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Non-secretory or low-secretory myeloma with intracellular kappa chains. Report of six cases and review of the literature

Turesson, I LU and Grubb, A LU orcid (1978) In Acta Medica Scandinavica 204(6). p.51-445
Abstract

This report concerns six cases of multiple myeloma characterized by either no demonstrable monoclonal immunoglobulin in plasma or urine or by trace amounts (less than or equal to 0.1 g/l) of monoclonal kappa chains in the urine. In all cases there was an infiltration of the bone marrow by plasma cells containing kappa chains but no heavy chains. A retrospective analysis was made of 126 consecutive cases of Bence Jones myeloma. The number of kappa and lambda cases was approximately the same. All cases secreting less than or equal to 0.1 g light chains per 1 urine were of kappa type. This contrasts with a kappa/lambda ratio of 1.4-1.9 among reported series of M-components containing both heavy and light chains. A review of reported cases... (More)

This report concerns six cases of multiple myeloma characterized by either no demonstrable monoclonal immunoglobulin in plasma or urine or by trace amounts (less than or equal to 0.1 g/l) of monoclonal kappa chains in the urine. In all cases there was an infiltration of the bone marrow by plasma cells containing kappa chains but no heavy chains. A retrospective analysis was made of 126 consecutive cases of Bence Jones myeloma. The number of kappa and lambda cases was approximately the same. All cases secreting less than or equal to 0.1 g light chains per 1 urine were of kappa type. This contrasts with a kappa/lambda ratio of 1.4-1.9 among reported series of M-components containing both heavy and light chains. A review of reported cases of non-secretory myeloma revealed a preserved capacity for Ig synthesis in the majority of cases and among these a preponderance of kappa chain producing clones. These observations might be explained by a higher tendency for kappa chain producing cells to mutate to low secretors or to cells producing abnormal light chains which are catabolized rapidly. The clinical data from our patients do not indicate a more pessimistic prognosis in non- or low-secretory myeloma, than in other cases of multiple myeloma.

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type
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publication status
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keywords
Aged, Bence Jones Protein/analysis, Bone Marrow Cells, Bone Neoplasms/immunology, Cell Count, Fluorescent Antibody Technique, Humans, Immunoglobulin A/analysis, Immunoglobulin G/analysis, Immunoglobulin Light Chains/analysis, Immunoglobulin M/analysis, Immunoglobulin kappa-Chains/analysis, Immunoglobulin lambda-Chains/analysis, Male, Middle Aged, Multiple Myeloma/immunology, Plasma Cells/immunology
in
Acta Medica Scandinavica
volume
204
issue
6
pages
51 - 445
publisher
Wiley-Blackwell
external identifiers
  • scopus:0018237174
  • pmid:104550
ISSN
0001-6101
DOI
10.1111/j.0954-6820.1978.tb08472.x
language
English
LU publication?
yes
id
a411f433-8d12-4fd9-be2c-c0f591e718d0
date added to LUP
2021-10-16 19:33:09
date last changed
2024-01-20 15:02:54
@article{a411f433-8d12-4fd9-be2c-c0f591e718d0,
  abstract     = {{<p>This report concerns six cases of multiple myeloma characterized by either no demonstrable monoclonal immunoglobulin in plasma or urine or by trace amounts (less than or equal to 0.1 g/l) of monoclonal kappa chains in the urine. In all cases there was an infiltration of the bone marrow by plasma cells containing kappa chains but no heavy chains. A retrospective analysis was made of 126 consecutive cases of Bence Jones myeloma. The number of kappa and lambda cases was approximately the same. All cases secreting less than or equal to 0.1 g light chains per 1 urine were of kappa type. This contrasts with a kappa/lambda ratio of 1.4-1.9 among reported series of M-components containing both heavy and light chains. A review of reported cases of non-secretory myeloma revealed a preserved capacity for Ig synthesis in the majority of cases and among these a preponderance of kappa chain producing clones. These observations might be explained by a higher tendency for kappa chain producing cells to mutate to low secretors or to cells producing abnormal light chains which are catabolized rapidly. The clinical data from our patients do not indicate a more pessimistic prognosis in non- or low-secretory myeloma, than in other cases of multiple myeloma.</p>}},
  author       = {{Turesson, I and Grubb, A}},
  issn         = {{0001-6101}},
  keywords     = {{Aged; Bence Jones Protein/analysis; Bone Marrow Cells; Bone Neoplasms/immunology; Cell Count; Fluorescent Antibody Technique; Humans; Immunoglobulin A/analysis; Immunoglobulin G/analysis; Immunoglobulin Light Chains/analysis; Immunoglobulin M/analysis; Immunoglobulin kappa-Chains/analysis; Immunoglobulin lambda-Chains/analysis; Male; Middle Aged; Multiple Myeloma/immunology; Plasma Cells/immunology}},
  language     = {{eng}},
  number       = {{6}},
  pages        = {{51--445}},
  publisher    = {{Wiley-Blackwell}},
  series       = {{Acta Medica Scandinavica}},
  title        = {{Non-secretory or low-secretory myeloma with intracellular kappa chains. Report of six cases and review of the literature}},
  url          = {{http://dx.doi.org/10.1111/j.0954-6820.1978.tb08472.x}},
  doi          = {{10.1111/j.0954-6820.1978.tb08472.x}},
  volume       = {{204}},
  year         = {{1978}},
}