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lymphoma相关的网络例句

查询词典 lymphoma

与 lymphoma 相关的网络例句 [注:此内容来源于网络,仅供参考]

alcl was not uncommon in children. the differential diagnoses included malgnant histiocytosis, t zone or pleomorphic t-cell lymphoma, hodgkins lymphoma, mycosis fungoides, and metastatic carcinoma. immunohistochemical study cd30, cd15, lca and ema were very helpful for diagnosis and differential diagnosis.

小儿间变性大细胞性淋巴瘤并不少见,需与恶性组织细胞增生症、t区或多形t淋巴瘤、霍奇金淋巴瘤、蕈样霉菌病和转移性癌等鉴别。cd30、cd15、lca和ema免疫酶标检查对诊断及鉴别诊断十分有用。

Methods: The expression of EOMES gene, ETS-1 gene and MEF (myeloid Elf-1 like factor) gene in 25 cases of N-NK/T-L and 25 control cases including 11 cases of B cell lymphoma (BCL, 6 cases of T cell lymphoma, 3 cases of normal spleen, 5 cases of chronic nasopharyngitis were detected by tissue microarray and in situ hybridization.

通过对EOMES,ETS-1和MEF基因进行克隆、探针制备和组织芯片制备,对25例N-NK/T-L以及同部位11例B细胞淋巴瘤、6例T细胞淋巴瘤、3例正常脾组织和5例慢性炎性鼻黏膜组织进行了原位杂交检测。

"In patients with splenic lymphoma with villous lymphocytes who are infected with HCV, treatment with interferon can lead to regression of the lymphoma," write Olivier Hermine, MD, PhD, from the Hopital Necker in Paris, and colleagues .

巴黎Necker 医院的Olivier Hermine医师,PhD及其同事写道:「对於HCV感染,并且有绒毛淋巴细胞的脾淋巴瘤患者,采用干扰素治疗,可以使淋巴瘤症状缓解。

Results In the gastric group,only one patient was confirmedly diagnosed with malignant lymphoma before operation,and in the intestinal group only two patients were suspected of malignant lymphoma.

本组通过49例原发性胃肠淋巴瘤的病理、临床分析,探讨其有关病变特征,旨在引导临床医生加深对本病的认识和重视,提高诊断正确率。1材料和方

There was no evidence of an extracranial non-Hodgkin lymphoma, so the conclusion was that this represented a primary central nervous system lymphoma.

目前还没有颅外非霍奇金淋巴瘤的证据,而且这是一个原发性中枢神经系统淋巴瘤的患者。

E studied expression levels of WAVE1 in six leukemia cell lines (the human Jurkat T leukemia cells, U937 histiocytic lymphoma cells, Burkitts lymphoma cell Raji, acute promyelocytic leukemia cell HL-60, chronic myelogenous leukemia cell K562 and K562/A02) by Western blotting analysis. Levels of WAVE1 expression were high in all six human leukemia cancer cell lines. In contrast, the constitutive expression levels of WAVE1 were noticeably lower in normal human peripheral blood mononuclear cells, or non-blood cancer cell-lines, including human lung A549 cancer cells, Hela cervical cancer cells, MG-63 osteosarcoma cells, CNE2 nasopharyngeal carcinoma cells, human umbilical vein endothelial cell, QSG7701 hepatocarcinoma cells, and WI-38 lung fibroblastoma cells.

AVE1在人类血液肿瘤细胞系(人T细胞白血病细胞系Jurkat、人组织细胞淋巴瘤细胞系U937、人Burkitts淋巴瘤细胞系Raji、人原髓细胞白血病细胞系HL-60、人慢性髓原白血病细胞系K562和K562/A02)中高表达,在非血液肿瘤细胞系(人肺腺癌细胞系A549、人宫颈癌细胞系Hela、人成骨肉瘤细胞系MG-63、人鼻咽癌细胞系CNE2、人脐静脉内皮细胞系HUVEC、人肺成纤维细胞系WI-38、人肝上皮细胞系QSG7701)以及正常人外周血单个核细胞中低表达或不表达。

Hydroa vacciniforme-like Cutaneous T cell lymphoma is a new kind of T cell lymphoma. This disorder may be related to the Epstein-Barr virus infection and mosquito bites.

种痘水疱病样皮肤T细胞淋巴瘤是一种新的恶性多系统疾病,发病可能与EBV感染以及蚊子叮咬有关。

Objective Primary lymphoma in the central nervous system is rare.In order to recognize it tree cases of primary leptomeningeal lymphoma were presented in this article.

目的 原发性中枢神经系统淋巴瘤很少见,本文报告3例原发性中枢神经系统淋巴瘤,以提高人们对本病的认识。

Three cases of advanced NHL associated with lymphomatous leptomeningitis were reported with a review of the literature.Two of the patients were poorly differenti- ated lymphocytic lymphoma,diffuse type,and the other Burkitt's lymphoma.

本文报告3例淋巴瘤性脑膜炎,并复习文献讨论淋巴瘤脑膜炎的诊断、治疗和预防。3例患者均为晚期非何杰金氏淋巴瘤。1例为低分化淋巴细胞淋巴瘤弥漫型,1例为 Burkitt's 淋巴瘤。

Results The pathology of all 10 cases of nasal lymphomas were T cell Non-Hodgkin's lymphoma, Ann Arbor stage Ⅰ~Ⅱin9 and 1 in stage IV. The locations of 10 lymphomae were in the anterior portion of one of the nasal cavities, and the lymphomae extended posteriorly along the inferior and/or media nasalis concha in different extent. No bone structure destruction was found in all stage I cases and the bone of the media nasalis concha as well as the uncinate process was partially absorbed in the stage IV nHL. The skin of the external noses adjacent to the lymphoma of the whole 10 cases were swollen in various severity with disappearance of the subcutaneous fat.

结果 10例鼻腔淋巴瘤病理均为T细胞非何杰金淋巴瘤,9例为Ann arbor I~II期,1例Ann Arbor IV期。10例病变均发生于一侧鼻腔前部,沿下鼻甲向后呈不同程度蔓延。9例I期病变均无骨质破坏,相邻鼻背侧皮肤不同程度肿胀,皮下脂肪消失,1例IV期病变可见患侧中鼻甲及钩突骨质部分吸收,同侧眶内肿瘤侵犯。

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