Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2022;22(2):96-103.
doi: 10.2174/1871529X22666220804155810.

Clinical Post-Transplant Lymphoproliferative Disorders

Affiliations
Review

Clinical Post-Transplant Lymphoproliferative Disorders

Ziba Aghsaeifard et al. Cardiovasc Hematol Disord Drug Targets. 2022.

Abstract

Post-transplant lymphoproliferative disorders (PTLDs) are characterized by hyperproliferation of B cells due to solid organ or allogeneic hematopoietic stem cell transplant. Based on histological findings, it is divided into 4 categories. Most PTLD patients are Epstein-Barr virus (EBV) positive. Additionally, aggressive immunosuppressive therapies can also lead to PTLD. Reducing immunosuppressive regimes, antivirals, monoclonal antibodies, chemotherapy, and radiotherapy are available therapeutic options, depending on the nature and phase of the disease. This review briefly highlights pathogenesis, risk factors, prevention, and therapeutic strategies regarding PTLDs.

Keywords: Epstein-Barr virus (EBV); hematopoietic stem cell; immunosuppression; lymphoma; post-transplant lymphoproliferative disorders (PTLD); transplant recipients.

PubMed Disclaimer

MeSH terms

LinkOut - more resources