Suppr超能文献

[一例与慢性活动性肝炎相关的多发性肌炎]

[A case of polymyositis associated with chronic active hepatitis].

作者信息

Fujitake J, Saida K, Nishitani H, Suginoshita T, Osaki S

机构信息

Department of Neurology, Utano National Hospital, Kyoto.

出版信息

Rinsho Shinkeigaku. 1990 Jan;30(1):55-61.

PMID:2184964
Abstract

A case of polymyositis associated with chronic active hepatitis was reported. A 53-year-old man, who had no previous history of blood transfusion nor hepatitis, noticed proximal dominant muscle weakness on January 29, 1985. He was admitted to Kyoto National Hospital on February 7, and laboratory studies disclosed the elevation of serum enzyme levels; creatine kinase (CK) 9845 IU/L (normal 54-263), glutamate oxaloacetate transaminase (GOT) 834 IU/L (9-31), glutamate pyruvate transaminase (GPT) 491 IU/L (4-34), lactate dehydrogenase (LDH) 2135 IU/L (248-464). Also serum gamma globulin was high (1.8 g/dl) and LE-like cell was found. The diagnosis of polymyositis was made and prednisolone therapy (60 mg/day) was started on February 23. The elevated serum enzymes decreased gradually, but severe muscle weakness persisted for about one month. On April 3, he was admitted to our hospital. Physical examination revealed moderate proximal dominant muscle weakness without skin eruption, jaundice or hepatosplenomegaly. The serum enzymes were still high; CK 1826, GOT 173, GPT 232 (GOT less than GPT), LDH 1548. However, alkaline phosphatase (ALP) and bilirubin were normal. Hepatitis B surface antigen (HBsAg) was not detected. Antinuclear antibody was positive. The electromyogram study showed myopathic change, and the muscle biopsy demonstrated myopathic change and cell infiltration, compatible with polymyositis. These results suggested liver dysfunction associated with polymyositis. Prednisolone therapy was continued and muscle weakness decreased. From December, 1985, serum enzymes (CK, GOT, GPT, LDH) elevated again and muscle weakness also slightly increased. Anti-smooth muscle antibody was positive. It was suggested that both polymyositis and liver dysfunction deteriorated.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

报告了1例与慢性活动性肝炎相关的多发性肌炎病例。一名53岁男性,既往无输血史及肝炎病史,于1985年1月29日出现以近端为主的肌肉无力。2月7日入住京都国立医院,实验室检查显示血清酶水平升高;肌酸激酶(CK)9845 IU/L(正常54 - 263),谷草转氨酶(GOT)834 IU/L(9 - 31),谷丙转氨酶(GPT)491 IU/L(4 - 34),乳酸脱氢酶(LDH)2135 IU/L(248 - 464)。血清γ球蛋白也升高(1.8 g/dl),并发现狼疮细胞样细胞。诊断为多发性肌炎,于2月23日开始泼尼松龙治疗(60 mg/天)。血清酶升高逐渐下降,但严重肌肉无力持续约1个月。4月3日,他入住我院。体格检查发现中度近端为主的肌肉无力,无皮疹、黄疸或肝脾肿大。血清酶仍高;CK 1826,GOT 173,GPT 232(GOT低于GPT),LDH 1548。然而,碱性磷酸酶(ALP)和胆红素正常。未检测到乙肝表面抗原(HBsAg)。抗核抗体阳性。肌电图检查显示肌病改变,肌肉活检显示肌病改变和细胞浸润,符合多发性肌炎。这些结果提示存在与多发性肌炎相关的肝功能障碍。继续泼尼松龙治疗,肌肉无力减轻。1985年12月起,血清酶(CK、GOT、GPT、LDH)再次升高,肌肉无力也略有增加。抗平滑肌抗体阳性。提示多发性肌炎和肝功能障碍均恶化。(摘要截取自250字)

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验