Search results for "DIAGNOSI"

showing 10 items of 2319 documents

Lipedema: an overview of its clinical manifestations, diagnosis and treatment of the disproportional fatty deposition syndrome - systematic review

2012

Lipedema is a disproportionate, symmetrical fatty swelling characterized by pain and bruising existing almost exclusively among women. We undertook a systematic review of the available literature about lipedema, given the lack of knowledge and little evidence about this disorder especially among obesity experts. Diagnosis of lipedema is usually based on clinical features. Symmetrical edema in the lower limbs with fatty deposits located to hips and thighs usually appears at puberty and often affects several members of the same family. Main disorders considered for differential diagnosis are lymphedema, obesity, lipohypertrophy and phlebedema. Treatment protocols comprise conservative (decong…

medicine.medical_specialtybusiness.industryEndocrinology Diabetes and Metabolismmedicine.medical_treatmentLipoedemaLipohypertrophyDecongestive lymphatic therapymedicine.diseaseDermatologySurgeryLymphedemaLiposuctionEdemamedicineLack of knowledgeDifferential diagnosismedicine.symptombusinessClinical Obesity
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Somatostatin-Rezeptor-Szintigraphie bei endokriner Orbitopathie

1994

Somatostatin receptor scintigraphy with 111In-labeled octreotide proves to be a very sensitive diagnostic tool for evaluation of inflammative activity in endocrine ophthalmopathy (EO). The results of somatostatin receptor scintigraphy (SRS) in 40 patients with EO show a high orbital accumulation of 111In-octreotide in clinically active EO (4 h-median/orbit-brain-ratio: 12.6; controls 4 h-median: 5.8) Patients with clinically inactive EO (4 h-median: 7.1) show a similar orbital accumulation of radioactivity compared to controls. 5 patients with active orbital myositis also revealed an even higher orbital accumulation of radioactivity (4 h-median: 42.3). The diagnostic value of SRS lies in it…

medicine.medical_specialtybusiness.industryGraves' diseaseOctreotidePeptide hormonemedicine.diseaseGastroenterologyeye diseasesEndocrinologySomatostatinOrbital MyositisInternal medicinemedicineRadiology Nuclear Medicine and imagingDifferential diagnosisReceptorbusinessMyositismedicine.drugRöFo - Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren
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Focal hepatic intrinsically hyperattenuating lesions at unenhanced CT: Not always calcifications.

2021

Due to the growing use of CT, there has been an increase in the frequency of detecting focal liver lesions. Intrinsically hyperattenuating hepatic lesions or pseudolesions are not uncommon at unenhanced CT. Hyperattenuating hepatic lesions can be divided into non-calcified and calcified. Causes of intrinsic hyperattenuation include hemorrhage, thrombosis, and calcifications. Focal liver lesions can show hyperattenuation on unenhanced CT in case of severe liver steatosis. Recognition of etiologies associated with hyperattenuation on unenhanced CT can help the radiologist in characterizing focal liver lesions and pseudolesions. In this paper, we describe the spectrum of intrinsically hyperatt…

medicine.medical_specialtybusiness.industryHyperattenuating hepatic pseudolesionLiver NeoplasmsCalcinosismedicine.diseaseThrombosisUnenhanced CTHepatic calcified lesionsDiagnosis DifferentialFatty LiverLiver steatosisIntrinsically hyperattenuating hepatic lesionLiver calcificationsmedicineHumansRadiology Nuclear Medicine and imagingRadiologyLiver calcificationsbusinessTomography X-Ray ComputedClinical imaging
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Musculoskeletal manifestations of childhood cancer and differential diagnosis with juvenile idiopathic arthritis (ONCOREUM): a multicentre, cross-sec…

2021

Summary Background Presenting symptoms of childhood cancers might mimic those of rheumatic diseases. However, the evidence available to guide differential diagnosis remains scarce. Preventing wrong or delayed diagnosis is therefore important to avoid incorrect administration of glucocorticoid or immunosuppressive therapy and worsening of prognosis. As such, we aimed to assess the prevalence and characteristics of presenting musculoskeletal manifestations in patients at cancer onset and to identify the factors that differentiate childhood malignancies with arthropathy from juvenile idiopathic arthritis. Methods We did a multicentre, cross-sectional study at 25 paediatric haemato-oncology cen…

medicine.medical_specialtybusiness.industryImmunologyArthritisCancerOdds ratioMusculoskeletal manifestationJuvenile idiopathic arthritismedicine.diseaseHistiocytosisRheumatologySettore MED/38 - PEDIATRIA GENERALE E SPECIALISTICAPrednisoneInternal medicineJoint painArthropathyMusculoskeletal manifestations childhood cancer juvenile idiopathic arthritismedicinechildhood cancerImmunology and AllergyDifferential diagnosismedicine.symptombusinessmedicine.drug
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AB1299-HPR THE RHEUMA-VOR APP: OPTIMIZING THE EARLY DIAGNOSIS OF RHEUMATIC DISEASES

2020

Background:The proof-of-concept network study “Rheuma-VOR” aims to improve the quality of rheumatological care through coordinated cooperation. In particular, rheumatic diseases should be diagnosed as early as possible and treated quickly in a targeted manner [3]. Smartphone apps have a potential to improve the management of chronic diseases. For example, they can be used to provide health information, or to offer self-monitoring and self-screening options [1, 2].Objectives:The Rheuma-VOR Screening-App study examines whether a smartphone-based app can increase the detection rate of the three most common chronic inflammatory rheumatic diseases: rheumatoid arthritis, psoriatic arthritis and s…

medicine.medical_specialtybusiness.industryImmunologyPsychological interventionmedicine.diseaseGeneral Biochemistry Genetics and Molecular BiologyRheumatologyPsoriatic arthritisRheumatologyInternal medicineFamily medicineCohortmedicineEtiologyImmunology and AllergyMedical diagnosisbusinesscomputermHealthDelphicomputer.programming_languageAnnals of the Rheumatic Diseases
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Dialyseassoziierte Amyloidosteopathie - Radiologische Aspekte

1991

Amongst the complications of dialysis, amyloid osteopathy is getting increasingly significant. It is due to deposition of beta 2-microglobulin. To determine the incidence and time of development of this complication, the skeletal radiographs of 185 patients undergoing dialysis, some for up to ten years, were analysed retrospectively. In about 10% of patients, the presence of beta 2-microglobulin osteopathy may be expected. The radiological features, sites of predilection and differential diagnosis of amyloid osteopathy and of other skeletal changes due to dialysis are discussed.

medicine.medical_specialtybusiness.industryIncidence (epidemiology)Amyloidosismedicine.medical_treatmentRetrospective cohort studymedicine.diseaseSurgeryOsteopathia striataOsteopathymedicineRadiology Nuclear Medicine and imagingDifferential diagnosisComplicationbusinessDialysisRöFo - Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren
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Chest Pain Unit Network in Germany

2017

![Figure][1] ![Figure][1] The fundamental goal of a chest pain unit (CPU) is to streamline the differential diagnosis of acute or newly symptomatic chest pain of unclear origin. Data from the United States [(1)][2] and the United Kingdom [(2)][3] demonstrated the superiority of CPUs

medicine.medical_specialtybusiness.industryMEDLINE030204 cardiovascular system & hematologyChest pain03 medical and health sciences0302 clinical medicinePatient satisfactionmedicine030212 general & internal medicineDifferential diagnosismedicine.symptomCardiology and Cardiovascular MedicineIntensive care medicinebusinessJournal of the American College of Cardiology
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2016 – European Society of Hypertension Guidelines for the management of high blood pressure in children and adolescents

2016

medicine.medical_specialtybusiness.industryMEDLINE030204 cardiovascular system & hematologyPediatricsRJ1-57003 medical and health sciences0302 clinical medicineBlood pressureManagement of Technology and InnovationEmergency medicinemedicine030212 general & internal medicineHypertension diagnosisbusinessAnales de Pediatría (English Edition)
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Treacher Collins syndrome-a case report and review of literature

2011

Treacher Collins syndrome (TCS) or Franceschetti syndrome is an autosomal dominant disorder of craniofacial development with variable expressivity. It is named after E Treacher Collins who described the essential components of the condition in 1900. Incidence of this syndrome is approximately 1 in 50,000 live births and it affects both genders equally. It affects structures which are derivatives of the first and second brachial arches. The most common manifestations of TCS are the antimongloid slanting of the palpebral fissures, colobomas of the lower eyelid, hypoplasia of zygoma and mandible; and a variety of ear abnormalities. This article describes clinical and radiographic features of T…

medicine.medical_specialtybusiness.industryMandiblePrenatal diagnosisOdontologíamedicine.disease:CIENCIAS MÉDICAS [UNESCO]DermatologyCiencias de la saludHypoplasiaSurgeryPalpebral fissuremedicine.anatomical_structureUNESCO::CIENCIAS MÉDICASMedicineEyelidCraniofacialDifferential diagnosisbusinessGeneral DentistryTreacher Collins syndrome
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Is It a Metastatic Disease: A Case Report and New Understanding of Rosai-Dorfman Disease?

2017

medicine.medical_specialtybusiness.industryNeoplasms Second PrimaryDermatologyGeneral MedicineDiseasemedicine.diseaseDermatologyPathology and Forensic MedicineDiagnosis Differential030207 dermatology & venereal diseases03 medical and health sciences0302 clinical medicine030220 oncology & carcinogenesisNeoplasmsMedicineHumansHistiocytosis SinusbusinessRosai–Dorfman diseaseThe American Journal of dermatopathology
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