Laftavi M R, Weber-Shrikant E, Kohli R, Patel S, Feng L, Said M, Dayton M, Pankewycz O
Department of Surgery, SUNY at Buffalo, New York, USA.
Transplant Proc. 2010 Sep;42(7):2547-50. doi: 10.1016/j.transproceed.2010.04.035.
The clinical and pathological experience with sirolimus is limited at this time. In this study, we report severe isometric vacuolization of the proximal tubules after sirolimus therapy in two kidney transplant patients. Patient 1 is a hepatitis C virus-positive, 30-year-old African American man who had end-stage renal disease (ESRD) of unknown etiology. Patient 2 is a 62-year-old white woman with ESRD due to unknown etiology. Both patients were initially placed on tacrolimus, mycophenolic acid, and prednisone immunosuppressive therapy. These patients were switched to sirolimus at 1 and 5 month posttransplant, respectively, due to the development of new-onset hyperglycemia and an elevated serum creatinine. Both patients presented with acute renal failure and high sirolimus levels at 5 years (patient 1) and 10 months posttransplant (patient 2). Biopsies of their kidney transplants showed widespread isometric tubular cytoplasmic vacuolization and severe arterial hyalinosis. Acute renal insufficiency improved after sirolimus dose reduction. In this case report, we introduce a new morphological appearance after sirolimus therapy of isometric cytoplasmic vacuolization of the renal tubules and severe arterial hyalinosis, similar to that seen in calcineurin inhibitor induced tubular toxicity.
目前,西罗莫司的临床和病理经验有限。在本研究中,我们报告了两名肾移植患者在接受西罗莫司治疗后近端肾小管出现严重的等距空泡化。患者1是一名30岁的丙型肝炎病毒阳性非裔美国男性,患有病因不明的终末期肾病(ESRD)。患者2是一名62岁的白人女性,患有病因不明的ESRD。两名患者最初均接受他克莫司、霉酚酸和泼尼松免疫抑制治疗。由于新发高血糖和血清肌酐升高,这两名患者分别在移植后1个月和5个月改用西罗莫司。两名患者分别在移植后5年(患者1)和10个月(患者2)出现急性肾衰竭且西罗莫司水平升高。对其肾移植组织进行活检显示广泛的等距肾小管细胞质空泡化和严重的动脉玻璃样变。降低西罗莫司剂量后,急性肾功能不全有所改善。在本病例报告中,我们介绍了西罗莫司治疗后出现的一种新的形态学表现,即肾小管等距细胞质空泡化和严重的动脉玻璃样变,类似于钙调神经磷酸酶抑制剂诱导的肾小管毒性所见。