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多发性软组织挫伤后对肺及其他脏器的影响 总被引:3,自引:1,他引:2
目的观察多发性软组织挫伤后短时间内死亡案例的脏器病理学改变。方法应用常规组织学及免疫组织化学染色技术进行光学显微镜检查。结果光镜检查见肺组织毛细血管扩张充血,白细胞集聚,肺组织散在片状出血、灶状坏死及透明膜形成;心脏间质血管扩张充血,点灶状纤维溶解;脑组织充血水肿,肝脾充血。免疫组化发现肺泡腔及部分血管内纤维蛋白染色阳性,部分脾脏血管内及肾髓质集合管中肌红蛋白染色阳性。结论本研究结果提示多发性软组织挫伤后短时间内死亡的死因为成人呼吸窘迫综合征(ARDS)合并多脏器功能衰竭。 相似文献
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Previous studies on cytoskeletal changes of in vitro and in vivo animal models of ischemic myocardium have suggested the possibility of using alterations in cytoskeleton proteins as an early marker for the post-mortem diagnosis of myocardial ischemia in cases of sudden death due to coronary artery disease (CAD). In the present study, using the technique of ABC-immunohistochemistry, we examine the changes of three cytoskeletal proteins: vinculin, desmin and α-actinin in human myocardial samples taken from 14 cases of CAD sudden death and 13 cases of non-CAD death. Results of these examinations are compared with immunohistochemical changes of myoglobin and histochemical staining of hematoxylin and eosin and phosphotungstic acid, and Masson trichrome. Patchy and extensive loss of the three cytoskeletal proteins was demonstrated in the myocardium of victims who died 1 h or later following the onset of symptoms of ischemic myocardium. The pattern of cytoskeleton change is equivocal in the cases of CAD who died less than 1 h after the onset of symptoms and of the cases of non-CAD. In these cases, no significant histological change was observed. With less non-specific background changes and stronger positive staining, immunohistochemical staining of the three cytoskeletal proteins is more reliable than myoglobin, which has attracted the attention of many pathologists searching for anatomic evidence of ischemic myocardium in coronary artery disease. 相似文献
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大鼠急性心肌缺血zif/268蛋白表达及其意义 总被引:2,自引:0,他引:2
目的 探讨急性心肌缺血早期不同时间不同区域心肌细胞内原癌基因蛋白zif/268的表达变化,为心肌早期缺血死后诊断提供新指标。方法 建立心肌早期缺血模型,大鼠分为正常、缺血组。采用免疫组化SABC法研究心肌细胞核蛋白zif/268的累积情况。结果 缺血 60min后,缺血区大鼠心肌细胞有部分心肌细胞核呈弱阳性着色,以后随缺血时间延长核阳性增强。正常和缺血30min组及未缺血区心肌细胞核未见有阳性反应。HE染色无明显病理改变。结论 免疫组化染色法检测心肌细胞核zif/268的表达对急性心肌缺血的死后诊断是一种有价值有意义的手段。 相似文献
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大鼠脊髓损伤后HIF—1α基因的表达 总被引:2,自引:0,他引:2
目的观察大鼠脊髓损伤后低氧诱导因子-1α(HIF—1α)的表达规律,探讨其在脊髓损伤发生发展过程中的作用及法医学应用。方法建立大鼠静压脊髓损伤模型,采用RT—PCR和免疫组化SP法对伤后不同时间(0、3、6、12h和1、3、5、7、11、14d)HIF-1α和HIF-1α mRNA的表达进行检测,BI2000图像分析系统分析结果。结果正常及假手术对照组大鼠脊髓组织内有低水平的HIF-1α mRNA表达,但几乎检测不到HIF-1α阳性细胞;脊髓损伤后,HIF-1α及HIF-1α mRNA表达开始升高,其中HIF-1α mRNA表达在伤后3h开始增加,3d达高峰,14d时恢复正常;HIF—1α表达在伤后3h开始增加,1d达高峰,较HIF—1α mRNA的达峰时间(伤后3d)提前。HIF-1α免疫阳性产物可见于脊髓神经元、胶质细胞、室管膜细胞及间质内的血管内皮细胞。结论脊髓损伤后HIF-1α基因表达开始升高,对组织和细胞起低氧保护作用,其表达的时序性规律可望用于法医学损伤时间推断。 相似文献