Discussion
Diagnosis With Brief Discussion
- Diagnosis
- Posttransplant lymphoproliferative disorder
- Radiologic Findings
- Chest CT scans shows multiple nodules in both lower lobes.
The patient underwent wedge resection of left lower lobe.
A Pathologic report revealed polymorphic posttransplant lymphoproliferative disorder.
The result of EBV in situ hybridization was positive.
- Brief Review
- Posttransplantation lymphoproliferative disorder (PTLD) is defined as an abnormal proliferation of lymphocytes, usually of B-cell origin, occurring in patients receiving immunosuppressants following organ or bone marrow transplantation. The disorder is strongly associated with Epstein-Barr virus infection. The estimated prevalence of PTLD in pediatric transplant recipients (4%) is higher than that in adults (0.8%). Under current immunotherapy regimens, PTLD may develop as early as 1 month after transplantation, but the median time from transplantation to diagnosis was reported as 4.4 months.
The Epstein-Barr virus infects B lymphocytes and stimulates their proliferation. The cytotoxic T lymphocytes that control B-cell proliferation in the healthy host are suppressed in the transplant recipient by agents such as cyclosporine-A, FK-506, and muromonab-CD3. This pathogenetic sequence undergirds the rationale for PTLD treatment, which is resection of tumor bulk and reduction of immunosuppression.
The histologic characteristics and immunocytochemistry of PTLD help guide therapy and gauge prognosis. Polymorphous, polyclonal tumors tend to regress spontaneously after immunosuppression has been reduced, but monomorphous, monoclonal tumors are more apt to behave like typical non-Hodgkin lymphoma and may require specific chemotherapy. Widely disseminated PTLD usually portends a fatal outcome. Treatment with acyclovir is directed toward the Epstein-Barr viral infection. Use of anti-B-cell monoclonal antibodies may be effective in selected patients.
The imaging features are similar to other lymphomas. CT may reveal retroperitoneal, mesenteric, mediastinal, or peripheral adenopathy or masses. Nodules in the liver, spleen, or kidneys are characteristically homogeneous and well-defined. Lung parenchymal involvement typically consists of discrete pulmonary nodules. Gastrointestinal involvement tends to produce ulcerative lesions leading to perforation and pneumoperitoneum.
- References
- Bowen et al. Cases of the Day. RadioGraphics 1992;12(2):393-395
- Keywords
- Lung, Lymphproliferative disorder,