Serous fluid cytology of multicentric Castleman’s disease and other lymphoproliferative disorders associated with Kaposi sarcoma-associated herpes virus: a review with case reports
Article first published online: 9 JUN 2011
© 2011 Blackwell Publishing Ltd
Volume 23, Issue 2, pages 76–85, April 2012
How to Cite
Lobo, C., Amin, S., Ramsay, A., Diss, T. and Kocjan, G. (2012), Serous fluid cytology of multicentric Castleman’s disease and other lymphoproliferative disorders associated with Kaposi sarcoma-associated herpes virus: a review with case reports. Cytopathology, 23: 76–85. doi: 10.1111/j.1365-2303.2011.00868.x
- Issue published online: 19 MAR 2012
- Article first published online: 9 JUN 2011
- Accepted for publication 25 March 2011
- Kaposi sarcoma-associated herpes virus;
- serous fluids;
- multicentric Castleman`s disease;
- plasmablastic lymphoma;
- primary effusion lymphoma
C. Lobo, S. Amin, A. Ramsay, T. Diss and G. KocjanSerous fluid cytology of multicentric Castleman’s disease and other lymphoproliferative disorders associated with Kaposi sarcoma-associated herpes virus: a review with case reports
Objective: The aim of this study is to describe and review the cytological features of Kaposi sarcoma-associated herpes virus (KSHV) related entities, such as multicentric Castleman’s disease (MCD), plasmablastic-lymphoma (PBL) and primary effusion lymphoma (PEL), which all may present as body cavity effusions. Serous fluid cytology of MCD and PBL has not, to our knowledge, thus far been described. Although different in nature, MCD, PBL and PEL are characterized by similar morphological features.
Materials and methods: Body cavity effusions from four different patients with previously known or unknown KSHV-related lymphoproliferations have been examined by routine cytology, immunocytochemistry (IC) and polymerase chain reaction (PCR).
Results: MCD, PBL and PEL are all characterized by increased cellularity, comprising mainly lymphoid and plasmacytoid cells with variable proportions of immunoblasts. Immunocytochemistry and PCR results show the MCD to be CD138 and KSHV positive, CD30 negative, IgM, IgH and lambda restricted but IgH polyclonal. PBL was CD138 positive, kappa restricted, weakly positive with VS38 and over 80% positive with MIB 1. PEL was CD45, EMA, CD138, KSHV, p53 and CD3 positive, CD20, EBV, CD30, CD2, CD4, ALK1, epithelial and mesothelial markers negative, and PCR monoclonal B-cell expanded (Ig-kappa bands).
Conclusion: Cytological examination of effusions in KSHV-related lymphoproliferative disorders may show similar morphological features but clonality studies and immunocytochemistry are very helpful in distinguishing between these rare benign and malignant lymphoproliferative diseases.