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Case Report: Two faces of gamma–delta mycosis fungoides: before and after renal transplantation

机译:病例报告:γ-δ真菌病真菌的两张脸:肾移植前后

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摘要

We describe a patient with a 30-year history of mycosis fungoides (MF) and renal transplantation performed 3 years before he presented with an ulcerated tumour in the lumbosacral area. Biopsy revealed a lymphatic infiltrate of medium-sized, pleomorphic T cells expressing the gamma–delta T-cell receptor. Radiological staging and bone marrow biopsy revealed no extracutaneous involvement. Despite reduction in systemic immunosuppressants, total skin electron beam radiotherapy and systemic chemotherapy, the disease followed a highly aggressive course and the patient died 31 years after initial diagnosis of MF. Pre-existing MF is not listed as a contraindication for solid organ transplantation. With an ever-increasing number of organ recipients, the number of MF patients undergoing solid organ transplantation will be likely to increase. Systematic collection and analysis of such cases is thus warranted to lead to a better understanding to what kind MF gets influenced by solid organ transplantation and ongoing immunosuppression.
机译:我们描述了一个有30年真菌病史(MF)的患者,在他的腰s部出现溃疡性肿瘤之前进行了3年的肾脏移植。活检显示,淋巴液浸润了表达γ-δT细胞受体的中等大小的多形性T细胞。放射学分期和骨髓活检均未发现皮肤外受累。尽管减少了全身性免疫抑制剂,进行了全皮肤电子束放射疗法和全身性化学疗法,但该病仍经历了高度侵袭性病程,患者在初步诊断为MF后31岁就死亡。现有的MF未列为实体器官移植的禁忌症。随着器官接受者的数量不断增加,进行实体器官移植的MF患者数量可能会增加。因此,有必要对此类病例进行系统的收集和分析,以使人们更好地了解实体器官移植和持续的免疫抑制对MF的影响。

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