Dear Editor,We read with interest the case report by Larson et al. [1] in the Journal of Hematopathology and would like to share a similarly challenging case of plasma cell leukemia encountered in a young patient at our center.A 36-year-old lady presented with a history of backache and generalized weakness for 3 months. She had severe pallor; however, there was no localized bony tenderness, lymphadenopathy, or organomegaly. Investigations revealed hemoglobin 51 g/L (reference range 120-160 g/L), total leukocyte count 243 × 10 9 /L (reference range 4-11 × 10 9 /L), and platelets 119 × 10 9 /L (reference range 150-400 × 10 9 /L). A peripheral blood smear showed marked lymphocytosis with absolute lymphocyte count of 206.6 × 10 9 /L (reference range 1.0-4.0 × 10 9 /L) and 3% cells showing lymphoplasmacytic morphology ( Fig. 1, left image). Biochemistry revealed normal renal function, albumin-corrected serum calcium (10.3 mg/ dL, reference range 9-11 mg/dL), and elevated lactate dehydrogenase (375 U/L, reference range 140-271 U/L). There was marked hypergammaglobulinemia and serum protein electrophoresis identified a monoclonal band (5.6 g/dl). Urine protein electrophoresis and immunofixation did not reveal an M-band and Bence Jones proteins were undetectable. Serum-free light chain assay showed κ = 12,400 mg/L (reference range 3.3-19.4 mg/L), λ = 6.11 mg/L (5.7-26.3 mg/L) with κ/λ ratio = 2029.46 (reference range 0.26-1.65). Bone marrow aspiration revealed massive infiltration by small * Prashant Sharma