Histological dating of subdural hematoma in infants.


Journal

International journal of legal medicine
ISSN: 1437-1596
Titre abrégé: Int J Legal Med
Pays: Germany
ID NLM: 9101456

Informations de publication

Date de publication:
Mar 2019
Historique:
received: 21 09 2018
accepted: 05 12 2018
pubmed: 17 12 2018
medline: 4 4 2019
entrez: 17 12 2018
Statut: ppublish

Résumé

After infant deaths due to non-accidental head injury (NAHI) with subdural hematoma (SDH), the magistrates ask experts to date the traumatic event. To do so, the expert only has tools based on adult series of NAHI. We aimed to develop an SDH dating system applicable to infants aged under 3 years. We studied a retrospective multicenter collection of 235 infants who died between the ages of 0 and 36 months, diagnosed with SDH by forensic pathological examination and with known posttraumatic interval (PTI). Two pathologists assessed blindly and independently 12 histomorphological criteria relating to the clot and 14 relating to the dura mater in 73 victims (31 girls, 42 boys) whose median age was 3.8 months. Histopathological changes were significantly correlated with PTI for the appearance of red blood cells (RBCs) and the presence or absence of siderophages, and regarding the dura mater, the quantity of lymphocytes, macrophages, and siderophages; presence or absence of hematoidin deposits; collagen and fibroblast formation; neomembrane thickness; and presence or absence of neovascularization. Dating systems for SDH in adults are not applicable to infants. Notably, neomembrane of organized connective tissue is formed earlier in infants than in adults. Our dating system improves the precision and reliability of forensic pathological expert examination of NAHI, particularly for age estimation of SDH in infants. However, the expert can only define a time interval. Histopathology is indispensable to detect repetitive trauma.

Sections du résumé

BACKGROUND BACKGROUND
After infant deaths due to non-accidental head injury (NAHI) with subdural hematoma (SDH), the magistrates ask experts to date the traumatic event. To do so, the expert only has tools based on adult series of NAHI. We aimed to develop an SDH dating system applicable to infants aged under 3 years.
METHODS AND RESULTS RESULTS
We studied a retrospective multicenter collection of 235 infants who died between the ages of 0 and 36 months, diagnosed with SDH by forensic pathological examination and with known posttraumatic interval (PTI). Two pathologists assessed blindly and independently 12 histomorphological criteria relating to the clot and 14 relating to the dura mater in 73 victims (31 girls, 42 boys) whose median age was 3.8 months. Histopathological changes were significantly correlated with PTI for the appearance of red blood cells (RBCs) and the presence or absence of siderophages, and regarding the dura mater, the quantity of lymphocytes, macrophages, and siderophages; presence or absence of hematoidin deposits; collagen and fibroblast formation; neomembrane thickness; and presence or absence of neovascularization. Dating systems for SDH in adults are not applicable to infants. Notably, neomembrane of organized connective tissue is formed earlier in infants than in adults.
CONCLUSION CONCLUSIONS
Our dating system improves the precision and reliability of forensic pathological expert examination of NAHI, particularly for age estimation of SDH in infants. However, the expert can only define a time interval. Histopathology is indispensable to detect repetitive trauma.

Identifiants

pubmed: 30554266
doi: 10.1007/s00414-018-1980-8
pii: 10.1007/s00414-018-1980-8
doi:

Substances chimiques

Reticulin 0
Fibrin 9001-31-4
Collagen 9007-34-5
Bilirubin RFM9X3LJ49

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

539-546

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Auteurs

Clémence Delteil (C)

Forensic Department, APHM, La Timone, 264 rue St Pierre, 13385, Marseille, Cedex 05, France. clemence.delteil@ap-hm.fr.
Aix-Marseille University, CNRS, EFS, ADES, Marseille, France. clemence.delteil@ap-hm.fr.

Sarah Humez (S)

Pathology Department, University Hospital of Lille, 2 Avenue Oscar Lambret, 59000, Lille, France.

Mohamed Boucekine (M)

Public Health Research Unit EA 3279, Aix-Marseille University, 3005, Marseille, France.

Anne Jouvet (A)

Pathology Department, University Hospital of Lyon-Est, 59 Boulevard Pinel, 69677, Bron, France.

Valery Hedouin (V)

Forensic Department and Social Medicine, Faculty of Medicine of Lille, 59045, Lille Cedex, France.

Laurent Fanton (L)

Forensic Department, 12 Avenue Rockefeller, 69437, Lyon 03, France.

Georges Leonetti (G)

Forensic Department, APHM, La Timone, 264 rue St Pierre, 13385, Marseille, Cedex 05, France.
Aix-Marseille University, CNRS, EFS, ADES, Marseille, France.

Lucile Tuchtan (L)

Forensic Department, APHM, La Timone, 264 rue St Pierre, 13385, Marseille, Cedex 05, France.
Aix-Marseille University, CNRS, EFS, ADES, Marseille, France.

Marie-Dominique Piercecchi (MD)

Forensic Department, APHM, La Timone, 264 rue St Pierre, 13385, Marseille, Cedex 05, France.
Aix-Marseille University, CNRS, EFS, ADES, Marseille, France.

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Classifications MeSH