体外丹参、藻酸双酯钠对脑血栓形成患者红细胞与内皮细胞粘附的影响

丹参、藻酸双酯钠是临床治疗脑血管病的常用药。本研究发现，在体外流场中用丹参、藻酸双酯钠分别处理脑血栓形成病人的红细胞后，此红细胞与培养的人脉静脉内皮细胞的粘附数目明显减少、粘附强度明显减弱；而且，在临床常用剂量下藻酸双酯钠的这种抗粘附作用优于丹参。认为丹参、藻酸双酯钠的这种抗粘附作用可能是临床用以治疗脑血栓形成的一个重要机理。     

山东省东南地区142例恙虫病病例分析

本文对１４２例恙虫病进行了分析。发现山东省东南地区的恙虫病患者在临床上具备焦痂、发热、皮疹和淋巴结肿大等四个特征；但临床表现比较轻缓，可能与该地区恙虫病立克次体的毒力较弱有关。治疗以四环素、氯霉素为主，疗效明显。     

异位甲状腺癌的诊断和治疗

目的　探讨异位甲状腺癌的发病特点、诊断和治疗方法。方法　对 2 9例异位甲状腺癌的临床及病理资料进行回顾性分析。结果　 2 9例均行手术治疗 ,术后辅以放、化疗。术后随访 ,5年存活率为 5 2 .0 % ,最长 1例已存活 2 4年。结论　早期发现并及时手术治疗是提高异位甲状腺癌患者生存率的关键 ,术后给予辅助性放、化疗有助于提高生存率。     

肝移植术后并发症的影像学评价

目的:采用多种影像学措施评价肝脏移植术后并发症。材料和方法:16例背驮式原位肝移植术患者,术后7天内每日行胸片及胸腹部超声检查。术后2周～12个月,当患者出现发烧、皮肤巩膜黄染及异常B型超声发现时,行上腹部CT检查5例8次、同时行胸部CT检查2例、上腹部MRI及MRCP检查6例、ERCP检查4例、PTC检查2例、“T”管造影2例和下腔静脉造影1例。结果:术后1周内诊断胸腔积液14例(14/16);术后1～2周诊断肺部感染7例(7/16);肺不张4例(4/16)。术后4个月和8个月诊断右肺和移植肝多发转移瘤各1例(2/6);术后3周～10个月诊断胆总管吻合口狭窄、胆管炎、胆泥形成等5例(5/16)。术后2周诊断下腔静脉狭窄1例(2/16)。结论:运用多种影像学检查方法有助于及时诊断肝移植术后并发症。     

门诊老年冠心病患者用药知识需求的调查

冠心病是老年人的常见病、多发病,致残或死亡率已居常见病之首[1]。目前,药物治疗仍是冠心病二级预防的主要措施。近年来研究发现,83·3%的冠心病患者无法正确使用药物,用药依从性差[2]。分析原因,87%的门诊老年慢性病患者包括冠心病患者在内,主观不遵医用药是由于在用药过程中出现诸多用药问题时得不到相关知识信息支持所导致[3]。另外,通过调查证实冠心病患者对用药知识的需求亦居前列,尤其是出院后用药知识是首要需求[2,4-6]。由此表明,对门诊老年冠心病患者进行用药知识教育十分必要。依据健康教育学方法,分析患者的教育需求是制定教育…     

呼出气氢测定试验对飞行人员乳糖酶缺乏症的研究

对66名汉族飞行人员进行乳糖呼出气氢测定试验,乳糖吸收不良的发生率为83.3％,其中乳糖不耐受者占34.6％;与一般汉族人群无明显差别。对10名确定为中度以上乳糖吸收不良的飞行人员进行250ml鲜牛奶的试验结果,有50％呼出气氢含量在正常范围,并无一例出现胃肠道症状。提示较长期食用牛奶未能使乳糖酶缺乏状态发生改变,但每日食用适量牛奶属合理营养。     

Genetic imbalances in pleomorphic xanthoastrocytoma detected by comparative genomic hybridization and literature review.

Pleomorphic xanthoastrocytoma (PXA) is a rare, low-grade astrocytic tumor found in the central nervous system. Histologically, the tumor is characterized by markedly pleomorphic and lipidized cells. Although most of the patients have a favorable prognosis, a small number of cases undergoing recurrence or progression to anaplastic astrocytoma were reported. Very few genetic studies have been performed on PXA because of its rarity and the pathogenesis of this neoplasm is largely unknown. In order to provide an overview of genetic alterations in PXA, we performed comparative genomic hybridization to identify chromosomal imbalances (DNA gains and losses) in three cases of PXA. Genetic imbalance was detected on at least one chromosome for each case. One case, which revealed multiple genetic alterations, showed a poor prognosis. DNA gain on chromosome 7 and loss on 8p were demonstrated in two of three cases, suggesting that the candidate gene(s) located on these regions may play a role in the development of PXA. Further studies are needed to identify the residing candidate genes that are involved in the tumorigenesis of PXA. In addition, the histopathological features and previous genetic studies on PXA are reviewed.