z-logo
open-access-imgOpen Access
Biclonal Gammopathy of IgA Kappa variants - A Case Report
Author(s) -
Manchana Lakshman Kumar,
Mahjabeen Salma,
P. Bhulaxmi,
K. Malathi,
Shaik Karimuddin Abdullah
Publication year - 2014
Publication title -
international journal of biomedical research
Language(s) - English
Resource type - Journals
eISSN - 2455-0566
pISSN - 0976-9633
DOI - 10.7439/ijbr.v5i10.795
Subject(s) - medicine , kappa , monoclonal gammopathy , dermatology , gammopathy , pathology , antibody , immunology , philosophy , linguistics , monoclonal , monoclonal antibody
Multiple myeloma is a clonal malignant neoplasm of plasma cells and is characterized by the secretion of monoclonal protein in plasma. Here, we report a case of biclonal multiple myeloma having two spikes on serum protein electrophoresis, one being in Beta-2 region and the other in gamma region. Further on immunofixation, both peaks were found to be of IgA-kappa variant. Biclonal gammopathy is a rare case, which accounts for only 1% of all myelomas but biclonal gammopathy of IgA kappa variant has not been described in the literature so far.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom