifesting as caudate hemorrhage without SAH has not previously been reported. Conclusion: This case highlights that the RAH aneurysm masquerading as caudate hemorrhage without SAH is exceedingly rare but can be encountered, representing a diagnostic and therapeutic challenge, and should be considered in the differential diagnosis. Moreover, early identifying and then eliminating such vascular anomaly if possible is of importance to prevent fatal hemorrhage.


2015 ◽  
Vol 84 (3) ◽  
pp. 865.e7-865.e11 ◽  
Author(s):  
Mohammad Samadian ◽  
Ehsan Alavi ◽  
Mehrdad Hosseinzadeh Bakhtevari ◽  
Omidvar Rezaei

2009 ◽  
Vol 32 (3) ◽  
pp. 349-354 ◽  
Author(s):  
Aman Singh Sohal ◽  
Manu Sundaram ◽  
Mac Mallewa ◽  
Mohamed Tawil ◽  
Rachel Kneen

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