基于适应症的肾移植活组织检查显示的组织病理学诊断:回顾性分析

Eryiğit Eren, Mehmet Tokac, Alaaddin Aydin, T. Sahin, Hikmet Bora Uslu, Selman Alkan, A. Dinckan
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摘要

目的:尽管在过去的二十年中,实体器官移植后免疫抑制药物取得了一些进展,但同种异体肾脏移植的长期生存率并没有显著提高。同种异体肾移植活检是确定移植物功能障碍的原因和调整患者管理的有用工具。方法:2017年1月至2023年1月期间在伊斯廷耶大学医院接受肾移植并行同种异体移植活检的患者构成本研究的目标人群。回顾性分析患者的人口学参数、临床资料、活检指征及组织病理学评估结果。结果:共纳入74例患者。组织病理学结果包括急性t细胞介导的排斥(TCMR) (n = 15, 20%),肾小管萎缩/慢性移植物肾病(IFTA) (n = 11, 15%),钙调磷酸酶抑制剂(CNI)毒性(n = 2, 3%),慢性抗体介入拒绝(ABMR) (n = 2, 3%),边缘病理学(n = 10, 13.5%),正常组织学(n = 5, 6.5%),移植glomerulopathy (TG) (n = 5, 6.5%),急性ABMR (n = 4, 5%),急性肾小管坏死(n = 7, 9%),多瘤病毒肾病(n = 3,4%)和非特异性变化(n = 10, 13.5%)。12% (n = 9)的移植物活检C4d阳性。73% (n = 54)的病例根据活检结果改变了治疗策略。随访期间,19例(25.6%)患者移植物丢失。结论:根据组织病理学分析结果,急性TCMR、IFTA和交界性病理是移植物肾功能障碍最常见的原因。同种异体肾移植活检导致了治疗策略的显著变化在相当数量的情况下。
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Histopathological diagnoses revealed by indication-based renal allograft biopsies: a retrospective analysis
Objectives: Although there have been several advances in post-solid organ transplantation immunosuppression medications over the last two decades, the long-term survival of renal allografts did not significantly improve. Renal allograft biopsy is a helpful tool for determining the cause of graft dysfunction and adjusting patient management. Methods: Patients who received kidney transplantation and underwent allograft biopsy in Istinye University Hospital between January 2017 and January 2023 constituted the target population of this study. Demographic parameters, clinical data and biopsy indications, and histopathological assessment results of the patients were retrospectively analyzed. Results: Overall, 74 patients were included. The histopathology results included acute T-Cell mediated rejection (TCMR) (n = 15, 20%), tubular atrophy/chronic allograft nephropathy (IFTA) (n = 11, 15%), calcineurin inhibitor (CNI) toxicity (n = 2, 3%), chronic antibody-mediated rejection (ABMR) (n = 2, 3%), borderline pathology (n = 10, 13.5%), normal histology (n = 5, 6.5%), transplant glomerulopathy (TG) (n = 5, 6.5%), acute ABMR (n = 4, 5%), acute tubular necrosis (n = 7, 9%), polyomavirus nephropathy (n = 3, 4%) and non-specific changes (n = 10, 13.5%). The C4d was positive in 12% (n = 9) of the graft biopsies. In 73% (n = 54) of cases, the treatment strategy was changed based on biopsy results. Among all patients, 19 (25.6%) lost their grafts during follow-up. Conclusions: According to the histopathological analysis results, acute TCMR, IFTA, and borderline pathology were the most common causes of renal graft dysfunction. Renal allograft biopsy led to a remarkable change in treatment strategies in a significant number of cases.
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