尿液细胞学在肾移植中还有作用吗?一家教学医院的经验报告

Ana Luisa Figueira Gouvêa, Fabiana Rabe Carvalho, Ana Lucia Rosa Nascimento, Rachel Ingrid Juliboni Cosendey, Camila de Melo Carvalho Nascimento, Jorge Reis Almeida
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引用次数: 0

摘要

简介尿液细胞学是一种非侵入性、低成本的方法,因此已被用作肾移植患者的监测策略。早期发现感染可预防可能出现的功能障碍和移植物损失。然而,这种方法的使用却在减少。方法:我们对连续接受肾移植手术的 29 名患者在移植后第一年内连续 17 个月的排空尿液样本进行了前瞻性研究。一名技术人员通过细胞离心和巴氏染色制备样本,一名病理学家对样本进行分析。诱饵细胞(DCs)阳性样本由另外两名技术人员制备,用于对比相分析、超微结构研究和 SV40 T 抗原免疫荧光。结果我们评估了 26 名患者的 252 份尿液样本。来自同一患者(3.8%)的 5 份尿液样本中,有 2 份样本(0.8%)在移植后第 4 周和第 5 周连续出现低级别鳞状上皮内病变;只有在移植后第 6 个月的样本中检测到罕见的上皮细胞,其不典型性尚未确定(0.4%)。患者随后的妇科检查和子宫颈抹片检查未发现任何变化。在四名患者(15.4%)的五份样本(2.0%)中发现了假丝酵母和真菌酵母。在其中一名患者的尿液中发现了三孢子虫。在 6 名患者(23.1%)的 25 份样本(9.9%)中检测到诱饵细胞。有两名患者出现持续的 DCs 脱落,其中一名患者的背景涂片很脏,后来发展为多瘤病毒相关性肾病。直流电的超微结构研究显示病毒颗粒呈二十面体。免疫荧光(SV40 T 抗原)在直流细胞核中呈阳性。对比相分析法在有大量直流细胞的样本中取得了成功。结论移植后系统性尿液细胞学检查有助于发现一些感染迹象。DC持续脱落和背景涂片不洁的患者值得临床特别关注。电子显微镜和免疫荧光(SV40 T 抗原)是检测多瘤病毒再活化的替代技术。研究结果表明,尿液细胞学仍在肾移植中发挥作用。
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Is There Still a Role for Urine Cytology in Kidney Transplantation? Experience Report in a Teaching Hospital
Introduction: Urinary cytology has been used as a monitoring strategy for kidney transplant patients, live under chronic immunosuppression, as it is a non-invasive and low-cost method. The early detection of infections can prevent possible dysfunction and graft loss. However, its use has been decreased. Methods: We conducted a prospective study on voided urine samples from 29 consecutive patients undergoing kidney transplantation over a continuous period of 17 months, collected during their first-year post-transplantation. One technician prepared the samples by cytocentrifugation, Papanicolaou staining, and one pathologist analyzed them. Decoy cells (DCs) positive samples were prepared, by other two technicians, for contrast phase analysis, ultrastructural study, and immunofluorescence for SV40 T antigen. Results: We evaluated 252 urine samples from 26 patients. Two consecutive samples (0.8%) out of five, from the same patient (3.8%), referring to the fourth- and fifth-week post-transplant, showed low-grade squamous intraepithelial lesions; only rare epithelial cells with atypia of undetermined significance were detected (0.4%) in the sample corresponding to the sixth month post-transplant. The patient’s subsequent gynecological examination and Pap smear revealed no changes. Pseudohyphae and fungus yeasts were found in five samples (2.0%) from four patients (15.4%). Trichosporon sp. was identified in the urine of one of these patients. Decoy cells were detected in 25 samples (9.9 %) from six patients (23.1%). Two patients had sustained DCs shedding; one of them, presenting dirty background smears, developed Polyomavirus-associated nephropathy. Ultrastructural study of DCs showed icosahedral viral particles. Immunofluorescence (SV40 T antigen) was positive in DCs nuclei. Analysis by contrast phase was successful in samples with numerous DCs. Conclusion: Systematic urinary cytology after transplantation helps detect some infection signs. Patients with sustained DCs shedding and dirty background smears deserve special clinical attention. Electron microscopy and immunofluorescence (SV40 T antigen) are alternative techniques to detect polyomavirus reactivation. The findings suggest that urinary cytology still plays a role in kidney transplantation.
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