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CD138- Plasmablastic Lymphoma: A Multi-institutional Study and Review of the Literature.

Authors :
Choudhuri J
Pan Z
Yuan J
Chen M
Wu X
Zheng G
Zhao C
Yuan Y
Agarwal B
Liu J
Ma MY
Wang Y
Shi Y
Source :
Archives of pathology & laboratory medicine [Arch Pathol Lab Med] 2023 Jun 01; Vol. 147 (6), pp. 643-654.
Publication Year :
2023

Abstract

Context.—: Plasmablastic lymphoma (PBL) is a rare aggressive lymphoma, usually positive for CD138 and frequently occurring in the oral cavity of human immunodeficiency virus (HIV) patients. Up to 10% of cases are negative for CD138 and diagnostically very challenging.<br />Objective.—: To investigate the appropriate approach to diagnose CD138- plasmablastic lymphoma and avoid misdiagnosis.<br />Design.—: We studied 21 cases of CD138- PBL from multiple large institutes in the United States and 21 cases from the literature.<br />Results.—: CD138- PBLs were positive for different B/plasma cell markers at various percentages: MUM1 (94.4%; 34 of 36), OCT2 (70.6%; 12 of 17), immunoglobulin light chains (68.8%; 22 of 32), CD38 (68.4%; 13 of 19), CD79a (34.2%; 13 of 38), and PAX5 (15.6%; 5 of 32), suggesting that MUM1, OCT2, immunoglobulin light chains, and CD38 are useful markers to help establish the lineage. A total of 83% of cases (30 of 36) were extraoral lesions. Extraoral lesions showed much lower Epstein-Barr virus (EBV) infection rates (16 of 30; 53.3%) and had worse prognosis. MYC was positive in 80% (8 of 10) of EBV+ cases and 40% (2 of 5) EBV- cases, indicating the importance of MYC in pathogenesis, especially in EBV+ cases.<br />Conclusions.—: Our study emphasizes that CD138- PBLs tend to be extraoral lesions, with much lower EBV infection rates, and diagnostically very challenging. Accurate diagnosis requires a thorough investigation and workup by using appropriate markers.<br /> (© 2023 College of American Pathologists.)

Details

Language :
English
ISSN :
1543-2165
Volume :
147
Issue :
6
Database :
MEDLINE
Journal :
Archives of pathology & laboratory medicine
Publication Type :
Academic Journal
Accession number :
36161544
Full Text :
https://doi.org/10.5858/arpa.2021-0462-OA