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  Vol. 7 No. 1, July 1962 TABLE OF CONTENTS
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Studies on Hepatocerebral Disease

IV. Portal-Systemic Encephalopathy in Chronic Schistosomiasis Japonica

SHIGEO OKINAKA, M.D.; MASAKI YOSHIKAWA, M.D.; TOSHIJI MOZAI, M.D.; KAZUTERU OGIHARA, M.D.; HARUO WATANABE, M.D.; TOSHIO TERAO, M.D.; SATOSHI UEDA, M.D.; SHUNSAKU HIRAI, M.D.

Arch Neurol. 1962;7(1):1a-9.

Since this article does not have an abstract, we have provided the first 150 words of the full text PDF and any section headings.

The development of neurological disorders in chronic schistosomiasis japonica with its well-known liver involvement presents an excellent opportunity to study the pathogenesis of neurological manifestations of liver disease, which has not been fully understood. Ariizumi1 in 1952 and Okinaka et al.2 in 1953 reported involvement of the nervous system in schistosomiasis not due to embolism of ova. A systematic study of schistosomiasis japonica from the neurological standpoint Was therefore attempted. Clinical records of 3 cases, autopsy findings of 2 cases, and the results of an epidemiological survey in the endemic area constitute the present communication.

Case Records

Three cases with well-developed neurological disorders associated with chronic schistosomiasis japonica were hospitalized and extensively studied with methods of clinical investigation, including determination of hepatic blood flow and splenic portography.

CASE 1.

—The patient was a 58-year-old female with positive reaction to the Schistosoma skin test. Family history was noncontributory except . . . [Full Text PDF of this Article]


Author Affiliations

TOKYO, JAPAN

The Third Department of Internal Medicine (Director: Prof. Dr. S. Okinaka), Faculty of Medicine, University of Tokyo.


Footnotes

Received for publication Jan. 22, 1962.



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