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Effects of human mesenchymal stem cell transplantation in the bilateral corpus striatum in a rat model of Tourette's syndrome 被引量:3
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作者 Xiumei Liu Yuwei Wang Mingji Yi 《Neural Regeneration Research》 SCIE CAS CSCD 2010年第17期1285-1290,共6页
Tourette's syndrome is treated by behavioral or pharmacological therapy.However,patients with malignant Tourette's syndrome also exhibit life-threatening symptoms,which are unresponsive to conservative treatments or... Tourette's syndrome is treated by behavioral or pharmacological therapy.However,patients with malignant Tourette's syndrome also exhibit life-threatening symptoms,which are unresponsive to conservative treatments or neurosurgical procedures,such as deep brain stimulation.In recent years,mesenchymal stem cells(MSCs)have shown therapeutic potential in many neurological diseases.Therefore,the present study proposed to use MSC transplantation as a novel therapy for Tourette's syndrome.Stereotypic behaviors in Tourette's syndrome rats decreased significantly at21 days after human MSCs transplantation into the striatum.Immunohistochemistry analyses revealed survival of transplanted human MSCs and differentiation into neurons and astrocytes in the rat brain.Results suggest that intrastriatal transplantation of human MSCs could provide therapeutic potential for Tourette's syndrome. 展开更多
关键词 tourette's syndrome sTEREOTYPY animal model mesenchymal stem cells TRANsPLANTATION neural regeneration
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Pulmonary amyloidosis and multiple myeloma mimicking lymphoma in a patient with Sjogren’s syndrome:A case report
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作者 Joa Kim Yun Sung Kim +1 位作者 Hee Jeong Lee Sang Gon Park 《World Journal of Clinical Cases》 SCIE 2022年第3期1016-1023,共8页
BACKGROUND Sjogren’s syndrome(SS),which affect salivary gland function,is an autoimmune disease.SS may involve extraglandular organs.Approximately 10 to 20 percent of SS patients have clinically significant lung dise... BACKGROUND Sjogren’s syndrome(SS),which affect salivary gland function,is an autoimmune disease.SS may involve extraglandular organs.Approximately 10 to 20 percent of SS patients have clinically significant lung disease,but presentation of pulmonary amylodosis is extremly rare.The incidence of benign monoclonal gammopathy in SS patients is high,but multiple myeloma is rare.No case involving the simultaneous occurrence of two rare diseases,pulmonary amyloidosis and multiple myeloma,in the same patient with SS has been reported so far.CASE SUMMARY A 41-year-old male patient was referred to our hematology department due to incidentally detected gastric plasmacytoma.He had been diagnosed with SS four years earlier.Multiple miliary nodules,ground glass opacity in both lung fields,and enlargement of both inguinal lymph nodes was observed on chest and abdomen computer tomography.Based on the pathological findings of lung and lymph node biopsied specimens,the patient was diagnosed with pulmonary amyloidosis and multiple myeloma.Pulmonary amyloidosis and multiple myeloma associated with SS has rarely been reported.CONCLUSION This is an extremely rare case of simultaneous pulmonary amyloidosis and multiple myeloma in the same patient with SS. 展开更多
关键词 Case report sjogren’s syndrome AMYLOIDOsIs multiple myeloma PLAsMACYTOMA
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Antibody-based immunotherapies for Parkinsonian syndromes
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作者 Lars Tonges Maria Angela Samis Zella 《Neural Regeneration Research》 SCIE CAS CSCD 2019年第11期1903-1904,共2页
What is the rationale for immunotherapies in Parkinsonian syndromes (PS)? PS are neurodegenerative diseases which are clinically characterized by a hypokinetic phenotype in combination with additional motor and non-mo... What is the rationale for immunotherapies in Parkinsonian syndromes (PS)? PS are neurodegenerative diseases which are clinically characterized by a hypokinetic phenotype in combination with additional motor and non-motor symptoms. One major pathological hallmark of all PS consists of a non-physiological detrimental accumulation of protein aggregates which appear intracellularly in neurons and glial cells but also in the extracellular space (Wong and Krainc, 2017). Depending on the pathogenic protein, PS can be divided into synucleinopathies, characterized by aggregation of the protein alpha-Synuclein (aSyn), and tauopathies, characterized by aggregation of the protein Tau (Levin et al., 2016;Poewe et al., 2017). Clinical syndromes of synucleinopathies include Parkinson’s disease (PD), multiple system atrophy (MSA) and dementia with Lewy bodies, and tauopathies include progressive supranuclear palsy (PSP) and corticobasal degeneration. 展开更多
关键词 Parkinsonian syndromes Parkinson’s disease(PD) multiple system atrophy(MsA)
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Tourette综合征伴发行为问题的初步研究 被引量:15
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作者 朱焱 苏林雁 +1 位作者 周明 赵爱玲 《中国神经精神疾病杂志》 CAS CSCD 北大核心 2004年第2期85-88,共4页
目的 探讨Tourette综合征 (TS)伴发的行为问题及与抽动严重程度的关系。方法 采用CBCL和YGTSS对 6 9例TS患儿和 6 9例对照组儿童进行评估 ,比较CBCL得分 ,并就TS的抽动严重程度与行为问题的关系进行相关和多元回归分析。结果 TS组社... 目的 探讨Tourette综合征 (TS)伴发的行为问题及与抽动严重程度的关系。方法 采用CBCL和YGTSS对 6 9例TS患儿和 6 9例对照组儿童进行评估 ,比较CBCL得分 ,并就TS的抽动严重程度与行为问题的关系进行相关和多元回归分析。结果 TS组社会能力各分量表分及总分低于对照组 (P <0 0 1) ,TS组存在广泛的行为问题 (P <0 0 1) ;抽动症状严重组的违纪、思维、外向性行为问题和行为问题总分明显高于轻度组 (P <0 0 5 ) ;抽动严重程度与患儿的学校情况和社会能力成负相关 (P <0 0 5 ) ;与社交、思维、注意、违纪、攻击性、外向性和行为问题总分成正相关 (P <0 0 1)。结论 TS患儿伴发有广泛的行为问题 。 展开更多
关键词 tourette综合征 伴发 行为问题 抽动程度 患儿
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Tourette综合征的认知功能研究 被引量:6
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作者 姚洪秀 包和华 +1 位作者 欧阳华 李国海 《中国行为医学科学》 CSCD 2005年第1期60-61,共2页
目的 探讨Tourette综合征患者认知功能障碍的特点。方法 分别对Tourette综合征患儿和正常儿童进行了韦氏儿童智力量表中的算术测验、数字广度测验、数字符号测验、图画填充测验、木块图测验;韦氏记忆量表中的逻辑记忆、逻辑记忆(延迟)... 目的 探讨Tourette综合征患者认知功能障碍的特点。方法 分别对Tourette综合征患儿和正常儿童进行了韦氏儿童智力量表中的算术测验、数字广度测验、数字符号测验、图画填充测验、木块图测验;韦氏记忆量表中的逻辑记忆、逻辑记忆(延迟)、视觉记忆、视觉记忆(延迟);数字划销测验(5个分量表)的净分和失误率;威斯康星卡片分类测验中的正确反应数、持续错误数、非持续错误数、分类数和神经系统软体征的测查。结果患儿组的以上所有认知测查结果(8.75±1.14,8.45±1.50,8.18±1.47,8.07±1.60,8.62±2.23;11.77±4.06,10.42±4.10,16.93±2.95,16.22±3.00;90.94±23.71,20.52±10.79;30.85±7.74,4.97±4.10,12.18±4.67,3.13±1.51,13.25±1.91)均较正常组(10.72±1.51,9.77±1.52,9.80±1.19,9.48±1.58,9.60±1.40;14.38±2.81,12.97±3.02,19.42±2.48,18.68±2.68;104.65±30.64,12.11±5.83;36.90±4.42,2.75±2.01,8.39±3.53,4.83±1.44,1.95±1.31)显著减退(P均<0.01)。结论Tourette综合征患儿存在注意、记忆、执行和运动协调功能方面的认知障碍。 展开更多
关键词 tourette综合征 认知功能障碍 韦氏记忆量表 儿童 逻辑记忆 视觉记忆
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重复性经颅磁刺激治疗Tourette综合征疗效及安全性研究 被引量:7
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作者 王珺 刘肖予 +3 位作者 陈倩 张烨 李尔珍 王立文 《临床和实验医学杂志》 2014年第16期1324-1326,共3页
目的探讨重复性经颅磁刺激治疗儿童Tourette综合征( TS)疗效及安全性。方法选择首都儿科研究所附属儿童医院神经内科门诊确诊的TS患儿30例,病程超过1年,正规药物治疗无效。在原药治疗基础上应用重复性经颅磁刺激( rTMS)治疗。rTM... 目的探讨重复性经颅磁刺激治疗儿童Tourette综合征( TS)疗效及安全性。方法选择首都儿科研究所附属儿童医院神经内科门诊确诊的TS患儿30例,病程超过1年,正规药物治疗无效。在原药治疗基础上应用重复性经颅磁刺激( rTMS)治疗。rTMS治疗参数:rTMS作用于辅助运动区( Cz前方3 cm),给予频率为0.5 Hz,磁场强度为50%~70%运动阈值,每序列20次脉冲,序列间隔2 s,60个序列,共1200次脉冲,一次性连续刺激。共治疗10天。rT-MS治疗前以及治疗后即刻、第4、8周内分别进行耶鲁综合抽动严重程度量表( YGTSS)评估。结果①治疗后即刻症状好转7例,显效、痊愈各3例;治疗后4周好转7例,显效7例,痊愈3例;治疗后8周好转7例,显效10例,痊愈3例,总有效率66.67%。②rTMS对发声抽动治疗的有效率显著高于运动抽动治疗的有效率( P ﹤0.001)。③所有患儿均能耐受治疗过程,无不良反应。结论应用低频的rTMS对辅助运动区进行刺激是辅助治疗TS的有效方法,本治疗方法对发声性抽动的改善情况明显好于运动性抽动。治疗过程不良反应少。 展开更多
关键词 tourette综合征 重复性经颅磁刺激 耶鲁综合抽动严重程度量表
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中药辅助托吡酯治疗Tourette综合征 被引量:2
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作者 戚小红 黄小波 田莉莉 《实用儿科临床杂志》 CAS CSCD 北大核心 2008年第15期1195-1196,1224,共3页
目的探讨托吡酯联合中药治疗对Tourette综合征患儿的疗效。方法将42例确诊为Tourette综合征的患儿随机分为研究组22例及对照组20例。对照组仅予口服托吡酯治疗,初始剂量0.5 mg/kg,1次/d,逐渐增加剂量,直到症状减轻或控制,最大量不超过5.... 目的探讨托吡酯联合中药治疗对Tourette综合征患儿的疗效。方法将42例确诊为Tourette综合征的患儿随机分为研究组22例及对照组20例。对照组仅予口服托吡酯治疗,初始剂量0.5 mg/kg,1次/d,逐渐增加剂量,直到症状减轻或控制,最大量不超过5.0 mg/(kg.d)。研究组在此基础上经中医辨证后加服中药止抽汤治疗,治疗第12周末评价疗效。治疗前后使用耶鲁抽动症整体严重度量表(YGTSS)及治疗中需处理的不良反应症状量表(TESS)评估其疗效及不良反应。采用SPSS 11.5软件进行统计学分析。结果治疗前2组YGTSS总分无统计学差异[研究组(48.20±10.42)分vs对照组(52.04±10.21)分P>0.05]。治疗第12周末,研究组YGTSS总分低于对照组[(27.88±14.24)分vs(36.53±17.45)分P<0.05],研究组减分率高于对照组[(43.12±18.42)%vs(33.49±14.38)%P<0.05]。治疗第12周末研究组TESS分值低于对照组[(2.16±2.25)vs(4.78±3.75)P<0.05]。结论托吡酯联合中药治疗能有效改善儿童Tourette综合征的抽动症状,不良反应相对较小。 展开更多
关键词 抽动-秽语综合征 托吡酯 中药 儿童
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Tourette综合征患儿血浆生长抑素测定及行为评价
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作者 徐向平 汪天柱 谷玲 《中国心理卫生杂志》 CSSCI CSCD 北大核心 1999年第6期359-360,共2页
目的 :了解生长抑素 ( SS)在本病发病中的作用及其与行为之间的关系。方法 :采用放射免疫法对 3 0例患儿进行了血浆生长抑素放射免疫活性 ( SL I)的测定及事件相关电位的检测 ,并用 Achenbach儿童行为量表进行评价。结果 :发现患儿血浆 ... 目的 :了解生长抑素 ( SS)在本病发病中的作用及其与行为之间的关系。方法 :采用放射免疫法对 3 0例患儿进行了血浆生长抑素放射免疫活性 ( SL I)的测定及事件相关电位的检测 ,并用 Achenbach儿童行为量表进行评价。结果 :发现患儿血浆 SL I明显增高 ,事件相关电位中 N1 0 0 、 P3 0 0 潜伏期显著延长。结论 :在本病发病机制中可能起一定作用 ,推测 SS是患儿异常行为的生化基础之一。 展开更多
关键词 生长抑素 行为 tourette综合征 事件相关电位
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Effects of Ningdong granule on DA,DRD2,and HVA in a rat model of Tourette's syndrome 被引量:2
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作者 吕红 林海燕 +3 位作者 赵辉 李安源 林莺 姚冰 《Journal of Traditional Chinese Medicine》 SCIE CAS CSCD 2012年第2期283-288,共6页
OBJECTIVE:Ningdong granule is a traditional Chinese medicine preparation for the treatment of Tourette's syndrome.METHODS:Sixty-four rats were randomly assigned to a control group and three experimental groups,res... OBJECTIVE:Ningdong granule is a traditional Chinese medicine preparation for the treatment of Tourette's syndrome.METHODS:Sixty-four rats were randomly assigned to a control group and three experimental groups,respectively.Rat models of Tourette's syndrome were established via intraperitoneal injection of apomorphine(Apo).The rats in the experimental groups were subsequently intragastrically injected with haloperidol at 10 mg/kg(haloperidol group),Ningdong granule at 370 mg/kg(NDG group),and normal saline(0.9%) at 10 mL/kg(Apo group),respectively.Rat behaviors were observed and recorded on a daily basis.After 12 w,all rats were sacrificed,and sera and striatal tissues were harvested.Homovanillic acid levels in sera,as well as dopamine and dopamine D2 receptor mRNA expression in the striatum,were measured to determine possible mechanisms of Ningdong granule on the dopamine system in a rat model of Tourette's syndrome.RESULTS:Following intervention,stereotype actions of the Tourette's syndrome rats were significantly inhibited in the haloperidol and NDG groups,respectively(P<0.01).Homovanillic levels were significantly greater in the haloperidol and NDG groups,respectively(P<0.05).In addition,dopamine levels were significantly less in the NDG group(P<0.01),and DRD2 mRNA expression was significantly reduced in the haloperidol and NDG groups,respectively(P<0.05).CONCLUSION:Results demonstrated that Ningdong granule effectively inhibited stereotype actions and Tourette's syndrome symptoms by promoting dopamine metabolism,reducing dopamine levels in the striatum,increasing homovanillic acid content in sera,and reducing mRNA expression of DRD2 in the striatum. 展开更多
关键词 Ningdong granule tourette's syndrome Rat models Dopamine Homovanillic acid Dopamine D2 receptor
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Observation on the Curative Effect of Acupuncture on Child Tourette's Syndrome
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作者 杜革术 朱函亭(翻译) 《Journal of Acupuncture and Tuina Science》 2007年第5期294-296,共3页
To investigate the efficacy of earth-reinforcing and wood-reducing acupuncture tbr child Tourette's syndrome. Methods: Forty-five children with Yourette's syndrome were randomly allocated, according to a random num... To investigate the efficacy of earth-reinforcing and wood-reducing acupuncture tbr child Tourette's syndrome. Methods: Forty-five children with Yourette's syndrome were randomly allocated, according to a random number table, into an acupuncture group (23 cases) and a Western medicine group (22 cases). Points Zhongwan (CV 12) and Siguan were selected in co-operation with acupuncture of other routine points in the acupuncture group. Haloperidol was orally administered for routine treatment in the Western medicine group. Results: The cure rate was 65.2% in the acupuncture group and 31.8% in the Western medicine group. There was a significant difference in cure rate between the two groups (P〈0.05). Conclusion: Earth-reinforcing and wood-reducing acupuncture has an exact curative effect on child Tourette's syndrome. 展开更多
关键词 CHILDREN tourette's syndrome AcupunctureTherapy
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Treatment of 102 Cases of Tourette's Syndrome with Acupuncture plus Herbal Medicine
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作者 马晓芃 赵粹英 +1 位作者 崔云华 朱毅 《Journal of Acupuncture and Tuina Science》 2007年第4期252-254,共3页
102 cases of Tourette's syndrome were divided into three types of the liver and kidney yin deficiency, phlegm and damp blockage and spleen and stomach deficiency. Acupuncture, auricular-plaster therapy, cupping thera... 102 cases of Tourette's syndrome were divided into three types of the liver and kidney yin deficiency, phlegm and damp blockage and spleen and stomach deficiency. Acupuncture, auricular-plaster therapy, cupping therapy and herbal medicine were combined to treat this syndrome. As a result, 30 cases were satisfactorily effective, 61 cases were improved and 11 cases were ineffective with a total effective rate of 98.2% and no side effects were noticed during treatment. 展开更多
关键词 tourette's syndrome Acupuncture-Moxibustion Therapy syndrome Differ Classification
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重症成人Still病1例报道并文献复习 被引量:1
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作者 王敏 郑瑶 杨旻 《中国急救医学》 CAS CSCD 北大核心 2018年第8期700-705,共6页
目的 探讨成人Still病(adult onset Still′s disease,AOSD)继发噬血细胞综合征(hemophagocytic syndrome,HPS)的临床资料及预后。 方法 以“adult onset Still′s disease”、“macrophage activation syndrome”、“hemophagocy... 目的 探讨成人Still病(adult onset Still′s disease,AOSD)继发噬血细胞综合征(hemophagocytic syndrome,HPS)的临床资料及预后。 方法 以“adult onset Still′s disease”、“macrophage activation syndrome”、“hemophagocytic lymphohistiocytosis” 和 “hemophagocytic syndrome”为检索词检索PubMed数据库,以“(成人斯蒂尔病 or 成人 Still′s病)、(巨噬细胞活化综合征 or 嗜血细胞综合征 or 噬血细胞综合征)”为检索词检索CNKI、WangFang Data和VIP数据库,时限为建库~2016年。 结果 患者,女,34岁,发热伴皮疹、咽痛、关节痛半个月,于2017-10-04入院。初步诊断发热待查,予以多种抗菌药物治疗后体温持续8 d未见下降,甲强龙使用48 h后体温再次上升,且出现血压下降、呼吸困难,骨穿见嗜血细胞,诊断AOSD、HPS、多脏器功能障碍综合征(MODS)。经地塞米松、环孢素(cyclosporine A, CsA)、依托泊苷(etoposide, VP16)治疗好转。检索文献54篇,其中5例因数据不全被排除,余下的49例,女39例,男10例,平均年龄(34.8±13.4)岁。HPS临床表现中发热、脾大、吞噬现象发生率高,血小板减少、铁蛋白、肝酶增高显著。HPS患者激素用量多,CsA、丙种球蛋白(IVIG)使用比例高,4例接受VP16治疗。11例死亡,5例死于MODS,3例死于中枢神经系统感染,余3例分别死于肠出血、呼吸衰竭、间质性心肌炎。 结论 HPS诊治关键在于早期诊断;早期激素联合免疫抑制剂治疗AOSD继发HPS(如出现持续血三系下降,积极应用VP16),合并MODS预后差。 展开更多
关键词 成人still病(AOsD) 嗜血细胞活化综合征(HPs) 多脏器功能障碍综合征(MODs) 依托泊苷(VP16)
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炎性脱髓鞘疾病患者S-100b和MBP的检测及其意义 被引量:4
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作者 吕志华 唐从峰 +2 位作者 汪保华 易继龙 文芳 《郧阳医学院学报》 2009年第1期29-31,35,共4页
目的:通过检测炎性脱髓鞘疾病患者脑脊液(CSF)中S-100b和碱性髓鞘蛋白(MBP)的含量及其相互关系,对炎性脱髓鞘疾病的发病机制进行探讨,并对S-100b的临床意义进行评价。方法:对43名多发性硬化患者(MS)、25名格林-巴利患者(GBS)和39名正常... 目的:通过检测炎性脱髓鞘疾病患者脑脊液(CSF)中S-100b和碱性髓鞘蛋白(MBP)的含量及其相互关系,对炎性脱髓鞘疾病的发病机制进行探讨,并对S-100b的临床意义进行评价。方法:对43名多发性硬化患者(MS)、25名格林-巴利患者(GBS)和39名正常对照者分别采用酶联免疫吸附试验检测脑脊液S-100b水平,同时应用改良的酶联免疫吸附同步法检测MBP含量以及应用改进的Thompson聚丙稀酰胺凝胶电泳法检测寡克隆IgG区带。结果:MS组和GBS组CSF中的S-100b及MBP水平均显著升高,与正常对照组比较有显著性差异(P<0.01),两者具有相关性(P<0.01);两组CSF IgG-OB阳性率(分别为83.7%、68.0%)也显著高于正常对照组(均为P<0.01)。结论:S-100b可能参与了炎性脱髓鞘疾病的发病机制,S-100b、MBP水平在一定程度上反映了脱髓鞘患者的严重程度,有助于病情预后的判断。 展开更多
关键词 s-100B蛋白 髓鞘碱性蛋白 脑脊髓液 多发性硬化 格林-巴利综合征
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Review of the evidence for the management of co-morbid Tic disorders in children and adolescents with attention deficit hyperactivity disorder 被引量:10
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作者 Michael O Ogundele Hani F Ayyash 《World Journal of Clinical Pediatrics》 2018年第1期36-42,共7页
Attention deficit hyperactivity disorder(ADHD) is the most common neurodevelopmental disorder in children and adolescents, with prevalence ranging between 5% and 12% in the developed countries. Tic disorders(TD) are c... Attention deficit hyperactivity disorder(ADHD) is the most common neurodevelopmental disorder in children and adolescents, with prevalence ranging between 5% and 12% in the developed countries. Tic disorders(TD) are common co-morbidities in paediatric ADHD patients with or without pharmacotherapy treatment. There has been conflicting evidence of the role of psychostimulants in either precipitating or exacerbating TDs in ADHD patients. We carried out a literature review relating to the management of TDs in children and adolescents with ADHD through a comprehensive search of MEDLINE, EMBASE, CINAHL and Cochrane databases. No quantitative synthesis(meta-analysis) was deemed appropriate. Metaanalysis of controlled trials does not support an association between new onset or worsening of tics and normal doses of psychostimulant use. Supratherapeutic doses of dextroamphetamine have been shown to exacerbate TD. Most tics are mild or moderate and respond to psychoeducation and behavioural management. Level A evidence support the use of alpha adrenergic agonists, including Clonidine and Guanfacine, reuptake noradrenenaline inhibitors(Atomoxetine) and stimulants(Methylphenidate and Dexamphetamines) for the treatment of Tics and comorbid ADHD. Priority should be given to the management of co-morbid Tourette's syndrome(TS) or severely disabling tics in children and adolescents with ADHD. Severe TDs may require antipsychotic treatment. Antipsychotics, especially Aripiprazole, are safe and effective treatment for TS or severe Tics, but they only moderately control the co-occurring ADHD symptomatology. Short vignettes of different common clinical scenarios are presented to help clinicians determine the most appropriate treatment to consider in each patient presenting with ADHD and co-morbid TDs. 展开更多
关键词 TICs disorders CHILDHOOD Attention DEFICIT HYPERACTIVITY disorder ADOLEsCENCE tourettes syndrome
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Diagnostic and surgical challenges of progressive neck and upper back painless masses in Madelung’s disease: A case report and review of literature 被引量:3
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作者 Ya-Jie Yan Shi-Qing Zhou +1 位作者 Chun-Qiao Li Yan Ruan 《World Journal of Clinical Cases》 SCIE 2022年第1期361-370,共10页
BACKGROUND Madelung’s disease(MD)is a chronic alcoholism-associated metabolic syndrome characterized by symmetrical subcutaneous deposition of adipose tissue in the head,neck,shoulders,back,trunk,and nerve roots of t... BACKGROUND Madelung’s disease(MD)is a chronic alcoholism-associated metabolic syndrome characterized by symmetrical subcutaneous deposition of adipose tissue in the head,neck,shoulders,back,trunk,and nerve roots of the upper and lower limbs.It is relatively rare in Asian individuals and is prone to misdiagnosis.Herein,we report a case of a patient with MD who had undergone surgical management at our hospital,and we discuss the pathogenesis,diagnosis,and treatment of MD.CASE SUMMARY We report a case of MD in a 65-year-old man of Han descent.The patient had multiple,painless progressive masses for more than five years in the neck and more than 30 years in the upper back.Because of neck mobility limitations and progressive cosmetic deformities caused by the masses,he was admitted to our hospital.He drank approximately 500 mL of liquor per day and smoked heavily for more than 30 years.Contrast-enhanced computed tomography of the neck and chest documented abundant unencapsulated,subcutaneous fatty deposits.We prepared a staged operation plan.The patient was diagnosed with MD;he was advised to abstain from alcohol and was followed up regularly.After a 3-month follow-up,no recurrence of fat accumulation was found in the surgical areas.CONCLUSION This report presents a case of surgical treatment for MD to improve clinicians'understanding of the disease. 展开更多
关键词 Madelung’s disease Benign symmetric lipomatosis Launois–Bensaude syndrome multiple symmetric lipomatosis LIPECTOMY Head and neck mass Case report
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Autologous mesenchymal stem cells applied on the pressure ulcers had produced a surprising outcome in a severe case of neuromyelitis optica 被引量:1
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作者 Adriana Octaviana Dulamea Mirela-Patricia Sirbu-Boeti +4 位作者 Coralia Bleotu Denisa Dragu Lucia Moldovan Ioana Lupescu Giancarlo Comi 《Neural Regeneration Research》 SCIE CAS CSCD 2015年第11期1841-1845,共5页
Recent studies provided evidence that mesenchymal stem cells(MSCs) have regenerative potential in cutaneous repair and profound immunomodulatory properties making them a candidate for therapy of neuroimmunologic dis... Recent studies provided evidence that mesenchymal stem cells(MSCs) have regenerative potential in cutaneous repair and profound immunomodulatory properties making them a candidate for therapy of neuroimmunologic diseases. Neuromyelitis optica(NMO) is an autoimmune, demyelinating central nervous system disorder characterized by a longitudinally extensive spinal cord lesion. A 46-year-old male diagnosed with NMO had relapses with paraplegia despite treatment and developed two stage IV pressure ulcers(PUs) on his legs. The patient consented for local application of autologous MSCs on PUs. MSCs isolated from the patient's bone marrow aspirate were multiplied in vitro during three passages and embedded in a tridimensional collagen-rich matrix which was applied on the PUs. Eight days after MSCs application the patient showed a progressive healing of PUs and improvement of disability. Two months later the patient was able to walk 20 m with bilateral assistance and one year later he started to walk without assistance. For 76 months the patient had no relapse and no adverse event was reported. The original method of local application of autologous BM-MSCs contributed to healing of PUs. For 6 years the patient was free of relapses and showed an improvement of disability. The association of cutaneous repair, sustained remission of NMO and improvement of disability might be explained by a promotion/optimization of recovery mechanisms in the central nervous system even if alternative hypothesis should be considered. Further studies are needed to assess the safety and efficacy of mesenchymal stem cells in NMO treatment. 展开更多
关键词 neuromyelitis optica Devic's syndrome mesenchymal stem cells multiple sclerosis pressure ulcers
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难治性Tourette′s综合征90例住院情况分析 被引量:2
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作者 张会会 金佩莹 +3 位作者 张久平 成鑫 徐萍 柯晓燕 《中华实用儿科临床杂志》 CAS CSCD 北大核心 2021年第19期1496-1500,共5页
目的分析难治性Tourette′s综合征(TS)患儿的诊疗过程、治疗方法及临床疗效,为综合性防治难治性TS提供依据。方法对2012年5月至2019年7月在南京医科大学附属脑科医院儿童心理卫生研究中心治疗的90例难治性TS患儿的一般情况、入院前后共... 目的分析难治性Tourette′s综合征(TS)患儿的诊疗过程、治疗方法及临床疗效,为综合性防治难治性TS提供依据。方法对2012年5月至2019年7月在南京医科大学附属脑科医院儿童心理卫生研究中心治疗的90例难治性TS患儿的一般情况、入院前后共患病的诊断、入院期间联合的非药物治疗、入院前后所使用药物种类、入院前及出院时主要抗抽动药物使用剂量及入院后有无共患病的治疗转归情况进行回顾性分析。根据耶鲁抽动症严重程度量表(YGTSS)评分评定患儿的抽动障碍严重程度,以YGTSS评分及减分率评定治疗效果,以临床疗效总评疗效指数(CGI-EI)评分作为最后的疗效评分。结果90例难治性TS患儿中,男82例,女8例;出入院时YGTSS评分比较(25.04±12.77比67.64±12.46),差异有统计学意义(t=27.55,P<0.05);所有患儿出院时有共患病诊断的比例(85.56%)较入院前(47.78%)显著升高,差异有统计学意义(χ^(2)=28.90,P<0.05);入院后联合的非药物治疗种类主要为心理健康教育(90例)、综合行为干预治疗(47例)及放松训练(19例);入院前后所使用药物种类相同,5种入院前及出院时的主要抗抽动药物使用剂量差异均无统计学意义(均P>0.05);入院后有无共患病患儿的治疗转归情况(YGTSS评分和减分率及CGI-EI评分)与入院前比较差异均无统计学意义(均P>0.05)。结论难治性TS患儿的门诊治疗与针对抽动的药物治疗并无疗效差别,而综合性干预的住院治疗可显著改善其临床症状。完善共患病的诊断治疗及联合综合性心理行为干预等非药物治疗是改善难治性TS患儿预后的关键。 展开更多
关键词 难治性tourettes综合征 儿童青少年 药物治疗 心理行为干预治疗
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速刺法治疗小儿多发性抽动症的临床效果及安全性
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作者 郑泳冰 林龄 张蕴 《中外医学研究》 2024年第24期62-65,共4页
目的:探讨小儿多发性抽动症采用速刺法治疗的临床效果以及治疗的安全性。方法:选取2020年1月—2023年5月福建中医药大学附属人民医院收治的74例多发性抽动症患儿作为研究对象,按双盲法分为对照组和试验组,每组各37例。对照组患儿采用盐... 目的:探讨小儿多发性抽动症采用速刺法治疗的临床效果以及治疗的安全性。方法:选取2020年1月—2023年5月福建中医药大学附属人民医院收治的74例多发性抽动症患儿作为研究对象,按双盲法分为对照组和试验组,每组各37例。对照组患儿采用盐酸硫必利片进行治疗,试验组患儿采用速刺法进行治疗。比较两组治疗总有效率、中医症候积分、抽动和不良反应发生情况。结果:相较于对照组,试验组治疗后精神倦怠、运动抽动、烦躁易怒等中医症候评分降幅更明显,差异有统计学意义(P<0.05);试验组治疗后总有效率高于对照组,差异有统计学意义(P<0.05)。相较于对照组,试验组治疗后发生抽动情况的减轻幅度更明显,差异有统计学意义(P<0.05);试验组不良反应发生率低于对照组,差异有统计学意义(P<0.05)。结论:速刺法在小儿多发性抽动症治疗中效果显著,可有效缓解患儿的临床症状,减少抽动情况的发生,且治疗安全性高。 展开更多
关键词 小儿多发性抽动症 速刺法 临床效果 安全性
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静安口服液为主治疗小儿多发性抽动症的临床研究 被引量:19
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作者 张骠 孔群 +4 位作者 林节 隆红艳 刘大为 司振阳 刘全胜 《南京中医药大学学报》 CAS CSCD 2008年第3期156-159,共4页
目的观察静安口服液为主治疗小儿多发性抽动症的临床疗效。方法采用随机分组的方法,以泰必利作为阳性对照组,从疾病症状、中医证候、起效率、病证疗效的相关性等方面比较2组的疗效,并做出评价。结果①2组的疾病临床症状和中医症候的综... 目的观察静安口服液为主治疗小儿多发性抽动症的临床疗效。方法采用随机分组的方法,以泰必利作为阳性对照组,从疾病症状、中医证候、起效率、病证疗效的相关性等方面比较2组的疗效,并做出评价。结果①2组的疾病临床症状和中医症候的综合疗效、愈显率、有效率、起效率均有显著差异(P<0.01)。②治疗组经治4周后病证疗效未见同步趋向性,经治12周后却显示出良的相关性。③治疗组起效较快。结论静安口服液是治疗肾虚肝旺、痰盛风动型小儿多发性抽动症的有效制剂。 展开更多
关键词 静安口服液 多发性抽动症 临床研究
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头皮针治疗多发性抽动症临床观察 被引量:29
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作者 单永华 姚维菊 《中国针灸》 CAS CSCD 北大核心 2001年第6期331-332,共2页
目的 :观察头皮针对多发性抽动症的临床效果。方法 :将 10 5例患者随机分为头皮针组、头针加中药组、西药组治疗并对照观察。结果 :头皮针组及头针加中药组与西药组相比差异有显著性意义 (P <0 0 5)。结论 :头皮针及头针加中药均对... 目的 :观察头皮针对多发性抽动症的临床效果。方法 :将 10 5例患者随机分为头皮针组、头针加中药组、西药组治疗并对照观察。结果 :头皮针组及头针加中药组与西药组相比差异有显著性意义 (P <0 0 5)。结论 :头皮针及头针加中药均对多发性抽动症有良好效果 ,疗效明显优于西药。 展开更多
关键词 多动秽语综合征 针灸疗法 头皮针 治疗
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