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- Kerasin histiocytosis 角苷脂组织细胞增多症
- 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。
- The article reports two cases of cutaneous malignant histiocytosis. 本文报告2例皮肤型恶性组织细胞增生症。
- 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。
- Histiocytosis X always had multiple bone lesions with osteolytic character. 此病常见有多处骨骼同时发生骨质溶解之病变。
- Inflammatory histiocytosis associated with disturbance of cholesterol metabolism,occurs chiefly in young children. 通常发生在年轻人身上的一种胆固醇代谢病症。
- Histiocytosis associated with disturbance of cholesterol metabolism, occurs chiefly in young children. 与胆固醇代谢障碍有关的组织细胞增多症，通常发生在年轻人身上。
- Objective To study the diagnosis and differential diagnosis of sea-blue histiocytosis(SBH). 目的探讨海蓝组织细胞增生症(SBH)的诊断及鉴别诊断。
- Pulmonary histiocytosis X is an uncommon interstitial lung disease that primarily affects young adults. 摘要肺组织细胞症X是一种罕见的间质性肺病，常影响年轻成人病患。
- 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。
- Histiocytosis associated with disturbance of cholesterol metabolism， occurs chiefly in young children. 与胆固醇代谢障碍有关的组织细胞增多症，通常发生在年轻人身上。
- 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。
- 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。
- It is an abnormal growth in the skin of histiocytes (histiocytosis), a cell that is part of the immune system. 它是一种皮肤组织细胞的非正常生长（组织细胞增生）。
- From Jan. 1980 to Oct. 1986, 23 cases of histiocytosis X, proven by pathology, were reviewed. 摘要从1980年1月到1986年10月，共收集23个已由病理证明为组织细胞症X的病例。
- To grasp pathological feature of the osteomyelitis、fibrous desplasia of bone、cemento-ossifying fibroma、osteoma、histiocytosis. 掌握颌骨骨髓炎、颌骨纤维结构不良、牙骨质-骨化纤维瘤、骨瘤及组织细胞增多症的病变特点及结局。
- 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。
- 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.
