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Posttransplantation lymphoproliferative disorder: changing manifestations of disease in a renal transplant population.

作者信息

Miller W T, Siegel S G, Montone K T

机构信息

Department of Radiology, Hospital of the University of Pennsylvania, Philadelphia 19104, USA.

出版信息

Crit Rev Diagn Imaging. 1997 Dec;38(6):569-85.

PMID:9442979
Abstract

OBJECTIVE

To review the changing manifestations of PTLD in patients with renal transplants.

METHODS

Review of 1954 records of the renal transplantation clinic from 1971 to 1993 produced 17 patients with the diagnosis of PTLD.

RESULTS

With changes in immunosuppression, the sites of involvement of PTLD have changed. Central nervous system involvement was the predominant site of disease prior to the use of cyclosporine. With the institution of cyclosporine, thoracic, and abdominal presentations became more common. PTLD isolated to the renal transplant is a new manifestation of disease that may be a result of immunosuppression with OKT3. Monomorphous PTLD was associated with a 78% PTLD related mortality. Polymorphous PTLD had a 0% PTLD related mortality. In patients with cross-sectional imaging abnormalities, PTLD presented as solitary or multiple masses in 78%. This is the finding most suggestive of PTLD in a transplant population.

CONCLUSION

Posttransplantation lymphoproliferative disorder is a heterogeneous grouping of lymphoid proliferation with variable clinical and radiographic manifestations. An understanding of the range of manifestations may lead to improved diagnosis of this unusual disorder.

摘要

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Clinical and pathological features of post-transplant lymphoproliferative disorders (PTLD).移植后淋巴细胞增生性疾病(PTLD)的临床和病理特征。
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