scholarly journals Moyamoya Disease Progressing from Unilateral to Bilateral Involvement —Case Report—

1992 ◽  
Vol 32 (12) ◽  
pp. 900-903 ◽  
Author(s):  
Shinzo YOSHIDA ◽  
Shigeo MATSUMOTO ◽  
Sadahiko BAN ◽  
Toyoshiro YAMAMOTO
Keyword(s):  
Case Report ◽  
Moyamoya Disease ◽  
Bilateral Involvement

Adult Moyamoya Disease which Progressed from Unilateral to Bilateral Involvement was Detected by MRA and was Treated with Prophylactic Revascularization : A Case Report

1998 ◽  
Vol 7 (5) ◽  
pp. 304-309
Author(s):  
Tatsunori KAWAI ◽  
Kanehisa KOHNO ◽  
Shiro OHUE ◽  
Noriyuki FUMOTO ◽  
Shinsuke OHTA ◽  
...  
Keyword(s):  
Case Report ◽  
Moyamoya Disease ◽  
Bilateral Involvement ◽  
Adult Moyamoya Disease

scholarly journals Magnetic Resonance Angiography Demonstrating Adult Moyamoya Disease Progressing from Unilateral to Bilateral Involvement-Case Report-

2004 ◽  
Vol 44 (4) ◽  
pp. 183-186 ◽  
Author(s):  
Reiko KAGAWA ◽  
Yoshikazu OKADA ◽  
Kouzo MORITAKE ◽  
Mutsuyo TAKAMURA
Keyword(s):  
Case Report ◽  
Magnetic Resonance ◽  
Magnetic Resonance Angiography ◽  
Moyamoya Disease ◽  
Bilateral Involvement ◽  
Adult Moyamoya Disease

scholarly journals Silent Moyamoya disease - A rare case report

2021 ◽  
Vol 16 (6) ◽  
pp. 1368-1373
Author(s):  
Juna Musa ◽  
Masum Rahman ◽  
Ali Guy ◽  
Angela Guy ◽  
Kristi Saliaj ◽  
...  
Keyword(s):  
Case Report ◽  
Moyamoya Disease ◽  
Rare Case ◽  
Rare Case Report

A Rare Presentation of Moyamoya Disease Mimicking Schizophrenia: A Case Report

2021 ◽  
pp. 102818
Author(s):  
Hung-Hsi Wu ◽  
Jia-Ying Shen ◽  
Ya-Hsuan Wang ◽  
Nian-Sheng Tzeng ◽  
Fang-Jung Wan ◽  
...  
Keyword(s):  
Case Report ◽  
Moyamoya Disease ◽  
Rare Presentation

Antepartum intracranial hemorrhage due to unrecognized unilateral moyamoya disease: a case report

2010 ◽  
Vol 283 (S1) ◽  
pp. 19-22 ◽  
Author(s):  
Jun Kakogawa ◽  
Miyuki Sadatsuki ◽  
Norio Masuya ◽  
Hideto Gomibuchi ◽  
Hiroyasu Ohno ◽  
...  
Keyword(s):  
Case Report ◽  
Intracranial Hemorrhage ◽  
Moyamoya Disease ◽  
Unilateral Moyamoya Disease

Wilms' Tumor Associated with Moyamoya Disease: A Case Report

1985 ◽  
Vol 40 (02) ◽  
pp. 114-116
Author(s):  
Y. Watanabe ◽  
T. Todani ◽  
T. Fujii ◽  
A. Toki ◽  
S. Uemura ◽  
...  
Keyword(s):  
Case Report ◽  
Moyamoya Disease ◽  
Wilms Tumor

scholarly journals A case report of moyamoya disease in children treated with encephalo-duro-myo-arterio-pericranial synangiosis

2021 ◽  
Author(s):  
Julius July
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
Magnetic Resonance Angiography ◽  
Moyamoya Disease ◽  
Internal Carotid ◽  
Language Function ◽  
Vascular Networks ◽  
Ischemic Event ◽  
Special Challenge ◽  
Ischemic Attack

Moyamoya disease that manifests during childhood may pose a special challenge for surgeons. We report a case of a 10-year-old girl who suffered from moyamoya disease and was successfully treated with encephalo-duro-myo-arterio-pericranial synangiosis (EDMAPS). She presented with a recurrent transient ischemic attack that worsened for 1 year. She was aphasic globally (sensory and motor) and had slightly weak right extremities. Her magnetic resonance angiography and computed tomography angiography showed the typical features of moyamoya disease with bilateral stenosis at the terminal internal carotid artery, bilaterally abnormal vascular networks, and a left ischemic event involving the temporoparietal region. She was recovered well after underwent bilateral EDMAPS, fully regained her language function after 3 months, and gathered her strength back. Therefore, EDMAPS could be a good, safe, and effective treatment for moyamoya disease in children.

scholarly journals Unusual presentation of moyamoya disease with popliteal involvement: case report and review of the literature

2021 ◽  
Vol 20 ◽  
Author(s):  
Mustafa Etli ◽  
Oguz Karahan
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
Moyamoya Disease ◽  
Doppler Sonography ◽  
Anticoagulant Treatment ◽  
Review Of The Literature ◽  
Peripheral Vascular ◽  
Bilateral Carotid Occlusion ◽  
Bilateral Carotid ◽  
Cerebrovascular System

Abstract Moyamoya disease is a rare disorder that involves the cerebrovascular system. Usually, it leads to occlusion of the arteries of the cerebral system and causes cerebral circulatory complaints. A 48-year-old female patient was admitted to our clinic with intermittent claudication in both legs. Biphasic and monophasic waveform patterns were detected bilaterally in distal (trifurcation arteries) lower extremities with Doppler sonography. The patient therefore underwent systemic vascular examination. Computed tomography angiography revealed bilateral carotid occlusion at the level of supraclinoid segments, and opacifications were detected at the distal segments of the bilateral anterior cerebellar and middle cerebellar arteries. The patient was diagnosed with moyamoya disease, and anticoagulant treatment was started. In conclusion, most previous reports have presented the cerebrovascular involvement of moyamoya disease. However, this disease can involve different peripheral vascular systems and careful and systemic vascular examination is necessary for an exact diagnosis.

scholarly journals Case Report: Acute Stroke in Young Adult Patient with Moyamoya Syndrome Secondary to Sickle Cell Disease

Blood ◽  
2020 ◽  
Vol 136 (Supplement 1) ◽  
pp. 13-13
Author(s):  
Oladipo Cole ◽  
Asia Filatov ◽  
Javed Khanni ◽  
Patricio Espinosa
Keyword(s):  
Case Report ◽  
Sickle Cell Disease ◽  
Sickle Cell ◽  
Moyamoya Disease ◽  
Conflicts Of Interest ◽  
Acute Chest Syndrome ◽  
African American Female ◽  
Moyamoya Syndrome ◽  
Cell Disease ◽  
Radiographic Findings

Moyamoya disease, well described in literature, is a chronic cerebrovascular occlusive disorder. It is characterized by progressive stenosis/occlusion of the terminal portions of the internal carotid arteries (ICA) and the proximal portions of the middle cerebral arteries (MCA). Less frequently described is Moyamoya syndrome, the name given to radiographic findings consistent with Moyamoya disease, but with an identifiable cause. The diseases associated with Moyamoya Syndrome include Sickle Cell Disease (SCD), Thalassemias, and Down's Syndrome to name a few. Common complications of Moyamoya include both ischemic and hemorrhagic strokes. Upon literature review, Moyamoya syndrome caused by SCD is not well described. When it is, the discussion is centered around the pediatric patient population and surgical management. Our case report describes a 22-year-old African American female with SCD who initially presented with Acute Chest Syndrome. Her hospital course was complicated by development of overt debilitating neurologic deficits. Subsequently, she was found to have Moyamoya Syndrome on neuroimaging. She was successfully treated with medical management without any surgical intervention. This case highlights the necessity of thorough examination, differential diagnosis, imaging findings, and consideration of predisposing syndromes in the work-up for Moyamoya syndrome; especially individuals with Sickle Cell Disease. Disclosures No relevant conflicts of interest to declare.

scholarly journals Bilateral involvement in patients with granulomatous mastitis: Surgical treatment and case report

2013 ◽  
Vol 02 (09) ◽  
pp. 525-529 ◽  
Author(s):  
P. Orsaria ◽  
F. De Sanctis ◽  
A. Esser ◽  
L. Dori ◽  
E. Bonanno ◽  
...  
Keyword(s):  
Case Report ◽  
Surgical Treatment ◽  
Granulomatous Mastitis ◽  
Bilateral Involvement
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