Plasma cell leukemia masquerading as ALL-L3--a case report

Kalpalata Tripathy1, Kalyani Prava Gouda, Sukumar Chakrabarty

  • 1Department of Pathology, S. C.B. Medical College, Cuttack, Orissa.

Insights

Plasma cell leukemia (PCL) is a rare plasma cell disorder. This case highlights PCL presenting with over 80% atypical Mott cells, mimicking Acute Lymphoid Leukemia-L3, and confirmed by bone marrow, serum, and imaging findings.

Area of Science:

  • Hematology
  • Oncology

Background:

  • Plasma cell leukemia (PCL) is an aggressive plasma cell dyscrasia characterized by over 20% circulating plasma cells.
  • PCL is rare, often presenting with advanced disease and poor prognosis.

Observation:

  • A 62-year-old female presented with a peripheral smear showing over 80% atypical vacuolated plasma cells (Mott cells).
  • These cells morphologically mimicked Burkitt cells seen in Acute Lymphoid Leukemia-L3 (ALL-L3).
  • Bone marrow aspirate showed few mature myeloma cells.

Findings:

  • Serum protein electrophoresis revealed a positive M-band.
  • Skeletal X-rays demonstrated lytic lesions in the femur and pelvic bones.
  • A definitive diagnosis of PCL was established based on the combined clinical and laboratory findings.

Implications:

  • This case underscores the importance of considering PCL in differential diagnoses, especially when atypical plasma cells are abundant.
  • Morphological mimicry of ALL-L3 by Mott cells in PCL necessitates comprehensive diagnostic workup.
  • Accurate diagnosis of PCL is crucial for appropriate treatment strategies and patient management.

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