Department of Advanced Biomedical Sciences, Legal Medicine Unit, University of Naples Federico II, Naples, Italy.
Department of Advanced Biomedical Sciences, Pathology Unit, University of Naples Federico II, Naples, Italy.
BMC Cardiovasc Disord. 2019 Nov 8;19(1):250. doi: 10.1186/s12872-019-1219-8.
Pulmonary embolism (PE) is associated to high mortality rate worldwide. However, the diagnosis of PE often results inaccurate. Many cases of PE are incorrectly diagnosed or missed and they are often associated to sudden unexpected death (SUD). In forensic practice, it is important to establish the time of thrombus formation in order to determine the precise moment of death. The autopsy remains the gold standard method for the identification of death cause allowing the determination of discrepancies between clinical and autopsy diagnoses. The aim of our study was to verify the morphological and histological criteria of fatal cases of PE and evaluate the dating of thrombus formation considering 5 ranges of time.
Pulmonary vessels sections were collected from January 2010 to December 2017. Sections of thrombus sampling were stained with hematoxylin and eosin. The content of infiltrated cells, fibroblasts and collagen fibers were scored using a semi-quantitative three-point scale of range values.
The 30 autopsies included 19 males (63.3%) and 11 females (36.7%) with an average age of 64.5 ± 12.3 years. The time intervals were as follows: early (≤1 h), recent (> 1 h to 24 h), recent-medium (> 24 h to 48 h), medium (> 48 h to 72 h) and old (> 72 h). In the first hour, we histologically observed the presence of platelet aggregation by immunofluorescence method for factor VIII and fibrinogen. The presence of lymphocytes has been identified from recent thrombus (> 1 h to 24 h) and the fibroblast cells were peripherally located in vascular tissue between 48 and 72 h, whereas they resulted central and copious after 72 h.
After a macroscopic observation and a good sampling traditional histology, it is important to identify the time of thrombus formation. We identified histologically a range of time in the physiopathology of the thrombus (early, recent, recent-medium, medium, old), allowing to determine the dating of thrombus formation and the exact time of death.
NCT03887819.
The trial registry is Cliniclatrials.gov, with the unique identifying number NCT03887819. The date of registration was 03/23/2019 and it was "Retrospectively registered".
肺栓塞(PE)是全球范围内导致高死亡率的疾病。然而,PE 的诊断往往不够准确。许多 PE 病例被误诊或漏诊,且这些病例通常与突发性意外死亡(SUD)相关。在法医学实践中,确定血栓形成的时间非常重要,以便确定确切的死亡时间。尸检仍然是识别死因的金标准方法,可确定临床诊断与尸检诊断之间的差异。我们的研究旨在验证致命性 PE 病例的形态学和组织学标准,并评估血栓形成的时间,考虑 5 个时间范围。
收集 2010 年 1 月至 2017 年 12 月的肺动脉段。对血栓取样进行苏木精和伊红染色。使用范围值的三分制半定量评分法对浸润细胞、成纤维细胞和胶原纤维的含量进行评分。
30 例尸检包括 19 名男性(63.3%)和 11 名女性(36.7%),平均年龄为 64.5±12.3 岁。时间间隔如下:早期(≤1 小时)、近期(>1 小时至 24 小时)、近期-中期(>24 小时至 48 小时)、中期(>48 小时至 72 小时)和晚期(>72 小时)。在第 1 小时,我们通过免疫荧光法检测因子 VIII 和纤维蛋白原观察到血小板聚集的存在。从近期血栓(>1 小时至 24 小时)中已经识别出淋巴细胞的存在,并且在 48 至 72 小时之间成纤维细胞位于血管组织的外周,而在 72 小时后则位于中央且丰富。
在进行宏观观察和良好的采样传统组织学检查后,确定血栓形成时间非常重要。我们在血栓形成的病理生理学中确定了一个时间范围(早期、近期、近期-中期、中期、晚期),从而可以确定血栓形成的时间,并确定确切的死亡时间。
NCT03887819。
该试验在 Cliniclatrials.gov 注册,唯一标识号为 NCT03887819。注册日期为 2019 年 3 月 23 日,为“回顾性注册”。