A Rare Case of Primary Plasma Cell Leukaemia with Monosomy XCorrespondence Address :
Dr. Smita Surendra Masamatti,
Assistant Professor, Department of Pathology, 3rd Floor, Sapthagiri Medical College, Bengaluru-560090, Karnataka, India.
Primary Plasma Cell Leukaemia (pPCL) is a very rare and aggressive subtype of plasma cell dyscrasias with a very poor outcome and characterized by presence of >2x109/l circulating plasma cells. Overall incidence being 1%-2% of all malignant plasma cell diseases and 0.9% of all acute leukaemias. Patients with primary and secondary PCL have similar clinical features but differences do exist. Here we report a rare and interesting case diagnosed as primary PCL in a 44-year-old female with unusual clinical presentation and complex karyotyping. Her serum electrophoresis showed a monoclonal IgG component and immunohistochemistry of bone marrow plasma cells showed CD 38 positive and CD 20 negative. The patient initially responded partially for combination chemotherapy, but succumbed after 20 days of diagnosis. We are presenting this case to highlight the importance of early diagnosis of such haematological malignancies in settings where treatment options like stem cell transplantation are limited.
Acute renal failure, Cytogenetics, Prognosis
Smita Surendra Masamatti, Aparna Narasimha, Archana C Shetty, C Vijaya. A RARE CASE OF PRIMARY PLASMA CELL LEUKAEMIA WITH MONOSOMY X. Journal of Clinical and Diagnostic Research [serial online] 2017 August [cited: 2018 Feb 24 ]; 11:ED06-ED07. Available from
Date of Submission: Mar 20, 2017
Date of Peer Review: Mar 21, 2017
Date of Acceptance: May 09, 2017
Date of Publishing: Aug 01, 2017
FINANCIAL OR OTHER COMPETING INTERESTS: None.
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