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Japanese

CEREBELLAR HEMORRHAGE: REPORT OF ONE SURVIVED CASE WITH OPERATION AND 8 AUTOPSIED CASES WITH REVIEW OF LITERATURES Takaomi Uemura 1 , Takashi Tomita 1 , Masahiro Mizukami 2 , Goro Araki 2 , Hiroshi Mihara 2 1Dept, of Neurosurgery, Keio Univ., School of Med. 2Mihara Memorial Hospital pp.879-888
Published Date 1973/7/1
DOI https://doi.org/10.11477/mf.1406203346
  • Abstract
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Cerebellar hemorrhage is classically thought to be a rare fatal disease. However, our data as well as those of others, indicate that its frequency is greater than is generally considered.

Recently we have encountered with 43 year old male who diagnosed as cerebellar hemorrhage angiographically and took satisfactory recovery by direct operative attack. Nine cases, one operated case and 8 autopsied cases, over the past 6 years were reviewed about incidence etc. with recent literatures reference.

He notes sudden onset of occipitalgia and dizzi-ness. At the time of admission neurological exa-mination revealed bilateral choked disk, nystagmus toward left, left sided dysdiadochokinesis and xanthochromia in the diagnostic spinal tap. Bi-lateral carotid angiograms showed ventricular dilatation. Bilateral retrograde brachial angio-grams revealed a space taking lesion in left cerebellar hemisphere. Preoperative pneumoven-triculography was not contributory. Suboccipital craniectomy was carried out and egg-sized intra-cerebellar hematoma was evacuated. Pathology of evacuated specimen demonstrated hemorrhage and gliosis surrounding hematoma without tumor cells or cryptic angiomatous malformations.

This case is the 4th successfully operated case in Japan. Though, all Japanese cases have chronicclinical course.

The clinical picture of all autopsied cases is not specifically characteristic comparing with those of subarachnoid hemorrhage or intracerebral hemor-rhage. The onset used to be abrupt, at times preceded by vomiting, headache and dizziness. Cerebellar signs are absent unexpectedly. The most common objective findings are initial loss of consciousness, meningeal and pyramidal signs. Blood was present in the cerebrospinal fluid in most cases. Five of patients died within the first 24 hours, 3 of them died between 8 days and 18 days.

Pathologically the highest incidence in autopsied cases was in the 5th to 6th decades. In 4 cases, location of hemorrhage was noted around dentate nucleus. Size of hemorrhage was variable from wall-nut to egg. Tonsillar herniation was noted in 4 cases. Ventricular hemorrhage was noted in5 cases. Associated lesions, though small hemor-rhage or infraction, found in the brain stem or cerebral hemisphere.

Etiologically 3 cases were attributed to hyper-tension with arteriosclerosis.

Clinically the diagnosis of cerebellar hemorrhage is quite difficult in acute stage. Most of our cases were diagnosed clinically as subarachnoid hemor-rhage. Therefore, retrograde brachial angiography is more valuable than pneumoventriculography in the point of differential diagnosis from aneurysm, arteriovenous malformation, intracerebral hema-toma etc.

We stressed the value of the retrograde brachial angiography as an useful diagnostic aid, if vessels of posterior fossa are adequately analysed by care-ful interpretation.


Copyright © 1973, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 2185-405X 印刷版ISSN 0006-8969 医学書院

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