致死性家族性肝内胆汁淤积症(拜勒病)慢性维生素E缺乏的病理研究。

K Saito, S Matsumoto, T Yokoyama, M Okaniwa, S Kamoshita
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引用次数: 11

摘要

致死性家族性肝内胆汁淤积症(拜勒病)发展为神经肌肉综合征,与实验性维生素E缺乏症和脂蛋白血症相似,死于肝和心力衰竭。血清维生素E水平极低。尸检显示肝内胆汁淤积性肝硬化,胆管系统无闭塞性病变,脾肿大伴脾瘤样结节。其他病理病变被认为是由于慢性维生素E缺乏:1。线粒体变化,尤指肝细胞和心肌的线粒体变化。2. 心肌病。3。肌病。4。血管病变。5。系统性lipofuscinosis。6. 生殖器官和内分泌器官的病变7. 脊柱后凸和足弓。8. 全身神经轴突营养不良伴周围神经病变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pathology of chronic vitamin E deficiency in fatal familial intrahepatic cholestasis (Byler disease).

A case of fatal familial intrahepatic cholestasis (Byler disease) developed a neuromuscular syndrome similar to that in experimental vitamin E deficiency and abetalipoproteinemia, and died of hepatic and cardiac failure. Serum vitamin E level was extremely low. Autopsy revealed intrahepatic cholestatic cirrhosis without obliterative lesions in the bile duct system and marked splenomegaly with splenoma-like nodules. The other pathological lesions were considered to be due to chronic vitamin E deficiency as follows:1. Mitochondrial changes especially of the hepatocyte and cardiac muscle. 2. Cardiomyopathy. 3. Myopathy. 4. Vasculopathy. 5. Systemic lipofuscinosis. 6. Lesions of the reproductive and endocrine organs. 7. Kyphoscoliosis and pes cavus. 8. Systemic neuroaxonal dystrophy with peripheral neuropathy.

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