Author/Authors :
Wadhwa, Heena Baba Farid University of Health Sciences - Faridkot - India , Singh, Navtej Baba Farid University of Health Sciences - Faridkot - India
Abstract :
Multiple Myeloma is a neoplasm of B cell lineage characterized by excessive proliferation of abnormal plasma cells. It is characterized by a clinical pentad of 1) anemia,
2) a monoclonal protein in the serum or the urine or both, 3) bone leisons and or bone
pain, 4) hypercalcemia>11.5g/dl and 5) renal insufficiency. Non secretory multiple
myeloma is a rare variant of the classic form of multiple myeloma and accounts for
1% to 5 % of all cases of multiple myeloma. The clinical presentation and radiographic findings of non-secretory multiple myeloma and multiple myeloma are the
same. The diagnosis of multiple myeloma requires the demonstration of monoclonal
gammopathy in the serum or urine. In non-secretory multiple myeloma, however no
such gammopathy can be demonstrated, making the diagnosis more difficult. We describe a 60 year old woman who initially presented with back pain which when further
investigated by complete blood count revealed hemoglobin of 13g/dl, Total Leukocyte
Count of 10,890 and platelet count of 1.5 lac/cmm. Viral markers revealed HCV positive. Hypercalcemia with a serum calcium level of 12.5g/dl was also demonstrated.
MRI revealed multiple lytic bony lesions. No monoclonal gammopathy was found in
the serum or urine and bone marrow biopsy showed marked plasmacytosis of > 45%.
We present a case of Non Secretory multiple myeloma because of its illusive nature
and rare entity.