Jimenez C, Rowe P C, Keene D
Department of Pediatrics, University of Ottawa School of Medicine, Ontario, Canada.
J Child Neurol. 1994 Jul;9(3):297-300. doi: 10.1177/088307389400900315.
Cerebral vasculitis and clinically important myocardial inflammation are rare in juvenile dermatomyositis. We report a previously healthy 6-year-old girl with dermatomyositis who died after a fulminating clinical deterioration. Postmortem examination of the heart revealed characteristic endothelial tubuloreticular aggregates and evidence of capillary necrosis and secondary thrombosis, associated with extensive hemorrhagic myocardial necrosis. Endothelial necrosis was also evident in the cerebrocortical capillaries.
脑脊髓炎和具有临床重要意义的心肌炎症在青少年皮肌炎中较为罕见。我们报告了一名先前健康的6岁皮肌炎女孩,她在病情急剧恶化后死亡。心脏的尸检显示有特征性的内皮管网状聚集物,以及毛细血管坏死和继发性血栓形成的证据,伴有广泛的出血性心肌坏死。脑皮质毛细血管中也明显存在内皮坏死。