中华医学杂志
2014年 · 第94卷第33期
中华医学杂志
肿瘤治疗理念及模式的变化
With the rapid development of biomedicine, especially molecular pathology, epigenetics, tumor stem cells[
CT引导下植入125I放射粒子治疗脊柱溶骨性转移瘤
经皮微波消融和二次手术治疗晚期复发型小肝癌的长期疗效观察
索拉非尼联合TACE治疗肝癌伴门静脉癌栓的临床观察
经肝动脉化疗栓塞肝细胞癌诱发肝源性糖尿病的危险因素分析
丙戊酸钠脑病的临床误诊分析
二维和三维超声测量胎儿胸腺在胎儿宫内生长迟缓时的应用
角膜共焦显微镜对于痛性糖尿病神经病变早期诊断的价值
老年2型糖尿病人群死亡风险的17年队列研究
体质指数和老年男性骨质疏松症的相关性分析
HIV阳性骨折患者手术切口愈合情况的临床分析
慢性肾衰竭患者认知损伤的评估与分析
靶向治疗用药顺序对转移性肾细胞癌患者无进展生存的影响
18F-FDG PET/CT评价初诊非霍奇金淋巴瘤代谢活性及其与免疫表型的相关性
房颤患者脑卒中的预防——新型抗凝药依度沙班与达比加群、利伐沙班、阿哌沙班疗效与安全性的比较
Warfarin is currently a commonly used drug for preventing embolism in patients with atrial fibrillation, but warfarin has limitations such as regular monitoring, narrow treatment window, and drug-drug interaction. Large-scale phase III clinical trials have confirmed that new oral anticoagulants (NOACs, dabigatran, rivaroxaban, apixaban, and edoxaban) are not inferior or even superior to warfarin in efficacy, respectively, while their bleeding incidence is similar or lower. However, there are no clinical trials that directly compare the efficacy and safety of these drugs with each other. Flemming Skjoth, Institute of Thrombosis, Aalborg University, Denmark, et al. used indirect comparative analysis to compare the differences in efficacy and safety between edoxaban and three other anticoagulants. "Efficacy and safety of edoxaban in comparison with dabigatran, rivaroxaban and apixaban for stroke prevention in atrial fibrillation-an indirect comparison analysis" Published in February 2014Journal of Thrombosis and HaemostasisOn.
替米沙坦对大鼠急性心肌梗死后炎症反应及纤维化的干预机制
卵巢特异性启动子调控白细胞介素-24基因对卵巢癌细胞系SKOV3的杀伤作用
miR-16对小鼠胶质母细胞瘤U87MG细胞增殖及新生血管化影响的在体实验研究
雌激素与铁在骨吸收中的拮抗效应及其机制
21-羟化酶缺乏致女性假两性畸形两姐妹的诊治
female pseudohermaphroditism is a common type of hermaphroditism. Patients have a normal female karyotype (46, XX), and there is only one gonad-ovary in the body, while the external genitalia and secondary sexual characteristics have male manifestations, such as clitoris enlargement, left and right fusion of labia majora, Adam's apple and beard, etc. The cause of female pseudohermaphroditism is that patients are exposed to excessive androgens since childhood, among which congenital adrenocortical hyperplasia, especially 21-hydroxylase (21-OHD) deficiency (which can lead to increased androgen synthesis in the body), is one of the main causes. This disease is not uncommon clinically, but familial rare. In January 2014, Peking Union Medical College Hospital admitted two cases of hermaphroditism in a family, which were biological sisters. The diagnosis and treatment results are reported as follows.
microRNA表达谱在动脉粥样硬化脑梗死调控中的研究进展
microRNA is a kind of 21-25 nucleotide long small non-coding ribonucleic acid encoded by endogenous genes widely existing in eukaryotic cells. After specific binding to target genes, it may induce the degradation of target mRNA by deadenylation, inhibit the initiation of protein translation or the extension of polypeptide chain, and degrade nascent proteins to regulate the role of target genes[
颅内隐球菌瘤一例
A 55-year-old male was admitted with headache for 2 months, aggravated with walking instability for 1 week. He has been in good health, has been exposed to radioactive elements, and has smoked for more than 30 years. Physical examination: Shen Qing Li, left isotropic hemianopia, bilateral limb muscle strength grade V, and no obvious abnormalities were found in the physical examination of the remaining nervous system. Laboratory tests: Hematuria routine, liver and kidney function were not abnormal, hepatitis B markers, human immunodeficiency virus antibody (Ⅰ + Ⅱ), Mycobacterium tuberculosis antibody and Treponema pallidum antibody were all negative, and pulmonary tumor markers were not abnormal. CT examination of the head showed that there was an irregular circular linear high-density shadow in the right occipital lobe, with low-density shadow in the ring, obvious edema around the lesion, and left deviation of the midline. MRI of the head showed that the right occipital lobe was about 6.5 cm ×5.5 cm ×5.0 cm in size, with cystic-solid lesions with long T1 and long T2 changes, uneven signals, clear boundaries, close relationship with the dura mater, and obvious edema around the tumor. After intravenous contrast, the lesions showed irregular annular enhancement, with a liquid dark area in the middle, see
超声诊断多睾症一例
A 27-year-old male came to our outpatient clinic in February 2014 due to infertility for 1 year after marriage. Specialist examination: the penis and scrotum develop normally, and the pubic hair is evenly distributed in an inverted triangle; The left testis, epididymis and spermatic cord are normal, and two masses can be accessed in the right scrotum. The texture is similar to that of the left testis, and there is no tactile tenderness. The scrotal ultrasound showed that the left testis was about 5.2 cm ×2.9 cm ×2.4 cm in size and 18.9 ml in volume, with normal shape, smooth capsule and uniform parenchymal echo. Two testicular echo masses can be detected in the sheath cavity of the right testis (
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