• 不 限
  • 期刊论文
  • 硕博论文
  • 会议论文
  • 报 纸
  • 英文论文
  2. 您的位置
  3. 首页
  4. 期刊论文
  5. Recurrent thrombosis in the lower extremities after thrombectomy in a patient with polycythemia vera

Recurrent thrombosis in the lower extremities after thrombectomy in a patient with polycythemia vera

来源 :世界临床病例杂志 | 被引量 : 0次 | 上传用户：skynini83
【摘 要】
：
BACKGROUND Acute arterial embolism of the extremities is a surgical emergency. Atrialfibrillation is the major etiology of acute arterial embolism of the extrem
【作 者】
：
Bu-Ping Jiang Guo-Bing Cheng Q 
【机 构】
：
DepartmentofVascularSurgery
【出 处】
：
世界临床病例杂志
【发表日期】
：
2020年24期
【关键词】
：
THROMBOSIS THROMBECTOMY Polycythemia vera Case report 
下载到本地 , 更方便阅读
下载此文 赞助VIP
声明 : 本文档内容版权归属内容提供方 , 如果您对本文有版权争议 , 可与客服联系进行内容授权或下架
论文部分内容阅读
BACKGROUND Acute arterial embolism of the extremities is a surgical emergency. Atrialfibrillation is the major etiology of acute arterial embolism of the extremities.Emergency femoral artery thrombectomy can successfully treat this issue.However, polycyth
其他文献
Minimally invasive maxillary sinus augmentation with simultaneous implantation on an elderly patient
BACKGROUND In this case study,a minimally invasive transalveolar approach using platelet-rich fibrin and bone substitute with simultaneous implantation was carr
期刊
MaxillarysinusaugmentationBonesubstituteBoneregenerationPlateletrichfibr
Sclerosing stromal tumor of the ovary with masculinization,Meig’s syndrome and CA125 elevation in an
BACKGROUND Sclerosing stromal tumor (SST) is an extremely rare sex cord stromal tumor of theovary. It was first reported and named in 1973. These tumors typical
期刊
OvariantumorSclerosingstromaltumorANDROGENSADOLESCENTVIRILIZATIONCasere
Extreme venous letting and cupping resulting in life-threatening anemia and acute myocardial infarct
BACKGROUND Wet cupping (WC) is a traditional therapy of skin suction-assisted bloodlettingthat is widely used in modern alternative medicine in Asia and the Mid
期刊
BLOODLETTINGST-elevationmyocardialinfarctionANEMIACUPPINGWetcuppingCase
Immunotherapies application in active stage of systemic lupus erythematosus in pregnancy:A case repo
BACKGROUND Pregnancy in the setting of systemic lupus erythematosus can worsen thecondition from the stable to active stage, with quality of life and fertility
期刊
PregnantwomenSystemiclupuserythematosusIMMUNOTHERAPIESCasereportActives
Novel conservative treatment for peritoneal dialysis-related hydrothorax:Two case reports
BACKGROUND Peritoneal dialysis (PD) is an important renal replacement therapy for patientswith end-stage renal disease. PD-related hydrothorax is a rare but ser
期刊
PeritonealdialysisEnd-stagerenaldiseaseHYDROTHORAXTREATMENTCONSERVATIVEC
Congenital nephrogenic diabetes insipidus due to the mutation in AVPR2(c.541C>T)in a neonate:A ca
BACKGROUND Congenital nephrogenic diabetes insipidus (CNDI) is a rare hereditary renaldisorder that is caused by mutations in AVPR2 or aquaporin 2 (AQP2). Up to
期刊
NEONATECongenitalnephrogenicdiabetesinsipidusAVPR2geneGenemutationMagne
Fracture of the scapular neck combined with rotator cuff tear:A case report
BACKGROUND Scapular fracture has a low incidence rate, accounting for 0.4%-0.9% of allfractures, and scapular neck fractures are extremely rare, comprisingappro
期刊
ScapularfracturesScapularneckfracturesRotatorcufftearGlenohumeraldisloc
Risk factors for de novo hepatitis B during solid cancer treatment
BACKGROUND Reactivation of hepatitis B virus(HBV)during anticancer treatment is a critical issue.When treating patients with solid tumors,it is unclear whether
期刊
HepatitisBREACTIVATIONSolidcancertreatmentDigestionandabsorptionorganH
Synchronous colonic mucosa-associated lymphoid tissue lymphoma found after surgery for adenocarcinom
BACKGROUND Mucosa-associated lymphoid tissue (MALT) lymphoma is a subtype of non-Hodgkin lymphoma that is mainly involved in the gastrointestinal tract. Thesync
期刊
Mucosa-associatedlymphoidtissuelymphomaADENOCARCINOMAColonSynchronousmali
Novel mutation in the ASXL3 gene in a Chinese boy with microcephaly and speech impairment:A case rep
BACKGROUND Bainbridge-Ropers syndrome (BRPS) is a severe disorder characterized by failureto thrive, facial dysmorphism, and severe developmental delay. BRPS is
期刊
Bainbridge-RoperssyndromeASXL3mutationWhole-exomesequencingCasereport