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首页> 外文期刊>Ultrastructural pathology >Macrophagic myofasciitis in childhood: the role of scanning electron microscopy/energy-dispersive spectroscopy for diagnosis.
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Macrophagic myofasciitis in childhood: the role of scanning electron microscopy/energy-dispersive spectroscopy for diagnosis.

机译:儿童期巨噬性肌筋膜炎:扫描电子显微镜/能量分散光谱法在诊断中的作用。

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摘要

Macrophagic myofasciitis (MMF) is an inflammatory myopathy related to aluminum-containing vaccines. Described in 1998, most cases were reported in adults, with only 22 cases being reported in children. Three children aged between 13 months and 3(1/2) years were investigated in our institution for neuromuscular symptoms. They underwent thorough clinical, familial, and laboratory investigations, electroneuromyography, muscle biopsy with transmission electron microscopy, scanning electron microscopy/energy dispersive spectroscopy (SEM/EDS), and, in one case, brain magnetic resonance imaging. They had received regular immunizations. Two patients were hypotonic and one presented with myotonia. Muscle biopsy of all patients presented macrophagic infiltrates with intracytoplasmic aluminum content as revealed by SEM/EDS analysis. Their diverse clinical picture does not support a direct relationship between local morphologic findings and systemic symptoms. The atypical clinical presentation of these children may not result from the superposition of MMF upon a background systemic neuromyopathy, suggesting instead that they are two coincident and independent conditions. Although the finding of macrophage infiltrates in muscle tissue is not new, the identification of aluminum content is recent. The use of tissue sections for aluminum detection and mapping by SEM/EDS is conclusive for, diagnosis; it has not been reported previously in a pathology journal, to the authors' knowledge.
机译:巨噬性肌筋膜炎(MMF)是一种与含铝疫苗有关的炎性肌病。描述于1998年,大多数病例报告于成人,仅22例报告于儿童。我们机构对三名年龄在13个月至3(1/2)岁之间的儿童进行了神经肌肉症状调查。他们进行了彻底的临床,家族和实验室研究,电子肌电图检查,透射电镜进行肌肉活检,扫描电子显微镜/能量色散光谱法(SEM / EDS),并在一种情况下进行了脑磁共振成像。他们已经接受了定期免疫。 2例低渗患者,1例出现肌强直。通过SEM / EDS分析显示,所有患者的肌肉活检均表现为巨噬细胞浸润,胞浆内铝含量较高。他们多样化的临床表现并不支持局部形态学发现与全身症状之间的直接关系。这些儿童的非典型临床表现可能不是由于背景系统性神经肌病引起的MMF叠加所致,而是表明他们是两个同时发生且独立的疾病。尽管在肌肉组织中发现巨噬细胞浸润并不新鲜,但是铝含量的鉴定是最近的。组织切片用于通过SEM / EDS进行铝检测和制图对于诊断具有决定性意义。据作者所知,以前没有在病理学杂志上报道过。

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