Severely Disseminated Kaposi Sarcoma after ABO-Incompatible Kidney Transplantation Treated Successfully with Paclitaxel and Gemcitabine Combined with Hemodialysis.
Tobias BomholtAnders Krarup-HansenMartin EgfjordSøren Schwartz SørensenNiels JunkerPublished in: Case reports in transplantation (2019)
Kaposi Sarcoma (KS) is driven by human herpes virus 8 causing vascular proliferation which is induced by loss of immune function most often due to HIV or immunosuppressants. KS occurs with increased incidence in kidney transplant recipients, but rarely is disseminated. We report a 64-year-old male who developed severely disseminated KS 5 months after ABO-incompatible kidney-transplantation. No guidelines for chemotherapy exist in this case and reduced kidney function and impaired immune system complicates the use of systemic chemotherapy in kidney transplant recipients. A combination of paclitaxel and gemcitabine followed by two days of hemodialysis treatment was chosen since paclitaxel can be given in full dose independently of kidney function and gemcitabine is metabolised to 2',2'-difluorodeoxyuridine which is found to be highly dialysable. The present treatment was well tolerated by the patient with one episode of leukopenia and elevated alanine transaminase during treatment which resolved. There were no serious adverse events and the patient obtained a complete remission verified by Positron Emission Tomography CT after ending chemotherapy and at one-year follow up.
Keyphrases
- kidney transplantation
- locally advanced
- positron emission tomography
- computed tomography
- rectal cancer
- chemotherapy induced
- endothelial cells
- case report
- peritoneal dialysis
- squamous cell carcinoma
- hiv infected
- chronic kidney disease
- hepatitis c virus
- magnetic resonance imaging
- antiretroviral therapy
- radiation therapy
- end stage renal disease
- human immunodeficiency virus
- contrast enhanced
- combination therapy
- magnetic resonance
- systemic lupus erythematosus
- clinical practice
- disease virus