Noonan phenotype associated with intracerebral hemorrhage and cerebral vascular anomalies: Case report

1993 ◽  
Vol 39 (1) ◽  
pp. 31-36 ◽  
Author(s):  
Tetsuo Hara ◽  
Tomio Sasaki ◽  
Hiroshi Miyauchi ◽  
Kintomo Takakura
Keyword(s):  
Case Report ◽  
Intracerebral Hemorrhage ◽  
Vascular Anomalies ◽  
Cerebral Vascular

P-OT021. Intracerebral hemorrhage in infective endocarditis, with dramatic response to dexamethasone: A case report

2021 ◽  
Vol 132 (8) ◽  
pp. e127
Author(s):  
Distya Nugrahening Pradhani ◽  
Ismail Setyopranoto ◽  
Indarwati Setyaningsih ◽  
Sri Sutarni
Keyword(s):  
Case Report ◽  
Infective Endocarditis ◽  
Intracerebral Hemorrhage

Pheochromocytoma Arising from the Organ of Zuckerkandl Associated with Intracerebral Hemorrhage (1 case report)

1984 ◽  
Vol 14 (1) ◽  
pp. 171
Author(s):  
Chong Ik Lee ◽  
Joo Hee Chang ◽  
Won Kun Park ◽  
In Kyun Han ◽  
Kwon Sam Kim ◽  
...  
Keyword(s):  
Case Report ◽  
Intracerebral Hemorrhage

scholarly journals Rete Middle Cerebral Artery Anomaly Presenting with a Large Intracerebral Hemorrhage: A Case Report

2021 ◽  
Author(s):  
Chandra Dev Sahu ◽  
Nishant Bhargava ◽  
Debabrata Sahana ◽  
Sanjeev Kumar
Keyword(s):  
Case Report ◽  
High Risk ◽  
Intracerebral Hemorrhage ◽  
Middle Cerebral Artery ◽  
Single Channel ◽  
Correct Diagnosis ◽  
Rare Condition ◽  
Haemorrhagic Stroke ◽  
Unilateral Involvement ◽  
Is Failure

AbstractRete MCA anomaly is extremely rare and has been seldomly discussed in literature. Embryologically MCA develops by fusion of multiple twigs which form a single channel. If there is failure to fuse a plexiform network of vessels persists known as rete MCA. This web like network of vessels is at high risk of haemorrhagic stroke and therefore for patients presenting incidentally correct diagnosis is paramount. Here we report a case of rete MCA anomaly in a 35-year-old gentle man who presented with a large haemorrhagic stroke in emergency. DSA showed unilateral involvement of proximal MCA, and otherwise normal intra-cranial vasculature. With this report we aim to correctly diagnose this rare condition and avoid misdiagnosis leading to unnecessary treatments.

Pulmonary Hyaline Membranes and Vascular Anomalies of the Lung: The "Lausanne Baby"

PEDIATRICS ◽  
1967 ◽  
Vol 39 (5) ◽  
pp. 791-792
Author(s):  
FORREST H. ADAMS ◽  
ADEL EL-SALAWY
Keyword(s):  
Blood Flow ◽  
Case Report ◽  
Pulmonary Blood Flow ◽  
Hyaline Membrane Disease ◽  
Vascular Anomalies ◽  
Hyaline Membranes ◽  
Hyaline Membrane

A very interesting brief case report, entitled "Pulmonary Hyaline Membranes and Vascular Anomalies of the Lung," was published in Pediatrics by Bozic. This case is commonly referred to as the "Lausanne baby" and is used by many to support the hypothesis that hyaline membrane disease is primarily related to reduced pulmonary blood flow. Although there are good reasons from observations in both man and animal to implicate reduced pulmonary blood flow as an important factor in the pathophysiology of hyaline membrane disease, we do not believe the "Lausanne baby" can be used to support this hypothesis.

scholarly journals Spontaneous Spinal Subdural and Subarachnoid Hemorrhage with Concomitant Intracerebral Hemorrhage: A Case Report

2019 ◽  
Vol 15 (1) ◽  
pp. 34 ◽  
Author(s):  
Young Lee ◽  
Jeongwook Lim ◽  
Sanghyun Han ◽  
Seung-Won Choi ◽  
Jin-Young Youm ◽  
...  
Keyword(s):  
Case Report ◽  
Subarachnoid Hemorrhage ◽  
Intracerebral Hemorrhage
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