Komatsuzaki Yo, Nakada Yasuyuki, Yamamoto Izumi, Kawabe Mayuko, Yamakawa Takafumi, Katsuma Ai, Katsumata Haruki, Mafune Aki, Kobayashi Akimitsu, Koike Yusuke, Yamada Hiroki, Miki Jun, Tanno Yudo, Ohkido Ichiro, Tsuboi Nobuo, Yokoyama Keitaro, Yamamoto Hiroyasu, Yokoo Takashi
Division of Nephrology and Hypertension, Department of Internal Medicine, The Jikei University School of Medicine, Tokyo, Japan.
Division of Urology, The Jikei University School of Medicine, Tokyo, Japan.
Case Rep Transplant. 2017;2017:1347052. doi: 10.1155/2017/1347052. Epub 2017 Jan 10.
Despite the recent development of immunosuppressive agents, plasma cell-rich acute rejection (PCAR) has remained refractory to treatment. Herein, we report an unusual case of PCAR that responded well to pulse steroid therapy alone. A 47-year-old man was admitted for a protocol biopsy three months after kidney transplantation, with a stable serum creatinine level of 1.6 mg/dL. Histological examination showed focal aggressive tubulointerstitial inflammatory cell infiltration of predominantly polyclonal mature plasma cells, leading to our diagnosis of PCAR. Three months following three consecutive days of high-dose methylprednisolone (mPSL) therapy, an allograft biopsy performed for therapy evaluation showed persistent PCAR. We readministered mPSL therapy and successfully resolved the PCAR. Although PCAR generally develops more than six months after transplantation, we diagnosed this case early, at three months after transplantation, with focally infiltrated PCAR. This case demonstrates the importance of early diagnosis and prompt treatment of PCAR to manage the development and severity of allograft rejection.
尽管近年来免疫抑制剂有所发展,但富含浆细胞的急性排斥反应(PCAR)对治疗仍具有难治性。在此,我们报告一例罕见的PCAR病例,该病例仅对脉冲类固醇疗法反应良好。一名47岁男性在肾移植术后三个月因方案活检入院,血清肌酐水平稳定在1.6mg/dL。组织学检查显示局灶性侵袭性肾小管间质性炎性细胞浸润,主要为多克隆成熟浆细胞,从而诊断为PCAR。在连续三天高剂量甲泼尼龙(mPSL)治疗三个月后,为评估治疗效果而进行的移植肾活检显示PCAR持续存在。我们再次给予mPSL治疗并成功解决了PCAR。尽管PCAR通常在移植后六个月以上发生,但我们在移植后三个月就早期诊断出该病例,其为局灶性浸润性PCAR。该病例证明了早期诊断和及时治疗PCAR对于控制移植肾排斥反应的发生和严重程度的重要性。