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pubmed-article:20656316pubmed:abstractTextPosttransplantation lymphoproliferative disorders (PTLD) are heterogeneous lesions with variable morphology, immunophenotype, and molecular characteristics. Multiple distinct primary lesions can occur in PTLD, rarely with both B-cell and T-cell characteristics. Lesions can involve both grafted organs and other sites; however, PTLD involving the pituitary gland has not been previously reported. We describe a patient who developed Epstein-Barr virus-negative PTLD 13 years posttransplantation involving the terminal ileum and pituitary, which was simultaneously involved by a pituitary adenoma. Immunohistochemistry of the pituitary lesion showed expression of CD79a, CD3, and CD7 with clonal rearrangements of both T-cell receptor gamma chain (TRG@) and immunoglobulin heavy chain (IGH@) genes. The terminal ileal lesion was immunophenotypically and molecularly distinct. This is the first report of pituitary PTLD and illustrates the potentially complex nature of PTLD.lld:pubmed
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pubmed-article:20656316pubmed:copyrightInfoCopyright © 2010 Elsevier Inc. All rights reserved.lld:pubmed
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pubmed-article:20656316pubmed:articleTitlePosttransplantation lymphoproliferative disease involving the pituitary gland.lld:pubmed
pubmed-article:20656316pubmed:affiliationDepartment of Pathology, University of Virginia Health System, PO Box 800214, Charlottesville, VA 22908, USA.lld:pubmed
pubmed-article:20656316pubmed:publicationTypeJournal Articlelld:pubmed
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pubmed-article:20656316pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed