Immunochemical studies in multiple myeloma.
Indian J Cancer
; 1997 Dec; 34(4): 151-8
Article
de En
| IMSEAR
| ID: sea-51204
The study deals with a total of 72 patients with Plasma cell dyscrasias (PCD) selected on the basis of atypical plasmacytosis in the bone marrow aspirate and radiological evidence of osteolytic lesions. Males(48) outnumbered the females (24). Pathological fracture and paraplegia was the commonest presenting symptom encountered in 38 patients. Electrophoresis of serum for 'M' band and Immunoelectrophoretic analysis of the serum revealed IgG myeloma in 40 patients followed by, IgA myeloma(13), Light chain disease (12) and other variants in remaining seven cases. The urinary Bence Jones proteins were detected in a total of 34 cases and was frequently encountered with IgA myeloma (7 out of 13) compared with IgG myeloma (13 out of 40) when analysed in Disc electrophoresis. Kappa light chain was observed in 21 cases and lambda counterpart in nine cases without any clinical significance. One case of solitary myeloma terminated in characteristic multicentric multiple myelomatosis within a span of six months in the sequential follow up study. We recommend the triangular approach to diagnosis of paraproteinemia with a special emphasis on immunoelectrophoresis for typing multiple myeloma and allied disorders along with disc electrophoresis for the demonstration of urinary Bence Jones protein in the routine set up.
Texte intégral:
1
Indice:
IMSEAR
Sujet Principal:
Sujet âgé de 80 ans ou plus
/
Sujet âgé
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Femelle
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Humains
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Mâle
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Protéine de Bence Jones
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Immunoglobuline A
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Immunoglobuline G
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Immunoglobuline M
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Immunoélectrophorèse
Type d'étude:
Clinical_trials
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Observational_studies
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Prognostic_studies
Limites du sujet:
Aged80
Pays comme sujet:
Asia
langue:
En
Texte intégral:
Indian J Cancer
Année:
1997
Type:
Article