Traumatic intracerebral hematoma—Which patients should undergo surgical evacuation? CT scan features and ICP monitoring as a basis for decision making

1989 ◽  
Vol 32 (3) ◽  
pp. 181-187 ◽  
Author(s):  
R. Bullock ◽  
J. Golek ◽  
G. Blake
2008 ◽  
Vol 55 (2) ◽  
pp. 123-127 ◽  
Author(s):  
B.M. Djurovic ◽  
G.M. Tasic ◽  
V.T. Jovanovic ◽  
I.M. Nikolic ◽  
R.V. Krunic-Protic ◽  
...  

In the period from 01.01.2000 until 31.12.2002 34 patients with spontaneous intracerebral hematoma (ICH) and with deeply disturbed state of consciousness were operated in the Department of neurosurgery of the Urgent Center, Clinical Center of Serbia. In all operated patients the indication for surgery was given on the basis of CT scan of the brain, state of consciousness, defined Glasgow coma score (GCS) and neurological status, but due to existing or threatening incarceration not even one patient was submitted to angiography of the blood vessels at the cerebral base, thus preoperatively we did not know the cause of the hemorrhage. Of 34 operated patients 22 or 64.7% died, and 12 or 35.3% survived. 14 patients were in the deepest phase of coma, where the preoperative GCS is from 3 to 5 points, and in the postoperative course only one survived, aged 25. The other survivors had somewhat less disturbed state of consciousness, they also were younger, CT scan of the brain was without blood in the chamber system. In the same period, in the Department of Neurosurgery of the Urgent Center, Clinical Center of Serbia 43 patients with traumatic intracerebral hematoma (TIH) were operated; 9 patients survived, 34 died. Only 4 patients had acute TIH. All of them were in the terminal stage of incarceration, and despite being immediately submitted to surgery all of them died. The remaining 39 patients had, the so called delayed TIH where the secondary CT scan of the brain showed development of the traumatic intracerebral haematoma that was not verified on the incipient scanner. Indication for a repeated CT scan was given in 19 patients due to focal or general neurological deterioration. However in 20 patients subsequent neurological disturbances were not registered. Those that survived were younger patients, and they were not in the deepest stage of coma, most often they had a temporal localization of hematoma.


1979 ◽  
Vol 19 (12) ◽  
pp. 1127-1137 ◽  
Author(s):  
TAKASHI TSUBOKAWA ◽  
JITSUHIRO YAMADA ◽  
NORITAMI TOMIZAWA ◽  
TOSHIKAZU GOTO ◽  
HIDEO SHINOZAKI ◽  
...  

2014 ◽  
Vol 21 (1) ◽  
pp. 109-112
Author(s):  
P. Sasikala ◽  
Bindu Menon ◽  
Amit Agarwal

Abstract Movement disorders are atypical and rare presentation of chronic subdural hematomas. We report a case of 60 year man who presented with intention tremors and altered sensorium. The patient had Kernohan-Woltman notch phenomenon on clinical examination. CT scan brain showed a large left fronto-temporo-parietal chronic subdural hematoma with significant mass effect and midline shift. His symptoms relieved completely after surgical evacuation of the hematoma.


1983 ◽  
Vol 23 (8) ◽  
pp. 644-650
Author(s):  
Yusuke SAWADA ◽  
Toshihisa SAKAMOTO ◽  
Daikai SADAMITSU ◽  
Kazuyuki NISHIDE ◽  
Katsumi IKEMURA ◽  
...  

2020 ◽  
Author(s):  
JIAYU SHEN ◽  
Changping Gan ◽  
R.D.T. Rajaguru ◽  
Dou Yuan ◽  
ZHENGHUA XIAO

Abstract Introduction: Marfan syndrome (MFS) is a common heritable connective tissue disease involving multiple organs. Even though the clinical manifestations of MFS can be various, aortic root aneurysm is estimated as one of the most serious complications. We herein describe an individualized treatment decision-making process for a 23-year-old male with MFS, suffering from a giant but stable aortic root aneurysm which is extremely rare at his age. Case: The patient, a 23-year-old male with a family history of MFS, presented to our cardiovascular department because of progressive exertional chest distress, fatigue and occasional precordial pain. Physical examinations revealed six-foot-three inches of height, high myopia, and a diastolic murmur at the aortic valve area. Laboratory examinations for systemic vasculitis and infectious diseases were negative. The transthoracic echocardiography (TTE) and enhanced thoracic computed tomography (CT) scan revealed the existence of a giant aortic root aneurysm (125.1 mm in short-axis), severe aortic valve regurgitation, cardiac dilatation (LV; 99 mm in diastolic diameter) and a poor ejection fraction (EF; 18%). Considering the risk of rupture or dissection of the dilated aortic root, we successfully performed the Bentall procedure based on the intraoperative exploration results. Postoperative thoracic CT scan revealed a normal sized reconstructed aortic root, and the patient was discharged uneventfully 7 days later. Conclusion It is extremely rare to report such a giant aortic root aneurysm in a young patient. In the treatment decision-making process, the patient’s specific situation should be taken into consideration. The composite replacement of the aortic valve and ascending aorta should be performed if the patient is not suitable for valve-sparing operation.


Nosotchu ◽  
1983 ◽  
Vol 5 (3) ◽  
pp. 180-185
Author(s):  
Masakazu Kitahara ◽  
Akira Ogawa ◽  
Shinro Komatsu ◽  
Yoshiharu Sakurai ◽  
Jiro Suzuki

1967 ◽  
Vol 9 ◽  
pp. 186-187
Author(s):  
Yuji MIYAZAKI ◽  
Toyoaki CHIBA ◽  
Hidehiko TAKAMATSU ◽  
Shinsho MATSUMOTO ◽  
Hiroshi TSUTSUMI ◽  
...  

2018 ◽  
Vol 37 (7) ◽  
pp. 1879-1884 ◽  
Author(s):  
M. Gamala ◽  
S. P. Linn-Rasker ◽  
M. Nix ◽  
B. G. F. Heggelman ◽  
J. M. van Laar ◽  
...  

PEDIATRICS ◽  
1981 ◽  
Vol 68 (3) ◽  
pp. 465-465
Author(s):  
T. H. Deonna

In their article on complications of sinusitis (Pediatrics 66:568, 1980) Brook and colleagues have discussed the "proper management of subdural empyemas which require prompt surgical evacuation." We want to call to the attention of Brook and colleagues as well as your readers, our article on nonsurgical treatment of interhemispheric subdural empyemas in children (published in English), which discusses the changing outlook of intracranial suppurations given earlier diagnosis with CT scan (Helv Paediatr Acta 32:577, 1979).


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