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病例报告:罕见 EBV 相关 T/NK 细胞单形性移植后淋巴增殖性疾病

英文原题:Case report: A rare EBV-associated T/NK cell monomorphic posttransplant lymphoproliferative disorder.

查看英文原题

Case report: A rare EBV-associated T/NK cell monomorphic posttransplant lymphoproliferative disorder.

PubMed 2024/10/24(内容时间) Front Immunol Q1 · IF 7(JCR 2025)

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研究概要

本罕见病例报告描述了 PTLD 伴咽部受累的一种表现。

中文摘要

肾移植(KT)是终末期肾病患者的最佳治疗方法。然而,术后并发症仍是肾移植恢复期面临的主要问题。移植后淋巴增殖性疾病(PTLD)是肾移植后接受免疫抑制治疗的受者可能发生的一种严重且危及生命的并发症。PTLD危险因素包括EB病毒(EBV)感染、累积免疫抑制程度及遗传因素。PTLD更常见于移植器官本身及其周围组织和中枢神经系统;累及咽部软组织则相对罕见,仅有少数病例报告。因此,关于其治疗或护理的系统经验十分有限。 病例介绍:我们报告一名41岁男性,因慢性肾功能不全接受肾移植。移植术后5年随访期间,患者反复出现发热、咽痛和双侧颈部淋巴结肿大。住院期间,患者从口咽部大量呕血,随后接受急诊手术结扎扁桃体动脉。通过血液EBV DNA检测、咽部活检及相应病理检查,最终诊断为EBV相关T/NK细胞单形性PTLD。接受6个周期R-CHOP化疗后,临床症状和实验室检查均恢复正常。之后随访3年,未见肿瘤复发,移植肾功能良好。

本罕见病例报告描述了累及咽部的PTLD表现。通过组织病理学检查早期诊断至关重要,可预防咽喉及气道损害,避免发生危及生命的情况。停用免疫抑制剂并开始全身治疗有助于疾病消退。鉴于该病发病率低、临床经验和数据有限,我们通过有效治疗和护理使患者顺利康复的经验,可为未来开发临床新药及制定PTLD患者诊疗方案提供参考。

展开英文摘要原文

Kidney transplantation (KT) is the best treatment for patients with end-stage renal disease. However, postoperative complications remain the main issues faced during KT recovery period. Posttransplant lymphoproliferative disorders (PTLD) are one of the severe and life-threatening complications that occur after KT while the recipient is undergoing immunosuppressive therapy. PTLD risk factors include Epstein-Barr virus (EBV) infection, the cumulative degree of immunosuppression, as well as genetic aspects. PTLD is more common in the transplanted organ itself and its surroundings, and the central nervous system, while PTLD involving the pharyngeal soft tissue is relatively rare, with only a few reported case reports. Therefore, systematic experience is scarce regarding whether the treatment or the care. CASE PRESENTATION: Herein, we report a 41-year-old male, underwent a reproductive KT due to chronic renal insufficiency. Recurrent fever, pharyngeal pain, and bilateral cervical lymph node enlargement were recurred during five years' follow-up after KT surgery. In this inpatient experience, the patient vomited a large amount of blood from the oropharynx, then the tonsil artery was ligated by emergency operation. EBV-associated T/NK cell monomorphic PTLD was eventually diagnosed by blood EBV DNA test, pharyngeal biopsy, and corresponding pathological examination. After six cycles of R-CHOP chemotherapy, the clinical symptoms and laboratory tests changed into normal. Subsequent three years' follow-up shows no tumor recurrence and good transplant kidney function.

This rare case report describes a manifestation of PTLD with pharyngeal involvement. Early diagnosis using histopathological examination is crucial to prevent damage to the throat and airway, and even life-threatening conditions. Discontinuing immunosuppression and starting systemic treatment can help in disease regression. Since the low incidence of this disease, limited clinical experience, and limited data, our experience with a smooth recovery through efficacy treatment and nursing can provide a reference for the development of new clinical drugs and diagnostic and treatment plans of patients with PTLD in the future.

论文信息

作者
Jiang X、Zhang YY、Li XW、Li XD、Li ZY、Meng WJ、Li SD
单位
Department of Urology, The General Hospital of Western Theater Command, Chengdu, China.China
文献类型
病例报告
期刊
Frontiers in immunology2024
原文标识
PubMed 39512350 · DOI 10.3389/fimmu.2024.1491681