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  Vol. 3 No. 5, November 1960 TABLE OF CONTENTS
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Neurologic Aspects of Waldenström's Macroglobulinemia

Report of a Case

JOHN LOGOTHETIS, M.D.; PAUL SILVERSTEIN, M.D.; JOHN COE, M.D.

Arch Neurol. 1960;3(5):564-573.

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

Introduction

In 1944 Waldenström described a clinical syndrome under the title "incipient myelomatosis"1 which he subsequently renamed "macroglobulinemia."2 S i n c e that time about 200 similar cases were reported principally in the foreign literature. A number of recent reviews3-6 have established the following as the outstanding characteristics of the disease.

1. It is a chronic debilitating illness primarily affecting males between the ages of 50 and 80. The usual life expectancy after the first manifestation of symptoms is 2 to 10 years.

2. The onset is insidious, usually characterized by progressive weakness, lassitude, weight loss, and pallor. Edema may be present.

3. Hemorrhagic diathesis is present in at least two-thirds of the cases and is manifested primarily by epistaxis, gingival and retinal hemorrhages, cutaneous p u r p u r a (usually late), and to a lesser extent bleeding from other organs.

4. Painless enlargement . . . [Full Text PDF of this Article]


Author Affiliations

Minneapolis

From the Division of Neurology, University of Minnesota Medical School, and the Department of Pathology, Minneapolis General Hospital.


Footnotes

Received for publication Aug. 8, 1960.



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