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Plasmablastic plasma cell myeloma mimicking plasmablastic lymphoma

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This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

223 DOI: 10.5045/kjh.2010.45.4.223

The Korean Journal of Hematology Volume 45ㆍNumber 4ㆍDecember 2010

Plasmablastic plasma cell myeloma mimicking plasmablastic lymphoma

Qute Choi, Hyun Kyung Kim

Department of Laboratory Medicine, Seoul National University College of Medicine, Seoul, Korea

A 54-year-old woman was admitted with compression fracture of thoracic vertebral bodies. Urine protein electro- phoresis revealed the presence of M protein and serum free κ/λ ratio was 0.01. Bone marrow aspiration (A) and biopsy (B) revealed diffuse infiltration of numerous large-sized blasts with basophilic cytoplasm, dispersed nuclear chromatin, high nuclear/cytoplasmic ratio and prominent nucleoli. Tumor cells showed strong expression of plasma cell (PC) antigen CD138 (C), monotypic light chain (D, κ negative; E, λ positive), negative expression of CD3, CD20, CD34, Tdt and CD30 by immunohistochemistry, mimicking a picture of plasmablastic lymphoma (PBL). PBL was ex- cluded on the basis of CD56 positivity (F) and absence of EBV-encoded RNA (G). The diagnosis of plasmablastic plasma cell myeloma (PBPCM) was made and the patient started chemotherapy. Morphologic features usually distin- guish PBL from well-differentiated plasma cell myeloma (PCM). However, highly aggressive PBPCM may show pre- dominance of plasma blasts, which can resemble PBL cells. Although both PB myeloma and PBL express PC antigens (CD138, monotypic light chain), positivity of EBV-encoded RNA is useful in establishing the diagnosis of PBL.

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