目的是介绍小儿胰岛细胞增生症的诊断和治疗经验。
The objective is to present the experience in the diagnosis and treatment of children's nesidioblastosis.
目的探讨恶性组织细胞增生症的X线表现。
Objective To study X-ray manifestations of malignant histiocytosis.
目的提高对郎格罕组织细胞增生症（LCH）的认识。
Objective To improve the identification of Langerhans cell histiocytosis (LCH).
目的总结小儿少见的胰岛细胞增生症的诊断和外科治疗要点。
Objective To present the experience in the diagnosis and treatment of children's nesidioblastosis.
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。
Skin biopsy and immunohistochemical study confirmed the diagnosis of Langerhans cell histiocytosis.
目的探讨胰岛细胞瘤与胰岛细胞增生症平扫与增强的影像特点。
Objective To study the MRI characteristics of islet cell tumor and islet cell hyperplasia with non enhanced and enhanced scans.
目的：总结郎格罕氏组织细胞增生症(LCH)的诊断与治疗经验。
Object: to summarize the experience of diagnosis and treatment of langerhans cell histiocytosis (LCH).
回顾性分析经手术与病理证实的13例胶质细胞增生症病人的临床资料。
Methods Clinical data of 13 patients with pathologically confirmed gliosis were analyzed retrospectively.
目的了解朗格·汉斯细胞组织细胞增生症(LCH)肺损害的临床情况。
Objective to understand the clinical manifestations of lung injury in Langerhans cell histocytosis (LCH).
目的探讨郎格罕组织细胞增生症(LCH)的临床特征，以提高诊断水平，减少误诊率。
Objective to explore the clinical and laboratory characteristics of langerhans cell histiocytosis (LCH) in children, so as to improve diagnosis level and decrease misdiagnosis rate.
临床鉴别诊断包括骨纤、骨瘤、皮样囊肿、脑膜瘤、嗜酸性肉芽肿、朗格·汉斯组织细胞增生症、以及转移瘤。
Clinical differential diagnosis includes fibrous dysplasia, osteoma, dermoid cyst, meningioma, eosinophilic granuloma, Lagerhan cell histiocytosis, and metastatic disease.
朗格·汉斯组织细胞增生症是一个特发性网状组织细胞增生性病变，主要累及朗格·汉斯细胞，一种起源于骨髓的幼稚树突细胞。
Langerhans cell histiocytosis is an idiopathic reticuloendothelial proliferative disorder involving the Langerhans cell, an immature dendritic cell of bone marrow origin.
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。
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.
羊水细胞DNA分析是先天性肾上腺皮质增生症21-羟化酶缺陷的产前诊断的可靠方法。
DNA analysis of amniocytes was a feasible method for the prenatal diagnosis of congenital adrenal hyperplasia with 21-hydroxylase deficiency.
目的探讨浆细胞型巨大淋巴结增生症的组织学发生、临床及病理特征。
ObjectiveTo discuss the histogenesis, clinical and pathological character of plasma-cell types of giant lympnode hyperplasia.
结论羊水细胞DNA分析是先天性肾上腺皮质增生症2 1羟化酶缺陷的产前诊断的可靠方法。
Conclusion DNA analysis of amniocytes was a feasible method for the prenatal diagnosis of congenital adrenal hyperplasia with 21-hydroxylase deficiency.
结论羊水细胞DNA分析是先天性肾上腺皮质增生症2 1羟化酶缺陷的产前诊断的可靠方法。
Conclusion DNA analysis of amniocytes was a feasible method for the prenatal diagnosis of congenital adrenal hyperplasia with 21-hydroxylase deficiency.
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