本文選題：包涵體肌炎　切入點(diǎn)：鑲邊空泡　出處：《中國神經(jīng)精神疾病雜志》2017年02期

【摘要】：正包涵體肌炎(inclusion body myositis,IBM)是一組成年發(fā)病的慢性、進(jìn)行性加重的骨骼肌炎性疾病,主要臨床表現(xiàn)為緩慢進(jìn)行性肌無力和肌萎縮,典型的病理改變是大量邊緣空泡(rimmed vacuole,RV),單核細(xì)胞浸潤非壞死組織,電鏡下可以觀察到包涵體~([1])。IBM罕見合并腫瘤報(bào)道,現(xiàn)報(bào)道1例我院發(fā)現(xiàn)的結(jié)腸癌合并的散發(fā)性包涵體肌炎
[Abstract]:Positive inclusion body myositis (IBM) is a group of chronic, progressive skeletal muscle inflammatory diseases that develop in adults. The main clinical manifestations are slow progressive myasthenia and muscular atrophy. The typical pathological changes are a large number of marginal vacuoles, a large number of marginal vacuoles, the infiltration of monocytes into non-necrotic tissues, and the presence of inclusion bodies under electron microscope ([1] .IBM rare complicated with tumor.) A case of sporadic inclusion body myositis with colon cancer found in our hospital is reported.
【作者單位】： 吉林大學(xué)第一醫(yī)院神經(jīng)內(nèi)科神經(jīng)科學(xué)中心;
【分類號】：R735.35;R685.2

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1 王曄;包涵體肌炎研究進(jìn)展[J];國外醫(yī)學(xué).神經(jīng)病學(xué)神經(jīng)外科學(xué)分冊;1999年01期

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