Tsuchimoto Akihiro, Matsukuma Yuta, Ueki Kenji, Nishiki Takehiro, Doi Atsushi, Okabe Yasuhiro, Nakamura Masafumi, Tsuruya Kazuhiko, Nakano Toshiaki, Kitazono Takanari, Masutani Kosuke
Department of Medicine and Clinical Science, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.
Department of Surgery, Fukuoka Red Cross Hospital, Fukuoka, Japan.
CEN Case Rep. 2019 Feb;8(1):1-7. doi: 10.1007/s13730-018-0354-x. Epub 2018 Aug 2.
Thrombotic microangiopathy (TMA) develops from various etiologies, and it is often difficult to distinguish the etiology of TMA in kidney transplantation. Antiphospholipid syndrome (APS) is one of the differential diagnoses for TMA that may cause acute loss of graft function or fatal thrombotic complications. This report details a 66-year-old male patient with polycythemia after ABO-incompatible kidney transplantation. Antibody screening tests were negative before transplant. Despite administration of an adequate desensitization therapy including plasmapheresis and rituximab, he developed acute graft dysfunction on postoperative day 112 and graft biopsy revealed prominent microvascular inflammation in the glomerular capillaries without immunoglobulin deposits. Flow cytometric panel-reactive antibody screening failed to detect donor-specific antibodies at both pre-transplant and episode biopsies. Anticardiolipin antibody was repeatedly positive, but neither thrombosis nor previous thrombotic episodes were detected. After excluding several differential diagnoses, the graft dysfunction with unexplained TMA was treated with steroid pulse, plasmapheresis and rituximab re-induction. Anticardiolipin antibody disappeared after this intensive treatment and graft function recovered gradually and stabilized for 52 months. This report suggests that asymptomatic anticardiolipin antibody may be associated with acute graft dysfunction. Even if thrombotic episodes are not observed, an exist of anticardiolipin antibody may be one of the risk factors of renal TMA after kidney transplantation.
血栓性微血管病(TMA)由多种病因引起,在肾移植中往往难以区分TMA的病因。抗磷脂综合征(APS)是TMA的鉴别诊断之一,可能导致移植肾功能急性丧失或致命的血栓并发症。本报告详细介绍了一名66岁男性患者,在ABO血型不相容肾移植后出现红细胞增多症。移植前抗体筛查试验为阴性。尽管给予了包括血浆置换和利妥昔单抗在内的充分脱敏治疗,但他在术后第112天出现急性移植肾功能障碍,移植肾活检显示肾小球毛细血管有明显的微血管炎症,无免疫球蛋白沉积。流式细胞仪检测群体反应性抗体筛查在移植前和发病时的活检中均未检测到供体特异性抗体。抗心磷脂抗体反复呈阳性,但未检测到血栓形成或既往血栓事件。在排除了几种鉴别诊断后,对原因不明的TMA伴移植肾功能障碍患者采用了类固醇冲击、血浆置换和利妥昔单抗再次诱导治疗。经过这种强化治疗后,抗心磷脂抗体消失,移植肾功能逐渐恢复并稳定了52个月。本报告表明,无症状抗心磷脂抗体可能与急性移植肾功能障碍有关。即使未观察到血栓事件,抗心磷脂抗体的存在也可能是肾移植后肾TMA的危险因素之一。