Shen Guang-li, Lv He, Bi Hong-yan, Zhang Wei, Yao Sheng, Yuan Yun
Department of Neurology, Peking University First Hospital, Beijing, China.
Neuropathology. 2007 Aug;27(4):309-13. doi: 10.1111/j.1440-1789.2007.00779.x.
Dermatomyositis (DM) is a systemic microvasculitis predominantly involving the capillaries. We investigated the expression of thrombomodulin (TM) and endothelial cell nitric oxide synthase (eNOS) in microvessels of DM patients. Twelve patients with acute or subacute onset of proximal muscle weakness and erythematous rash over their faces and shoulders were included in this study. Serum creatine phosphokinase was elevated in almost all patients. Electromyograph showed a myopathic pattern in all patients. Muscle biopsies were performed in all patients and 10 non-DM controls and studied with histological, enzyme histochemical and immunohistochemical staining. von Willebrand factor, TM and eNOS antibodies were used as the primary antibodies. Perifascicular degeneration and inflammatory cell infiltration in the perimysium were noted in almost all patients. Non-special esterase staining was markedly positive in capillary and microvascular endothelium. Marked reduction in TM and eNOS staining was noted in DM patients in perimysium microvessels and perifascicular area capillaries. Vascular lesions in DM were not only limited to capillaries. The low expression of TM and eNOS in microvessels suggests the anticoagulation and vasodilation functions of vascular endothelium is reduced. DM is an inflammatory vascular endothelial disease.
皮肌炎(DM)是一种主要累及毛细血管的系统性微血管炎。我们研究了皮肌炎患者微血管中血栓调节蛋白(TM)和内皮细胞一氧化氮合酶(eNOS)的表达。本研究纳入了12例急性或亚急性起病的近端肌无力且面部和肩部出现红斑皮疹的患者。几乎所有患者的血清肌酸磷酸激酶均升高。所有患者的肌电图均显示肌病模式。对所有患者以及10名非皮肌炎对照者进行了肌肉活检,并采用组织学、酶组织化学和免疫组织化学染色进行研究。使用血管性血友病因子、TM和eNOS抗体作为一抗。几乎所有患者均可见束周变性和肌束膜炎症细胞浸润。非特异性酯酶染色在毛细血管和微血管内皮中呈明显阳性。在皮肌炎患者的肌束膜微血管和束周区域毛细血管中,TM和eNOS染色明显减少。皮肌炎中的血管病变不仅局限于毛细血管。微血管中TM和eNOS的低表达提示血管内皮的抗凝和血管舒张功能降低。皮肌炎是一种炎症性血管内皮疾病。