包涵体肌炎

1
inclusion body myositis
讨论：包涵体肌炎(inclusion body myositis,IBM)是一种起病隐袭，病程长，原因不明的特发性慢性炎症性肌病，多发生于中老年人，表现为缓慢持续进展的肢体肌...
2
amyopathic&nbsp
...炎；多发性肌炎；幼年型皮肌炎；无肌病型皮肌炎；无肌病型皮肌炎；包涵体肌炎；dermatomyositis；polymyositis；amyopathic ; dermatomyositis；amyopathic ; dermatomyositis；inclusion body myositis；DM；PM；ADM；EAM；JDM；IBM）老年人原发性肝...
3
dermatomyositis
...皮肌炎与多发性肌炎（皮肌炎；多发性肌炎；幼年型皮肌炎；无肌病型皮肌炎；无肌病型皮肌炎；包涵体肌炎；dermatomyositis；polymyositis；amyopathic dermatomyositis；amyopathic dermatomyositis；inclusion body myositis；DM；PM；ADM；...
4
DM
...包涵体肌炎；dermatomyositis；polymyositis；amyopathic dermatomyositis；amyopathic dermatomyositis；inclusion body myositis；DM；PM；ADM；EAM；JDM；IBM）联合免疫缺陷病（严重联合免疫缺陷病；伴有血小板减少及湿疹的免疫缺陷病；共济失调毛细血管扩张症；...

短语

1
目的探讨包涵体肌炎（IBM）的临床与病理特点。
Objective The study was to investigate the clinical and pathological features of inclusion body myositis(IBM).
2
目的探讨包涵体肌炎(ibm)的临床表现与病理特点。
Objective: To investigate the clinical and pathological features of inclusion body myositis (IBM).
3
近来，包涵体肌炎、皮肌炎、多发性肌炎中几种免疫细胞类型和免疫反应过程被认定。
Several immune system cell types and processes have been recently identified in muscle in inclusion body myositis dermatomyositis and polymyositis.

包涵体肌炎
是一种慢性炎症性肌病。其主要病理特点是肌浆或肌核内有管状细丝包涵体。包涵体肌炎起病隐匿，缓慢进展，首发症状约70%为下肢近端无力，也可为下肢远端、上肢或四肢均匀无力起病。肌无力可对称或不对称，随着病情进展，远端肌无力可达50%，但仅有35%其远端无力的程度达到或超过近端无力。最易受累的肌肉是肱二头肌、肱三头肌、髂腰肌、股四头肌和胫前肌，而三角肌、胸大肌、骨间肌、颈屈肌、腓肠肌及足趾屈肌受累较轻。腱反射常减低，尤以膝反射减退最为常见。

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