scholarly journals Transient unilateral facial paralysis induced by perimesencephalic non-aneurysmal subarachnoid hemorrhage: A case report and review of the literature

2015 ◽  
Vol 10 (4) ◽  
pp. 1541-1543 ◽  
Author(s):  
HUI-JUN WEN ◽  
JIN-SHUO YANG ◽  
YONG-QIANG LI
Keyword(s):  
Case Report ◽  
Subarachnoid Hemorrhage ◽  
Facial Paralysis ◽  
Aneurysmal Subarachnoid Hemorrhage ◽  
Review Of The Literature

Aneurysmal Subarachnoid Hemorrhage with Spinal Subdural Hematoma: A Case Report and Systematic Review of the Literature

2019 ◽  
Vol 128 ◽  
pp. 240-247
Author(s):  
Robert J. Rothrock ◽  
Adam Y. Li ◽  
Jamie Rumsey ◽  
Johanna T. Fifi ◽  
Christopher P. Kellner ◽  
...  
Keyword(s):  
Systematic Review ◽  
Case Report ◽  
Subarachnoid Hemorrhage ◽  
Subdural Hematoma ◽  
Aneurysmal Subarachnoid Hemorrhage ◽  
Review Of The Literature ◽  
Spinal Subdural Hematoma

Coarctation of the Aorta as a Rare Indirect Cause of Aneurysmal Subarachnoid Hemorrhage in the Adolescent: A Case Report and Review of the Literature

2021 ◽  
Author(s):  
Michael Veldeman ◽  
Anke Höllig ◽  
Hans Clusmann ◽  
Gerrit Alexander Schubert
Keyword(s):  
Case Report ◽  
Subarachnoid Hemorrhage ◽  
Aortic Arch ◽  
Ct Angiography ◽  
Cerebral Angiography ◽  
Aneurysmal Subarachnoid Hemorrhage ◽  
Coarctation Of The Aorta ◽  
Review Of The Literature ◽  
Anterior Circulation ◽  
Anterior Circulation Aneurysms

AbstractAneurysmal subarachnoid hemorrhage (SAH) is rare in teenagers. We present the case of a 19-year-old woman with an aneurysmal SAH and four anterior circulation aneurysms. Due to the urgency of operative treatment, no initial conventional cerebral angiography was performed. The CT angiography depicted the aortic arch incompletely. The coarctation was discovered on day 5 after ictus in a cerebral angiography for vasospasm surveillance. We believe that in young SAH patients without an explainable predilection for aneurysm formation, imaging of the aortic arch during the initial CT angiography, not to miss a coarctation of the aorta, is highly recommended.

scholarly journals Congenital unilateral facial palsy revealing a facial nerve agenesis: a case report and review of the literature

2019 ◽  
Vol 5 (1) ◽  
pp. 20180029
Author(s):  
Yaotse Elikplim Nordjoe ◽  
Ouidad Azdad ◽  
Mohamed Lahkim ◽  
Laila Jroundi ◽  
Fatima Zahrae Laamrani
Keyword(s):  
Case Report ◽  
Facial Nerve ◽  
Temporal Bone ◽  
Facial Paralysis ◽  
Facial Palsy ◽  
Rare Condition ◽  
Review Of The Literature ◽  
Moebius Syndrome ◽  
Temporal Bone Ct

Facial nerve aplasia is an extremely rare condition that is usually syndromic, namely, in Moebius syndrome. The occurrence of isolated agenesis of facial nerve is even rarer, with only few cases reported in the literature. We report a case of congenital facial paralysis due to facial nerve aplasia diagnosed on MRI, while no noticeable abnormality was detected on the temporal bone CT.

scholarly journals Sick sinus syndrome following aneurysmal subarachnoid hemorrhage. A case report.

Nosotchu ◽  
1991 ◽  
Vol 13 (5) ◽  
pp. 400-404
Author(s):  
Masaaki Yamamoto ◽  
Tsuyomi Mizoguchi ◽  
Kouichi Shinohara ◽  
Akihiko Sakaue ◽  
Masamichi Tomonaga
Keyword(s):  
Case Report ◽  
Subarachnoid Hemorrhage ◽  
Sick Sinus Syndrome ◽  
Aneurysmal Subarachnoid Hemorrhage

Multiple Cerebral Angiomas and Rendu-Osler-Weber Disease: Case Report

Neurosurgery ◽  
1991 ◽  
Vol 29 (4) ◽  
pp. 599-602 ◽  
Author(s):  
B. Aesch ◽  
E. Lioret ◽  
B. de Toffol ◽  
M. Jan
Keyword(s):  
Case Report ◽  
Subarachnoid Hemorrhage ◽  
Surgical Treatment ◽  
Arteriovenous Malformations ◽  
Review Of The Literature ◽  
Disease Case

Abstract A 25-year-old man was hospitalized after suffering a subarachnoid hemorrhage. Arteriograms disclosed two arteriovenous malformations, one of which was asymptomatic. Rendu-Osler-Weber disease was suspected because of the concomitant existence of cutaneous telangiectases, Review of the literature shows that in 12 previously published cases involving multiple arteriovenous malformations, this diagnosis was established five times. The indications for surgical treatment are discussed.

Lethal Vertebral Artery Dissection in Pregnancy: A Case Report and Review of the Literature

2006 ◽  
Vol 130 (4) ◽  
pp. 533-535 ◽  
Author(s):  
Madalina Tuluc ◽  
Daniel Brown ◽  
Bruce Goldman
Keyword(s):  
Case Report ◽  
Pregnant Woman ◽  
Subarachnoid Hemorrhage ◽  
Vertebral Artery ◽  
Fatal Outcome ◽  
Vertebral Artery Dissection ◽  
Rare Event ◽  
Artery Dissection ◽  
Review Of The Literature ◽  
In Pregnancy

Abstract Subarachnoid hemorrhage represents a rare event in pregnancy with a high mortality rate. We present the case of a 39-year-old pregnant woman who developed right vertebral artery dissection with subsequent massive subarachnoid hemorrhage with fatal outcome. The macroscopic and microscopic autopsy findings are described. A review of the literature with a discussion of the varied predisposing factors for vertebral artery dissection and subarachnoid hemorrhage and the rarity of these events in pregnancy is provided.

Sign in / Sign up

Export Citation Format

Share Document