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- Clinical Features and Diagnosis of Langerhans Cell Hyperplasia 郎格罕细胞组织细胞增生症的临床特征与诊断
- Langerhans cell hyperplasia 郎格罕细胞组织细胞增生症
- 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。
- 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。
- Basal cell hyperplasia is usually seen in the transition zone. Occasionally, it may be encountered in needle biopsies (which sample peripheral zone). 基底细胞增生通常见于前列腺移行区。在前列腺针刺活检标本中偶尔可以见到。
- 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。
- Psoriasis is a chronic illness that charactered by prostate of malpighian cell hyperplasia and Inflammatory cell infiltration of dermis. 银屑病是一种以角质形成细胞良性增生和真皮炎症细胞浸润为病理特征的慢性复发性疾病。
- 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。
- P504S was negative in entire 8 cases of basal cell hyperplasia (BCH) and in 3 cases of ASAP. 在3例ASAP中未见阳性。
- 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。
- Methods Specimens from 26 cases of basal cell hyperplasia and tumor of prostate were studied with HE and immunohistochemical stains by light-microscopy. 方法选取26例的前列腺基底细胞增生和肿瘤标本，分别作HE和免疫组化染色，光镜下观察。
- Objective To study the characteristics of morphology and immunohistochemistry of basal cell hyperplasia and tumor of prostate in order to provide evidences for its diagnostis. 目的探讨前列腺基底细胞增生和肿瘤的形态学和免疫组化特征，提供诊断依据。
- 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。
- The morphology of other lesions including atrophy, adenosis and basal cell hyperplasia, and also seminal vesicle epithelium was studied. 同时也研究其他病灶，如萎缩、腺体增生、基底细胞增生，以及贮精囊上皮之形态。
- 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。
- Work done previously by Professor Mackay on BAFF showed that levels correlate with B cell hyperplasia (expansion) and cancer. 麦凯教授先期针对BAFF所做的工作表明体内BAFF的水平同B细胞超常增生（增殖）和癌症相关。
- 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。
