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古德综合征与复发性利什曼病:一例病例报告及文献综述

Good's syndrome and recurrent leishmaniasis: A case report and review of literature.

作者信息

Tolomeo Manlio, Bonura Silvia, Abbott Michelle, Anastasia Antonio, Colomba Claudia, Cascio Antonio

机构信息

Department of Health Promotion Sciences, Section of Infectious Diseases, University of Palermo, Via del Vespro 129, 90127, Palermo, Italy.

出版信息

Heliyon. 2020 Sep 29;6(9):e05061. doi: 10.1016/j.heliyon.2020.e05061. eCollection 2020 Sep.

DOI:10.1016/j.heliyon.2020.e05061
PMID:33024862
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7527582/
Abstract

We report the case of a 56-year-old Caucasian male affected by thymoma and myasthenia gravis that developed recurrent visceral leishmaniasis 11 years after thymectomy. After treatment of each relapse with liposomal amphotericin B the PCR- was negative and the patient showed clinical improvement. An immunologic work-up was performed showing lymphopenia with an important decrease in CD4+ T cells (52 cells/μ) and CD4/CD8 ratio (0.2). HIV test was negative. On the basis of previous thymoma and myasthenia gravis and on the basis of the immunological profile a diagnosis of Good's syndrome was made. Since IFNγ plays a main role in the control of infection the production of IFNγ was evaluated. After mitogen stimulation of peripheral blood mononuclear cells the production of IFNγ was lower than normal. This is the second reported case of Good's syndrome with recurrent leishmaniasis and indicates that a definitive cure for leishmaniasis in patients with Good's syndrome is not possible. Immunologic work-up in our patient strongly suggests that relapses could be correlated with the low CD4+ T cell number and with the low IFNγ production. Immunotherapy with IFNγ or with compounds able to block the Th2 interleukin production could be a therapeutic option in these patients.

摘要

我们报告了一例56岁的白种男性患者,患有胸腺瘤和重症肌无力,在胸腺切除术后11年发生复发性内脏利什曼病。每次复发后用脂质体两性霉素B治疗,PCR结果为阴性,患者临床症状改善。进行了免疫检查,结果显示淋巴细胞减少,CD4 + T细胞(52个细胞/μ)和CD4/CD8比值显著降低(0.2)。HIV检测为阴性。基于既往的胸腺瘤和重症肌无力以及免疫检查结果,诊断为古德综合征。由于IFNγ在控制感染中起主要作用,因此评估了IFNγ的产生。外周血单个核细胞经丝裂原刺激后,IFNγ的产生低于正常水平。这是第二例报告的伴有复发性利什曼病的古德综合征病例,表明古德综合征患者的利什曼病无法彻底治愈。我们患者的免疫检查强烈提示复发可能与CD4 + T细胞数量低和IFNγ产生低有关。用IFNγ或能够阻断Th2白细胞介素产生的化合物进行免疫治疗可能是这些患者的一种治疗选择。