病例报告:一种罕见的 EBV 相关 T/NK 细胞单形性移植后淋巴组织增生性疾病。

IF 5.7 2区 医学 Q1 IMMUNOLOGY
Frontiers in Immunology Pub Date : 2024-10-24 eCollection Date: 2024-01-01 DOI:10.3389/fimmu.2024.1491681
Xin Jiang, Yao-Yu Zhang, Xiao-Wei Li, Xiao-Dong Li, Zhan-Yuan Li, Wen-Jun Meng, Sha-Dan Li
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引用次数: 0

摘要

背景:肾移植(KT)是治疗终末期肾病患者的最佳方法。然而,术后并发症仍是肾移植恢复期面临的主要问题。移植后淋巴组织增生性疾病(PTLD)是肾移植术后受者接受免疫抑制治疗期间出现的严重并危及生命的并发症之一。PTLD 的风险因素包括 Epstein-Barr 病毒(EBV)感染、免疫抑制的累积程度以及遗传因素。PTLD多见于移植器官本身及其周围和中枢神经系统,而涉及咽部软组织的PTLD则相对罕见,仅有少数病例报告。因此,无论是治疗还是护理方面都缺乏系统的经验:在此,我们报告了一名 41 岁男性患者,因慢性肾功能不全接受了生殖 KT。KT 手术后的五年随访期间,患者反复出现发热、咽痛和双侧颈淋巴结肿大。在这起住院病例中,患者口咽部大量呕血,随后通过急诊手术结扎了扁桃体动脉。通过血液 EBV DNA 检测、咽部活检和相应的病理检查,最终确诊为 EBV 相关 T/NK 细胞单形 PTLD。经过六个周期的 R-CHOP 化疗后,临床症状和实验室检查均恢复正常。随后三年的随访显示肿瘤未复发,移植肾功能良好:这份罕见病例报告描述了咽部受累的 PTLD 表现。采用组织病理学检查进行早期诊断对于防止咽喉和气道受损甚至危及生命至关重要。停止免疫抑制并开始系统治疗有助于疾病的消退。由于该病发病率低、临床经验有限、数据有限,我们通过疗效治疗和护理顺利康复的经验,可为今后开发新的临床药物和 PTLD 患者的诊疗方案提供参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Case report: A rare EBV-associated T/NK cell monomorphic posttransplant lymphoproliferative disorder.

Background: 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.

Conclusion: 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.

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来源期刊
CiteScore
9.80
自引率
11.00%
发文量
7153
审稿时长
14 weeks
期刊介绍: Frontiers in Immunology is a leading journal in its field, publishing rigorously peer-reviewed research across basic, translational and clinical immunology. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Immunology is the official Journal of the International Union of Immunological Societies (IUIS). Encompassing the entire field of Immunology, this journal welcomes papers that investigate basic mechanisms of immune system development and function, with a particular emphasis given to the description of the clinical and immunological phenotype of human immune disorders, and on the definition of their molecular basis.
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