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Spontaneous Heparin-Induced Thrombocytopenia Presenting as Concomitant Bilateral Cerebrovascular Infarction and Acute Coronary Syndrome
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作者 Jong Kun Park Ilan Vavilin +4 位作者 Jacob Zaemes Araba Ofosu-Somuah Raghav Gattani Camila Sahebi Alexander G.Truesdell 《Cardiovascular Innovations and Applications》 2023年第1期44-48,共5页
Background:Spontaneous heparin-induced thrombocytopenia is a pro-thrombotic syndrome in which anti-heparin antibodies develop without heparin exposure.Case presentation:A 78-year-old man who underwent a successful lum... Background:Spontaneous heparin-induced thrombocytopenia is a pro-thrombotic syndrome in which anti-heparin antibodies develop without heparin exposure.Case presentation:A 78-year-old man who underwent a successful lumbar laminectomy presented to the hospital 5 days after discharge for stroke-like symptoms and was found to have acute infarcts of the bilateral frontal lobes.The patient was found to be severely thrombocytopenic and was incidentally found to have an inferior wall myocardial infarction.Further investigation led to the diagnosis of bilateral lower extremity deep vein thromboses.His overall clinical presentation prompted a detailed hematologic workup that indicated positivity for heparin-induced thrombocy-topenia despite no previous exposure to heparin products.Conclusions:This case illustrates a patient with no prior lifetime heparin exposure who underwent laminectomy with subsequent development of acute infarcts of the bilateral frontal lobes,an inferior wall myocardial infarction,and bilateral lower extremity deep vein thromboses,with concern for sequelae of spontaneous heparin-induced thrombo-cytopenia. 展开更多
关键词 Acute coronary syndrome deep vein thrombosis myocardial infarction cerebrovascular infarction spontaneous heparin-induced thrombocytopenia
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Rivaroxaban for the treatment of heparin-induced thrombocytopenia with thrombosis in a patient undergoing artificial hip arthroplasty:A case report
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作者 Fang-Fang Lv Mei-Ye Li +1 位作者 Wei Qu Zhao-Shun Jiang 《World Journal of Clinical Cases》 SCIE 2023年第26期6147-6153,共7页
BACKGROUND Anticoagulation treatment after lower limb surgery is one of the key methods to avoid thrombosis,and low-molecular-weight heparin is the treatment that is most frequently used in clinical practice.But one u... BACKGROUND Anticoagulation treatment after lower limb surgery is one of the key methods to avoid thrombosis,and low-molecular-weight heparin is the treatment that is most frequently used in clinical practice.But one uncommon side effect of lowmolecular-weight heparin is heparin-induced thrombocytopenia(HIT),which can develop into thrombosis if not caught early or managed incorrectly.CASE SUMMARY We present a case of a patient who underwent hip arthroplasty and experienced thrombocytopenia due to HIT on the 9th d following the application of lowmolecular-weight heparin anticoagulation.We did not diagnose HIT in time and applied 1 unit of platelets to the patient,which led to thrombosis.Luckily,the patient recovered following effective and timely surgery and treatment with rivaroxaban.CONCLUSION Patients using low-molecular-weight heparin after lower limb surgery need to have their platelet counts regularly checked.If HIT develops,platelet treatment should be given with caution. 展开更多
关键词 Low-molecular-weight heparin heparin-induced thrombocytopenia with thrombosis PLATELET Case report
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Cerebral venous thrombosis and heparin-induced thrombocytopenia in an 18-year old male with severe ulcerative colitis 被引量:4
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作者 Gudrun Scheving Thorsteinsson Maria Magnussson +4 位作者 Lena M Hallberg Nils Gunnar Wahlgren Fredrik Lindgren Petter Malmborg Thomas H Casswall 《World Journal of Gastroenterology》 SCIE CAS CSCD 2008年第28期4576-4579,共4页
The risk of thromboembolism is increased in inflammatory bowel disease and its symptoms may be overlooked. Furthermore, its treatment can be complex and is not without complications. We describe a case of an adolescen... The risk of thromboembolism is increased in inflammatory bowel disease and its symptoms may be overlooked. Furthermore, its treatment can be complex and is not without complications. We describe a case of an adolescent boy who developed a cerebral sinus venous thrombosis during a relapse of his ulcerative colitis and who, while on treatment with heparin, developed heparin-induced thrombocytopenia (HIT). The treatment was then switched to fondaparinux, a synthetic and selective inhibitor of activated factor . 展开更多
关键词 Inflammatory bowel disease Ulcerative colitis Cerebral venous thrombosis heparin-induced thrombocytopenia FONDAPARINUX
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Successful treatment in one myelodysplastic syndrome patient with primary thrombocytopenia and secondary deep vein thrombosis:A case report
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作者 Wen-Bin Liu Jian-Xiong Ma Hong-Xuan Tong 《World Journal of Clinical Cases》 SCIE 2022年第14期4640-4647,共8页
BACKGROUND The contradictory process of coagulation and anticoagulation maintains normal physiological function,and platelets(PLTs)play a key role in hemostasis and bleeding.When severe thrombocytopenia and deep vein ... BACKGROUND The contradictory process of coagulation and anticoagulation maintains normal physiological function,and platelets(PLTs)play a key role in hemostasis and bleeding.When severe thrombocytopenia and deep vein thrombosis(DVT)occur simultaneously,the physician will be confronted with a great challenge,especially when interventional thrombectomy fails.CASE SUMMARY We describe a 52-year-old woman who suffered from myelodysplastic syndrome with severe thrombocytopenia and protein S deficiency with right lower extremity DVT.In this patient,the treatment of DVT was associated with numerous contradictions due to severe thrombocytopenia,especially when interventional thrombectomy was not successful.Fortunately,fondaparinux sodium effectively alleviated the thrombus status of the patient and gradually decreased the D-dimer level.In addition,no increase in bleeding was noted.The application of eltrombopag stimulated the maturation and differentiation of megakaryocytes and increased the peripheral blood PLT count.The clinical symptoms of DVT in the right lower extremities in this patient significantly improved.The patient resumed daily life activities,and the treatment effects were independent of PLT transfusion.CONCLUSION This is a contradictory and complex case,and fondaparinux sodium and eltrombopag may represent a good choice for the treatment of DVT in patients with severe thrombocytopenia. 展开更多
关键词 thrombocytopenia Deep vein thrombosis Fondaparinux sodium THROMBOPHILIA Myelodysplastic syndrome ELTROMBOPAG Case report
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Challenging anticoagulation therapy for multiple primary malignant tumors combined with thrombosis:A case report and review of literature
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作者 Jia-Xin Chen Ling-Ling Xu +1 位作者 Jing-Ping Cheng Xun-Hua Xu 《World Journal of Clinical Cases》 SCIE 2024年第9期1704-1711,共8页
BACKGROUND Venous thromboembolism significantly contributes to patient deterioration and mortality.Management of its etiology and anticoagulation treatment is intricate,necessitating a comprehensive consideration of v... BACKGROUND Venous thromboembolism significantly contributes to patient deterioration and mortality.Management of its etiology and anticoagulation treatment is intricate,necessitating a comprehensive consideration of various factors,including the bleeding risk,dosage,specific anticoagulant medications,and duration of therapy.Herein,a case of lower extremity thrombosis with multiple primary malignant tumors and high risk of bleeding was reviewed to summarize the shortcomings of treatment and prudent anticoagulation experience.CASE SUMMARY An 83-year-old female patient was admitted to the hospital due to a 2-wk history of left lower extremity edema that had worsened over 2 d.Considering her medical history and relevant post-admission investigations,it was determined that the development of left lower extremity venous thrombosis and pulmonary embolism in this case could be attributed to a combination of factors,including multiple primary malignant tumors,iliac venous compression syndrome,previous novel coronavirus infection,and inadequate treatment for prior thrombotic events.However,the selection of appropriate anticoagulant medications,determination of optimal drug dosages,and establishment of an appropriate duration of anticoagulation therapy were important because of concurrent thrombocytopenia,decreased quantitative fibrinogen levels,and renal insufficiency.CONCLUSION Anticoagulant prophylaxis should be promptly initiated in cases of high-risk thrombosis.Individualized anticoagulation therapy is required for complex thrombosis. 展开更多
关键词 Venous thromboembolism Cancer-associated thrombosis Anticoagulation therapy iliac vein compression syndrome COVID-19 thrombocytopenia Case report
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Successful Treatment of Severe Heparin-induced Thrombocytopenia with Intravenous Immunoglobulin, Platelet Transfusion and Rivaroxaban: A Case Report 被引量:2
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作者 黄河 林颖 +2 位作者 姚荣欣 何牧卿 林晓骥 《Chinese Medical Sciences Journal》 CAS CSCD 2019年第1期60-64,共5页
Heparin-induced thrombocytopenia(HIT) is a relatively infrequent complication of heparin administration. HIT can cause devastating thrombosis, making it one of the most serious adverse drug reactions encountered in cl... Heparin-induced thrombocytopenia(HIT) is a relatively infrequent complication of heparin administration. HIT can cause devastating thrombosis, making it one of the most serious adverse drug reactions encountered in clinical practice. We successfully treated a case of severe HIT presenting with thrombosis and life-threatening bleeding complications with intravenous immunoglobulin(IVIG), platelet transfusion and oral anticoagulant Rivaroxaban. In this case, we considered that IVIG played the most important role by preventing further thrombosis, increasing the platelet count, and ensuring the efficacy of Rivaroxaban. We therefore suggest that IVIG might be the optimal treatment for patients with this urgent condition. 展开更多
关键词 heparin-induced thrombocytopenia thrombosis INTRAVENOUS IMMUNOGLOBULIN platelet TRANSFUSION RIVAROXABAN
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Factors predisposing to thrombosis after major joint arthroplasty
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作者 Zoe H Dailiana Nikolaos Stefanou +6 位作者 Sokratis Varitimids Nikolaos Rigopoulos Apostolos Dimitroulias TheofilosKarachalios Konstantinos N Malizos Despoina Kyriakou Panagoula Kollia 《World Journal of Orthopedics》 2020年第9期400-410,共11页
BACKGROUND Total joint arthroplasty is one of the most common options for end stage osteoarthritis of major joints.However,we must take into account that thrombosis after hip/knee arthroplasty may be related to mutati... BACKGROUND Total joint arthroplasty is one of the most common options for end stage osteoarthritis of major joints.However,we must take into account that thrombosis after hip/knee arthroplasty may be related to mutations in genes encoding for blood coagulation factors and immune reactions to anticoagulants[heparininduced thrombocytopenia(HIT)/thrombosis].Identifying and characterizing genetic risk should help to develop diagnostic strategies or modify anticoagulant options in the search for etiological mechanisms that cause thrombophilia following major orthopedic surgery.AIM To evaluate the impact of patients’coagulation profiles and to study specific pharmacologic factors in the development of post-arthroplasty thrombosis.METHODS In 212(51 male and 161 female)patients that underwent primary total hip arthroplasty(100)or total knee arthroplasty(112)due to osteoarthritis during a period of 1 year,platelet counts and anti-platelet factor 4(PF4)/heparin antibodies were evaluated pre/postoperatively,and antithrombin III,methylenetetrahydrofolate reductase,factor V and prothrombin gene mutations were evaluated preoperatively.In a minimum follow-up of 3 years,196 patients receiving either low-molecular-weight heparins(173)or fondaparinux(23)were monitored for the development of thrombocytopenia,anti-PF4/heparin antibodies,HIT,and thrombosis.RESULTS Of 196 patients,32 developed thrombocytopenia(nonsignificant correlation between anticoagulant type and thrombocytopenia,P=0134.)and 18 developed anti-PF4/heparin antibodies(12/173 for low-molecular-weight heparins and 6/23 for fondaparinux;significant correlation between anticoagulant type and appearance of antibodies,P=0.005).Odds of antibody emergence:8.2%greater in patients receiving fondaparinux than low-molecular-weight heparins.Gene mutations in factor II or V(two heterozygotes for both factor V and II)were identified in 15 of 196 patients.Abnormal low protein C and/or S levels were found in 3 of 196(1.5%)patients,while all patients had normal levels of von Willebrand factor,lupus anticoagulant,and antithrombin III.Four patients developed HIT(insignificant correlation between thrombocytopenia and antibodies)and five developed thrombosis(two had positive antibodies and two were heterozygotes for both factor II&V mutations).Thrombosis was not significantly correlated to platelet counts or HIT.The correlation of thrombosis to antibodies,factor II,factor V was P=0.076,P=0.043,P=0.013,respectively.CONCLUSION Screening of coagulation profile,instead of platelet monitoring,is probably the safest way to minimize the risk of post-arthroplasty thrombosis.In addition,fondaparinux can lead to the formation of anti-PF4/heparin antibodies or HIT. 展开更多
关键词 ARTHROPLASTY thrombosis heparin-induced thrombocytopenia Coagulation factors Low-molecular-weight heparin FONDAPARINUX
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Hypereosinophilia with cerebral venous sinus thrombosis and intracerebral hemorrhage:A case report and review of the literature
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作者 Xiu-Hua Song Tian Xu Guo-Hua Zhao 《World Journal of Clinical Cases》 SCIE 2021年第28期8571-8578,共8页
BACKGROUND Hypereosinophilia(HE)is defined as a peripheral blood eosinophil count of>1.5×109/L and may be associated with tissue damage.The clinical presentations of HE vary;however,myocardial fibrosis and thr... BACKGROUND Hypereosinophilia(HE)is defined as a peripheral blood eosinophil count of>1.5×109/L and may be associated with tissue damage.The clinical presentations of HE vary;however,myocardial fibrosis and thrombosis can threaten the lives of patients with sustained eosinophilia.Cerebral venous sinus thrombosis(CVST)in the setting of eosinophil-related diseases has seldom been reported.Here,we review the literature on HE with CVST to increase knowledge and encourage early diagnosis.CASE SUMMARY A previously healthy 41-year-old man was admitted to hospital with diarrhea and abdominal pain.He was treated with antibiotics for suspected acute colitis.Three days later,he experienced headache and vomiting.Brain computed tomography(CT)revealed thrombosis of the left jugular vein to the left transverse sinus vein.Platelet(PLT)count decreased to 60×1012/L,and absolute eosinophil count(AEC)increased to 2.41×109/L.He was treated with low-molecular-weight heparin.PLT count progressively decreased to 14×109/L,and we terminated anticoagulation and performed PLT transfusion.Six days after admission,he complained of a worsening headache.Brain CT revealed right temporal lobe and left centrum semiovale intracerebral hemorrhage,and AEC increased to 7.65×109/L.We used prednisolone for HE.The level of consciousness decreased,so emergency hematoma removal and decompressive craniectomy for right cerebral hemorrhage were performed.The patient was alert 2 d after surgery.He was treated with anticoagulation again 2 wk after surgery.Corticosteroids were gradually tapered without any symptomatic recurrence or abnormal laboratory findings.CONCLUSION HE can induce CVST,and we need to focus on eosinophil counts in patients with CVST. 展开更多
关键词 Cerebral venous sinus thrombosis Intracerebral hemorrhage HYPEREOSINOPHILIA Hypereosinophilic syndrome thrombocytopenia COLITIS Case report
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A rare case of arterial thrombosis due to heparin-induced thrombocytopenia
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作者 LI Lei GAO Wei ZHANG Fu-chun HAN Jiang-li ZHANG Yuan WANG Gui-song SHE Fei GUO Li-jun 《Chinese Medical Journal》 SCIE CAS CSCD 2011年第22期3830-3833,共4页
A 78-year-old man presented with an eight-hour history of chest distress. Electrocardiograph and serum cardiac enzymes were suggestive of acute inferior myocardial infarction with right ventricular infarction. The pat... A 78-year-old man presented with an eight-hour history of chest distress. Electrocardiograph and serum cardiac enzymes were suggestive of acute inferior myocardial infarction with right ventricular infarction. The patient, who underwent emergency percutaneous coronary intervention, suffered from thrombocytopenia presenting with cerebral infarction and myocadial reinfarction during haparin exposure. The laboratory test for heparin-induced thrombocytopenia (HIT) specific antibodies (heparin-platelet factor, PF4) was positive. The case was diagnosed as arteries thrombosis due to heparin-induced thrombocytopenia; the patient died after cessation of heparin. 展开更多
关键词 heparin-induced thrombocytopenia arterial thrombosis
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Heparin-induced thrombocytopenia occurring early after living donor liver transplantation:a case report
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作者 Naoya Iwasaki Motohiro Sekino +11 位作者 Takanobu Hara Akihiko Soyama Masaaki Hidaka Yusuke Kasai Miki Suzumura Hiroshi Araki Rintaro Yano Sojiro Matsumoto Taiga Ichinomiya Ushio Higashijima Susumu Eguchi Tetsuya Har 《Emergency and Critical Care Medicine》 2023年第4期198-202,共5页
Background:Thrombocytopenia commonly occurs early after liver transplantation.Heparin,usually administered as anticoagulant ther-apy for thrombosis,a common complication after liver transplantation,may cause heparin-i... Background:Thrombocytopenia commonly occurs early after liver transplantation.Heparin,usually administered as anticoagulant ther-apy for thrombosis,a common complication after liver transplantation,may cause heparin-induced thrombocytopenia.Heparin-induced thrombocytopenia is a rare but life-threatening complication,and its diagnosis after liver transplantation is challenging.Case presentation:We report a case of heparin-induced thrombocytopenia after living donor liver transplantation with a good out-come because of early diagnosis and discontinuation of heparin.After liver transplantation,the platelet count usually reaches a nadir on postoperative days 3–5 and gradually recovers.In contrast,heparin-induced thrombocytopenia typically occurs 5–10 days after heparin administration;therefore,if heparin is started intraoperatively,then thrombocytopenia will occur on postoperative days 5–10.Conclusion:Monitoring the trend and timing of thrombocytopenia and detailed examination for thrombosis may help confirm the diag-nosis of heparin-induced thrombocytopenia in the early stage after liver transplantation. 展开更多
关键词 Case report HEPARIN heparin-induced thrombocytopenia Liver transplantation thrombocytopenia thrombosis
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Diagnostic Approach of Thrombocytopenia in Pregnancy: A Review
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作者 John Alexander Yela Cono Sandra Ximena Olaya +2 位作者 David Ricardo Murillo-Garcia Brahyan Osorio Juan David Hernández 《Open Journal of Obstetrics and Gynecology》 CAS 2022年第8期784-792,共9页
Thrombocytopenia (defined as platelet count <sup>9</sup>/L) is present in 7% - 12% of pregnant women at delivery. Although there are mild etiologies of this condition that are often diagnosed incidentally,... Thrombocytopenia (defined as platelet count <sup>9</sup>/L) is present in 7% - 12% of pregnant women at delivery. Although there are mild etiologies of this condition that are often diagnosed incidentally, there are more severe causes that can be life threating. Thrombocytopenia also has a great implication in surgical risk and regional anesthesia. A structured evaluation of thrombocytopenia is necessary to allow an adequate diagnostic approach. Here we summarized the current knowledge of thrombocytopenia in pregnancy. 展开更多
关键词 PREGNANCY thrombocytopenia Gestational thrombocytopenia PREECLAMPSIA HELLP syndrome Immune thrombocytopenia Thrombotic Microangiopathy heparin-induced thrombocytopenia Disseminated Intravascular Coagulation
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下肢深静脉血栓介入治疗发生肝素诱发血小板减少伴血栓形成综合征一例 被引量:9
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作者 田玉龙 张曦彤 《介入放射学杂志》 CSCD 北大核心 2012年第1期53-54,共2页
临床资料患者女,70岁。因右下肢胀痛1周,渐进性加重活动受限3 d入院。查体:右侧下肢肿胀明显,肌张力较对侧高,皮色加深,右侧深静脉走形区压痛。彩色多普勒超声检查示:右侧下肢深静脉血栓形成(DVT)急性期。治疗方案:①右髂股静脉导... 临床资料患者女,70岁。因右下肢胀痛1周,渐进性加重活动受限3 d入院。查体:右侧下肢肿胀明显,肌张力较对侧高,皮色加深,右侧深静脉走形区压痛。彩色多普勒超声检查示:右侧下肢深静脉血栓形成(DVT)急性期。治疗方案:①右髂股静脉导管溶栓; 展开更多
关键词 静脉血栓形成 介入治疗 肝素诱发血小板减少伴血栓形成综合征
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阿加曲班研究进展 被引量:24
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作者 张子彦 张宏卫 《国际内科学杂志》 CAS 2007年第8期483-485,共3页
阿加曲班是合成的小分子药物,为一价直接凝血酶抑制剂,阿加曲班直接与凝血酶的催化活性位点结合,不但灭活液相凝血酶,还能够灭活与纤维蛋白血栓结合的凝血酶,目前已批准用于肝素诱导的血小板减少及血栓症、经皮冠状动脉介入治疗、脑卒... 阿加曲班是合成的小分子药物,为一价直接凝血酶抑制剂,阿加曲班直接与凝血酶的催化活性位点结合,不但灭活液相凝血酶,还能够灭活与纤维蛋白血栓结合的凝血酶,目前已批准用于肝素诱导的血小板减少及血栓症、经皮冠状动脉介入治疗、脑卒中溶栓等血栓性疾病。体内外研究表明,它还抑制凝血酶的其他作用,如可以抑制肿瘤转移、炎症过程及血管成形术后的再狭窄等。 展开更多
关键词 阿加曲班 肝素诱导的血小板减少及血栓症 缺血性脑卒中 经皮冠状动脉介入
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T_H17细胞及IL-17在原发性抗磷脂综合征中的表达及临床意义 被引量:1
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作者 解鸿翔 陈素峰 +1 位作者 朱里洁 孙青阳 《临床检验杂志》 CAS CSCD 2016年第4期260-263,共4页
目的观察T_H17细胞及相关细胞因子IL-17在原发性抗磷脂综合征(PAPS)中的表达水平,并初步探讨其临床意义。方法收集32例PAPS患者及33例健康对照者静脉血标本,分离外周血单个核细胞(PBMC),流式细胞术检测T_H17细胞百分率,ELISA法检测血浆I... 目的观察T_H17细胞及相关细胞因子IL-17在原发性抗磷脂综合征(PAPS)中的表达水平,并初步探讨其临床意义。方法收集32例PAPS患者及33例健康对照者静脉血标本,分离外周血单个核细胞(PBMC),流式细胞术检测T_H17细胞百分率,ELISA法检测血浆IL-17的表达水平,并分析IL-17水平与PAPS患者临床病理特征及实验室指标[抗心凝脂抗体(a CL)、抗β2糖蛋白Ⅰ(β2GPⅠ)和狼疮抗凝物(LA)]的关系。结果 PAPS患者外周血T_H17细胞百分率为(1.98±0.78)%,血浆IL-17水平为(60.72±18.71)pg/m L,均显著高于健康人对照组(P均<0.01),且T_H17细胞百分率与血浆IL-17水平呈正相关(r=0.586,P<0.01)。PAPS患者血浆IL-17水平与患者a CL、抗β2GPⅠ抗体和LA均无明显相关性(P均>0.05)。与近期(≥3月)无相关临床事件发生的PAPS患者相比,新近(≤1月)发生动脉血栓事件的患者血浆IL-17水平差异无统计学意义(P=0.074),静脉血栓和血小板减少的PAPS患者IL-17蛋白水平显著升高(P<0.01)。结论 T_H17细胞及IL-17与PAPS血栓形成和血小板减少密切相关,提示T_H17细胞及IL-17参与了PAPS脉管症状的发病机制。 展开更多
关键词 抗磷脂综合征 TH17细胞 白细胞介素-17 血栓 血小板减少
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儿童嗜酸性粒细胞增多综合征并多发动静脉血栓形成1例并文献复习 被引量:1
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作者 王勇 林明星 +2 位作者 林晓霞 陈燕惠 李健 《中国小儿血液与肿瘤杂志》 CAS 2018年第3期137-142,共6页
目的提高对儿童嗜酸性粒细胞增多综合征(HES)并血小板减少及多发动静脉血栓的认识。方法回顾性分析1例HES并血小板减少、肺栓塞及下肢深静脉血栓患儿的病例资料,并复习相关文献,总结其临床特征及诊治经验。结果患儿,男,12岁,临床表现包... 目的提高对儿童嗜酸性粒细胞增多综合征(HES)并血小板减少及多发动静脉血栓的认识。方法回顾性分析1例HES并血小板减少、肺栓塞及下肢深静脉血栓患儿的病例资料,并复习相关文献,总结其临床特征及诊治经验。结果患儿,男,12岁,临床表现包括皮疹、发热、胸痛、下肢肿胀及破溃;辅助检查:血常规提示反复嗜酸性粒细胞增多及血小板减少,D-二聚体升高,3P+FDPP阳性,双下肢血管彩超提示深静脉多发血栓形成,肺动脉CT提示肺栓塞;予短程糖皮质激素联合静脉注射用人血免疫球蛋白治疗,嗜酸性粒细胞及血小板虽可恢复正常,但易反复;予低分子肝素钠抗凝2个月,血栓进展;维持抗凝同时口服强的松2个月,症状消失、血常规恢复正常、血栓完全吸收。结论 HES本身可引起血小板低下;HES合并D二聚体升高时,需警惕深静脉血栓形成及脏器栓塞,尽早抗凝治疗联合糖皮质激素治疗成功率高,可减少严重血栓性事件发生。 展开更多
关键词 嗜酸粒细胞增多综合征 儿童 肺栓塞 血小板减少 下肢深静脉血栓形成
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急性冠状动脉综合征合并血小板减少症 被引量:1
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作者 韩雅君 王丽媛 +1 位作者 朱慧 何涛 《医学综述》 2015年第12期2215-2217,共3页
急性冠状动脉综合征(ACS)合并血小板减少症时明显增加患者住院期间出血率和病死率,同时影响ACS治疗。而血小板减少症人群仍有发生血栓事件的可能。血小板减少症患者发生ACS时,血小板计数<30×109/L时出血概率增加,不宜应用抗血... 急性冠状动脉综合征(ACS)合并血小板减少症时明显增加患者住院期间出血率和病死率,同时影响ACS治疗。而血小板减少症人群仍有发生血栓事件的可能。血小板减少症患者发生ACS时,血小板计数<30×109/L时出血概率增加,不宜应用抗血小板药物。当血小板>30×109/L应用双联抗血小板药物治疗的同时应积极提高血小板治疗,评价出血风险,密切监测血小板变化。如果进行冠状动脉介入治疗建议裸支架治疗。ACS患者治疗期间出现血小板减少症主要的原因是药物导致血小板减少,包括肝素、血小板糖蛋白Ⅱb/Ⅲa受体拮抗剂、氯吡格雷等,但应及时诊断方能准确治疗,要与弥散性血管内凝血等进行鉴别。 展开更多
关键词 急性冠状动脉综合征 血小板减少症 血栓
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系统性红斑狼疮继发抗磷脂综合征的中西医诊治进展 被引量:1
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作者 韦锦松 荣晓凤 《中医药临床杂志》 2021年第9期1828-1833,共6页
抗磷脂综合征(the antiphospholipid syndrome,APS)是以动静脉血栓事件、病理妊娠、血小板减少以及持续存在抗磷脂抗体(antiphospholipid antibodies,aPL)为特征的一种自身免疫性疾病。APS常继发于系统性红斑狼疮(system ic lupus eryth... 抗磷脂综合征(the antiphospholipid syndrome,APS)是以动静脉血栓事件、病理妊娠、血小板减少以及持续存在抗磷脂抗体(antiphospholipid antibodies,aPL)为特征的一种自身免疫性疾病。APS常继发于系统性红斑狼疮(system ic lupus erythematosus,SLE),因SLE继发APS的不良预后越来越引起重视,寻找新的治疗手段已迫在眉睫。虽然目前诸多中医大家证实了活血化瘀、补肾健脾等治疗方法对SLE继发APS的临床疗效,但西医抗凝及抗血小板仍是最有效、最主流的治疗手段,因此中西医结合治疗可能成为另一种极富前景的治疗方法。 展开更多
关键词 系统性红斑狼疮 抗磷脂综合征 血栓形成 复发性流产 血小板减少 中西医
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血小板减少并深静脉血栓形成
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作者 徐玫丽 霍继荣 周雨迁 《中国实用内科杂志》 CAS CSCD 北大核心 2009年第1期89-91,共3页
关键词 血小板减少 系统性红斑狼疮 深静脉血栓形成 抗磷脂抗体综合征
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血小板减少与抗磷脂综合征临床及实验室特点的关联分析 被引量:3
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作者 李煜子 姜承瑞 +1 位作者 李春 栗占国 《中华风湿病学杂志》 CAS CSCD 北大核心 2021年第1期8-14,共7页
目的探讨以血小板减少为主要表现的APS患者的临床及实验室特点,以及将血小板减少纳入分类标准对APS诊断率的影响。方法回顾性分析2003年1月至2017年8月于北京大学人民医院住院的临床资料齐全的APS患者161例,根据血小板减少病史,分为血... 目的探讨以血小板减少为主要表现的APS患者的临床及实验室特点,以及将血小板减少纳入分类标准对APS诊断率的影响。方法回顾性分析2003年1月至2017年8月于北京大学人民医院住院的临床资料齐全的APS患者161例,根据血小板减少病史,分为血小板减少组和血小板正常组,采用χ^(2)检验或Fisher确切概率法及t检验进行统计学处理。结果161例APS患者中,原发性APS 48例(29.8%),继发性APS 113例(70.2%)。91例(56.5%)患者出现血小板减少,62例(38.5%)患者以血小板减少首发。原发性APS患者血小板减少组发生血栓(40.0%和69.6%,χ^(2)=4.218,P=0.040)的比例相对较低,静脉血栓(20.0%和47.8%,χ^(2)=4.174,P=0.041)的发生率明显低于血小板正常组;继发性APS患者血小板减少组发生血栓(43.9%和80.9%,χ^(2)=15.496,P<0.01)的比例相对较低,其中动脉血栓(21.2%和42.6%,χ^(2)=5.944,P=0.015)及静脉血栓(22.7%和51.1%,χ^(2)=9.753,P=0.002)的发生率均明显低于血小板正常组。在实验室检查方面,原发性APS患者血小板减少组较易出现抗心磷脂抗体(aCL)阳性(80.0%和52.2%,χ^(2)=4.174,P=0.041),继发性APS患者血小板减少组较易出现白细胞减少(25.8%和10.6%,χ^(2)=4.002,P=0.045)、补体C3下降(78.7%和44.4%,χ^(2)=13.205,P<0.01)和补体C4下降(74.6%和46.7%,χ^(2)=8.485,P=0.004)。在本组患者中,符合1988年、1989年、1999年及2006年APS的分类标准的患者比例分别为88.2%、87.0%、64.0%及70.8%,若将血小板减少纳入到2006年APS分类标准中,将使该比例提高到96.3%。结论伴有血小板减少的APS患者发生血栓的风险显著低于血小板正常者。血小板减少是APS的重要表现,可提高APS的临床诊断率。 展开更多
关键词 抗磷脂综合征 血小板减少 血栓形成 分类
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新冠病毒疫苗诱导的伴有血小板减少的免疫性血栓综合征的报告率 被引量:2
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作者 曲畅达 颜畅 潘玉君 《国际免疫学杂志》 CAS 2022年第2期113-118,共6页
新冠肺炎疫情催生了新冠病毒疫苗的快速研发和应用,2020年年底以来国内外陆续有4类11款新冠疫苗已获批附条件紧急上市。上市前,这些疫苗的有效性和安全性评价都表现良好。但是疫苗上市后,在真实世界(real-world)随着接种剂次的增加,某... 新冠肺炎疫情催生了新冠病毒疫苗的快速研发和应用,2020年年底以来国内外陆续有4类11款新冠疫苗已获批附条件紧急上市。上市前,这些疫苗的有效性和安全性评价都表现良好。但是疫苗上市后,在真实世界(real-world)随着接种剂次的增加,某些疫苗接种后陆续出现罕见的不良反应,引起了人们的广泛关注。在所有的不良反应中,尤以疫苗诱导的伴有血小板减少免疫性血栓最为严重。此病虽然发生几率低,但一旦发病比较危重,死亡率高。欧美国家使用的主流4款疫苗,阿斯利康黑猩猩腺病毒载体疫苗、强生人26型腺病毒载体疫苗、Moderna mRNA疫苗和辉瑞mRNA疫苗,接种后引起的伴有血小板减少免疫性血栓的报告率分别为每百万人5.7~21.7、0.9~11.5、0.9~5.6和0.4~1.9例。我国使用的4款灭活疫苗、1款人5型腺病毒载体疫苗和1款基因工程重组蛋白疫苗以及俄罗斯使用的人5型/26型腺病毒载体疫苗,到目前为止没有此病的病例报告。但随着接种剂次的增加,应密切注意和随访可能出现的、罕见的不良反应的发生。 展开更多
关键词 新冠病毒疫苗 接种 副作用 免疫性血栓综合征 血小板减少的免疫性血栓
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