肾移植后出现的皮肤 T 细胞淋巴瘤 (CTCL):文献中的临床变异综述

IF 1.1 Q4 HEMATOLOGY
Jordan Pilkington, S. Shalin, H. K. Wong
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引用次数: 0

摘要

移植后淋巴组织增生性疾病是一种罕见疾病,年发病率为 0.5% 至 3.7%。这种疾病的预后很差。在本报告中,我们描述了一例罕见的肾移植后原发性皮肤T细胞淋巴瘤(PT-CTCL)真菌病IIB期病例,并对文献中报道的PT-CTCL进行了回顾。确诊后的治疗包括贝沙罗汀、环孢素和泼尼松。目前,患者已摆脱疾病困扰。这些信息旨在增加人们对PT-CTCL发病率和治疗的了解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cutaneous T-Cell Lymphoma (CTCL) Arising Post Kidney Transplant: A Review of Clinical Variants in the Literature
Post-transplant lymphoproliferative disease is a rare disorder with an annual incidence of 0.5% to 3.7%. Development of this disorder carries with it a poor prognosis. In this report, we describe a rare case of post-transplant primary cutaneous T-cell lymphoma (PT-CTCL) mycosis fungoides stage IIB in a patient following kidney transplantation, as well as a review of PT-CTCL reported in the literature. The treatment following diagnosis included bexarotene, cyclosporine, and prednisone. Currently, the patient is free from disease. This information aims to add to the knowledge of the prevalence and management of PT-CTCL.
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来源期刊
Hematology Reports
Hematology Reports HEMATOLOGY-
CiteScore
0.90
自引率
0.00%
发文量
47
审稿时长
10 weeks
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