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抗胸腺细胞球蛋白治疗后再生障碍性贫血伴 EBV 再激活。

Aplastic Anemia with Epstein-Barr Virus Reactivation after Anti-thymocyte Globulin Therapy.

机构信息

Department of Hematology, Ebina General Hospital, Japan.

Division of Hematology/Oncology, Department of Internal Medicine, Tokai University School of Medicine, Japan.

出版信息

Intern Med. 2023 Sep 1;62(17):2553-2557. doi: 10.2169/internalmedicine.0539-22. Epub 2023 Feb 1.

Abstract

Lymphoproliferative disorders and Epstein-Barr virus reactivation (EBV-LPDs) have various forms of onset, ranging from infectious mononucleosis-like syndrome (IM-like) to lymphoma, although whether or not IM-like progresses to lymphoma remains unclear. A 61-year-old man was diagnosed with aplastic anemia (AA). Polyclonal atypical B-lymphocytes were observed in the peripheral blood, and IM-like was diagnosed. Atypical lymphocytes disappeared, but a gastrointestinal examination revealed diffuse large B-cell lymphoma (DLBCL). Rituximab was initiated but later discontinued because of severe acute respiratory syndrome coronavirus 2 infection. Pancytopenia due to AA exacerbation recurred. The patient ultimately died of multiple organ failure due to bacterial infection.

摘要

淋巴组织增生性疾病和 EBV 再激活(EBV-LPDs)有多种发病形式,从传染性单核细胞增多症样综合征(IM 样)到淋巴瘤不等,尽管 IM 样是否进展为淋巴瘤尚不清楚。一位 61 岁男性被诊断为再生障碍性贫血(AA)。在外周血中观察到多克隆非典型 B 淋巴细胞,并诊断为 IM 样。非典型淋巴细胞消失,但胃肠检查显示弥漫性大 B 细胞淋巴瘤(DLBCL)。由于严重急性呼吸综合征冠状病毒 2 感染,开始使用利妥昔单抗,但后来停止。由于 AA 恶化导致的全血细胞减少再次发生。患者最终因细菌感染导致多器官衰竭而死亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1d8/10518559/5db09190980d/1349-7235-62-2553-g001.jpg

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