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Post‐transplant lymphoproliferative disorders in lung transplant recipients: 20‐yr experience at the University of Minnesota
Author(s) -
Wudhikarn Kitsada,
Holman C.J.,
Linan M.,
Blaes A.H.,
Dunitz J.M.,
Hertz M.E.,
Peterson B.A.
Publication year - 2010
Publication title -
clinical transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.918
H-Index - 76
eISSN - 1399-0012
pISSN - 0902-0063
DOI - 10.1111/j.1399-0012.2010.01332.x
Subject(s) - medicine , lymphoproliferative disorders , transplantation , lung transplantation , lung , post transplant lymphoproliferative disorder , retrospective cohort study , organ transplantation , immunosuppression , lymphoma , surgery , gastroenterology , rituximab
Wudhikarn K, Holman CJ, Linan M, Blaes AH, Dunitz JM, Hertz ME, Peterson BA. Post‐transplant lymphoproliferative disorders in lung transplant recipients: 20‐yr experience at the University of Minnesota.
Clin Transplant 2011: 25: 705–713. © 2010 John Wiley & Sons A/S. Abstract: Post‐transplant lymphoproliferative disorders (PTLD) are potentially fatal complications of solid organ transplantation. The natural history of PTLD varies considerably among the different types of organs transplanted. While lung transplant recipients are highly susceptible to PTLD, there are only a few small studies that detail PTLD in this setting. We undertook this study to better describe the characteristics and treatment response in PTLD after lung transplantation. We conducted a retrospective chart review of lung and heart/lung‐transplant recipients between 1985 and 2008. A total of 32 cases (5%) of PTLD were identified in 639 patients. The median interval after transplantation to the diagnosis was 40 (3–242) months. Eight patients (25%) were diagnosed within one yr of transplantation and had PTLD predominantly within the thorax and allograft. Twenty‐four patients (75%) were diagnosed more than one yr after transplantation and their tumors mainly affected the gastrointestinal tract. Monomorphic PTLD, diffuse large B‐cell lymphoma, was diagnosed in 91%. Treatment of PTLD varied according to stage and clinical circumstances. Twenty‐four patients (75%) have died. The median overall survival was 10 (0–108) months. PTLD after lung transplantation remains a challenge as a result of its frequency, complexity and disappointing outcome.