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[Kaposi's sarcoma after kidney transplantation]
P Heering1, R Meschig, S Glück
1Abteilung für Nephrologie, Medizinische Universitätsklinik und Poliklinik, Düsseldorf.
Deutsche Medizinische Wochenschrift (1946)
|September 15, 1989
Summary
A kidney transplant recipient developed Kaposi
Area of Science:
- Immunosuppression and Oncology
- Transplantation Medicine
- Dermatology
Background:
- Post-transplant lymphoproliferative disorders (PTLD) are a known complication following organ transplantation.
- Kaposi's sarcoma (KS) is a PTLD associated with human herpesvirus 8 (HHV-8) infection, often seen in immunosuppressed individuals.
- Management of PTLD typically involves reducing immunosuppression and/or antiviral therapy.
Observation:
- A 44-year-old male developed cutaneous Kaposi's sarcoma with nodular and follicular lesions nine months post-haplo-identical kidney transplantation.
- The patient was on a regimen of methylprednisolone and cyclosporin A, with no evidence of HIV.
- No visceral involvement of the Kaposi's sarcoma was detected.
Findings:
- Reducing the dosage of methylprednisolone and cyclosporin A halted the progression of skin lesions while maintaining kidney transplant function.
- Radiotherapy (48 Gy) led to regression of lesions in the lower legs.
- Recurrence of Kaposi's sarcoma ten months later required additional radiotherapy, which controlled growth without impacting transplant function.
Implications:
- Immunosuppression reduction is a key strategy in managing post-transplant Kaposi's sarcoma.
- Radiotherapy can be an effective treatment modality for cutaneous Kaposi's sarcoma in transplant recipients.
- Careful monitoring and tailored treatment are crucial for managing PTLD while preserving graft function.