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Acute or chronic pulmonary emphysema? Or both?-A contribution to the diagnosis of death due to violent asphyxiation in cases with pre-existing chronic emphysema.
Gava, Giuseppe; Eickhoff, Simon B; Filler, Timm J; Mayer, Felix; Mahlke, Nina S; Ritz-Timme, Stefanie.
Afiliación
  • Gava G; Institute of Legal Medicine, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
  • Eickhoff SB; Institute of Systems Neuroscience, Medical Faculty, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
  • Filler TJ; Institute of Neuroscience and Medicine, Brain & Behaviour (INM-7), Research Centre Jülich, Jülich, Germany.
  • Mayer F; Institute for Anatomy I, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
  • Mahlke NS; Institute of Legal Medicine, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
  • Ritz-Timme S; Institute of Legal Medicine, Heinrich Heine University Düsseldorf, Düsseldorf, Germany. ninasophia.mahlke@med.uni-duesseldorf.de.
Int J Legal Med ; 136(1): 133-147, 2022 Jan.
Article en En | MEDLINE | ID: mdl-34181078
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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfisema Pulmonar / Enfisema Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Int J Legal Med Asunto de la revista: JURISPRUDENCIA Año: 2022 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfisema Pulmonar / Enfisema Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Int J Legal Med Asunto de la revista: JURISPRUDENCIA Año: 2022 Tipo del documento: Article País de afiliación: Alemania