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- A case of Langerhans cell histiocytosis is reported. 报告1例朗格汉斯细胞组织细胞增生症。
- A clinical study of 7 cases of pulmonary Langerhans cell histiocytosis. 肺郎格罕细胞组织细胞增多症7例临床分析。
- Clinical analysis on 23 cases of solitary Langerhans cell granuloma of long bone. 长骨孤立性朗格罕细胞肉芽肿23例临床分析。
- Langerhans cell histiocytosis is diagnosed by histological examination and immunohistochemical study. 藉由病理检查及免疫组织学检查证实为兰格罕氏组织细胞增生症。
- A similar disease in humans, Hashimoto-Pritzker disease, is also a Langerhans cell histiocytosis. 人类也有类似的疾病，称为朗格汉斯组织细胞增多病。
- Cell depletion can be fixed in three main ways. 修理细胞消耗有三个主要方法。
- Skin biopsy and immunohistochemical study confirmed the diagnosis of Langerhans cell histiocytosis. 经病理及免疫组化检查证实为朗格汉斯细胞组织细胞增生症。
- Purpose : To investigate the long-term treatment outcome of patients of Langerhans cell histiocytosis (LCH). 摘要目的：研究兰格汉氏组织细胞增多症患者治疗后的长期追踪结果。
- The skin biopsy and immunohistochemical examination confirmed the diagnosis of Langerhans cell histiocytosis. 躯干部出现丘疹2个月,经组织病理及免疫组化检查证实为朗格汉斯细胞组织细胞增生症。
- Congenital self-healing reticulohistiocytosis, also known as Hashimoto-Pritzker disease) is a rare variant of Langerhans cell histiocytosis. 摘要先天性自愈性网状组织细胞增生症是兰格罕氏组织细胞增生症中罕见的一种型态。
- To explore the clinic and laboratory characteristics of Langerhans cell histocytosis(LCH), so as to improve its diagnosis and treatment level. 摘要目的探讨朗格罕细胞组织细胞增生症的临床和实验室特点，进一步提高其诊疗水平。
- Langerhans cell histiocytosis is an uncommon disease, involvement of the thyroid by langerhans cell histiocytosis is rare. 摘要朗格汉斯细胞增生症是一种较少见的疾病，累及甲状腺者更为罕见。
- Bone marrow examination could be helpful for diagnosis.It had been misdiagnosed as urticaria or Langerhans cell histiocytosis. 本例曾先后误诊为荨麻疹、郎格罕细胞组织细胞增生症，骨髓检查可确诊。
- Objective To investigate the clinical value of bone scintigraphy in the diagnosis and follow-up of Langerhans cell histiocytosis (LCH). 目的探讨骨显像在诊断儿童郎格尔汉斯细胞组织细胞增生症(LCH)及其随访中的临床价值。
- non -T cell depleted haploidentical BMT 单倍相合未去T细胞骨髓移植
- Objective Explore the result of modified DAL-HX83/90 protocol in childhood Langerhans cell histiocytosis (LCH) in order to improve the treatment result of LCH patients. 目的为提高儿童郎格罕细胞组织细胞增生症(LCH)的预后,在复习文献基础上对DAL-HX83/90方案进行改良并观察其初步疗效。
- The team found that DNA replication was reduced by about 50% in cells depleted of TROY, the report indicates, further suggesting an important role for TROY in the growth of melanoma cells. 报告指出，DNA复制在TROY缺失细胞降低大约50%25，进一步提示TROY在黑素瘤细胞生长中的重要作用。
- Langerhans cell histiocytosis of bone causes bone destruction and frequent bone reactions Hat mimic benign and malignant neoplasms as well as osteomyelitis. 摘要骨的蓝格罕士氏细胞组织球症造成骨结构破坏，在临床变化上类似恶性肿瘤或骨髓炎。
- Langerhans' cell histiocytosis (LCH) is a proliferative histiocytosis disorder.The clinical severity of LCH ranges from fatal disorders to isolated bone lesions. 摘要组织细胞增生症是一种罕见的疾病，临床严重度从致命到只有单一骨病灶。
- Langerhans cell histiocytosis of bone causes bone destruction and frequent bone reactions that mimic benign and malignant neoplasms as well as osteomyelitis. 骨的蓝格罕士氏细胞组织球症造成骨结构破坏，在临床变化上类似恶性肿瘤或骨髓炎。
