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Japanese

Chronic Subdural Hematoma Associated with Primary Thrombocythemia; Report of an operated case, using plateletpheresis Atsushi SUGAWARA 1 , Kazuo EBINA 1 , Hiroshi OHI 1 , Jun SAWATAISHI 1 , Mitsuyuki FUKUDA 2 1Departments of Neurosurgery, Nakadoori Hospital 2Departments of Internal Medicine, Nakadoori Hospital Keyword: Primary thrombocythemia , Chronic subdural hematoma , Plateletpheresis pp.851-855
Published Date 1991/9/10
DOI https://doi.org/10.11477/mf.1436900321
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Abstract

Primary thrombocythemia is a chronic proliferative disorder of the bone marrow in which either thrombo-tic or paradoxically hemorrhagic symptoms or both may occur due to the pathological increase in the num-ber of platelets. The mechanism of hemorrhagic diath-esis in this disorder is not fully defined. We presented a rare case of primary thrombocythemia developing chro-nic subdural hematoma which was surgically managed with the use of plateletpheresis. It was believed that platelepheresis was useful in controlling hemorrhagic complications during surgery associated with primary thrombocythemia.

A 62-year-old man was admitted to the hospital forevaluation of motor weakness on the right side. The patient had no episode of head trauma. CT scan de-monstrated the presence of subdural hematoma in the left frontotemporal region with significant ventricular shift and deformity. No definite abnormalities were dis-closed on laboratory examination except for the hemo-gram in which platelet count was extremely elevated and read 109 × 104/mm3. Examination of bone marrow smears disclosed an abnormal increase in megakary-ocytes. Despite the increase in the number of the platelets, other coagulation studies gave normal results. Prior to surgery plateletpheresis was attempted in hopes of reducing the number of peripheral platelets and eventually avoiding the risk of hemorrhagic com-plications during sugery. As a result surgery for aspira-tion of the hematoma was successfully performed. The postoperative course remained uneventful as the patient continuously underwent two courses of plateletpheresis and chemotherapy, The patient was discharged with no neurological deficits and the peripheral platelets re-mained reduced in number at 50 × 104/mm3 two months after discharge.


Copyright © 1991, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1251 印刷版ISSN 0301-2603 医学書院

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