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- histiocytic dermatoarthritis 组织细胞性皮肤关节炎(家族性)
- Erdheim-Chester disease (ECD) is a rare systemic histiocytic disease. (ECD是一种罕见的全身性组织细胞疾病。
- Objective:To discuss the clinical and haematological characteristics of sea-blue histiocytic syndrome(SBH). 目的:探讨海蓝组织细胞综合征(SBH)的临床及血液学特点。
- The tumor cells were focally positive for CD68 immunostaining, suggesting possible histiocytic origin. 局部肿瘤细胞CD68免疫染色呈阳性,显示细胞来源可能是组织细胞。
- Objective: To discuss the clinical and haematological characteristics of sea-blue histiocytic syndrome (SBH). 摘要目的:探讨海蓝组织细胞综合征(SBH)的临床及血液学特点。
- Both epithelial mid histiocytic, markers were co-expressed, positive for AE1/AE3, EMA and CD68. 免疫表型:瘤细胞呈上皮和组织细胞双表达,AE1/AE3、EMA和CD68阳性。
- Histiocytic disorders refer to diseases that are caused by abnormal behavior of these cells. 组织细胞疾病指这些细胞的非正常行为所引起的疾病。
- In contrast to malignant histiocytosis, VAHS is usually a benign self-limiting illness, in which histiocytic proliferation is reversible. 比起恶性的血球吞嗜症候群;病毒并发的血球吞嗜症候群通常是良性;有自限性的疾病;而此种组织增生是可以回复的.
- Objective To summary 9 cases of histiocytic necrotizing lymphadenitis(HNL) of children and discuss the diagnosis and therapy. 目的通过对9例小儿组织细胞坏死性淋巴结炎(HNL)进行总结分析,探讨其诊断和治疗方法。
- To investigate the clinical menifestation, diagnosis and therapy of the disease of histiocytic necrotizing lymphadenitis (HNL). 目的探讨组织细胞坏死性淋巴结炎的临床表现、诊断、治疗。
- These findings support the idea that some cases of ECD are clonal neoplastic disorders of putative histiocytic differentiation. 这些发现支持这一设想,即某些ECD病例为假定组织细胞分化的克隆性肿瘤性病变。
- Erdheim-Chester disease (ECD) is a rare histiocytic disorder of unknown etiology that involves predominantly bone and viscera. (ECD是一种罕见的病因不明的组织细胞疾病,主要累及骨和内脏。
- Other canine myositides, associated with infectious and histiocytic diseases, may also be relevant to similar human disorders. 其他犬类的肌病,无论是感染相关性肌病还是遗传的疾病,也都可能和人类的相似的疾病相关。
- Purpose To investigate the morphogenesis of histiocytic necrotizing lymphadenitis(HNL) at an angle of molecular biology in order to increase knowledge and avoid misdiagnosis. 目的从分子生物学角度,探讨组织性坏死性淋巴结炎的组织发生,提高认识,避免误诊。
- Purpose To investigate the morphogenesis of histiocytic necrotizing lymphadenitis (HNL) at an angle of molecular biology in order to increase knowledge and avoid misdiagnosis. 摘要目的从分子生物学角度,探讨组织性坏死性淋巴结炎的组织发生,提高认识,避免误诊。
- Langerhans cell histiocytosis (LCH) is a proliferative histiocytic disorder of unknown cause characterized by the accumulation of Langerhan cells in various tissues. 郎格罕细胞性组织细胞增生症是一种不明成因的增生性组织细胞疾病,其特徵为郎格罕细胞积聚于多个不同组织。
- Risdall RJ.Virus-associated hemopliagocytic syndrome: a benign histiocytic proliferation distinct from malignant histiocytosis [J].Cam Cer 1979,44: 993. 龚新顺;李淑萍.;病毒相关吞噬血细胞综合症两例报道[J]
- Virus-associated hemophagocytic syndrome (VAHS) is characterized by histiocytic hyperplasia, marked hemophagocytosis, and cytopenia, in association with a systemic viral illness (269). 病毒并发的血球吞嗜症候群以组织增生;显著的血球吞嗜现象和红血球减少为特徵;并同时有全身性病毒疾病.
- Objective To summary 9 cases of histiocytic necrotizing lymphadenitis(HNL) of children and discuss the diagnosis and therapy.Methods Reviewed clinical data and histological findings. 摘要目的通过对9例小儿组织细胞坏死性淋巴结炎(HNL)进行总结分析,探讨其诊断和治疗方法。
- Subsequent pathological examination indicated a histiocytic proliferation positive for CD68 and factor VIII, and negative for CD1a and S100, with Touton giant cells characteristic of ECD. 其后的病理检查表现出ECD特征性的组织细胞增生:CD68和VIII因子阳性,CD1a和S100阴性,伴Touton巨细胞。