首页> 外文期刊>International Journal of Clinical and Experimental Pathology >Nocardia otitidiscaviarum meningitis in a diffuse large B-cell lymphoma patient with CD4-positive lymphocytopenia and persistent oligoclonal CD8-positive lymphocytes in the peripheral blood
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Nocardia otitidiscaviarum meningitis in a diffuse large B-cell lymphoma patient with CD4-positive lymphocytopenia and persistent oligoclonal CD8-positive lymphocytes in the peripheral blood

机译:弥漫性B细胞淋巴瘤弥漫性大B细胞淋巴瘤患者外周血CD4阳性CD4阳性和持续性寡克隆CD8阳性淋巴细胞

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Nocardiosis, sometimes presenting with multiple granulomatous lesions, is a rare opportunistic infection occurring in immunocompromised patients. However, its immunological features remain largely unaddressed. We investigated the immunological characteristics of human nocardiosis and examined the component cells of the granulomatous lesions. A 66-year-old man with diffuse large B-cell lymphoma presented with fever and multiple nodules in the lung during chemotherapy. The blood culture formed white colonies, but their characterization was difficult by routine microbiological laboratory methods. Matrix-assisted laser desorption ionization-time of flight mass spectrometry identified the colonies as Nocardia otitidiscaviarum. Meanwhile, the patient suddenly experienced an epileptic seizure without a brain abscess. His cerebrospinal fluid (CSF) showed neutrophilic pleocytosis (108/mm3). The conventional agar culturing failed to isolate colonies, but culturing with brain-heart infusion agar generated colonies. These colonies were completely concordant with those from the blood, as confirmed by 16S rRNA gene sequencing. Therefore, the patient had developed meningitis through sepsis induced by N. otitidiscaviarum. His CD4-positive T-lymphocyte counts were low, and oligoclonal CD8-positive αβ T-lymphocytes were present in the blood prior to the first and after three cycles of chemotherapy. He had bone marrow granulomatous lesions comprising lymphoma and CD8-positive αβ T-cells. Treatment with sulfamethoxazole/trimethoprim relieved all of his symptoms. The combined analysis by microbiological and molecular methods determined the cause of his epileptic seizure. His immunological characteristics, including low CD4-positive or CD8-positive αβ T-lymphocytes, may have contributed to the unusual clinical presentations by N. otitidiscaviarum, which rarely involves the central nervous system.
机译:诺卡氏病有时会出现多个肉芽肿性病变,是免疫功能低下患者中罕见的机会性感染。但是,其免疫学特征仍未解决。我们调查了人类诺卡氏菌的免疫学特征,并检查了肉芽肿性病变的组成细胞。一名66岁的男子,患有弥漫性大B细胞淋巴瘤,在化疗期间出现发烧和肺部多个结节。血液培养物形成白色菌落,但是通过常规的微生物实验室方法很难表征它们。基质辅助激光解吸电离飞行时间质谱法确定的菌落为诺卡氏菌。同时,患者突然经历了癫痫发作,没有脑脓肿。他的脑脊液(CSF)显示嗜中性粒细胞增多(108 / mm3)。传统的琼脂培养无法分离菌落,但脑心浸液琼脂培养产生菌落。这些菌落与血液中的菌落完全一致,如16S rRNA基因测序所证实。因此,该患者已通过由奥氏杆菌引起的败血症发展为脑膜炎。他的CD4阳性T淋巴细胞计数低,并且在第一个化疗周期和三个化疗周期后的血液中存在低克隆CD8阳性αβT淋巴细胞。他患有骨髓肉芽肿性病变,包括淋巴瘤和CD8阳性αβT细胞。用磺胺甲恶唑/甲氧苄啶治疗可缓解他的所有症状。通过微生物学和分子方法的综合分析确定了他的癫痫发作的原因。他的免疫学特征,包括低CD4阳性或CD8阳性αβT淋巴细胞,可能导致了耳鼻咽喉癌的罕见临床表现,这种疾病很少涉及中枢神经系统。

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