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Paraneoplastic syndromes associated with lung cancer 被引量:12
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作者 Nobuhiro Kanaji Naoki Watanabe +5 位作者 Nobuyuki Kita Shuji Bandoh Akira Tadokoro Tomoya Ishii Hiroaki Dobashi Takuya Matsunaga 《World Journal of Clinical Oncology》 CAS 2014年第3期197-223,共27页
Paraneoplastic syndromes are signs or symptoms that occur as a result of organ or tissue damage at locations remote from the site of the primary tumor or metastases. Paraneoplastic syndromes associated with lung cance... Paraneoplastic syndromes are signs or symptoms that occur as a result of organ or tissue damage at locations remote from the site of the primary tumor or metastases. Paraneoplastic syndromes associated with lung cancer can impair various organ functions and include neurologic, endocrine, dermatologic, rheumatologic, hematologic, and ophthalmological syndromes, as well as glomerulopathy and coagulopathy(Trousseau's syndrome). The histological type of lung cancer is generally dependent on the associated syndrome, the two most common of which are humoral hypercalcemia of malignancy in squamous cell carcinoma and the syndrome of inappropriate antidiuretic hormone secretion in small cell lung cancer. The symptoms often precede the diagnosis of the associated lung cancer, especially when the symptoms are neurologic or dermatologic. The proposed mechanisms of paraneoplastic processes include the aberrant release of humoral mediators, such as hormones and hormone-like peptides, cyto-kines, and antibodies. Treating the underlying cancer is generally the most effective therapy for paraneoplastic syndromes, and treatment soon after symptom onset appears to offer the best potential for symptom improvement. In this article, we review the diagnosis, potential mechanisms, and treatments of a wide variety of paraneoplastic syndromes associated with lung cancer. 展开更多
关键词 paraneoplastic SYNDROME Small CELL LUNG CANCER Non-small CELL LUNG CANCER Symptom Diagnosis Treatment Endocrine Neurologic HEMATOLOGIC Trousseau’s SYNDROME
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Immunohistochemical study on gastroenteric nervous system in trisomy 16 mice:an animal model of Down syndrome 被引量:1
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作者 LC Busch W Kuhnel 《World Journal of Gastroenterology》 SCIE CAS CSCD 2000年第6期793-799,共7页
AIM To study the development of gastroentericnervous system in trisomy 16 mouse embryos.The gastroenteric nervous system in trisomy 16mice and their normal littermates,serving ascontrols from embryonic days 13 to 18(E... AIM To study the development of gastroentericnervous system in trisomy 16 mouse embryos.The gastroenteric nervous system in trisomy 16mice and their normal littermates,serving ascontrols from embryonic days 13 to 18(ED13-18)was identified by using primary antibody againstprotein gene product(PGP)9.5.METHODS Trisomy 16 mouse breeding andtrisomy 16 mouse embryos were identified fromtheir normal littermates by chromosomeexamination;PGP 9.5 immunohistochemicalstainning.CONCLUSION Trisomy 16 mice, as an animal model for Down syndrome, has abnormality not only in several systems and organs but also in gastroenteric innervation. This report describes for the first time that the development of the gastroenteric nervous system was not only delayed but also pathological. 展开更多
关键词 GASTROINTESTINAL system down syndrome IMMUNOHISTOCHEMISTRY TRISOMY 16 mouse nervous system protein gene product 9.5
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Two uncommon manifestations of leptospirosis:Sweet's syndrome and central nervous system vasculitis 被引量:1
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作者 Peter George 《Asian Pacific Journal of Tropical Medicine》 SCIE CAS 2011年第1期83-84,共2页
To leptospirosis is the commonest spirocheatal infection in the tropical and temperate countries of Indian sub-continent and Africa and the most common zoonosis worldwide.The protean manifestation of this infectious d... To leptospirosis is the commonest spirocheatal infection in the tropical and temperate countries of Indian sub-continent and Africa and the most common zoonosis worldwide.The protean manifestation of this infectious disease is a challenge for practising clinicians across the world. In poor developing countries,at most clinical suspicion it is essential in the diagnosis of this disease.In this report,we are able to document two uncommon manifestations of leptospirosis, namely Sweet’s syndrome and central nervous system vasculitis. 展开更多
关键词 LEPTOSPIROSIS Sweet’s syndrome Central nervous system VASCULITIS
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Paraneoplastic syndromes in cholangiocarcinoma
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作者 Saad Ur Rahman Muhammad Khawar Sana +2 位作者 Zabreen Tahir Aamir Ali Pir Ahmad Shah 《World Journal of Hepatology》 2020年第11期897-907,共11页
Paraneoplastic syndromes are the symptoms or signs which result from damage to tissues that are distant from the site of malignancy,due to complex interactions between the body’s immune system and malignant neoplasm.... Paraneoplastic syndromes are the symptoms or signs which result from damage to tissues that are distant from the site of malignancy,due to complex interactions between the body’s immune system and malignant neoplasm.Cholangiocarcinoma(CCA)is an aggressive epithelial malignancy of hepatobiliary tree and it is found to be associated with various paraneoplastic syndromes.These syndromes can present as dermatological,neurological,renal,hematological,or multi-systemic manifestations.Clinical suspicion and timely recognition of these syndromes can lead to early diagnosis of covert malignancies like CCA.The management plan remains the removal of the underlying cause which in this case is CCA. 展开更多
关键词 CHOLANGIOCARCINOMA paraneoplastic syndrome MALIGNANCY Immune system Biliary tree MULTI-ORGAN
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Paraneoplastic Syndromes of Hypercalcemia and Leukocytosis Associated with Colonic Metastases from Squamous Cell Carcinoma of the Lung: a Case Report
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作者 Xiangtao Ma Xu Wang +4 位作者 Liwei Yu Jing Fu Shan Wang Ruyu Du Zhirong Cui 《Chinese Journal of Clinical Oncology》 CSCD 2006年第1期66-69,共4页
Lung cancer is the most common cancer-related death in both men and women in the world. Approximately 25% of all cancer deaths are attributable to lung carcinoma. Moreover, about one-half of patients with lung cancer ... Lung cancer is the most common cancer-related death in both men and women in the world. Approximately 25% of all cancer deaths are attributable to lung carcinoma. Moreover, about one-half of patients with lung cancer have metastases at the time of initial diagnosis, most frequently of lymph nodes, adrenals, liver, bone and brain. However metastasis to the colon is very rare. Over the past 25 years about 13 cases of symptomatic colonic metastases from lung malignancies of all types have been reported in the literature. Hypercalcemia and leukocytosis are two of the most common paraneoplastic syndromes associated with various malignancies. However, concomitant manifestation of hypercalcemia and leukocytosis are occasionally observed in the same cancer patients. Here, we present a rare case of colonic metastasis from a squamous cell carcinoma of the lung associated with paraneoplastic syndromes of hypercalcemia and leukocytosis. 展开更多
关键词 paraneoplastic syndrome lung cancer HYPERCALCEMIA LEUKOCYTOSIS prognosis.
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An overview on CV2/CRMP5 antibody-associated paraneoplastic neurological syndromes 被引量:1
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作者 Sai Wang Haiman Hou +5 位作者 Yao Tang Shuang Zhang Gege Wang Ziyan Guo Lina Zhu Jun Wu 《Neural Regeneration Research》 SCIE CAS CSCD 2023年第11期2357-2364,共8页
Paraneoplastic neurological syndrome refers to certain malignant tumors that have affected the distant nervous system and caused corresponding dysfunction in the absence of tumor metastasis.Patients with this syndrome... Paraneoplastic neurological syndrome refers to certain malignant tumors that have affected the distant nervous system and caused corresponding dysfunction in the absence of tumor metastasis.Patients with this syndrome produce multiple antibodies,each targeting a different antigen and causing different symptoms and signs.The CV2/collapsin response mediator protein 5(CRMP5)antibody is a major antibody of this type.It damages the nervous system,which often manifests as limbic encephalitis,chorea,ocular manifestation,cerebellar ataxia,myelopathy,and peripheral neuropathy.Detecting CV2/CRMP5 antibody is crucial for the clinical diagnosis of paraneoplastic neurological syndrome,and anti-tumor and immunological therapies can help to alleviate symptoms and improve prognosis.However,because of the low incidence of this disease,few repo rts and no reviews have been published about it so far.This article intends to review the research on CV2/CRMP5antibody-associated paraneoplastic neurological syndrome and summarize its clinical features to help clinicians comprehensively understand the disease.Additionally,this review discusses the curre nt challenges that this disease poses,and the application prospects of new detection and diagnostic techniques in the field of paraneoplastic neurological syndrom e,including CV2/CRMP5-associated paraneoplastic neurological syndrome,in recent years. 展开更多
关键词 AUTOIMMUNITY CRMP5 CV2 CV2/CRMP5 antibody paraneoplastic neurological syndromes paraneoplastic syndromes TUMOR
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Studies on Plasma Norepinephrine and EpinephrineContents and Vegetative Nervous SystemFunction in Various Liver Syndrome
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作者 金益强 胡随瑜 +4 位作者 张翔 王勇华 鄢东红 刘爱平 朱崇学 《Chinese Journal of Integrative Medicine》 SCIE CAS 1999年第2期111-114,共4页
Objective: To study the characteristics of plasma norepinephrine (NE) and epinephrine (E) contents alternation and vegetative nervous function disturbance in patients with various Liver Syndrome of TCM.Methods: Subjec... Objective: To study the characteristics of plasma norepinephrine (NE) and epinephrine (E) contents alternation and vegetative nervous function disturbance in patients with various Liver Syndrome of TCM.Methods: Subjects were selected on the principle of combination of disease diagnosis and Syndrome Differentiation. Plasma NE and E contents were determined by high performance liquid chromatography (HPLC) and electrochemical detector. The vegetative nervous function were assessed by comprehensive analysis of sympathetic and parasympathetic hyperfunction symptoms, physiologic indexes and physical loading tests.Results: Patients of Liver Excess Syndrome had an elevated plasma NE and E contents and those with the vegetative nervous system disturbance mainly hypersympathetic. On the contrary, patients of Liver Deficiency Syndrome had lowered plasma NE and E contents and those with the vegetative nervous system disturbance mainly hyper-parasympathetic.Conclusion: Plasma NE and E contents and vegetative nervous function disturbance can be taken as the auxiliary laboratory diagnostic indexes for Syndrome Differentiation of Liver Excess and Liver Deficiency. 展开更多
关键词 Liver Syndrome of TCM plasma norepinephrine plasma epinephrine vegetative nervous function
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Role of F-18 FDG PET/CT imaging in the diagnosis of paraneoplastic neurological syndromes
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作者 Lei Kang Xiaojie Xu +1 位作者 Hongwei Sun Rongfu Wang 《The Chinese-German Journal of Clinical Oncology》 CAS 2014年第10期494-498,共5页
Paraneoplastic neurological syndromes(PNS) is a series of rare neurologic disorders which happen with an underlying malignancy. It has various clinical symptoms proceding to the diagnosis of tumors. Although the abnor... Paraneoplastic neurological syndromes(PNS) is a series of rare neurologic disorders which happen with an underlying malignancy. It has various clinical symptoms proceding to the diagnosis of tumors. Although the abnormality of anti-neuronal antibodies is suggestive of PNS and tumors, there exist many false positive and false negative cases. The diagnosis of PNS is usually a challenge in clinic. Positron emission tomography/computed tomography(PET/CT) imaging is an anatomical and functional fusion imaging method, which provides the whole-body information by single scan. Fluorodeoxyglucose(FDG) PET/CT imaging can not only detect potential malignant lesions in the whole body, but also assess functional abnormality in the brain. In this review, the mechanism, clinical manifestation, diagnostic procedure and the recent progress of the utility of FDG PET/CT in PNS are introduced respectively. 展开更多
关键词 paraneoplastic neurological syndrome (PNS) fluorodeoxyglucose (FDG) positron emission tomography/com-puted tomography (PET/CT) anti-neuronal antibody
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Metastatic gastric cancer from breast carcinoma presenting with paraneoplastic rheumatic syndrome:A case report
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作者 Marília Bortoluz Rech Eduarda Renz da-Cruz +3 位作者 Karina Salgado Raul Angelo Balbinot Silvana Sartori Balbinot Jonathan Soldera 《World Journal of Clinical Cases》 SCIE 2023年第14期3282-3287,共6页
BACKGROUND Breast cancer is the most frequently diagnosed cancer worldwide.It is the leading cause of death by malignant disease in women.CASE SUMMARY A female patient,73 years of age,sought care due to weakness,mild ... BACKGROUND Breast cancer is the most frequently diagnosed cancer worldwide.It is the leading cause of death by malignant disease in women.CASE SUMMARY A female patient,73 years of age,sought care due to weakness,mild abdominal pain,arthralgia,and weight loss.She was taking anastrazole as maintenance therapy for localized breast cancer and had moderate anemia and elevated acutephase markers.Upper digestive endoscopy showed isolated erosion in the gastric corpus.This lesion was compatible with signet-ring cell adenocarcinoma in anatomopathological study and was confirmed as metastasis of a breast carcinoma in immunohistochemistry,which was positive for estrogen antibody.Further imaging studies determined numerous proximal bone metastases.The patient was treated with prednisone for paraneoplastic syndrome,which improved the anemia and rheumatic disease,and with chemotherapy,which greatly improved the symptoms.She has been followed-up for 6 mo,and her anemia,arthralgias,and acute phase markers have normalized.CONCLUSION Systemic treatment strategies seem to be the best choice for gastric metastasis from breast cancer,resulting in disease control and relapse-free survival.Prospective studies with longer follow-up are needed to better understand the biological,pathological,and clinicopathological characteristics and outcomes of the endoscopic features associated with metastatic gastric cancer from breast carcinoma. 展开更多
关键词 Breast cancer Gastric metastasis ANEMIA paraneoplastic syndrome Case report
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胸腺瘤相关重症肌无力合并炎性肌病三例报道并文献复习
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作者 蒋云 侯世芳 +3 位作者 张华 苏闻 张劲松 国红 《中国神经免疫学和神经病学杂志》 CAS 2024年第1期1-7,共7页
目的分析重症肌无力(myasthenia gravis,MG)合并炎性肌病(inflammatory myopathy,IM)患者的临床特点及其与胸腺瘤的相关性。方法分析北京医院2010-3-1—2020-3-31收治的3例MG合并IM患者的临床特点,并结合文献进行复习。结果3例MG-IM中1... 目的分析重症肌无力(myasthenia gravis,MG)合并炎性肌病(inflammatory myopathy,IM)患者的临床特点及其与胸腺瘤的相关性。方法分析北京医院2010-3-1—2020-3-31收治的3例MG合并IM患者的临床特点,并结合文献进行复习。结果3例MG-IM中1例合并谷氨酸脱羧酶抗体阳性的僵肢综合征(stiff limb syndrome,SLS)。3例患者均有胸腺瘤,血清肌酸激酶和肌酸激酶同工酶升高,横纹肌抗体和心肌抗体阳性,而肌炎特异性抗体(myositis specific antibodies,MSA)和肌炎相关抗体(myositis associated antibodies,MAA)均阴性;肌电图提示肌源性损害和神经肌肉接头受累;心电图和超声心动图提示心肌受累;肌肉病理诊断多发性肌炎。联合46篇文献中的93例患者,共96例MG-IM患者纳入汇总分析。MG与IM同时发生者占42.7%,以MG症状首发者占34.4%,以IM症状首发者占22.9%。EMG检查提示肌源性损害和神经肌肉接头突触后膜疾病。乙酰胆碱受体(acetylcholine receptor,AChR)抗体阳性者占91.3%(84/92),MSA抗体阳性者仅占3.0%(2/66),MAA抗体阳性者仅占6.3%(2/32),横纹肌抗体阳性者占95.2%(20/21),6例行心肌抗体检测者均呈阳性。CT检查发现胸腺瘤者占64.4%(58/90)。53例行胸腺瘤手术的患者中,47例描述了胸腺瘤病理分型,以胸腺瘤B2型最常见(19例,40.4%),其次为B1型10例(21.3%),B3型9例(19.1%),AB型8例(17.0%),C型1例(2.1%)。89例行骨骼肌病理检查,其中以多发性肌炎最常见(62例,69.7%),其次为皮肌炎13例(14.6%),肉芽肿性肌炎9例(10.1%),免疫坏死性肌病2例(2.2%),嗜酸性粒细胞肌炎2例(2.2%),包涵体肌炎1例(1.1%)。7例尸体解剖患者行心肌病理检查,均诊断巨细胞性心肌炎。结论MG-IM多见于胸腺瘤患者,部分MG-IM患者同时合并心肌炎。大多数MG-IM患者血MSA和MAA抗体阴性。血横纹肌抗体和心肌抗体阳性提示骨骼肌和心肌受累,巨细胞性心肌炎是MG-IM患者死亡的主要原因之一。MG、IM和SLS全面准确的诊断依赖于临床、电生理、免疫学和肌肉病理的综合评估。 展开更多
关键词 重症肌无力 炎性肌病 僵肢综合征 胸腺瘤 副肿瘤综合征 肌炎
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抗SOX1抗体相关神经系统副肿瘤综合征的临床异质性分析
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作者 杨柳 陈瑞玲 +3 位作者 赵媛 赵莹莹 易立 脱厚珍 《北京医学》 CAS 2024年第5期350-354,共5页
目的总结抗Y染色体性别决定区相关高迁移率超家族1(SRY⁃like high⁃mobility group superfamily of developmental transcription factors 1,SOX1)抗体相关神经系统副肿瘤综合征(paraneoplastic neurological syndrome,PNS)的临床表现、... 目的总结抗Y染色体性别决定区相关高迁移率超家族1(SRY⁃like high⁃mobility group superfamily of developmental transcription factors 1,SOX1)抗体相关神经系统副肿瘤综合征(paraneoplastic neurological syndrome,PNS)的临床表现、影像学特征和预后。方法选取2019年1月至2023年1月首都医科大学附属北京友谊医院抗SOX1抗体相关PNS患者6例,回顾性分析患者的相关资料。结果6例患者中,男5例、女1例,年龄42~76岁。6例患者中,感觉运动周围神经病合并小细胞肺癌(small cell lung cancer,SCLC)2例、边缘叶脑炎2例、副肿瘤小脑变性1例和Lam⁃bert-Eaton肌无力综合征合并SCLC 1例。6例患者血清抗SOX1抗体均阳性,其中合并其他抗体阳性1例、合并脑脊液抗SOX1抗体阳性2例。6例患者神经系统症状均早于肿瘤发现前,均于发现抗SOX1抗体后行肿瘤筛查,其中3例SCLC患者进行治疗后病情较稳定;截至随访时间,余3例患者经检查未发现肿瘤(其中病例5随访>2年,病例2和病例4随访<2年),进行治疗后,症状未见明显进展。结论抗SOX1抗体相关PNS患者存在高度临床异质性,部分患者伴发肿瘤。可增加副肿瘤抗体的检测,以提高早期诊断潜在肿瘤的可能性。 展开更多
关键词 Y染色体性别决定区相关高迁移率超家族1 副肿瘤综合征 副肿瘤性小脑变性 小细胞肺癌 Lam⁃bert-Eaton肌无力综合征 副肿瘤性边缘叶脑炎
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21例神经系统副肿瘤综合征临床分析
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作者 李才明 李丽英 +3 位作者 许倩 沈士媛 吴楚妍 刘以恒 《广州医药》 2024年第10期1198-1204,共7页
目的分析神经系统副肿瘤综合征(PNS)的临床特点以提高对该病的早期诊断和治疗效果。方法回顾性分析惠州市第一人民医院和惠州市中心人民医院神经内科2019年10月—2022年10月收治的21例PNS患者的临床表现、实验室检查结果和治疗效果,并... 目的分析神经系统副肿瘤综合征(PNS)的临床特点以提高对该病的早期诊断和治疗效果。方法回顾性分析惠州市第一人民医院和惠州市中心人民医院神经内科2019年10月—2022年10月收治的21例PNS患者的临床表现、实验室检查结果和治疗效果,并作文献回顾。结果21例患者中出现了10种副肿瘤综合征,其中经典综合征占比28.6%(6/21),最多见的是边缘叶脑炎;20例在血液或脑脊液中发现检测到抗神经元抗体,非特征性抗体阳性率最高(12/20),其中以半定量脑组织切片TBA检测阳性率最高(7/20);有特征性抗体的8例以抗Yo抗体阳性率最高(6/8)。21例患者均随访至2023年3月,8例发现原发肿瘤,其中4例在神经系统病变之后。69.25%(9/13)的患者使用糖皮质激素治疗和(或)丙种球蛋白治疗有效。结论21例PNS患者中以非经典综合征占比较多,经典与非经典副肿瘤综合征均应进行肿瘤筛查,未发现肿瘤者应密切随访。非特征性抗体阳性率最高,提示PNS可能仍有许多相关抗体未明确,临床工作中也应对非特征性抗体阳性予以重视。 展开更多
关键词 神经系统副肿瘤综合征 相关神经元抗体 神经系统损害
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合并皮肤色素沉着的抗Hu、抗Amphiphysin抗体阳性副肿瘤性感觉神经元病一例
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作者 徐宁康 兰希福 +2 位作者 赵曼丽 徐谦 孙翀 《脑与神经疾病杂志》 CAS 2024年第9期547-551,共5页
目的 提高对合并罕见临床症状的双抗体阳性副肿瘤感觉神经元病(PSN)的认识。方法 报道1例合并皮肤色素沉着的双抗体阳性PSN患者,分析其临床资料。结果 患者女性,58岁,以四肢不对称性麻木无力为主要表现,查血清副肿瘤抗体谱:抗Hu抗体(+)... 目的 提高对合并罕见临床症状的双抗体阳性副肿瘤感觉神经元病(PSN)的认识。方法 报道1例合并皮肤色素沉着的双抗体阳性PSN患者,分析其临床资料。结果 患者女性,58岁,以四肢不对称性麻木无力为主要表现,查血清副肿瘤抗体谱:抗Hu抗体(+)、抗Amphiphysin抗体(+),查体发现患者双手及腹部皮肤色素沉着,结合病史及检查结果高度怀疑副肿瘤综合征,但初步检查未发现肿瘤病灶,应用地塞米松及免疫球蛋白后效果不佳,行血浆置换后症状减轻。6个月后患者复查PET-CT发现存在肺部肿瘤,纵隔淋巴结活检病理证实为小细胞肺癌,诊断为“PSN”,后患者转入肿瘤科进一步治疗。结论 高风险副肿瘤自身抗体如抗Hu、抗Amphiphysin抗体对副肿瘤综合征的诊断具有重要意义,不明原因的皮肤色素沉着应引起临床医生的重视,警惕副肿瘤综合征的可能。 展开更多
关键词 副肿瘤神经系统综合征 副肿瘤自身抗体 皮肤色素沉着
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以急性多发性脑梗死为主要表现的特鲁索综合征3例
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作者 颜谈 许静 +2 位作者 汝宁 陈巨罗 王幼萌 《安徽医药》 CAS 2024年第2期386-389,共4页
目的 分析以急性多发性脑梗死为主要表现的特鲁索综合征(Trousseau’s syndrome,TS)的临床及影像学特征。方法回顾分析2019年12月至2021年12月阜阳市人民医院神经内科收治的3例以急性多发性脑梗死为主要表现的TS病人的临床资料,并结合... 目的 分析以急性多发性脑梗死为主要表现的特鲁索综合征(Trousseau’s syndrome,TS)的临床及影像学特征。方法回顾分析2019年12月至2021年12月阜阳市人民医院神经内科收治的3例以急性多发性脑梗死为主要表现的TS病人的临床资料,并结合相关文献分析该病的临床和影像特征。结果 其中男1例,女2例;发病年龄范围为52~85岁;3例病人D-二聚体均明显升高;头颅MRI均显示为以“三流域征”为特点的急性多发性脑梗死;伴腹腔转移瘤1例,伴静脉系统血栓2例;1例予低分子肝素抗凝+双抗抗血小板聚集,2例予低分子肝素抗凝治疗。结论 急性多发性脑梗死是TS的一个重要表现;对于不符合血管分布的急性多发性脑梗死,病因需考虑恶性肿瘤所致高凝状态可能;D-D是诊断TS的重要线索。 展开更多
关键词 副肿瘤综合征 神经系统 栓塞和血栓形成 特鲁索综合征 脑梗死 三流域征 恶性肿瘤
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免疫检查点抑制剂相关抗神经元抗体阳性副肿瘤神经综合征临床特征分析
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作者 张乐 范思远 +3 位作者 任海涛 徐燕 柏琳 关鸿志 《中国现代神经疾病杂志》 CAS 北大核心 2024年第5期346-351,共6页
目的 分析抗神经元抗体阳性免疫检查点抑制剂相关副肿瘤神经综合征(ICI-PNS)的临床特征。方法与结果 纳入2012年1月至2024年3月中国医学科学院北京协和医院诊断与治疗的5例抗神经元抗体阳性ICI-PNS患者,肿瘤类型包括小细胞肺癌(2例)、... 目的 分析抗神经元抗体阳性免疫检查点抑制剂相关副肿瘤神经综合征(ICI-PNS)的临床特征。方法与结果 纳入2012年1月至2024年3月中国医学科学院北京协和医院诊断与治疗的5例抗神经元抗体阳性ICI-PNS患者,肿瘤类型包括小细胞肺癌(2例)、恶性黑色素瘤(1例)、霍奇金淋巴瘤(1例)、宫颈癌(1例),免疫检查点抑制剂包括程序性死亡蛋白-1抑制剂(3例)、程序性死亡蛋白配体-1抑制剂(1例)、程序性死亡蛋白-1/细胞毒性T细胞相关抗原4双抑制剂(1例)。5例患者均出现副肿瘤神经综合征的高风险表型,其中4例表现为边缘性脑炎,1例表现为快速进展的小脑综合征。血清和(或)脑脊液中检出的抗神经元抗体包括抗Hu、γ-氨基丁酸B型受体、Y染色体性别决定区相关高迁移率组盒蛋白1、代谢型谷氨酸受体5型、Yo抗体。4例神经系统症状出现在应用免疫检查点抑制剂2周内。4例病情达峰时改良Rankin量表评分为3分,1例为5分。5例患者常见不良事件评价标准分级(CTCAE)均为3级。治疗方面,停用免疫检查点抑制剂,给予糖皮质激素联合静脉注射免疫球蛋白治疗,神经系统症状均有改善。结论 中高风险抗神经元抗体是ICI-PNS的诊断标志物,可依据ICI-PNS临床表型及CTCAE分级等综合制定免疫治疗方案,停用免疫检查点抑制剂,应用糖皮质激素、静脉注射免疫球蛋白可以改善患者预后。 展开更多
关键词 副肿瘤综合征 神经系统 免疫检查点抑制剂(非MeSH词) 神经元 自身抗体 药物相关性副作用和不良反应
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结肠腺癌致异位促肾上腺皮质激素综合征1例报道
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作者 楚立园 吕丽媛 +2 位作者 李潇 邬日新 田劭丹 《现代肿瘤医学》 CAS 2024年第10期1898-1902,共5页
异位促肾上腺皮质激素综合征(ectopic ACTH syndrome, EAS)又称异位ACTH综合征,是副肿瘤综合征内分泌系统的一种特殊类型,与垂体以外的肿瘤组织分泌过量有生物活性的ACTH或其类似物,刺激肾上腺皮质增生有关。临床观察发现,多种不同起源... 异位促肾上腺皮质激素综合征(ectopic ACTH syndrome, EAS)又称异位ACTH综合征,是副肿瘤综合征内分泌系统的一种特殊类型,与垂体以外的肿瘤组织分泌过量有生物活性的ACTH或其类似物,刺激肾上腺皮质增生有关。临床观察发现,多种不同起源的肿瘤与EAS相关,其中以支气管类癌和小细胞肺癌最为常见,其次是胸腺肿瘤、胰腺神经内分泌肿瘤、甲状腺髓样癌等,这些肿瘤多具有神经内分泌特征[1-2]。 展开更多
关键词 异位ACTH综合征 结肠癌 副肿瘤综合征 临床病例报道
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Anti-N-methyl-D-aspartate receptor-associated encephalitis: A review of clinicopathologic hallmarks and multimodal imaging manifestations 被引量:1
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作者 Bryce David Beutler Alastair E Moody +4 位作者 Jerry Mathew Thomas Benjamin Phillip Sugar Mark B Ulanja Daniel Antwi-Amoabeng Lucas Anthony Tsikitas 《World Journal of Radiology》 2024年第1期1-8,共8页
Anti-N-methyl-D-aspartate receptor-associated encephalitis(NMDARE)is a rare immune-mediated neuroinflammatory condition characterized by the rapid onset of neuropsychiatric symptoms and autonomic dysfunction.The mecha... Anti-N-methyl-D-aspartate receptor-associated encephalitis(NMDARE)is a rare immune-mediated neuroinflammatory condition characterized by the rapid onset of neuropsychiatric symptoms and autonomic dysfunction.The mechanism of pathogenesis remains incompletely understood,but is thought to be related to antibodies targeting the GluN1 subunit of the NMDA receptor with resultant downstream dysregulation of dopaminergic pathways.Young adults are most frequently affected;the median age at diagnosis is 21 years.There is a strong female predilection with a female sex predominance of 4:1.NMDARE often develops as a paraneoplastic process and is most commonly associated with ovarian teratoma.However,NMDARE has also been described in patients with small cell lung cancer,clear cell renal carcinoma,and other benign and malignant neoplasms.Diagnosis is based on correlation of the clinical presentation,electro-encephalography,laboratory studies,and imaging.Computed tomography,positron emission tomography,and magnetic resonance imaging are essential to identify an underlying tumor,exclude clinicopathologic mimics,and predict the likelihood of long-term functional impairment.Nuclear imaging may be of value for prognostication and to assess the response to therapy.Treatment may involve high-dose corticosteroids,intravenous immunoglobulin,and plasma exchange.Herein,we review the hallmark clinicopathologic features and imaging findings of this rare but potentially devastating condition and summarize diagnostic criteria,treatment regimens,and proposed pathogenetic mechanisms. 展开更多
关键词 Anti-N-methyl-D-aspartate receptor-associated encephalitis Autoimmune encephalitis ENCEPHALITIS Ovarian teratoma paraneoplastic syndrome TERATOMA
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奥法妥木单抗治疗免疫检查点抑制剂相关副肿瘤性小脑性共济失调综合征1例
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作者 刘雅菁 冯双浩 +2 位作者 江佳佳 杨伊 卜晖 《中国神经精神疾病杂志》 CAS CSCD 北大核心 2024年第3期159-161,共3页
报告应用奥法妥木单抗(Ofatumumab,OFA)治疗免疫检查点抑制剂(immune checkpoint inhibitors,ICI)引起的副肿瘤性小脑性共济失调综合征1例。患者,男,57岁,既往小细胞肺癌病史,应用“卡瑞丽珠单抗”免疫治疗,主因“行走不稳1年余,头部不... 报告应用奥法妥木单抗(Ofatumumab,OFA)治疗免疫检查点抑制剂(immune checkpoint inhibitors,ICI)引起的副肿瘤性小脑性共济失调综合征1例。患者,男,57岁,既往小细胞肺癌病史,应用“卡瑞丽珠单抗”免疫治疗,主因“行走不稳1年余,头部不自主晃动1月余”入院。入院后完善头颅核磁、胸部CT、脑电图、腰椎穿刺等相关检查,副肿瘤综合征抗体谱抗GAD65抗体IgG(+),确诊免疫检查点抑制剂相关神经系统副肿瘤综合征(paraneoplastic neurological syndromes,PNS),给予OFA治疗(20mg/次)后症状明显改善。本文通过分析该病例的临床特点及诊疗思路,以提高临床医师对该疾病的认识,为类似病例的临床诊治提供参考。 展开更多
关键词 奥法妥木单抗 神经系统副肿瘤综合征 免疫检查点抑制剂 小脑共济失调 CD20单克隆抗体
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抗Hu抗体对胃肠动力障碍性疾病神经系统损伤机制的研究进展
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作者 付铭玉 方秀才 《胃肠病学》 2024年第2期104-108,共5页
越来越多的研究提示靶向神经元抗体特别是抗Hu抗体可对中枢神经系统和(或)肠神经系统造成不同程度的损伤,影响相关疾病的发生、发展和预后,因此明确这类抗体对神经系统损伤的机制及其与疾病的相关性对个体化诊断和治疗具有重要指导意义... 越来越多的研究提示靶向神经元抗体特别是抗Hu抗体可对中枢神经系统和(或)肠神经系统造成不同程度的损伤,影响相关疾病的发生、发展和预后,因此明确这类抗体对神经系统损伤的机制及其与疾病的相关性对个体化诊断和治疗具有重要指导意义。本文就抗Hu抗体与副肿瘤性胃肠动力障碍性疾病、慢性假性肠梗阻、肠易激综合征等疾病的相关性及其对神经元的损伤机制作一综述。 展开更多
关键词 抗Hu抗体 神经系统损伤 胃肠动力障碍 副肿瘤综合征 神经系统 肠假性梗阻 肠易激综合征
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Analysis of metabolic characteristics of metabolic syndrome in elderly patients with gastric cancer by non-targeted metabolomics
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作者 Huan Zhang Wen-Bing Shen Lin Chen 《World Journal of Gastrointestinal Oncology》 SCIE 2024年第6期2419-2428,共10页
BACKGROUND The relationship between metabolic syndrome(MetS)and gastric cancer(GC),which is a common metabolic disease,has attracted much attention.However,the specific metabolic characteristics of MetS in elderly pat... BACKGROUND The relationship between metabolic syndrome(MetS)and gastric cancer(GC),which is a common metabolic disease,has attracted much attention.However,the specific metabolic characteristics of MetS in elderly patients with GC remain unclear.AIM To investigate the differentially abundant metabolites and metabolic pathways between preoperative frailty and MetS in elderly patients with GC based on nontargeted metabolomics techniques.METHODS In this study,125 patients with nonfrail nonmeal GC were selected as the control group,and 50 patients with GC in the frail group were selected as the frail group.Sixty-five patients with GC combined with MetS alone were included in the MetS group,and 50 patients with GC combined with MetS were included in the MetS group.Nontargeted metabolomics techniques were used to measure plasma metabolite levels by ultrahigh-performance liquid chromatography-mass spectrometry.Multivariate statistical analysis was performed by principal component analysis,orthogonal partial least squares,pattern recognition analysis,cluster analysis,and metabolic pathway annotation.RESULTS A total of 125 different metabolites,including amino acids,glycerophospholipids,sphingolipids,fatty acids,sugars,nucleosides and nucleotides,and acidic compounds,were identified via nontargeted metabolomics techniques.Compared with those in the control group,there were 41,32,and 52 different metabolites in the MetS group,the debilitated group,and the combined group,respectively.Lipid metabolites were significantly increased in the MetS group.In the weak group,amino acids and most glycerol phospholipid metabolites decreased significantly,and fatty acids and sphingosine increased significantly.The combined group was characterized by significantly increased levels of nucleotide metabolites and acidic compounds.The alanine,aspartic acid,and glutamate metabolic pathways were obviously enriched in the asthenic group,and the glycerol and phospholipid metabolic pathways were obviously enriched in the combined group.CONCLUSION Elderly GC patients with simple frailty,simple combined MetS,and frailty combined with MetS have different metabolic characteristics,among which amino acid and glycerophospholipid metabolite levels are significantly lower in frail elderly GC patients,and comprehensive supplementation of fat and protein should be considered.Many kinds of metabolites,such as amino acids,lipids,nucleotides,and acidic compounds,are abnormally abundant in patients with MetS combined with fthenia,which may be related to tumor-related metabolic disorders. 展开更多
关键词 nervous breakdown Metabolic syndrome Elderly individuals Gastric cancer Nontargeted metabolomics
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