Development of Biclonal Gammopathy in a Patient with von Recklinghausen's Neurofibromatosis
- 12 January 1979
- journal article
- research article
- Published by Wiley in Acta Medica Scandinavica
- Vol. 205 (1-6) , 243-245
- https://doi.org/10.1111/j.0954-6820.1979.tb06038.x
Abstract
A well-established case of von Recklinghausen''s neurofibromatosis, in which a biclonal gammopathy developed, was studied. One paraprotein was characterized as Ig[immunoglobulin]G .kappa., the other as IgG .lambda.. This combination of anomalies was not described previously in the literature.This publication has 11 references indexed in Scilit:
- IgM‐Producing Lymphocytes in Peripheral Nerve in a Patient with Benign Monoclonal GammopathyScandinavian Journal of Haematology, 1973
- Oligoclonal MacroglobulinaemiaScandinavian Journal of Immunology, 1972
- Agarose Gel ElectrophoresisScandinavian Journal of Clinical and Laboratory Investigation, 1972
- PYODERMA GANGRENOSUM WITH A MONOCLONAL IgM RED CELL AGGLOMERATING FACTORBritish Journal of Dermatology, 1971
- Monoclonal Hypergammaglobulinemia of theγM Type in a Nine-year-old Girl with Ataxia-TelangiectasiaAmerican Journal of Clinical Pathology, 1970
- Neurofibromatosis in childhoodThe Journal of Pediatrics, 1970
- Myasthenia gravis with a myeloma-type, gamma-G (IgG) immunoglobulin abnormalityThe American Journal of Medicine, 1969
- Multiple Myeloma Associated with Two Serum M Components, γG Type K and γA Type LNew England Journal of Medicine, 1967
- Axillary Freckling as a Diagnostic Aid in NeurofibromatosisAnnals of Internal Medicine, 1964