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Monomorphic epitheliotropic intestinal T-cell lymphoma with bone marrow involved: A case report
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作者 Fen-Juan Zhang Wen-Juan Fang Cang-Jian Zhang 《World Journal of Clinical Cases》 SCIE 2024年第4期814-819,共6页
BACKGROUND Monomorphic epithelial intestinal T-cell lymphoma(MEITL)is a rare type of peripheral T-cell lymphoma.The clinical manifestations are diarrhea,abdominal pain,perforation and an abdominal mass.CASE SUMMARY We... BACKGROUND Monomorphic epithelial intestinal T-cell lymphoma(MEITL)is a rare type of peripheral T-cell lymphoma.The clinical manifestations are diarrhea,abdominal pain,perforation and an abdominal mass.CASE SUMMARY We present a 52-year-old female patient who was diagnosed with MEITL.Further disease progression was observed after multiline chemotherapy.Eventually,the patient died of a severe infection.CONCLUSION MEITL is a rare intestinal primary T-cell lymphoma with aggressive behavior,a high risk of severe life-threatening complications,and a poor prognosis. 展开更多
关键词 monomorphic epithelial intestinal T-cell lymphoma Autologous stem cell transplantation CHEMOTHERAPEUTICS Case report
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Monomorphic epitheliotropic intestinal T-cell lymphoma presenting as melena with long-term survival: A case report and review of literature 被引量:5
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作者 Sotaro Ozaka Kunimitsu Inoue +6 位作者 Tomoya Okajima Takako Tasaki Shimpei Ariki Hideki Ono Takeaki Ando Tsutomu Daa Kazunari Murakami 《World Journal of Gastroenterology》 SCIE CAS 2021年第38期6501-6510,共10页
BACKGROUND Monomorphic epitheliotropic intestinal T-cell lymphoma(MEITL)is a rare primary intestinal T-cell lymphoma,previously known as enteropathy-associated T-cell lymphoma type II.MEITL is an aggressive T-cell lym... BACKGROUND Monomorphic epitheliotropic intestinal T-cell lymphoma(MEITL)is a rare primary intestinal T-cell lymphoma,previously known as enteropathy-associated T-cell lymphoma type II.MEITL is an aggressive T-cell lymphoma with a poor prognosis and high mortality rate.The known major complications of MEITL are intestinal perforation and obstruction.Here,we present a case of MEITL that was diagnosed following upper gastrointestinal bleeding from an ulcerative duodenal lesion,with recurrence-free survival for 5 years.CASE SUMMARY A 68-year-old female was admitted to our hospital with melena and mild anemia.An urgent esophagogastroduodenoscopy(EGD)revealed bleeding from an ulcerative lesion in the transverse part of the duodenum,for which hemostatic treatment was performed.MEITL was diagnosed following repeated biopsies of the lesion,and cyclophosphamide,doxorubicin,vincristine,and prednisone(CHOP)chemotherapy was administered.She achieved complete remission after eight full cycles of CHOP therapy.At the last follow-up examination,EGD revealed a scarred ulcer and 18Fluorodeoxyglucose(18FDG)positron emission tomography/computed tomography showed no abnormal FDG accumulation.The patient has been in complete remission for 68 mo after initial diagnosis.CONCLUSION To rule out MEITL,it is important to carefully perform histological examination when bleeding from a duodenal ulcer is observed. 展开更多
关键词 monomorphic epitheliotropic intestinal T-cell lymphoma Enteropathyassociated T-cell lymphoma type II Gastrointestinal bleeding Intestinal lymphoma Duodenal ulcer Case report
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Chidamide based combination regimen for treatment of monomorphic epitheliotropic intestinal T cell lymphoma following radical operation:Two case reports 被引量:8
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作者 Ting-Zhi Liu Yi-Jia Zheng +4 位作者 Zhan-Wen Zhang Shan-Shan Li Jiao-Ting Chen Ai-Hua Peng Ren-Wei Huang 《World Journal of Clinical Cases》 SCIE 2020年第7期1278-1286,共9页
BACKGROUND Monomorphic epitheliotropic intestinal T cell lymphoma(MEITL)is a rare extranodal T-cell lymphoma that has uniformly aggressive features with a poor prognosis.No standardized treatment protocols have been e... BACKGROUND Monomorphic epitheliotropic intestinal T cell lymphoma(MEITL)is a rare extranodal T-cell lymphoma that has uniformly aggressive features with a poor prognosis.No standardized treatment protocols have been established.Previous experience has demonstrated favorable outcomes with combination chemotherapy followed by autologous hematopoietic stem cell transplant.However,many patients are unable to tolerate the toxicities.Chidamide is a new histone deacetylase inhibitor that has shown preferential efficacy in mature T-cell lymphoma.CASE SUMMARY We herein present two cases of MEITL who were both intermediate risk according to enteropathy-associated T cell lymphoma prognostic index.Case one was a 61-year-old man.He complained of upper abdominal pain and intermittent black stool for 2 mo.Imaging examination revealed that the intestinal wall was thickened.He received a partial excision of the small intestine.A chidamidebased combination regimen was given postoperatively.Eleven months later,he presented with recurrence in the bilateral lungs.He passed away 15 mo after his diagnosis.Case two was a 35-year-old woman who complained of abdominal distention for 1 mo.Positron emission tomography/computed tomography demonstrated wall thickening of the small intestine and upper sigmoid colon.Colon perforation and septic shock occurred on the fourth day of her admission.She was treated by sigmoid colostomy.Chidamide-based combination therapy was then provided.She was recurrence-free for 6 mo until lesions were found in the bilateral brain and lived for 17 mo since her diagnosis.Compared to historical data,chidamide seems to improve the prognosis of MEITL slightly.CONCLUSION MEITL is a type of aggressive lymphoma.Chidamide is a new promising approach for the treatment of MEITL. 展开更多
关键词 monomorphic epitheliotropic INTESTINAL T CELL lymphoma HISTONE DEACETYLASE inhibitor CHIDAMIDE Intensive chemotherapy Stem CELL transplantation Case report
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Surgical management of monomorphic epitheliotropic intestinal Tcell lymphoma followed by chemotherapy and stem-cell transplant:A case report and review of the literature 被引量:1
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作者 Abdul Saad Bissessur Ji-Chun Zhou +4 位作者 Ling Xu Zhao-Qing Li Si-Wei Ju Yun-Lu Jia Lin-Bo Wang 《World Journal of Gastrointestinal Oncology》 SCIE 2022年第11期2273-2287,共15页
BACKGROUND Monomorphic epitheliotropic intestinal T-cell lymphoma(MEITL)is a rare and rapidly progressive intestinal T-cell non-Hodgkin lymphoma associated with a very poor prognosis and a median survival of 7 mo.Adva... BACKGROUND Monomorphic epitheliotropic intestinal T-cell lymphoma(MEITL)is a rare and rapidly progressive intestinal T-cell non-Hodgkin lymphoma associated with a very poor prognosis and a median survival of 7 mo.Advances in the identification of MEITL over the last two decades have led to its recognition as a separate entity.MEITL patients,predominantly male,typically present with vague and nonspecific symptoms and diagnosis is predominantly confirmed at laparotomy.Currently,there are no standardized treatment protocols,and the optimal therapy remains unclear.CASE SUMMARY We report a case of MEITL that was initially considered to be gastrointestinal stromal tumor(GIST)and Imatinib was administered for one cycle.The 62-yearold man presented with abdominal pain,abdominal distension,and weight loss of 20 pounds.Within 2 wk,the size of the mass considerably increased on computed tomography scans.The patient underwent surgery followed by chemotherapy with CHOP(cyclophosphamide,doxorubicin,vincristine,and prednisone)and stem-cell transplant.A correct diagnosis of MEITL was established based on postoperative pathology.Immunophenotypically,the neoplastic cells fulfilled the diagnostic criteria for MEITL as they were CD3+,CD4+,CD8+,CD56+,and TIA-1+.CONCLUSION Given that MEITL has no predisposing factor and presents with vague symptoms with rapid progression,the concomitant presence of abdominal symptoms and B symptoms(weight loss,fever,and night sweats)with hypoalbuminemia,anemia,low lymphocytic count and endoscopic findings of diffuse infiltrating type lesions should alert physicians to this rare disease,especially when it comes to Asian patients.Immediate laparotomy should then be carried out followed by chemotherapy and stem-cell transplant. 展开更多
关键词 monomorphic epitheliotropic intestinal T-cell lymphoma Gastrointestinal stromal tumor Immunophenotypically CHEMOTHERAPY Stem-cell transplant Case report
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Aryepiglottic Fold as a Rare Location for a Monomorphic Adenoma—Case Report
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作者 Hosaagrahara Subbegowda Satish Niveditha Jayanna +1 位作者 Borlingegowda Viswanatha Ramabhadraiah Anil Kumar 《International Journal of Otolaryngology and Head & Neck Surgery》 2013年第2期61-62,共2页
We report a case of Monomorphic adenoma of aryepiglottic fold. Histopathological findings are described. This is the first case, to our knowledge, of a Monomorphic adenoma presenting at aryepiglottic fold. Complete ex... We report a case of Monomorphic adenoma of aryepiglottic fold. Histopathological findings are described. This is the first case, to our knowledge, of a Monomorphic adenoma presenting at aryepiglottic fold. Complete excision of the mass was done through laryngofissure approach. 展开更多
关键词 monomorphic ADENOMA Laryngofissure Aryepiglottic FOLD
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The stable Auslander-Reiten components of certain monomorphism categories
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作者 Rasool Hafezi Yi Zhang 《Science China Mathematics》 SCIE CSCD 2024年第3期505-526,共22页
Let Λ be an Artin algebra and let Gprj-Λ denote the class of all the finitely generated Gorenstein projective Λ-modules. In this paper, we study the components of the stable Auslander-Reiten quiver of a certain sub... Let Λ be an Artin algebra and let Gprj-Λ denote the class of all the finitely generated Gorenstein projective Λ-modules. In this paper, we study the components of the stable Auslander-Reiten quiver of a certain subcategory of the monomorphism category S(Gprj-Λ) containing boundary vertices. We describe the shape of such components. It is shown that certain components are linked to the orbits of an auto-equivalence on the stable category Gprj. In particular, for the finite components, we show that under certain mild conditions,their cardinalities are divisible by 3. We see that this three-periodicity phenomenon reoccurs several times in the paper. 展开更多
关键词 monomorphism category almost split sequence Auslander-Reiten quiver Gorenstein projective module
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CD56阴性单形性结外NK/T细胞淋巴瘤1例 被引量:1
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作者 吴仕收 高源 +1 位作者 张立彦 于国华 《临床与病理杂志》 2025年第5期649-654,共6页
结外NK/T细胞淋巴瘤被归类为一种非霍奇金淋巴瘤,以其侵袭性强和异质性著称,此类患者预后差,常见的组织学特点包括肿瘤细胞浸润破坏血管、凝固性坏死及肿瘤细胞多形性。现报告1例就诊于烟台毓璜顶医院的女性结外NK/T细胞淋巴瘤,主要特... 结外NK/T细胞淋巴瘤被归类为一种非霍奇金淋巴瘤,以其侵袭性强和异质性著称,此类患者预后差,常见的组织学特点包括肿瘤细胞浸润破坏血管、凝固性坏死及肿瘤细胞多形性。现报告1例就诊于烟台毓璜顶医院的女性结外NK/T细胞淋巴瘤,主要特征为以单形性为组织学特点且免疫标记CD56[即神经细胞黏附分子(neural cell adhesion molecule,NCAM)]阴性,这在结外NK/T细胞淋巴瘤患者中极为罕见。患者入院后行内镜下病损切除术。术后病理证实为结外NK/T细胞淋巴瘤,患者术后随访6个月,接受COEP-L(环磷酰胺+长春新碱+依托泊苷+泼尼松+左旋门冬酰胺酶)化学治疗+放射治疗方案治疗,目前生存良好。基于临床表现、组织病理形态、免疫组织化学染色结果及原位杂交结果进行综合病理诊断至关重要,能够避免漏诊、误诊。 展开更多
关键词 单形形 CD56 EPSTEIN-BARR病毒感染 非霍奇金淋巴瘤 结外NK/T细胞淋巴瘤
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Radiofrequency catheter ablation at the left coronary cusp in treatment of repetitive monomorphic tachycardia of the left ventricular outflow tract 被引量:2
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作者 唐恺 马坚 +4 位作者 张澍 楚建民 张奎俊 王方正 陈新 《Chinese Medical Journal》 SCIE CAS CSCD 2004年第2期168-171,共4页
Background The aim of this study was to clarify the electrocardiographic characteristics of repetitive monomorphic ventricular tachycardia (RMVT) originating from the left ventricular outflow tract, and to describe th... Background The aim of this study was to clarify the electrocardiographic characteristics of repetitive monomorphic ventricular tachycardia (RMVT) originating from the left ventricular outflow tract, and to describe the results of treatment with radiofrequency catheter ablation (RFCA).Methods Routine 12-lead surface electrocardiography and electrophysiological studies were performed on 11 RMVT patients with no organic heart disease, who were subsequently treated with RFCA directed at targets identified by pace mapping.Results The surface electrocardiogram QRS characteristics of RMVT included an atypical left bundle branch block and right axis deviation, with a low amplitude 'rs' or 'rS' pattern in lead I , an 'rS' or 'RS' pattern in V1, and a precordial R wave transition zone in V2 or V3. In 1 patient, a small S wave was observed in V5. Using pace mapping techniques, we selected the left coronary cusp as the ablation target. RMVT was eliminated in all 11 patients immediately after radiofrequency energy delivered. During a follow-up of 13 ±7 months, RMVT recurred in only 1 patient.Conclusion RMVT originating from the left ventricular outflow tract has specific electrocardiographic characteristics, and can be successfully and safely cured using RFCA directed at the left coronary cusp. 展开更多
关键词 repetitive monomorphic ventricular tachycardia ELECTROCARDIOGRAM catheter ablation left coronary cusp
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肠道单形性亲上皮性T细胞淋巴瘤11例临床病理分析
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作者 何银环 汪小霞 +3 位作者 叶胜兵 程平 饶秋 鲍炜 《临床与实验病理学杂志》 北大核心 2025年第6期795-798,共4页
目的探讨肠道单形性亲上皮性T细胞淋巴瘤(monomorphic epitheliotropic intestinal T-cell lymphoma,MEITL)的临床病理特征。方法收集11例患者的临床资料,行HE、免疫组化、原位杂交、Ig和TCR基因重排检测,分析其临床病理特征并复习相关... 目的探讨肠道单形性亲上皮性T细胞淋巴瘤(monomorphic epitheliotropic intestinal T-cell lymphoma,MEITL)的临床病理特征。方法收集11例患者的临床资料,行HE、免疫组化、原位杂交、Ig和TCR基因重排检测,分析其临床病理特征并复习相关文献。结果11例MEITL患者年龄28~71岁,中位年龄53岁;发病部位:小肠9例,结肠2例。临床症状主要表现为腹痛、腹胀。镜下肿瘤细胞弥漫浸润肠壁全层,形态单一,小-中等大小,核圆形深染,胞质淡染或透明,染色质颗粒状,核仁不明显,核分裂象多见,周边黏膜绒毛萎缩,上皮内淋巴细胞增多,部分具有亲上皮性。免疫表型:肿瘤细胞CD3、CD8、CD43、CD56、Gran B和TIA-1均阳性,CD4、CD5、perforin、CD20、CD79α均阴性,其中2例CD20、CD79α散在异常阳性,Ki67增殖指数高。EBER原位杂交均阴性;9例TCR重排检测均阳性,7例Ig基因重排均阴性。结论MEITL是罕见的肠道高度侵袭性T细胞淋巴瘤,临床表现无特异性,活检诊断困难,需结合临床资料、形态学特点、免疫表型、原位杂交和基因检测。 展开更多
关键词 肠肿瘤 肠道单形性亲上皮性T细胞淋巴瘤 免疫组织化学 T细胞受体
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Localization of homotopy epimorphisms and homotopy monomorphisms
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作者 沈文淮 左再思 《Chinese Science Bulletin》 SCIE EI CAS 1995年第12期984-987,共4页
Recall that f: X→Y is a homotopy epimorphism (monomorphism), if given u, v: Y→W (u, v: W→X), uofvof implies uv (foufov implies uv). In this note, we shall consider the localization of homotopy epimorphisms andmonom... Recall that f: X→Y is a homotopy epimorphism (monomorphism), if given u, v: Y→W (u, v: W→X), uofvof implies uv (foufov implies uv). In this note, we shall consider the localization of homotopy epimorphisms andmonomorphism, 1.e. the following is considered. Problem. If f:X→Y is a homotopy epimorphism (monomorphism), then is any 展开更多
关键词 LOCALIZATION HOMOTOPY EPIMORPHISM HOMOTOPY monomorphism.
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Monomorphism categories associated with symmetric groups and parity in finite groups
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作者 ZHANG YueHui 《Science China Mathematics》 SCIE 2013年第3期525-530,共6页
Monomorphism categories of the symmetric and alternating groups are studied via Cayley's Em-bedding Theorem. It is shown that the parity is well defined in such categories. As an application, the parity in a finit... Monomorphism categories of the symmetric and alternating groups are studied via Cayley's Em-bedding Theorem. It is shown that the parity is well defined in such categories. As an application, the parity in a finite group G is classified. It is proved that any element in a group of odd order is always even and such a group can be embedded into some alternating group instead of some symmetric group in the Cayley's theorem. It is also proved that the parity in an abelian group of even order is always balanced and the parity in an nonabelian group is independent of its order. 展开更多
关键词 monomorphism categories Cayley’s theorem PARITY balanced group
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Injective objects of monomorphism categories
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作者 Keyan SONG Yuehui ZHANG 《Frontiers of Mathematics in China》 SCIE CSCD 2016年第2期401-409,共9页
For an acyelic quiver Q and a finite-dimensional algebra A, we give a unified form of the indecomposable injective objects in the monomorphism category Mon(Q, A) and prove that Mon(Q, A) has enough injective objects.
关键词 monomorphism categories injective objects
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Silting Objects over the Stable Monomorphism Category of Higher Differential Objects
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作者 Nan Gao Xuanyu Liu Jing Ma 《Algebra Colloquium》 SCIE CSCD 2023年第2期225-236,共12页
Higher differential objects are investigated and used for addressing three gen-eral problems.Torsionless differential modules over path algebras are characterized.The adjoint triples between triangulated categories,in... Higher differential objects are investigated and used for addressing three gen-eral problems.Torsionless differential modules over path algebras are characterized.The adjoint triples between triangulated categories,involving derived categories and singularity categories,are allowed to be constructed from those between the abelian categories C and C[ε]^(n).The partial silting properties between an abelian category C and C[ε]^(n)are trans-ferred,and if moreover,C is Frobenius,the partial silting objects of the stable monomor-phism categories of C[ε]^(n)are constructed from those of C. 展开更多
关键词 higher differential object stable monomorphism category partial silting object
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On homotopy regular monomorphisms 被引量:2
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作者 CHEN Jixiang Department of Mathematics, Nankai University, Tianjin 300071, China 《Chinese Science Bulletin》 SCIE EI CAS 1998年第1期27-30,共4页
A concept of homotopy regular monomorphism is introduced which is strictly between homotopy monomorphism and homotopy equivalence. And it characterizes homotopy equivalence in some sense.
关键词 HOMOTOPY monomorphISM HOMOTOPY EQUALIZER HOMOTOPY REGULAR monomorphISM HOMOTOPY PULL back.
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单形性嗜上皮性肠道T细胞淋巴瘤3例临床病理观察 被引量:1
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作者 兰秋霞 马强 肖华亮 《诊断病理学杂志》 2024年第2期110-113,118,共5页
目的探讨单形性嗜上皮性肠道T细胞淋巴瘤(MEITL)的临床病理特征、诊断与鉴别诊断,以提高对单形性嗜上皮性肠道T细胞淋巴瘤的认识。方法收集本院诊断的3例MEITL的临床资料,进行组织学及免疫组化观察,并复习相关文献,归纳该肿瘤的诊断和... 目的探讨单形性嗜上皮性肠道T细胞淋巴瘤(MEITL)的临床病理特征、诊断与鉴别诊断,以提高对单形性嗜上皮性肠道T细胞淋巴瘤的认识。方法收集本院诊断的3例MEITL的临床资料,进行组织学及免疫组化观察,并复习相关文献,归纳该肿瘤的诊断和鉴别诊断要点。结果镜下见淋巴细胞弥漫浸润肠壁全层,肠黏膜糜烂伴溃疡形成,可见淋巴上皮病变,肿瘤细胞大小较为一致,细胞中等大小,核仁可见,细胞膜不规则,胞质淡染,可见核分裂象及核碎裂。免疫组化:3例均表达CD3、CD2、CD7、CD8、CD56、TIA-1,均不表达CD20、PAX-5、CD30、EBER、H3k36me,Ki-67增殖指数约70%,p53散在弱阳。结论MEITL较为罕见,临床症状不特异,早期易漏诊,晚期易与其他恶性肿瘤混淆,大多为术后病理诊断明确。 展开更多
关键词 单形性嗜上皮性肠道T细胞淋巴瘤 诊断 鉴别诊断 淋巴瘤 治疗
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一种简单通用的鸟类性别分子鉴定技术(简报) 被引量:23
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作者 胡锐颖 耿昕 +3 位作者 马珺 陈云霜 李仲逵 丁小燕 《实验生物学报》 CSCD 北大核心 2003年第5期401-404,共4页
我国幅员辽阔,生物类型多种多样,是世界上拥有鸟类种类最多的国家之一.截至1999年底,已知有鸟类1253种948亚种,隶属于21目83科,其中有多种为我国特有或珍稀濒危的鸟类[1,2].
关键词 鸟类 性别 分子鉴定技术 聚合酶链式反应 单态性鸟
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关于同伦正则态射 被引量:13
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作者 曹永知 郭驼英 朱萍 《数学物理学报(A辑)》 CSCD 北大核心 2000年第2期274-277,共4页
该文在点标拓扑空间的范畴中引进了同伦正则态射的概念 ,研究了它存在的条件、性质以及它与同伦单 (满 )态、同伦正则单 (满 )
关键词 同伦论 同伦正则态射 同伦单态 同伦满态
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体表心电图两步法快速判定流出道室性早搏的起源 被引量:13
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作者 贾玉和 马坚 +6 位作者 李贤 聂玲 方丕华 姚焰 张奎俊 楚建民 张澍 《中国循环杂志》 CSCD 北大核心 2010年第3期208-211,共4页
目的:本文通过回顾既往消融成功的室性早搏(室早)病例,将其体表心电图与成功消融靶点部位比对,得出用两步法快速判定室早起源的心腔,以期在以后的室早射频消融治疗前能帮助确定消融策略。方法:66例成功消融的室早或室性心动过速患者,男3... 目的:本文通过回顾既往消融成功的室性早搏(室早)病例,将其体表心电图与成功消融靶点部位比对,得出用两步法快速判定室早起源的心腔,以期在以后的室早射频消融治疗前能帮助确定消融策略。方法:66例成功消融的室早或室性心动过速患者,男30例,平均年龄(36.9±13.9)岁。其中经股静脉途径在右心室消融成功32例(右心室消融组),经股动脉途径在左心室消融成功34例(左心室消融组)。结合文献,对明确了起源点的室早患者的四个心电图特征利用SPSS10.0软件进行分析。特征1:肢体导联Ⅰ、aVR、aVL和Ⅱ、Ⅲ、aVF导联及胸前导联V1的形态;特征2:V1导联r或R波时程;特征3:V1导联r或R波时程占总QRS时程的百分比(Dr/DQRS);特征4:R/S移行的胸前导联(即出现R/S≥1时的胸前导联)。结果:R/S移行的胸前导联和Dr/DQRS两项体表心电图特征性指标对预测室早起源具有很强的指导性。其中R/S移行导联在V4~6导联判定起源点在右心室侧的敏感度只有37.5%,但是其判定室早起源点不在左心室侧(即在右心室侧)的特异度却达100%,相应地其判定起源点在右心室侧的阳性预测值为100%,阴性预测值为63%。进一步对余下的54例R/S移行在V1、V2、V3导联的病例采用Dr/DQRS进行分析,发现将这些患者以Dr/DQRS<0.5(n=19)和Dr/DQRS≥0.5(n=35)分为两部分。其中以Dr/DQRS<0.5来判别消融靶点在右心室侧的敏感度是90.0%,特异度为97.1%,阳性预测值为94.7%,阴性预测值为94.3%;而用Dr/DQRS≥0.5来判定消融靶点在左心室侧的敏感度为97.1%,特异度为90.0%,阳性预测值为94.3%,阴性预测值为94.7%。结论:本研究提示在室早射频消融手术前可依据R/S移行的胸前导联和Dr/DQRS两项体表心电图指标,只用两步即可对室早起源得到初步判定。 展开更多
关键词 室性早搏 射频消融 心电图
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微卫星BAT-26位点单态性的分析 被引量:3
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作者 狄金明 张一楚 +1 位作者 顾琴龙 陈蕾 《肿瘤防治研究》 CAS CSCD 2001年第2期124-125,共2页
目的 微卫星不稳定性 (Microsatellite Instability,MSI)在许多肿瘤的发生中具很重要的作用 ,大多数微卫星 (Microsatellite,MS)位点在正常人群中多态性明显 ,有报道表明 BAT- 2 6位点单态性很好 ,据此我们分析了 60例正常肠粘膜标本中... 目的 微卫星不稳定性 (Microsatellite Instability,MSI)在许多肿瘤的发生中具很重要的作用 ,大多数微卫星 (Microsatellite,MS)位点在正常人群中多态性明显 ,有报道表明 BAT- 2 6位点单态性很好 ,据此我们分析了 60例正常肠粘膜标本中 BAT- 2 6位点 MSDNA的情况 ,以便了解 BAT- 2 6位点单态性情况。方法 组织 DNA提取后 PCR扩增 ,扩增产物行 6%变性聚丙烯酰胺凝胶电泳 ,最后银染。结果 所有标本在 BAT- 2 6位点 MSDNA长度无明显改变。结论 BAT- 2 6具有较好的单态性。 展开更多
关键词 微卫星 微卫星不稳定性 BAT-26 单态性 肿瘤 聚合酶链反应
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单形性亲上皮性肠道T细胞淋巴瘤16例临床病理学分析 被引量:4
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作者 张景航 薛云 +4 位作者 张延平 高子芬 黄欣 李敏 苏蔚 《新乡医学院学报》 CAS 2021年第11期1043-1047,共5页
目的探讨单形性亲上皮性肠道T细胞淋巴瘤(MEITL)的临床病理特点、免疫表型及分子遗传学改变。方法选择新乡医学院第一附属医院及北京大学第三医院收治的16例MEITL患者,采用免疫组织化学、原位杂交及T细胞受体(TCR)基因克隆性重排检测等... 目的探讨单形性亲上皮性肠道T细胞淋巴瘤(MEITL)的临床病理特点、免疫表型及分子遗传学改变。方法选择新乡医学院第一附属医院及北京大学第三医院收治的16例MEITL患者,采用免疫组织化学、原位杂交及T细胞受体(TCR)基因克隆性重排检测等方法检测其组织病理学,分析患者的临床病理学特点。结果16例MEITL患者中男女比例为9:7,中位发病年龄为54岁。13例患者病变部位位于小肠,1例位于升结肠近回盲部,1例位于降结肠,1例位于乙状结肠;临床表现以腹胀、腹痛、腹泻为主,部分出现腹部肿块及肠穿孔,无特异性改变;镜下肿瘤细胞形态较单一,小至中等大,细胞质淡染,核圆形、核仁不明显,染色质细腻;可见“亲上皮现象”,核分裂象及坏死易见。免疫组织化学检测结果显示,CD3、CD8、CD56、T细胞胞内抗原1(TIA-1)、B淋巴细胞瘤-2(Bcl-2)呈阳性表达,CD5、Granzyme B呈阴性表达,Ki-67增殖指数50%~90%;原位杂交结果显示,EB病毒编码的小RNA阴性。TCR重排检测阳性14例,阴性2例。结论METCL是罕见的原发胃肠道的高侵袭性淋巴瘤,多位于小肠,无特异性的临床表现,肿瘤细胞形态较单一,可见“亲上皮现象”,核分裂象及坏死易见,CD3、CD8、CD56、TIA-1、Bcl-2呈阳性表达,CD5、Granzyme B呈阴性表达,Ki-67增殖指数及TCR重排检测阳性率较高。 展开更多
关键词 单形性亲上皮性肠道T细胞淋巴瘤 免疫组织化学 原位杂交 T细胞受体
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