| Literature DB >> 31995186 |
Declan McGuone1, Dominique Leitner2, Christopher William3,4, Arline Faustin3, Nalin Leelatian1, Ross Reichard5, Timothy M Shepherd6, Matija Snuderl4, Laura Crandall2,7, Thomas Wisniewski3,8, Orrin Devinsky2.
Abstract
Sudden unexplained death in childhood (SUDC) affects children >1-year-old whose cause of death remains unexplained following comprehensive case investigation and is often associated with hippocampal abnormalities. We prospectively performed systematic neuropathologic investigation in 20 SUDC cases, including (i) autopsy data and comprehensive ancillary testing, including molecular studies, (ii) ex vivo 3T MRI and extensive histologic brain samples, and (iii) blinded neuropathology review by 2 board-certified neuropathologists. There were 12 girls and 8 boys; median age at death was 33.3 months. Twelve had a history of febrile seizures, 85% died during apparent sleep and 80% in prone position. Molecular testing possibly explained 3 deaths and identified genetic mutations in TNNI3, RYR2, and multiple chromosomal aberrations. Hippocampal abnormalities most often affected the dentate gyrus (altered thickness, irregular configuration, and focal lack of granule cells), and had highest concordance between reviewers. Findings were identified with similar frequencies in cases with and without molecular findings. Number of seizures did not correlate with hippocampal findings. Hippocampal alterations were the most common finding on histological review but were also found in possibly explained deaths. The significance and specificity of hippocampal findings is unclear as they may result from seizures, contribute to seizure pathogenesis, or be an unrelated phenomenon.Entities:
Keywords: Dentate gyrus; Hippocampal abnormalities; Neuropathology; Pediatric; Seizure; Sudden unexplained death in childhood
Mesh:
Year: 2020 PMID: 31995186 PMCID: PMC7036658 DOI: 10.1093/jnen/nlz136
Source DB: PubMed Journal: J Neuropathol Exp Neurol ISSN: 0022-3069 Impact factor: 3.685