{micro}-Chain Disease

doi:10.1001/archinte.1975.00330010073010

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Vol. 135 No. 1, January 1975

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SYMPOSIUM ON MYELOMA

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µ-Chain Disease

Edward C. Franklin, MD

Arch Intern Med. 1975;135(1):71-72.

Abstract

The clinical and laboratory features of the seven known patientswith heavy chain disease showed that all but one had chroniclymphocytic leukemia. Two common and striking features are thepresence of ${kappa}$ -type Bence Jones proteins and vacuolated plasmacells in the marrow.

Author Affiliations

From Irvington House Institute, Rheumatic Diseases Study Group, Department of Medicine, New York University School of Medicine.

Footnotes

Received for publication March 7, 1974; accepted May 16.

Read before the Symposium on Myeloma, Atlanta, Oct 22, 1973.

Reprint requests to 550 First Ave, New York, NY 10016 (Dr. Franklin).

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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Plasma Cell Dyscrasias and Cryoglobulins
Bloch and Franklin
JAMA 1982;248:2670-2676.
ABSTRACT

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