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.
本文报告三例先天性精阜增生症。
This paper reports 3 cases of congenital hyperplasia of the verumontanum.
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.
纤腺囊性增生症亦为双侧乳腺癌的危险因素。
Fibrocystic proliferation was risky factor of double-sides breast cancer.
目的探讨肾上腺皮、髓质增生症的诊断和治疗。
Objective To study the diagnosis and treatment of adrenal cortical and medullary hyperplasia.
本文报道21例精阜增生症尿流动力学检查结果。
Urodynamic studies in 21 cases of verumontanum hyperplasia were presented.
目的：探讨小儿精阜增生症的病因、诊断和治疗。
Objective: To study the etiology, diagnosis and treatment of congenital hyperplasia of verumontanum(CHV) in children.
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：探讨巨大淋巴结增生症（CD）的CT表现特点。
Objective:To assess the CT findings of the Castleman disease(CD).
目的提高对肾上腺髓质增生症(amh)的诊断与治疗水平。
Objective To study the diagnosis and treatment of adrenal medullary hyperplasia (AMH).
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.
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.
方法回顾性分析9例经病理证实的巨淋巴结增生症的CT表现。
Methods:CT findings in 9 cases with castleman disease confirmed by pathology were retrospectively analyzed.
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：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).
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.
目的了解巨大淋巴结增生症的CT和MRI表现以及与病理改变的联系。
Objective To study ct and MRI characteristics of giant lymph node hyperplasia and their pathologic basis.
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.
前言：目的：探讨超声内镜(EU S)对胆囊腺肌增生症的诊断价值。
Objective: to evaluate endoscopic ultrasonography (EUS) in the diagnosis of gallbladder adenomyomatosis.
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).
目的明确口腔粘膜良性淋巴组织增生症（BLOM）的临床病理特征及其本质。
Objective To reveal the clinicopathological and immunohistochemical features of benign lymphadenosis of oral mucosa (BLOM).
艺术被看作象牙之塔，某种孤立于生活的气泡，或者一个发达了的文明的增生症。
Art has been regarded as the ivory tower, some bubble isolated from life, or some hyperplasia of a developed civilization.
结果11例患者中颅底肿瘤6例，颅底骨纤维异常增生症3例，脑膜脑膨出2例。
Results Among 11 patients, there were 6 patients with skull base tumor, 3 patients with fibrosis hyperplasia, 2 patients with encephalomeningocele.
目的开展新生儿先天性肾上腺皮质增生症筛查，降低残疾儿童的发生率，提高人口素质。
Objective to develop the neonatal screening for congenital adrenal hyperplasia in order to prevent children from congenital disability and improve the aristogenesis in our country.
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.
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.
肾上腺病变11例，其中良性肿瘤7例，恶性肿瘤2例，2例肾上腺增生症在随访观察中。
Of 11 cases adrenal diseases, there were 7 cases adrenal malignant tumor and 2 cases benign tumor, 2 cases adrenal 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.
目的提高纵隔巨淋巴结增生症的认识水平，探讨纵隔巨淋巴结增生症的影像学表现及诊断价值。
Objective To improve mediastinal giant lymph node hyperplasia, discuss the understanding level on mediastinal giant lymph node hyperplasia of imaging manifestations and diagnostic value.
淋巴血管肌肉增生症是罕见的、病因未知的疾病，其通常发生在生育年龄的女性和患有结节硬化症的人。
Lymphangioleiomyomatosis (LAM) is a rare disease of unknown origin that usually occurs in women of reproductive age and people with tuberous sclerosis.
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