Search results for "rare"

showing 10 items of 2778 documents

Relationship between Skin Temperature, Electrical Manifestations of Muscle Fatigue, and Exercise-Induced Delayed Onset Muscle Soreness for Dynamic Co…

2020

Delayed onset muscle soreness (DOMS) indicates the presence of muscle damage and impairs force production and control. Monitorization of DOMS is useful to improving recovery intervention plans. The magnitude of DOMS may relate to muscle fatigue, which can be monitored by surface electromyography (EMG). Additionally, growing interest has been expressed in determining whether the skin temperature over a muscle group during exercise to fatigue could be a non-invasive marker for DOMS. Here we determine whether skin temperature and manifestations of muscle fatigue during exercise are correlated and can predict DOMS after concentric&ndash

AdultMalemedicine.medical_specialtyDynamic contractionselectromyographyHealth Toxicology and Mutagenesislcsh:MedicinePhysical exerciseExerciciElectromyographyBicepsArticle03 medical and health sciencesYoung AdultTemperatura corporal0302 clinical medicinePhysical medicine and rehabilitationphysical exerciseDelayed onset muscle sorenessmedicineHumansMuscle SkeletalExerciseMuscle fatiguemedicine.diagnostic_testbusiness.industrylcsh:RPublic Health Environmental and Occupational Healthexercise recoverySkin temperatureMuscle activationbiceps brachialisBayes Theorem030229 sport sciencesMyalgiaCross-Sectional Studiesinfrared thermographyMuscle Fatiguemedicine.symptombusinessSkin Temperature030217 neurology & neurosurgery
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Wilson's disease in Spain: validation of sources of information used by the Rare Diseases Registries

2021

[ES] Objetivo: Evaluar las fuentes de información empleadas por los Registros Autonómicos de Enfermedades Raras (RAER) para la captación de la enfermedad de Wilson en España, calcular su prevalencia y mortalidad, y describir las características sociodemográficas de las personas afectadas. Método: Estudio epidemiológico transversal, periodo 2010-2015. Se captaron los posibles casos mediante los códigos 275.1 (CIE-9-MC), E83.0 (CIE-10) y 905 ORPHA en 15 RAER y el Registro de Pacientes de Enfermedades Raras del Instituto de Salud Carlos III. Los diagnósticos fueron validados revisando la documentación clínica. Se calcularon el valor predictivo positivo (VPP) de las fuentes de información, la p…

AdultMalemedicine.medical_specialtyHealth information systemsEpidemiologyPopulationEnfermedad de WilsonPrimary careSistemas de información en saludYoung Adult03 medical and health sciences0302 clinical medicineHepatolenticular DegenerationClinical historyPrevalencemedicineEpidemiologíaHumansRegistries030212 general & internal medicineFuentes de datoseducationWilson diseaseGynecologyeducation.field_of_study030505 public healthEnfermedades rarasbusiness.industryPublic Health Environmental and Occupational HealthHospital discharge databaseData sourcesAtencion primariaPredictive valueRare diseasesCross-Sectional StudiesSpainFemalePublic aspects of medicineRA1-1270Prevalencia0305 other medical sciencebusinessGaceta Sanitaria
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Inflammatory implant periapical lesion: etiology, diagnosis, and treatment--presentation of 7 cases.

2008

Purpose To investigate implant periapical lesions, and to describe their treatment. The hypothesis of this evaluation is that implant periapical lesions are disorders of the area surrounding the apex of a dental implant, and that their etiology can be multifactorial (ie, vascular impairment, vascular ischemia, overheating of bone during drilling, and implant surface contamination). The diagnosis is based on the clinical manifestations and x-ray findings. The x-ray findings usually involve a periapical radiotransparency. Materials and Methods Seven patients with implant periapical lesions (3 in the upper jaw, and 4 in the mandible) after implant placement are described. All patients reported…

AdultMalemedicine.medical_specialtyMaxillary sinusRadiographymedicine.medical_treatmentDentistryMandibleLesionmedicineMaxillaHumansDental Restoration FailureDental implantAgedDental Implantsbusiness.industryPeriapical DiseasesDental Implantation EndosseousMiddle AgedSurgeryPeriapical lesionRadiographymedicine.anatomical_structureRarefying osteitisTreatment OutcomeOtorhinolaryngologyEtiologySurgeryFemaleImplantOral Surgerymedicine.symptombusinessJournal of oral and maxillofacial surgery : official journal of the American Association of Oral and Maxillofacial Surgeons
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Intraperitoneal Onlay Mesh Technique for Spigelian Hernia in an Outpatient and Short-Stay Surgery Unit: What's New in Intraperitoneal Meshes?

2018

Spigelian hernia (SH) is a rare entity, but its surgical treatment is essential because of its high complication risk. Laparoscopic approaches have become the option in elective surgery because it has less morbidity and requires a shorter stay. Several laparoscopic techniques have been employed, but there is no gold standard technique for this kind of hernia. We report, in this study, our experience with intraperitoneal onlay mesh (IPOM) repair.Fifteen patients underwent elective surgery for SH between 2008 and 2015 in a Short-Stay Surgical Unit. Laparoscopic IPOM technique was performed in all patients. The technique, epidemiological data, operative findings, hospital stay, morbidity, and …

AdultMalemedicine.medical_specialtyOperative Time030230 surgeryAmbulatory Care Facilities03 medical and health sciences0302 clinical medicineSpigelian herniaMedicineHumansSurgical treatmentHerniorrhaphyAgedRetrospective Studiesbusiness.industryRare entityLength of StayMiddle AgedSurgical Meshmedicine.diseaseShort stay surgeryHernia VentralSurgeryTreatment Outcome030220 oncology & carcinogenesisSurgeryFemaleLaparoscopyComplicationbusinessJournal of laparoendoscopicadvanced surgical techniques. Part A
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Occupational risk factors for mycosis fungoides: a European multicenter case-control study.

2004

Mycosis fungoides (MF) is a rare disease with an unknown etiology. Its distribution suggests that occupational exposures may play a role. In the present study, we searched for occupational factors associated with MF. A European multicenter case-control study on seven rare cancers, including MF, was conducted from 1995 to 1997. Patients between 35 and 69 years of age diagnosed with MF (n = 134) were identified and their diagnoses were checked by a reference pathologist who classified 83 cases as definitive, 35 cases as possible, and 16 cases as not histologically verified. Of the 118 histologically verified cases, 104 were interviewed, of which 76 were definitive cases. As controls, we selec…

AdultMalemedicine.medical_specialtySkin NeoplasmsPopulationMedizinOccupational medicineMycosis FungoidesRare DiseasesRisk FactorsInternal medicineEpidemiologymedicineHumansOccupationseducationAgededucation.field_of_studyMycosis fungoidesbusiness.industryPublic Health Environmental and Occupational HealthCase-control studyOdds ratioMiddle Agedmedicine.diseaseConfidence intervalSurgeryEuropeOccupational DiseasesLogistic ModelsCase-Control StudiesEtiologyFemalebusinessJournal of occupational and environmental medicine
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Multiple periscope and chimney grafts to treat ruptured thoracoabdominal and pararenal aortic aneurysms

2011

Purpose: To report midterm outcomes after urgent endovascular repair of ruptured pararenal or thoracoabdominal aortic aneurysms using multiple periscope and chimney grafts to preserve renovisceral branch perfusion and facilitate aneurysm exclusion. Methods: Nine consecutive men (mean age 72614 years, range 40–88) presenting with ruptured thoracoabdominal (n56), pararenal (n52), or infrarenal (n51) aortic aneurysm underwent urgent endovascular repair with at least 1 periscope graft delivered via a transfemoral access; chimney grafts were installed from an axillary access. In all, 17 periscope and 7 chimney grafts were used to reperfuse 11 renal and 13 visceral arteries in the 9 patients. The…

AdultMalemedicine.medical_specialtyTime Factorsmedicine.medical_treatmentAortic RuptureLess invasive610 Medicine & healthRuptured Aortic AneurysmProsthesis DesignEndovascular aneurysm repairSettore MED/22 - Chirurgia VascolareAortography2705 Cardiology and Cardiovascular Medicinelaw.inventionBlood Vessel Prosthesis ImplantationlawmedicineHumans2741 Radiology Nuclear Medicine and ImagingRadiology Nuclear Medicine and imagingChimneyAgedRetrospective Studiesendodebranching renovisceral arteries chimney graft periscope graft stentgraft endograft ruptured aortic aneurysm ruptured thoracoabdominal aortic aneurysm ruptured pararenal aortic aneurysm ruptured AAA endovascular aneurysm repairAged 80 and overAortic Aneurysm Thoracicbusiness.industry10042 Clinic for Diagnostic and Interventional RadiologyEndovascular ProceduresChimney graftBlood flowMiddle AgedSurgeryBlood Vessel Prosthesis10020 Clinic for Cardiac Surgery2746 SurgeryTreatment Outcomecardiovascular systemSurgeryFemaleStentsRadiologyPeriscopeCardiology and Cardiovascular MedicinebusinessTomography X-Ray ComputedAortic Aneurysm Abdominal
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“Puffy hand syndrome”

2016

Resume La toxicomanie intraveineuse est responsable de nombreuses complications notamment cutanees et infectieuses. Il existe un syndrome rarement observe en rhumatologie se traduisant par des « grosses mains » : le puffy hand syndrome. Nous en rapportons deux cas rencontres en consultation de rhumatologie chez deux patients toxicomanes. Il s’agit d’un œdeme des mains, bilateral, indolore, ne prenant pas le godet, survenant chez un de nos patients pendant l’intoxication par heroine, et chez l’autre 2 ans apres avoir arrete ses injections. Chez nos deux patients les bilans complementaires (biologiques, radiologiques, echographiques) etaient sans particularite, ce qui a permis dans le context…

AdultMalemedicine.medical_specialtymedia_common.quotation_subjectContext (language use)Physical examinationSeverity of Illness IndexSampling Studies030218 nuclear medicine & medical imagingLymphatic System030207 dermatology & venereal diseases03 medical and health sciencesRare Diseases0302 clinical medicineRheumatologyInternal medicineEdemaSeverity of illnessmedicineHumansLymphedema030212 general & internal medicinePhysical Examinationmedia_commonmedicine.diagnostic_testHeroin Dependencebusiness.industryAddictionSyndromeHandmedicine.diseaseDermatologyRheumatologySurgeryLymphedemaEtiologyFemalemedicine.symptombusinessJoint Bone Spine
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Ménétrier's disease in a patient with refractory ulcerative colitis: a clinical challenge and review of the literature

2023

Ménétrier’s disease (MD) is a rare disease of the stomach, characterised by hypertrophic gastric folds leading to protein loss. The association with ulcerative colitis (UC) is rare but has been reported in the literature. We report a case of a 29-year-old male affected by UC with an additional diagnosis of MD 3 years after UC diagnosis. UC was refractory to several treatment lines (thiopurines, infliximab, vedolizumab and ustekinumab), and the patient underwent colectomy. Octreotide was administered for MD normalising blood biochemistry, but it was not effective in inducing endoscopic remission of the stomach. Treatment options in patients with MD and UC are discussed.

AdultMalemedicine.medical_specialtymedicine.medical_treatmentGastroenterologyInflammatory bowel diseaseVedolizumabInternal medicineUstekinumabmedicineHumansGastritis HypertrophicColectomybusiness.industryGeneral Medicinemedicine.diseaseUlcerative colitisInfliximabInfliximabMénétrier's diseaseColitis UlcerativeUstekinumabbusinessRare diseasemedicine.drugdrugs: gastrointestinal system; gastroenterology; inflammatory bowel disease
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Survival and prognostic factors in patients with oral squamous cell carcinoma

2020

Background This study aimed to evaluate sociodemographic and clinical factors influencing overall survival (OS) in patients with oral squamous cell carcinoma (OSCC). Material and Methods Medical charts of 547 patients with OSCC from a public hospital in northeastern Brazil seen between 1999 and 2013 were evaluated. Survival analysis was performed using the Kaplan-Meier method. The influence of age, sex, ethnicity, clinical stage, anatomical location, type of treatment, and comorbidities on the patients’ prognosis was evaluated. Cox proportional hazards regression model was used to identify independent prognostic factors. Results The 5-year OS was 39%. Multivariate analysis showed that age <…

AdultOncologymedicine.medical_specialtyPoor prognosisYounger ageMultivariate analysisneoplasmsglandular and epithelial03 medical and health scienceshead and neck neoplasms0302 clinical medicineOral Cancer and Potentially malignant disordersInternal medicinefollow up studiesCox proportional hazards regressionHumansMedicineBasal cellIn patientStage (cooking)General DentistryUNESCO:CIENCIAS MÉDICASSurvival analysisRetrospective StudiesSquamous Cell Carcinoma of Head and Neckbusiness.industryResearchrare diseases030206 dentistryPrognosisstomatognathic diseasesOtorhinolaryngologyCarcinoma Squamous CellMouth NeoplasmsepidemiologySurgerybusinessBrazilMedicina Oral Patología Oral y Cirugia Bucal
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Autoimmune polyglanduläre Syndrome

2013

The autoimmune polyglandular syndrome (APS) is defined as the manifestation of at least two endocrine autoimmune diseases. In order to take the wide spectrum of components and the variations of the disease fully into account, APS is usually divided up into the rare juvenile type (APS I) and the more common adult type (APS II-IV). APS I is caused by a monogenetic mutation whereas APS II-IV has a multifactorial genesis with combination related subgroups. Early diagnosis, individual adjustment of therapy and screening of high risk patients in particular are regarded as clinically relevant. In addition to the patient's history, the diagnosis of APS encompasses serologic measurement of organ-spe…

AdultPediatricsmedicine.medical_specialtyEndometriosisPhysical examinationHashimoto DiseaseDiseaseDiagnosis DifferentialHypothyroidismPregnancyHumansMass ScreeningMedicineHashimoto DiseasePolyendocrinopathies AutoimmuneMass screeningAutoantibodiesmedicine.diagnostic_testbusiness.industryIncidence (epidemiology)AutoantibodyGeneral MedicineDiabetes GestationalFemaleDifferential diagnosisbusinessInfertility FemaleRare diseaseDMW - Deutsche Medizinische Wochenschrift
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