Clinical Analysis of Intravenous Cyclophosphamide Therapy for Steroid-Resistant Polymyositis/Dermato

来源 :The 12th Annual Asian and Oceanian Myology Center (AOMC)Scie | 被引量 : 0次 | 上传用户:phpzen
下载到本地 , 更方便阅读
声明 : 本文档内容版权归属内容提供方 , 如果您对本文有版权争议 , 可与客服联系进行内容授权或下架
论文部分内容阅读
Purpose To acquire the tolerance, efficacy and safety indications of oral glucocorticoid and pulse intravenous cyclophosphamide (CTX) therapy for polymyositis (PM) or dermatomyositis (DM)patients, who are resistant ortolerant to glucocorticoid.Methods 20 patients were clinically and pathologically diagnosed as PM or DM according to the principle made by Bohan and Peter in 1975.Most of them were followed up for over 12 months with clinical manifestations, serum creatine kinase (CK) levels, electromyography (EMG) characteristics and muscle biopsy findings.All the adverse effects conforms to NCI-CTCAE 3.0.
其他文献
Background Mitochondrial thymidine kinase 2(TK2) is one of human deoxynucleoside kinases catalyzing the primary phosphorylation of thymidine and deoxycytidine to the corresponding nucleoside monophosp
会议
Objective To investigate the effects of collagen contents, peroxisome proliferator-activated receptor alpha (PPARalpha) and retinoid X receptor alpha (RXRct) expressions in a rat prolonged alcoholic m
会议
Case A 40-year-old man was admitted to our hospital complaining of weakness and atrophy in his both hands.He experienced weakness abruptly in bilateral hands, resulting in decreased grip strength and
会议
Objective SBMA is traditionally considered as a motoneuron disease.But elevation of serum creatine kinase (CK) has been reported in SBMA patients in different cohorts.Since many neuromuscular disorder
会议
Background Miller Fisher syndrome (MFS) is a variant of Guillain-Barre syndrome with a good natural outcome.However, some patients do not recover completely and have residual deficits.The purpose of t
会议
Objective To determine whether the addition of dexmedetomidine to caudal with ropivacaine promote the analgesia against acute visceral pain in children with Hirschsprungs disease undergoing Soave oper
会议
Objective To investigate the SOD1 gene mutations in patients with sporadic ALS.Methods In this study, we screened for the SOD1 mutations in 51 patients who had been clinically diagnosed with sporadic
会议
Objective:Duchenne muscular dystrophy (DMD) is a severe progressive muscular disorder caused by mutations in thedystrophingene.Stem cells transplanted into lethally irradiatedmdxmice and double knock
会议
Objective and Method to report a case of classical juvenile neuronal ceroid lipofuscinoses(JNCL,also known as Batten disease).Results A 19-year-old girl developed progressive visual impairment at the
会议
Objectiv To assess the value of bulbocavernosus reflex (BCR) and pudendal nerve somatosenso ry evoked potential (SSEP) in the patients withdiabeticneurogenic bladder.Methylcobalamininterv entiontreatm
会议