Non-Secretory Multiple Myeloma in a Hemodialysis Patient with Hypercalcemia
Journal Title: Turkish Journal of Hematology - Year 2012, Vol 29, Issue 3
Abstract
To the Editor, Multiple myeloma (MM) develops due to clonal expansion of malign plasma cells. Abnormal plasma cells secrete abnormal immunoglobulins that can be detected monoclonally (M peak) in serum and/or urine via electrophoresis. MM manifests clinically and radiologically with anemia, hypercalcemia, renal failure, and lytic lesions in bones [1]. When the characteristic MM clinical and radiological findings are observed, but there is no monoclonal M peak based on electrophoresis, it is known as non-secretory multiple myeloma (NSMM)—a rare variant of MM [2,3]. NSMM is observed 1%-5% of all MM patients [4]. Hypercalcemia, which can present as mild to severe and life threatening, is the most common metabolic abnormality associated with MM, occurring in approximately 33% of patients [5]. Herein we report a patient diagnosed with NSMM after detecting hypercalcemia during follow-up 7 months after the start of hemodialysis treatment.
Oyun Çocuğunda, Geç Bulgu Veren Doğumsal Diyafram Hernisine Bağlı Ağır Demir Eksikliği Anemisi
An Unusual Presentation of Hairy Cell Leukemia
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Türkiye’de Klinik Araştırmalar
Annular Erythematous Patches as the Presenting Sign of Extranodal Natural Killer/T-Cell Lymphoma
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Miyelodisplastik Sendrom, Psöriazis, Hipogamaglobulinemi ve Monozomi 7’si Olan Bir Çocuk Miyelodisplastik Sendrom Olgusu