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The Annals of Thoracic Surgery, Vol 56, 527-538, Copyright © 1993 by The Society of Thoracic Surgeons
JM Chen, ML Barr, A Chadburn, G Frizzera, FA Schenkel, RR Sciacca, DS Reison, LJ Addonizio, EA Rose and DM Knowles
We conducted a retrospective study of 516 cardiac recipients who underwent
transplantation between April 1983 and April 1992, 19 of whom had
development of post-transplantation lymphoproliferative disorders (PTLDs).
These 19 patients presented with involvement of lung (5), gastrointestinal
tract (5), disseminated disease (6), and adenoids and lymph nodes (3).
B-cell proliferations ranging from an atypical hyperplasia to malignant
lymphoma developed in 18 patients, and mixed cellularity Hodgkin's disease
developed in 1 patient. The 19 patients with PTLD displayed a predominance
of both women and cardiomyopathy as the indication for transplantation when
compared with two separate control populations. No correlation was found
between demographic criteria analyzed and (1) early versus late diagnosis
of PTLD after transplantation, (2) the site of PTLD involvement, or (3) the
histopathologic category of the PTLD lesion. Patients with gastrointestinal
tract and lung PTLD involvement enjoyed an improved survival after both
transplantation and PTLD diagnosis when compared with patients with PTLD
involvement of all other extranodal sites. We report a high incidence of
PTLD involving the lung and gastrointestinal tract in our cohort study.
These sites of involvement responded better to a reduction in
immunosuppression than did the other extranodal sites of involvement.
ARTICLES
Management of lymphoproliferative disorders after cardiac transplantation
Department of Cardiothoracic Surgery, Columbia University College of Physicians and Surgeons, New York, NY 10032.
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