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  Vol. 110 No. 5, Nov 1962 TABLE OF CONTENTS
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Active Recovery from Hepatic Disease of the Alcoholic

CHARLES S. DAVIDSON, M.D.; RICHARD A. MacDONALD, M.D.

Arch Intern Med. 1962;110(5):592-595.

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

Active hepatic insufficiency of the alcoholic, when severe, is often fatal.1,2 The cause is unknown, and treatment with alcohol withdrawal and a nutritious diet has doubtful specificity. The disease is characterized histologically by liver-cell necrosis, "alcoholic hyalin" (Mallory),3 polymorphonuclear infiltration, and parenchymal disorganization. Hepatic fat is usually present in large amounts, but the necrotic lesion appears to be independent of the amount of fat. Outstanding clinical features are jaundice (sometimes simulating extrahepatic obstruction),4,5 polymorphonuclear leukocytosis, as well as other evidences of severe liver disease.

This report concerns a patient with histologic and clinical abnormalities as marked as we have seen, yet recovery occurred with restitution of almost normal liver function and histology.

A 49-year-old male was admitted to the II and IV (Harvard) Medical Services, Boston City Hospital, after about 2 months of progressive fatigue, weakness, and anorexia. A week earlier he had observed light stools, dark . . . [Full Text PDF of this Article]


Author Affiliations

BOSTON

Associate Professor of Medicine, Harvard Medical School, Associate Director, Second and Fourth (Harvard) Medical Services, and Associate Physician, Thorndike Memorial Laboratory, Boston City Hospital (Dr. Davidson); Assistant Professor of Pathology, Harvard Medical School; Associate Pathologist, Mallory Institute of Pathology, Boston City Hospital (Dr. MacDonald).; From the Thorndike Memorial Laboratory and the Second and Fourth (Harvard) Medical Services and the Mallory Institute of Pathology, Boston City Hospital, and the Departments of Medicine and Pathology, Harvard Medical School.


Footnotes

Supported in part by the United States Army Medical Research and Development Command, Department of the Army, under Contract No. DA-49-193-MD-2013.



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