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Posttransplantation Lymphoproliferative Disorder

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Molecular Pathology of Lung Diseases

Part of the book series: Molecular Pathology Library ((MPLB,volume 1))

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Abstract

Lymphoproliferative disorders are known complications of congenital and acquired immunodeficiency and/or iatrogenic-induced immunosuppression. A lymphoplasmacytic proliferation or lymphoma developing as a consequence of continuous iatrogenic immunosuppression following solid organ transplantation and hematopoietic stem cell transplantation (HSCT) is called posttransplantation lymphoproliferative disorder (PTLD). Posttransplantation lymphoproliferative disorders are a morphologically and clinically heterogenous group of disorders, many of which are associated with the Epstein-Barr virus (EBV). Morphologically the spectrum ranges from polyclonal lymphoplasmacytic proliferations resembling infectious mononucleosis to frankly neoplastic lymphomas. These lymphomas are commonly EBV positive B cell and less commonly EBV negative (B or T cell) in origin. Clinically, some of these disorders regress after reduction of the immunosuppressive regimen, and others progress to serious and potentially fatal lymphomas requiring chemotherapy.

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Ehsan, A., Herrick, J.L. (2008). Posttransplantation Lymphoproliferative Disorder. In: Zander, D.S., Popper, H.H., Jagirdar, J., Haque, A.K., Cagle, P.T., Barrios, R. (eds) Molecular Pathology of Lung Diseases. Molecular Pathology Library, vol 1. Springer, New York, NY. https://doi.org/10.1007/978-0-387-72430-0_31

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