Gemelli A, Paciolla A, Oliosi F, Basso A, Moscardin R, Tineo M C, Romano P, Alaibac M, Aversa S, Furian L, D'Angelo A, Bonfante L
Clinica Nefrologica, Dipartimento di Scienza Mediche e Chirurgiche, Universita' degli Studi di Padova, Padova, Italy.
G Ital Nefrol. 2009 Jan-Feb;26(1):90-3.
We report a case of Kaposi's sarcoma in a patient who received a double kidney transplant in 2005. Immunosuppression was induced with rapamycin and antilymphocyte serum while maintenance therapy consisted of rapamycin, corticosteroids and mycophenolic acid. The patient developed delayed graft function but no rejection. In November 2006 and March 2007 two graft biopsies were taken because of a significant rise in serum creatinine; they revealed chronic allograft nephropathy and polyomavirus infection. Meanwhile a skin biopsy of the leg was performed to determine the nature of a discolored lesion. The morphohistological diagnosis was Kaposi's sarcoma. For this reason rapamycin was stopped and steroid treatment gradually reduced. Specific therapy with doxorubicin was started; radiological and endoscopic examination excluded disseminated disease while serological tests were positive for antibodies to HHV-8, a virus known to cause Kaposi's sarcoma. Unfortunately, withdrawal of antirejection therapy caused loss of the graft, so the patient had to start dialysis. In this report we stress the possible development of malignancy in transplanted patients who are given rapamycin. Rapamycin is known to be an antirejection drug and to have antineoplastic activity; the major risk of malignancy is probably related to immunosuppression rather than the type of drugs used to obtain it.
我们报告一例2005年接受双肾移植患者发生卡波西肉瘤的病例。诱导免疫抑制采用雷帕霉素和抗淋巴细胞血清,维持治疗包括雷帕霉素、皮质类固醇和霉酚酸。该患者出现移植肾功能延迟恢复,但无排斥反应。2006年11月和2007年3月,因血清肌酐显著升高进行了两次移植肾活检;结果显示为慢性移植肾肾病和多瘤病毒感染。与此同时,对腿部进行了皮肤活检以确定一处变色病变的性质。形态组织学诊断为卡波西肉瘤。因此停用了雷帕霉素,并逐渐减少类固醇治疗。开始使用阿霉素进行特异性治疗;影像学和内镜检查排除了播散性疾病,而血清学检测显示抗人疱疹病毒8型(已知可引起卡波西肉瘤的一种病毒)抗体呈阳性。不幸的是,停用抗排斥治疗导致移植肾丧失,因此患者不得不开始透析。在本报告中,我们强调接受雷帕霉素治疗的移植患者可能发生恶性肿瘤。已知雷帕霉素是一种抗排斥药物且具有抗肿瘤活性;发生恶性肿瘤的主要风险可能与免疫抑制有关,而非用于实现免疫抑制的药物类型。