PMID- 27496505 OWN - NLM STAT- MEDLINE DCOM- 20170426 LR - 20211204 IS - 1873-2623 (Electronic) IS - 0041-1345 (Linking) VI - 48 IP - 5 DP - 2016 Jun TI - Kaposi Sarcoma in the Genital Area in a Kidney Transplant Patient: A Case Report and Literature Review. PG - 1843-8 LID - S0041-1345(16)00329-8 [pii] LID - 10.1016/j.transproceed.2016.01.070 [doi] AB - BACKGROUND: Kaposi sarcoma (KS) is a cancer with an incidence in patients after transplantation (Tx) that is 500 times greater than that in the healthy population. The risk of KS increases significantly during therapy, especially when immunosuppressive therapy with cyclosporine A (CsA) is used. Most cases of KS develop during the first 2 years after transplantation. After a KS diagnosis, it is recommended to reduce the doses of immunosuppressive medications. Conversion of immunosuppressive treatment into mammalian target of rapamycin (m-TOR) inhibitors is strongly suggested. PATIENTS AND METHODS: We present the case of a 65-year-old man with end-stage renal disease (ESRD) of unknown etiology, who had kidney transplantation in 2008. Immunosuppressive protocol was based on CsA, mycophenolate mofetil (MMF) and prednisolone (PRE). In 2011, during the dermatological consultation, on the penis glans a purple stain of uneven surface was noted. Histology study revealed the presence of KS. The treatment was modified. The patient was converted from CsA to everolimus. Before converting, the creatinine concentration was 1.79 mg/dl and proteinuria less than 0.3 g/day. RESULTS: The change in the scheme of immunosuppresion from CsA to everolimus was performed to treat the Kaposi sarcoma. Gradually, within a year, the KS was cured. However, the graft function deteriorated, and the graft was lost in one-years' time. CONCLUSION: We present the first documented case of KS in the genital area of a kidney patient. The reduction in the strength of immunosuppression, and the introduction of an m-TOR inhibitor, may have contributed to the deterioration of kidney function, however it was substantial in the treatment of KS. CI - Copyright (c) 2016 Elsevier Inc. All rights reserved. FAU - Imko-Walczuk, B AU - Imko-Walczuk B AD - Copernicus-Independent Public Healthcare Centre, Dermatology & Venereology Clinic, Gdansk, Poland; College of Health, Beauty and Education in Poznan, Poland. Electronic address: bimko@wp.pl. FAU - Kielbowicz, M AU - Kielbowicz M AD - College of Health, Beauty and Education in Poznan, Poland. FAU - Malyszko, J AU - Malyszko J AD - 1st Department of Nephrology and Transplantology with Dialysis Unit, Medical University, Bialystok, Poland. FAU - Malyszko, J AU - Malyszko J AD - 2nd Department of Nephrology Medical University, Bialystok, Poland. FAU - Barczyk, M AU - Barczyk M AD - 1st Department of Nephrology and Transplantology with Dialysis Unit, Medical University, Bialystok, Poland. FAU - Debska-Slizien, A AU - Debska-Slizien A AD - Chair & Clinic of Nephrology, Transplantology and Internal Medicine, Gdansk University of Medical Sciences, Gdansk, Poland. FAU - Mysliwiec, M AU - Mysliwiec M AD - 1st Department of Nephrology and Transplantology with Dialysis Unit, Medical University, Bialystok, Poland. FAU - Rutkowski, B AU - Rutkowski B AD - Chair & Clinic of Nephrology, Transplantology and Internal Medicine, Gdansk University of Medical Sciences, Gdansk, Poland. LA - eng PT - Case Reports PT - Journal Article PT - Review PL - United States TA - Transplant Proc JT - Transplantation proceedings JID - 0243532 RN - 0 (Immunosuppressive Agents) RN - 83HN0GTJ6D (Cyclosporine) RN - 9HW64Q8G6G (Everolimus) RN - 9PHQ9Y1OLM (Prednisolone) RN - HU9DX48N0T (Mycophenolic Acid) SB - IM MH - Aged MH - Cyclosporine/adverse effects MH - Everolimus/*therapeutic use MH - Female MH - Humans MH - *Immunocompromised Host MH - Immunosuppression Therapy/adverse effects MH - Immunosuppressive Agents/therapeutic use MH - Kidney Transplantation/*adverse effects MH - Male MH - Mycophenolic Acid/adverse effects MH - Penile Neoplasms/*immunology MH - Prednisolone/therapeutic use MH - Sarcoma, Kaposi/*immunology EDAT- 2016/08/09 06:00 MHDA- 2017/04/27 06:00 CRDT- 2016/08/07 06:00 PHST- 2015/11/29 00:00 [received] PHST- 2016/01/21 00:00 [accepted] PHST- 2016/08/07 06:00 [entrez] PHST- 2016/08/09 06:00 [pubmed] PHST- 2017/04/27 06:00 [medline] AID - S0041-1345(16)00329-8 [pii] AID - 10.1016/j.transproceed.2016.01.070 [doi] PST - ppublish SO - Transplant Proc. 2016 Jun;48(5):1843-8. doi: 10.1016/j.transproceed.2016.01.070.