在青少年皮肌炎中,甲襞毛细血管脱落先于肠肺病和微穿孔的出现

Andi Wang , Amer Khojah , Gabrielle Morgan , Lauren M. Pachman
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引用次数: 4

摘要

青少年皮肌炎(JDM)是一种罕见的自身免疫性疾病,其特征是皮肤和肌肉血管系统的慢性炎症。甲襞毛细血管末端行环(ERL)的缺失与疾病活动有关。我们现在首次报道了两名JDM患者的严重胃肠道(GI)事件,这两名患者的ERL都急剧下降,这有助于将JDM视为肌病血管炎组的一员。这些病例表明,在选定的JDM儿童中,ERL密度的突然显著损失似乎是严重系统性微血管病(包括胃肠道血管病)的一个新的可靠指标。
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Nailfold capillary dropout precedes the presentation of pneumatosis intestinalis and micro-perforation in juvenile dermatomyositis

Juvenile dermatomyositis (JDM) is a rare autoimmune disease characterized by chronic inflammation of the skin and muscle vasculature. Loss of nailfold capillary end row loops (ERL) is associated with disease activity. We now present the first report of serious gastrointestinal (GI) events in two JDM patients, both preceded by a precipitous drop in their ERL, which contributes to the consideration of JDM as a member of the vasculitis group of myopathies. These cases demonstrate that the sudden and significant loss of ERL density appears to be a novel and reliable indicator of severe systemic microangiopathy, including gastrointestinal vasculopathy, in selected children with JDM.

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