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Updated: Jul 8, 2026

Murine Full-thickness Skin Transplantation
Published on: January 2, 2017
Regression of Post-transplant Kaposi's sarcoma after Replacing Cyclosporine with Mycophenolate Mofetil
M M Hussein1, J M Mooij, H M Roujouleh
1Department of Nephrology and Dialysis, Al Hada Armed Forces Hospital, Taif, Saudi Arabia.
Abstract:
Kaposi's sarcoma (KS) has been recently linked with human herpes virus-8 (HHV-8) infection. Other risk factors include the use of cyclosporine and polyclonal anti-lymphocyte sera. Reduction of the immunosuppression, in particular cyclosporine, leads to regression or disappearance of the tumor in a significant number of patients. There are few publications about the response of the tumor to the newer immunosuppressive agent mycophenolate mofetil (MMF). We describe here a 52-year-old woman, who developed KS 22 months after living related transplantation. The sarcoma lesions disappeared after replacing cyclosporine and azathioprine by MMF, while the allograft function remained stable. This case suggests the importance of discontinuation of cyclosporine in the treatment of post-transplant KS. MMF, while maintaining allograft function in the absence of cyclosporine, apparently did not interfere with the regression of the tumor.
Insights
This study shows that stopping cyclosporine and switching to mycophenolate mofetil (MMF) can help post-transplant Kaposi's sarcoma (KS) disappear. MMF maintained transplant function without hindering KS regression.
Area of Science:
- Oncology
- Immunology
- Transplantation
Background:
- Kaposi's sarcoma (KS) is linked to human herpes virus-8 (HHV-8).
- Cyclosporine use is a known risk factor for post-transplant KS.
- Limited data exists on newer immunosuppressants like mycophenolate mofetil (MMF) for KS treatment.
Purpose of the Study:
- To report a case of post-transplant Kaposi's sarcoma (KS).
- To evaluate the effect of switching from cyclosporine to mycophenolate mofetil (MMF) on KS regression and allograft function.
Main Methods:
- A 52-year-old female patient developed KS post-living related transplantation.
- Treatment involved replacing cyclosporine and azathioprine with MMF.
- Allograft function and KS lesion status were monitored.
Main Results:
- Kaposi's sarcoma lesions disappeared after initiating MMF.
- Allograft function remained stable throughout the treatment period.
- MMF facilitated KS regression without compromising graft survival.
Conclusions:
- Discontinuation of cyclosporine is crucial for treating post-transplant KS.
- Mycophenolate mofetil (MMF) is a viable alternative immunosuppressant that supports KS regression and maintains allograft function.
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