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伊德拉利司布联合皮质类固醇治疗滤泡性淋巴瘤期间播散性隐球菌病。

Disseminated cryptococcal disease during treatment with idelalisib and corticosteroids for follicular lymphoma.

机构信息

Immunology, Erasmus MC, Rotterdam, The Netherlands

Internal Medicine, Albert Schweitzer Hospital, Dordrecht, The Netherlands.

出版信息

BMJ Case Rep. 2020 Jul 5;13(7):e235216. doi: 10.1136/bcr-2020-235216.

Abstract

A patient on a regimen of idelalisib and corticosteroids for a relapse of follicular lymphoma presented to our emergency ward with a fever of unknown origin. Despite the initiation of broad-spectrum antibiotics and fluids, the patient's clinical condition deteriorated. Eventually, a diagnosis of disseminated cryptococcosis was established and immunophenotyping revealed complete absence of circulating B and CD4-T lymphocytes, and a markedly diminished CD8-T lymphocyte count. In this case, treatment with idelalisib and corticosteroids likely resulted in profound lymphopenia and the first reported instance of disseminated cryptococcosis under this regimen. After the withdrawal of idelalisib and steroids and initiation of antifungal therapy, lymphocyte counts partially recovered. After clinical improvement, the patient could be discharged from the hospital. This case highlights that the combination of idelalisib and corticosteroids can cause significant immunocompromise and opportunistic infections. Additionally, we illustrate the rate of lymphocyte reconstitution after withdrawal from idelalisib and corticosteroids.

摘要

一位滤泡性淋巴瘤复发患者正在接受idelalisib 和皮质类固醇治疗,因不明原因发热来到我们的急诊病房。尽管开始使用广谱抗生素和补液,但患者的临床状况恶化。最终,诊断为播散性隐球菌病,免疫表型显示循环 B 和 CD4-T 淋巴细胞完全缺失,CD8-T 淋巴细胞计数明显减少。在这种情况下,idelalisib 和皮质类固醇的治疗可能导致严重的淋巴细胞减少症,并且是该方案下首例播散性隐球菌病的报告。在停用 idelalisib 和类固醇并开始抗真菌治疗后,淋巴细胞计数部分恢复。在临床改善后,患者可以出院。本病例强调了 idelalisib 和皮质类固醇的联合使用会导致严重的免疫抑制和机会性感染。此外,我们还说明了停用 idelalisib 和皮质类固醇后淋巴细胞重建的速度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b13a/7337623/42b1e6d3b390/bcr-2020-235216f01.jpg

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