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Rationale:  Among patients with post-transplant lymphoproliferative disorder (PTLD), there is a high incidence of immunosuppressed transplant recipients. It is necessary to make an early diagnosis to increase the likelihood of a good prognosis.    Patient concerns:  We report a case of a 54-year-old female patient who developed PTLD after liver and kidney transplantation.    Diagnoses:  We aimed to analyze the standard diagnosis and follow-up of PTLD with imaging. Radiologists need to be familiar with all imaging modalities when dealing with PTLD, including ultrasonography, computed tomography, magnetic resonance imaging, positron-emission tomography/computed tomography.    Interventions:  The initial treatment included both reduction of immunosuppression and rituximab. Then the treatment strategy changed to rituximab and chemotherapy. Finally, the treatment strategy combined glucocorticoid therapy.    Outcomes:  The patient was in a stable condition at the 3-month follow-up.    Lessons:  Systematic evaluation of the various imaging modalities, treatment options, and prognoses of PTLD in renal allografts suggested that in cases with a poor prognosis, the proper imaging modalities provide essential information with regard to the determination of the appropriate treatment.

Multimodality imaging features, treatment, and prognosis of post-transplant lymphoproliferative disorder in renal allografts