1) hemophagocytic lymphohistiocytosis
嗜血淋巴组织细胞增生症
1.
Objective To analyze virological features of Epstein-Barr virus associated hemophagocytic lymphohistiocytosis in children cases.
目的了解儿童EB病毒(Epstein-Barr virus,EBV)相关性嗜血淋巴组织细胞增生症(EBV-associated hemophagocyticlymphohistiocytosis,EBV-HLH)的血清学EB病毒抗体和病毒复制水平等病毒学特征。
2.
Objective: To provide clinical data for controlling Epstein-Barr virus associated hemophagocytic lymphohistiocytosis(EBV-HLH) by investigat- -ing the clinical features, diagnosis, treatment and outcome of EBV associated severe infectious mononucleosis(severe IM) and EBV-HLH, and analyzing the risk factors for the presence of EBV-HLH.
目的:探讨EB病毒相关性重症传染性单核细胞增多症(severe infectious mononucleosis,简称重症IM)和EB病毒相关性嗜血淋巴组织细胞增生症(Epstein-Barr virus associated hemophagocytic lympho- -histiocytosis,EBV-HLH)的临床特点、诊断标准、治疗及疗效,并分析预测EBV-HLH发生的危险因素,为防治EBV-HLH提供临床依据。
2) hemophagocytic lymphohistiocytosis
噬血细胞性淋巴组织细胞增生症
1.
Objective To discuss the clinical characteristic and prognosis of the hemophagocytic lymphohistiocytosis(HLH).
目的探讨噬血细胞性淋巴组织细胞增生症(HLH)的临床特点及预后,初步评价早期化疗疗效。
2.
Objective: To Investigate the clinical features,risk factors and rational administrations of hemophagocytic lymphohistiocytosis(HLH).
目的:探讨噬血细胞性淋巴组织细胞增生症的临床表现特征,影响HLH预后的危险因素及合理用药。
3.
Objective To explore the clinical characteristics and influential factors on prognosis of hemophagocytic lymphohistiocytosis(HLH)in children.
目的探讨儿童噬血细胞性淋巴组织细胞增生症(HLH)的临床特点及预后影响因素。
3) hemophagocytic lymphohistiocytosis
噬血细胞淋巴组织细胞增生症
1.
Diagnosis,immunochemotherapy and analysis of associated causes for hemophagocytic lymphohistiocytosis:reports of 23 pediatric cases
儿童噬血细胞淋巴组织细胞增生症23例临床分析
5) Hemophagocytic lymphohistiocytosis
噬血淋巴组织细胞增生症
1.
Clinical Study on Severe Infectious Mononucleosis and Hemophagocytic Lymphohistiocytosis;
重症传染性单核细胞增多症及噬血淋巴组织细胞增生症临床研究
6) hemophagocytic lymphohistiocytosis
噬血细胞性淋巴组织细胞增多症
1.
This study was aimed to explore the level of glycosylated ferritin in the patients with secondary hemophagocytic lymphohistiocytosis(HLH) and its diagnostic significance.
本研究探讨血清糖化铁蛋白在诊断继发性噬血细胞性淋巴组织细胞增多症(HLH)中的意义。
2.
The aim of study was to establish an accurate and stable technique for the detection of NK cell activity in the diagnosis of hemophagocytic lymphohistiocytosis(HLH).
本研究目的旨在建立一种准确、稳定的NK细胞杀伤活性检测方法,应用于获得性噬血细胞性淋巴组织细胞增多症诊断。
3.
The aim of this study was to investigate the clinical features of acquired hemophagocytic lymphohistiocytosis(HLH) complicated with hepatic dysfunction.
本研究探讨获得性噬血细胞性淋巴组织细胞增多症(hemophagocytic lymphohistiocytosis,HLH)肝功能损害的临床特点。
补充资料：家族性嗜血性网状细胞增生症
家族性嗜血性网状细胞增生症
familial hemophagocytic reticulosis
又称为“家族性嗜红细胞性淋巴组织细胞增生症”(familial erythrophagocytic lymphohistiocytosis），是一种少见的常染色体隐性遗传性疾病。病理特点是全身各组织器官呈弥漫性淋巴组织细胞浸润，并有明显的吞噬(吞噬红细胞、白细胞、血小板和细胞碎片）。患儿于生后几个月内出现反复腹泻、腹胀、呕吐、烦躁等症状，6个月至1岁时突然高热、肝脾肿大、出血、黄疸，甚至惊厥，多在短期内死于出血和败血症。实验室检查全血减少、网织红正常，肝功异常，凝血酶原时间延长，血脂增高，骨髓检查可见巨噬网状细胞增多以及吞噬红细胞、白细胞、血小板及细胞碎片。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条