Monoclonal Gammopathy in a Child with Leukemia

Author:

STOOP JAN W.12,ZEGERS BEN J. M.13,VAN DER HEIDEN CEES12,BALLIEUX RUDY E.13

Affiliation:

1. University Children’s Hospital and the Division of Clinical Immunochemistry, Department of Internal Medicine, University Hospital, Utrecht, The Netherlands.

2. University Children's Hospital.

3. Division of Clinical Immunochemistry, University Hospital.

Abstract

Abstract This paper describes the case history of a boy found to suffer from acute blastic leukemia at the age of two years. Manifestations of an intracranial localization of the leukemic process occurred several times in the course of the next 18 months; a generalized relapse responded well to therapy. The boy subsequently developed a severe refractory virus infection of the skin and suffered a few other virus infections, without any of the usual changes in the morphology of the blood. A few weeks later he developed a monoclonal gammopathy of the IgG class type L with Bence Jones proteinuria, likewise of type L. The possible causes of this clinical course and of the paraproteinemia are discussed.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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1. Stem Cell Leukaemia in Myelomatosis;Scandinavian Journal of Haematology;2009-04-24

2. Transitorische oligoklonale Paraproteinämie bei Virusinfektion und maligner lymphatischer Erkrankung;DMW - Deutsche Medizinische Wochenschrift;2008-03-25

3. T‐ALL with monoclonal gammopathy and hairy cell features;American Journal of Hematology;2000-09-14

4. Monoclonal gammopathies in children;Journal of Clinical Immunology;1989-07

5. Monoclonal gammopathy in chronic myeloproliferative disorders;Blut;1989-01

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