性母细胞

性母细胞瘤与45，XO/47，XYY嵌合体（1例报道及5例文献复习）

Gonadoblastoma and 45 , xo / 47 , XYY mosaicism ( a case report and review of five oases )

本文报道1例核型为45，XO/47，XYY的性母细胞瘤，结合近30年文献中该类核型7例报道中发生性母细胞瘤的5例。

A case of gonadoblastoma with 45 , XO / 47 , XYY mosaicism is reported . Another 7 cases of the same mosaicism in the literature during the last 30 years are reviewed .

8例中6例发生性母细胞瘤。

Of these 8 cases , 6 had gonadoblastoma .

结论性母细胞瘤是一种罕见的混合性生殖-性索间质肿瘤，具有独特的病理形态特征。

Conclusions GB is a rare mixed germ cell-sex cord-stromal tumor with distinct pathological features .

方法采用光镜、免疫组化对3例性母细胞瘤进行观察，并复习相关文献。

Methods Three cases of GB were investigated by light microscopy and the related literature was reviewed .

性腺二期是性腺中脂肪大量积累的阶段，同时也出现了大量的初级性母细胞，此阶段发育时间较长，可长至数年。

At the second stage the fat was accumulating a lot , and a large number of auxocyte had emerged . This period lasted a long time to several years .

多形性胶质母细胞瘤（GBM）显示肿瘤细胞深染和多形性

This glioblastoma multiforme ( GBM ) demonstrates marked cellularity with marked hyperchromatism and pleomorphism .

人类多形性胶质母细胞瘤中变异型IκBα基因抑制血管新生的研究

Mutant-type I κ B α gene inhibits angiogenesis in human glioblastoma multiform cells

X射线诱导多形性胶质母细胞瘤细胞系的凋亡

Apoptosis induced by X-ray in glioblastoma multiform cell lines

资料与方法搜集经MRI诊断、临床及病理证实的12例髓母细胞瘤，其中8例为原发性髓母细胞瘤，4例为髓母细胞瘤转移；

Materials and Methods MRI findings in 12 cases with pathologically-proved myeloblastoma were retrospectively analyzed .

结果：多形性胶质母细胞瘤CT表现为低密度影，瘤内卒中表现为高密度；

Results : CT appearance of glioblastoma multiforme was low density image , intratumorally apoplexy was high density image .

变异型IκBα抑制人类多形性胶质母细胞瘤细胞中血管生长因子VEGF及IL-8的表达

Mutant-type I κ B α inhibit the expression of VEGF and IL-8 in human glioblastoma multiform cells

原发与继发性胶质母细胞瘤中survivin表达及其意义

Expression of survivin in primary and secondary glioblastoma and its significance

~（60）Coγ射线对多形性胶质母细胞瘤中的肿瘤干细胞的影响

Sensitivity of Brain Tumor Stem Cells from Multiform Glioblastomas to ~ ( 60 ) Co γ - ray in Vitro

磷酸化JNK与磷酸化c-Jun在多形性胶质母细胞瘤中的表达及意义

Clinical significance of p-c-Jun N-terminal kinase and p-c-Jun expression in glioblastoma

CD44变异型在自发颅外转移性胶质母细胞瘤中的表达

Variant CD44 Adhesion Molecules Are Expressed in a Human Glioblastoma with Spontaneous Extraneural Metastases

RNA干扰抑制多型性胶质母细胞瘤FGF-2和B7-H1表达的研究

The Inhibition of FGF-2 and B7-H1 in the Glioblastoma Multiforme by RNA Interference

方法：经手术病理证实的多形性胶质母细胞瘤21例，其中20例行CT扫描，18例行MRI检查，分别分析其影像学表现。

Methods : 21 cases of glioblastoma multiforme were proved by surgical and pathologic findings.20 of them were performed by CT , 18 performed by MRI , analysing the imaging manifestations of them .

结论IκBαM基因可有效抑制胶质瘤中的血管新生从而抑制肿瘤的生长，这可作为人类多形性胶质母细胞瘤抗血管治疗的理论基础。

Conclusion I κ B α M gene transfer could inhibit in vivo angiogenesis , therefore , suppress tumorigenicity of human glioma cells . This could be a theoretical basis in the anti-vascular therapy of human glioma .

目的研究变异型IκBα（IκBαM）基因在人类多形性胶质母细胞瘤（GBM）中对血管新生的抑制作用。

Objective To investigate the inhibitory effects of mutant-type I κ B α( I κ B α M ) gene on angiogenesis in human glioblastoma multiform ( GBM ) cells .

目的探讨survivin蛋白在原发与继发性胶质母细胞瘤（glioblastoma，GBM）中的表达及其临床病理学意义。

Purpose To investigate the expression of survivin in primary and secondary glioblastoma ( GBM ) and its clinicopathological significance .

多形性胶质母细胞瘤（GBM）是最常见的致命性的脑部肿瘤。

Glioblastoma multiforme ( GBM ) is the most common and lethal type of brain cancer .

结论：小剂量VM-26即对体外培养人多形性胶质母细胞BT325产生抑制作用。

Conclusion : Glioblastoma multiforme BT325 can be effectively inhibited by low dose of VM-26 in vitro .

目的探讨磷酸化JNK（p-JNK）与磷酸化c-Jun（p-c-Jun）在多形性胶质母细胞瘤（GBM）中的表达及意义。

Objective To explore the clinical significance and the expression of phosphorylated c-Jun N-terminal kinase ( p-JNK ) and phosphorylated c-Jun ( p-c-Jun ) in glioblastoma ( GBM ) .

多形性胶质母细胞瘤（GBM）是一类具有高侵袭特点的原发性脑肿瘤，肿瘤组织常常入侵周围正常组织，外科手段治疗效果不理想，术后常复发，患者预后差。

Glioblastoma multiform ( GBM ) is a highly malignant , lethal primary brain tumor . The therapeutic efficacy of surgery is not ideal because it infiltrates the surrounding normal tissue , thus GBMs have also associated with poor prognosis and short life expectance .

按组织学分型，弥漫性淋巴母细胞型2例和弥漫性混合细胞型淋巴肉瘤、结节性前淋巴细胞型、结节性淋巴母细胞型、Lennert氏淋巴瘤及混合细胞型何杰金氏病各1例。

Two cases were classified as diffuse lymphoblastic lymphosarcoma and one each as nodular prolymphocytic , nodular lymphoblastic , diffuse mixed cell type lymphosarcoma , Lennert 's lymphoma , mixed cell type Hodgkin 's disease .

并且，高级别胶质瘤（间变型星形细胞瘤WHOm；多形性胶质母细胞瘤WHOW）患者的预后情况依然不佳。因此，临床上期待有更加行之有效的治疗方式。

The prognosis for patients with high-grade gliomas , which include anaplastic astrocytoma ( WHO ⅲ) and glioblastoma multiforme ( GBM , WHO IV ), remains dismal . Hence , there is a great hope for novel therapeutic approaches .

骨骺侵袭性骨母细胞瘤并动脉瘤样骨囊肿1例报告

One Case : Invasive Osteoblastoma in Osteoepiphysis with Aneurysmal Bone Cyst

侵袭性骨母细胞瘤2例报告暨文献复习

Invasive osteoblastoma : radiotherapy results in 2 cases and literature review

福建省畲族人群永久性淋巴母细胞株的建立

Establishment of Lymphoblastoid Cell Strains from She Population in Fujian of China