紫杉醇、吉西他滨联合血液透析成功治疗abo血型不相容肾移植后严重播散性卡波西肉瘤。

Case Reports in Transplantation Pub Date : 2019-12-11 eCollection Date: 2019-01-01 DOI:10.1155/2019/8105649
Tobias Bomholt, Anders Krarup-Hansen, Martin Egfjord, Søren Schwartz Sørensen, Niels Junker
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引用次数: 1

摘要

卡波西肉瘤(KS)由人类疱疹病毒8驱动,引起血管增生,而血管增生通常是由HIV或免疫抑制剂引起的免疫功能丧失引起的。KS在肾移植受者中发病率增高,但很少播散。我们报告一例64岁男性患者在abo血型不相容肾移植5个月后发生严重弥散性KS。在这种情况下,没有化疗指南,肾功能下降和免疫系统受损使肾移植受者全身化疗的使用复杂化。选择紫杉醇和吉西他滨的联合治疗,然后进行两天的血液透析治疗,因为紫杉醇可以独立于肾功能给予全剂量,吉西他滨被代谢为2',2'-二氟脱氧尿苷,这被发现是高度可透析的。患者在治疗期间出现过一次白细胞减少和谷丙转氨酶升高,目前的治疗耐受性良好。无严重不良事件发生,化疗结束后随访1年,经正电子发射断层扫描CT证实患者完全缓解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Severely Disseminated Kaposi Sarcoma after ABO-Incompatible Kidney Transplantation Treated Successfully with Paclitaxel and Gemcitabine Combined with Hemodialysis.

Severely Disseminated Kaposi Sarcoma after ABO-Incompatible Kidney Transplantation Treated Successfully with Paclitaxel and Gemcitabine Combined with Hemodialysis.

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.

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