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It also is related to bone marrow structural damage resulting from tumor invasion,large proliferation of granulation or fibrous tissue,which often affect hemopoiesis.Leukemoid reaction occurred in the majority of malignancies is myeloid leukemia response,among which some are.neutropenia,and even agranulocytosis and increasion or decreasion of platelets.These are all have close relationship with marrow invasion of malignant tumor,immune reaction of the body and chemotherapy as well as radiotherapy.
亦与骨髓被恶性肿瘤细胞浸润、肉芽和纤维组织大量增生,使骨髓结构破坏,影响红系造血有关;绝大多数恶性肿瘤并发的类白血病反应是粒细胞性的,部分患者白细胞减少,甚至粒细胞缺乏,以及血小板增高或减少,均与恶性肿瘤细胞骨髓浸润、机体的免疫反应、放化疗有关。
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Features of the related myeloproliferative disorder included isolated erythrocytosis, distinctive bone marrow morphology, and reduced serum erythropoietin levels.
相关骨髓增生碍的主要特征为:独立的红细胞增多,特征性的骨髓心态学以及血清中促红细胞生成素的减少。
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As a result penicillium of Ma Erni humble is double photograph bacterium, mould bacterium colony can discover the broom shape mycelial of diagnostic sex,; of pigment of rose of water-solubility of the generation after sanded Paul fosters 3 days is medullary inside and outside of cell of blood of the week outside mixing all can discover spore;PAS coloring sees bacterium body show circle, elliptic or sausage shape, size is differ, it is 2~8 μ M about, color of afterbirth wall incarnadine and clear and successive, it is thus clear that inside the cell of sausage shape one apparent horizontal stroke is lain between, afterbirth is qualitative not easy and chromatic.
结果马尔尼菲青霉菌为双相菌,霉菌型菌落可发现特征性的扫帚状菌丝,沙保罗培养3天后产生水溶性玫瑰色素;骨髓和外周血细胞内外均可发现孢子;PAS染色可见菌体呈圆形、椭圆形或腊肠状,大小不一,约为2~8μm,胞壁染红色且清楚连续,在腊肠状的细胞内可见一明显的横隔,胞质不易着色。
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Candida colonisation did not enhance oalbumin permeation in mast cell deficient W/W mice but did in congenic littermate control +/+ mice. Reconstitution of mast cells in W/W mice by transplantation of bone marrow deried mast cells restored the ability to increase oalbumin permeation in response to Candida colonisation.
念珠菌定植不加强肥大细胞缺陷W/W小鼠的蛋白通透性,而其同系同窝对照+/+小鼠则有加强,W/W小鼠通过骨髓肥大细胞移植重建肥大细胞功能可恢复念珠菌定植后对卵白蛋白通透性的增强作用。
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The diagnosis of ITP is made clinically by exclusion of other causes of thrombocytopenia, the absence of splenomegaly, and the finding of normal or increased megakaryopoiesis on bone marrow examination. The nonimmune thrombocytopenia is caused by some nonimmune factors, such as acute leukemia, hypersplenism and post-chemotherapic bone marrow suppression.
特发性血小板减少性紫癜的诊断仍只是一种排除性的临床诊断,其国内诊断标准为多次化验检查血小板计数减少,脾脏不增大或仅轻度增大,骨髓检查巨核细胞数增多或正常,有成熟障碍,并且具备以下五点中的任何一点:泼尼松治疗有效,切脾治疗有效,血小板相关抗体增多,血小板相关补体增多,血小板寿命测定缩短,同时应排除继发性血小板减少症。
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Tender, erythematous, edematous plaques that may centrally vesiculate on the upper part of the body associated with fever and leukocytosis characterize Sweet's syndrome.
身体上部压痛性水肿性红斑块伴发热和白细胞增多为Sweet综合征的特征,这可能是骨髓性白血病的早期征象。
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Tender, erythematous, edematous plaques that may centrally vesiculate on the upper part of the body associated with fever and leukocytosis characterize Sweet's syndrome.
身体上部触痛、红斑块、水肿性斑块伴发热和白细胞增多为 Sweet 综合征的特征,这也可能是骨髓性白血病的早期征象。
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Acute myelocytic leukemia is a malignant neoplasm of hematopoietic cells characterized is an abnormal proliferation of myeloid precursor cells.
急性前骨髓性白血病,是一种造血组织的恶性疾病,其治病原因乃骨髓性前趋细胞不正常的大量增生,并有细胞分化停止的病变。
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However, this approach conferred the resistance to not only myelopoietic cells but also tumor cells that have invaded or metastasized into bone marrow or circulating blood for nonspecific expression of the exogenous genes.
详细骨髓造血细胞中导入耐药耐辐射基因是克服放化疗对造血系统抑制作用的有效手段,但外源基因的非特异性表达也增加了残存在血液或者侵犯至骨髓中的肿瘤细胞耐受性。
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ResultsCharacteristic features at the presentation of AITL included generalized lymphadenopathy, fever, splenomegaly, and skin rashes with polyclonal hyper-gammaglobulinemia and other hematological abnormalities (such as Coombs-positive hemolytic anemia), which often involved the bone marrow and had well-described histologic features.The positive rate for CXCL13 was 93.3%.
结果:AITL主要表现为淋巴结肿大、发热、脾大和皮疹,伴有多克隆性高球蛋白血症和其他血液学异常如白细胞升高、Coombs试验阳性,常累及骨髓,具有特征性的病理组织学表现,免疫组织化学实验显示B-淋巴细胞趋化因子CXCL13阳性率为93.3%。
- 更多网络解释与骨髓性的相关的网络解释 [注:此内容来源于网络,仅供参考]
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megaloblastic anemia:巨幼细胞性贫血
巨幼细胞性贫血(megaloblastic anemia)系脱氧核糖核酸(DNA)合成的生物化学障碍及DNA复制速度减缓所致的疾病. 影响到骨髓造血细胞--红细胞系、粒细胞系及巨核细胞系而形成贫血,甚至全血细胞减少. 骨髓造血细胞的特点是胞核与胞质的发育及成熟不同步,
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Arsenic Trioxide:氧化砷
三氧化砷(arsenic trioxide)为我国古老药方,最近在中国被发现可以治疗急性前骨髓性白血病. 另外在西方Soignet医生证实,若给予低剂量的三氧化砷,可以使前骨髓性白血病的病人得到惊人的完全缓解结果(12中有11人),而且低剂量的砷有良好的耐受性,
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bone marrow suppression:骨髓抑制
综合上述,复发性或是转移性子宫颈癌的传统治疗效果是很有限的,而这些治疗会引起很大的并发症例如骨髓抑制 (bone marrow suppression)的副作用,这类副作用容易有时会引起败血症而造成病患死亡,而标靶治疗的药物一般副作用病患的耐受度较好,
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lienomedullary:脾骨髓的
lienomalacia 脾软化 | lienomedullary 脾骨髓的 | lienomyelogenousleukemia 脾骨髓性白血病
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myelocyst:骨髓囊肿
myelocone 脑脂尘 | myelocyst 骨髓囊肿 | myelocystic 髓性囊性的
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myelocystic:髓性囊性的
myeloblastoma 成骨髓细胞瘤 | myelocystic 髓性囊性的 | myelocytosis 髓细胞增多症
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myelogenesis:脑脊髓形成,髓鞘(质)形成
\\"脊髓发育不良\\",\\"myelodysplasia\\" | \\"脑脊髓形成,髓鞘(质)形成\\",\\"myelogenesis\\" | \\"骨髓性的\\",\\"myelogenic,myelogenous,myelogenitic\\"
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myelogenous:骨髓性的
31. bladder 膀胱 | 32. myelogenous 骨髓性的 | 33. fusion gene 融合基因
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osteonecrosis:骨坏死
骨坏死( osteonecrosis)是指骨的有活力成分(包括骨细胞、骨髓造血细胞及脂肪细胞)的死亡. 人体内骨髓系统很多部位可以发生骨坏死,以股骨头、腕舟骨、足距骨最多见. 各种骨缺血时都是同样具有特征性的,各种骨缺血时的差别只不过是在数量、部位和受累骨的年龄方面有些变化c.
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Myelodysplastic Syndromes:骨髓增生异常综合征
[关键词] 反应停 骨髓增生异常综合征 骨髓增生异常综合征(myelodysplastic syndromes)是一组异质性的克隆性造血干细胞疾病,具有难治性全血细胞减少、骨髓病态造血及向白血病转化高风险特征.