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特发性婴儿动脉钙化:儿童期意外猝死的罕见原因。

Idiopathic infantile arterial calcification: a rare cause of sudden unexpected death in childhood.

作者信息

Guimarães Susana, Lopes José Manuel, Oliveira José Bessa, Santos Agostinho

机构信息

Institute of Molecular Pathology and Immunology, University of Porto (IPATIMUP), Porto, Portugal.

出版信息

Patholog Res Int. 2010 Jul 27;2010:185314. doi: 10.4061/2010/185314.

Abstract

Unexpected child death investigation is a difficult area of forensic practice in view of the wide range of possible genetic, congenital, and acquired natural and nonnatural causes. Idiopathic infantile arterial calcification (IIAC) is a rare autosomic recessive disease usually diagnosed postmortem. Inactivating mutations of the ENPP1 gene were described in 80% of the cases with IIAC. We report a case of a 5-year-old girl submitted to a forensic autopsy due to sudden death and possible medical negligence/parents child abuse. Major alterations found (intimal proliferation and deposition of calcium hydroxyapatite around the internal elastic lamina and media of arteries; acute myocardial infarct, stenotic and calcified coronary artery; perivascular and interstitial myocardial fibrosis; and subendocardial fibroelastosis) were diagnostic of IIAC. We reviewed IIAC cases published in the English literature and highlight the importance of adequate autopsy evaluation in cases of sudden child death.

摘要

鉴于可能的遗传、先天性以及后天性自然和非自然病因范围广泛,意外儿童死亡调查是法医实践中的一个难题领域。特发性婴儿动脉钙化(IIAC)是一种罕见的常染色体隐性疾病,通常在死后诊断。在80%的IIAC病例中发现了ENPP1基因的失活突变。我们报告一例5岁女孩因猝死以及可能的医疗疏忽/父母虐待儿童而接受法医尸检的病例。发现的主要病变(内膜增生以及动脉内弹性膜和中膜周围羟基磷灰石钙的沉积;急性心肌梗死、狭窄和钙化的冠状动脉;血管周围和间质心肌纤维化;以及心内膜下纤维弹性组织增生)可诊断为IIAC。我们回顾了英文文献中发表的IIAC病例,并强调了在儿童猝死病例中进行充分尸检评估的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5013/2991079/507a55cd0206/PRI2010-185314.001.jpg

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