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Epstein-Barr virus-associated Hodgkin's disease following renal transplantation

Authors
Choi, Jung-HyeAhn, Myung-JuOh, Young-HaHan, Sang-WoongKim, Ho-JungLee, Young-YeulKim, In-Soon
Issue Date
Mar-2006
Publisher
대한내과학회
Keywords
Hodgkin's disease; Post-transplant lymphoproliferative disorder; Renal transplantation
Citation
The Korean Journal of Internal Medicine, v.21, no.1, pp 46 - 49
Pages
4
Indexed
SCOPUS
KCICANDI
Journal Title
The Korean Journal of Internal Medicine
Volume
21
Number
1
Start Page
46
End Page
49
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/181683
DOI
10.3904/kjim.2006.21.1.46
ISSN
1226-3303
2005-6648
Abstract
Post-transplant lymphoproliferative disorders (PTLD) have been recognized as a complication of immunosuppression and occur with a reported incidence of 1 to 8% of recipients receiving solid organ transplantation. PTLD are classified into two major categories, polymorphic and monomorphic PTLD. The majority of the monomorphic PTLD cases are non-Hodgkin's lymphoma of B-cell origin. Hodgkin's disease is not part of the typical spectrum of PTLD; however, it has been rarely reported. We describe a case of Hodgkin's disease following renal transplantation. A 41-year-old man developed right cervical lymphadenopathy following renal transplantation 116 months previously for chronic renal failure of unknown origin. He had been taking cyclosporine, mycophenolate mofetil and prednisone. A lymph node biopsy revealed mixed cellularity Hodgkin's disease. Immunohistochemical staining was positive for CD30 and EBV-latent membrane protein-1. No other site of disease was identified. The immunosuppressive agents were reduced (mycophenolate mofetil was discontinued, cyclosporine dose reduced from 200 mg to 150 mg and prednisone continued at 5 mg). After 2 cycles of ABVD followed by radiation therapy (3600 cGy), he achieved complete remission.
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