Institute of Legal Medicine, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Institute of Systems Neuroscience, Medical Faculty, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Int J Legal Med. 2022 Jan;136(1):133-147. doi: 10.1007/s00414-021-02619-7. Epub 2021 Jun 28.
The diagnosis of death due to violent asphyxiation may be challenging if external injuries are missing, and a typical acute emphysema (AE) "disappears" in pre-existing chronic emphysema (CE). Eighty-four autopsy cases were systematically investigated to identify a (histo-) morphological or immunohistochemical marker combination that enables the diagnosis of violent asphyxiation in cases with a pre-existing CE ("AE in CE"). The cases comprised four diagnostic groups, namely "AE", "CE", "acute and chronic emphysema (AE + CE)", and "no emphysema (NE)". Samples from all pulmonary lobes were investigated by conventional histological methods as well as with the immunohistochemical markers Aquaporin 5 (AQP-5) and Surfactant protein A1 (SP-A). Particular attention was paid to alveolar septum ends ("dead-ends") suspected as rupture spots, which were additionally analyzed by transmission electron microscopy. The findings in the four diagnostic groups were compared using multivariate analysis and 1-way ANOVA analysis. All morphological findings were found in all four groups. Based on histological and macroscopic findings, a multivariate analysis was able to predict the correct diagnosis "AE + CE" with a probability of 50%, and the diagnoses "AE" and "CE" with a probability of 86% each. Three types of "dead-ends" could be differentiated. One type ("fringed ends") was observed significantly more frequently in AE. The immunohistochemical markers AQP-5 and SP-A did not show significant differences among the examined groups. Though a reliable identification of AE in CE could not be achieved using the examined parameters, our findings suggest that considering many different findings from the macroscopical, histomorphological, and molecular level by multivariate analysis is an approach that should be followed.
如果没有外伤,暴力性窒息导致的死亡诊断可能具有挑战性,而且典型的急性肺气肿 (AE) 在预先存在的慢性肺气肿 (CE) 中“消失”。系统地研究了 84 例尸检病例,以确定一种(组织学)形态或免疫组织化学标志物组合,使在预先存在的 CE 中具有 AE(CE 中的 AE)的情况下能够诊断暴力性窒息。这些病例包括四个诊断组,即“AE”、“CE”、“急性和慢性肺气肿 (AE + CE)”和“无肺气肿 (NE)”。使用常规组织学方法以及 Aquaporin 5 (AQP-5) 和 Surfactant protein A1 (SP-A) 等免疫组织化学标志物对所有肺叶的样本进行了研究。特别关注疑似破裂点的肺泡隔末端(“死端”),并用透射电子显微镜对其进行了额外分析。使用多变量分析和单向方差分析比较了四个诊断组的发现。所有形态学发现均见于四个组。基于组织学和宏观发现,多变量分析能够以 50%的概率预测正确的诊断“AE + CE”,并以 86%的概率预测“AE”和“CE”的诊断。可以区分三种类型的“死端”。一种类型(“边缘末端”)在 AE 中观察到的频率明显更高。免疫组织化学标志物 AQP-5 和 SP-A 在检查组之间没有显示出显著差异。尽管使用检查参数无法可靠地识别 CE 中的 AE,但我们的研究结果表明,通过多变量分析考虑宏观、组织形态学和分子水平的许多不同发现是一种应该遵循的方法。