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Japanese

A CASE OF SUBCLAVIAN STEAL SYNDROME WITH CEREBELLAR HEMANGIOBLASTOMA Satoru Watanabe 1 , Tomohiro Matsuzawa 1 , Shigeru Ishikawa 1 , Shozo Ishii 1 , Takao Suzuki 2 , Humio Shiratsu 2 1Department of Neurosurgery, Juntendo University School of Medicine 2Department of Thoracic Surgery, Juntendo University School of Medicine pp.607-613
Published Date 1972/5/1
DOI https://doi.org/10.11477/mf.1406203120
  • Abstract
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This is a report of a case who has suffered from the cerebellar tumor convined with the "subclavian steal syndrome" due to obstruction of the right subclavian artery.

The patient, 45 years old male, was suddenly developed severe headache associated with vomiting and admitted to the Juntendo University Hospital with additional symptom of gradual drop of conscious level on August 17 in 1969.

On admission, examinations revealed the increased intracranial pressure, paresis of the left 8th through 12th cranial nerves, left cerebellar hemisphere signs and left hemiparesis. Radial pulsation on both side was not synchronous and systolic blood pressure on the right side was 14 mmHg lower than that on the left side.

Ventriculo-auriculostomy was immediately fol-lowed by clearing of consciousness and disappear-ance of the signs of intracranial hypertension.

Retrograde vertebral angiogram demonstrated a tumor stain surrounded by the round avascular area in the left cerebellar hemisphere.

Retrograde vertebral angiogram showed that the contrast medium did go up until the basilar artery then flow down the right vertebral artery to the right brachial artery via subclavian artery. When a retrograde angiography was made from the right brachial artery neither left common carotid nor innominating artery was demonstrated and the right subclavian artery ended blindly. Contrast medium which once did go up the right vertebral artery returned on the same route again after the completion of injection.

On September 21, suboccipital craniectomy was carried out and cystic tumor with thumb-tip sized mural nodule on the left cerebellar hemisphere was removed. Histological diagnosis of the tumor was hemangioblastoma.

Postoperative course was uneventful and the patient showed continuous improvement until No-vember 5 when he developed rather suddenly the paresis of lower cranial nerves, cerebellar and pyramidal signs associated with headache.

On December 10, reconstruction of the right subclavian artery was carried out. Using a piece from the internal iliac artery an autograft was made between the proximal end of right carotid artery and subclavian artery. Following the second surgery, almost complete disappearance of neurolo-gical abnormalities resulted and no recurrence of symptoms occurs for 8 months follow-up period.


Copyright © 1972, 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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