Qamar Syeda Hania, Khara Maliha, Herath Jayantha C
Department of Laboratory Medicine and Pathobiology, Faculty of Medicine, University of Toronto, Toronto, ON, Canada.
Tanz Centre for Research in Neurodegenerative Diseases, University of Toronto, Toronto, ON, Canada.
Forensic Sci Med Pathol. 2025 Jan 14. doi: 10.1007/s12024-025-00942-8.
Spontaneous pneumothorax (SP) is a condition defined by abnormal gas accumulation in the chest cavity. Mutations of the collagen type III alpha 1 chain, COL3A1 gene, are primarily linked to vascular Ehlers-Danlos syndrome (vEDS); however, they can also contribute to structural changes in the tissue, like bullae of the lungs. In this case report, we present a young, thinly built boy who died due to a spontaneous pneumothorax. Post-mortem genetic testing revealed a novel COL3A1 mutation, likely contributing to the pathogenic events underlying death due to spontaneous pneumothorax. We recommend implementing genetic testing of correlative or causative genes in the context of SP.
自发性气胸(SP)是一种由胸腔内异常气体积聚所定义的病症。III型胶原蛋白α1链(COL3A1基因)的突变主要与血管型埃勒斯-当洛综合征(vEDS)相关;然而,它们也可能导致组织的结构变化,如肺大疱。在本病例报告中,我们呈现了一名身材消瘦的年轻男孩,他因自发性气胸死亡。尸检基因检测发现了一种新的COL3A1突变,可能是导致其因自发性气胸死亡的致病事件的原因。我们建议在自发性气胸的背景下对相关或致病基因进行基因检测。