Search results for "Systemic disease"

showing 10 items of 58 documents

M2 Polarized Macrophages and Giant Cells Contribute to Myofibrosis in Neuromuscular Sarcoidosis

2011

The etiopathogenesis of sarcoidosis, a systemic granulomatous disease, still remains obscure. A multitude of organs have been described to be affected in systemic sarcoidosis. Skeletal muscles may also be affected, leading to myalgia and weakness. A workup of the specific immune response with emphasis on the macrophage response is provided herein. Affected muscle tissue from seven patients with systemic sarcoidosis was analyzed and compared with that from seven patients with other myopathies containing macrophagocytic infiltration. Monocytes/macrophages and giant cells in granulomas of muscle tissue from patients with sarcoidosis show a status of alternative activation (M2) based on their e…

MalePathologymedicine.medical_specialtySystemic diseaseSarcoidosismedicine.medical_treatmentBiologyGiant CellsMonocytesPathology and Forensic MedicineTh2 CellsImmune systemmedicineHumansMacrophageRNA MessengerMuscle SkeletalAgedGranulomaMacrophagesCCL18Cell PolarityEpithelial CellsRegular ArticleNeuromuscular DiseasesMacrophage ActivationMiddle Agedmedicine.diseaseAcquired immune systemFibrosisPhenotypeCytokineGene Expression RegulationGiant cellChemokines CCGranulomaImmunologyCytokinesFemaleThe American Journal of Pathology
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Maxillofacial nodular fasciitis: a report of 3 cases.

2002

MalePathologymedicine.medical_specialtySystemic diseasebusiness.industryNodular fasciitisMiddle Agedmedicine.diseaseConnective tissue diseaseTongue DiseasesDiagnosis DifferentialOtorhinolaryngologyClinical investigationmedicineHumansSurgeryHistopathologyFemaleOral SurgeryFasciitisbusinessMouth DiseasesMouth FloorNeckAgedJournal of oral and maxillofacial surgery : official journal of the American Association of Oral and Maxillofacial Surgeons
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Coronary artery bypass grafting in adult coronary artery disease due to suspected Kawasaki disease in childhood

2000

Development of coronary artery aneurysms is one typical complication of Kawasaki disease and can cause coronary artery disease even in early childhood. Information about course and outcome in adults is rare. Here, we present a 49-year-old man with serious three-vessel coronary artery disease and giant coronary artery aneurysms following suspected Kawasaki disease.

MalePulmonary and Respiratory MedicineSystemic diseasemedicine.medical_specialtyCoronary DiseaseMucocutaneous Lymph Node SyndromeCoronary artery diseaseAneurysmhemic and lymphatic diseasesInternal medicinemedicineHumanscardiovascular diseasesCoronary Artery BypassVascular diseasebusiness.industryCoronary AneurysmMiddle Agedmedicine.diseaseSurgerymedicine.anatomical_structurecardiovascular systemCardiologySurgeryKawasaki diseaseCardiology and Cardiovascular MedicinebusinessComplicationVasculitisArteryThe Annals of Thoracic Surgery
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Antigens of the major histocompatibility complex in patients with chronic discoid lupus erythematosus.

1990

summary The frequencies of the major histocompatability complex class I, class II and class III antigens were determined in 130 patients (88 women and 42 men) with chronic discoid lupus erythematosus, and compared with those of 764 healthy controls. A significant increase in HLA-B7 (38.0% in the patients vs. 25·8% in the control group), HLA-B8 (29·5% vs. 17·4%), HLA-Cw7 (58·9% vs. 26·1%), HLA-DR2 (46·9% vs. 29·7%), HLA-DR3 (32·0% vs. 19·4%), HLA-DQwi (76·6% vs. 60·5%), and a decrease in HLA-A2 (41·9% vs. 55·7%) was found. The calculated relative risk values for the respective antigens markedly increased when two or more antigens were present in one patient, with a maximum relative risk valu…

MaleRiskmedicine.medical_specialtySystemic diseaseDermatologyHLA-C AntigensMajor histocompatibility complexGastroenterologyHLA-B8 AntigenHLA-B7 AntigenHLA-DR3 AntigenLupus Erythematosus DiscoidAntigenHLA AntigensInternal medicineHLA-DQ AntigensHLA-A2 AntigenmedicineHumansIn patientHLA-DR2 AntigenLupus erythematosusbiologybusiness.industrymedicine.diseaseConnective tissue diseaseRelative riskImmunologyChronic Diseasebiology.proteinFemaleDisease SusceptibilitybusinessChronic discoid lupus erythematosusThe British journal of dermatology
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IgG4 Related Syndrome: Another Multiorgan Disease in the Interest Field of Internal Medicine.

2016

BACKGROUND: IgG4-related disease is a rare, clinical and pathologic disease entity of unknown etiology. Its main features are increased serum concentrations of IgG4 > 1,35 g/l, lymphocyte and IgG4+plasma-cell infiltration within tissues, fibrosis or sclerosis. The classical presentation of IgG4-RSD is pancreatitis which is combined with the involvement of biliary ducts in 74 percent of patients. Extrapancreatic manifestations include: abdominal or mediastinal lymphadenopathy; the involvement of salivary glands and lacrimal glands, kidneys, lung, retroperitoneum. Since IgG4-related disease is a multiorgan lymphoproliferative syndrome, it requires a careful differential diagnosis from othe…

MaleSystemic diseasePathologymedicine.medical_specialtySettore MED/09 - Medicina InternaCholangitis SclerosingLymphadenopathyAzathioprineRetroperitoneal fibrosisSialadenitisIgG4 syndrome Internal MedicineDrug DiscoveryInternal MedicinemedicineHumansEosinophiliaAgedPharmacologybusiness.industryRetroperitoneal FibrosisSyndromemedicine.diseaseImmunoglobulin GPancreatitisIgG4-related diseaseSarcoidosismedicine.symptomDifferential diagnosisbusinessmedicine.drug
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Clinical course and symptomatic prediagnostic period of patients with Wegener's granulomatosis and microscopic polyangiitis.

1998

The clinical course of 15 patients with Wegener's granulomatosis (WG) and eight patients with microscopic polyangiitis (MPA) from one nephrological clinical center is presented for the period from 1984 to 1993, when testing for antineutrophil cytoplasmic antibodies (ANCA) was gradually introduced into routine clinical practice. We found a high degree of prolonged time periods with symptoms attributable to WG or MPA until the specific diagnosis was made. Nine patients with WG and one patient with MPA had symptomatic prediagnostic periods of more than three years, which extended in one case up to twenty years. In these prediagnostic periods, often even severe flares of vasculitic activity res…

MaleVasculitisPediatricsmedicine.medical_specialtySystemic diseaseTime Factorsmedicine.medical_treatmentRemission SpontaneousSpontaneous remissionCritical Care and Intensive Care MedicineAntibodies Antineutrophil CytoplasmicRenal DialysismedicineRapidly progressive glomerulonephritisHumansCyclophosphamideDialysisAnti-neutrophil cytoplasmic antibodyRetrospective StudiesImmunosuppression Therapybusiness.industryGranulomatosis with PolyangiitisGeneral MedicineMiddle Agedmedicine.diseaseSurgeryNephrologyFemaleMicroscopic polyangiitisComplicationVasculitisbusinessImmunosuppressive AgentsRenal failure
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Epistaxis and systemic disease

2008

Abstract We report the case of a 77-year-old man who presented nasal obstruction sensation and epistaxis. Otorhinolaryngologic examination revealed occupation of the left nasal passage and the left maxillary sinus by an inflammatory tumour, the biopsy results of which were inconclusive. While diagnostic tests were being carried out, the patient presented a severe systemic condition consisting mainly of anemia, acute renal failure, and cavitated diffuse bilateral lung infiltrates. In the light of the results of anti-neutrophilic cytoplasmic antibodies and renal biopsy, Wegener's granulomatosis was diagnosed and treatment for the disease was instituted, with a favourable response. Finally, cl…

Malemedicine.medical_specialtySystemic diseaseMaxillary Sinus NeoplasmsAnemiaBiopsyComorbidityDiseaseRenal DialysisTrimethoprim Sulfamethoxazole Drug CombinationBiopsyHumansMedicineCyclophosphamideGlucocorticoidsAgedNasal passagesLungPapillomamedicine.diagnostic_testGlomerulosclerosis Focal Segmentalbusiness.industryGranulomatosis with PolyangiitisAnemiaGeneral MedicineAcute Kidney Injurymedicine.diseaseLeft maxillary sinusDermatologySurgeryEpistaxismedicine.anatomical_structureRenal biopsyNasal ObstructionLung Diseases InterstitialTomography X-Ray ComputedbusinessActa Otorrinolaringologica (English Edition)
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Cardiac involvement in rheumatoid arthritis: Evidence of silent heart disease

1995

Background : Rlieumatoid arthritis (RA) is a systemic disease involving many organ systems and is frequently accompanied by cardiac alterations. However, there is considerable disagreement concerning the cardiac abnormalities found in patients with RA. The purpose of our investigation was to determine, by a non-invasive method such as echocardiography, the nature and extent of cardiac involvement in RA patients with no symptoms of cardiac disease, in comparison with a control sample. Methods : We selected 35 patients affected by rheumatoid arthritis (five men, 30 women), aged 51 ± 11 years. No patient had either symptoms of cardiac disease or extra cardiac complaint. As a control group we s…

Malemedicine.medical_specialtySystemic diseaseSettore MED/09 - Medicina InternaHeart DiseasesHeart diseaseArthritisDiseaseAsymptomaticPericardial effusionRheumatoid arthritis Cardiac abnormalities EchocardiographyArthritis RheumatoidInternal medicinemedicineHumansSinus rhythmbusiness.industryMiddle Agedmedicine.diseaseSettore MED/45 - Scienze Infermieristiche Generali Cliniche E PediatricheSettore MED/11 - Malattie Dell'Apparato CardiovascolareSurgerySettore MED/16 - ReumatologiaEchocardiographyRheumatoid arthritiscardiovascular systemCardiologyFemalemedicine.symptomCardiology and Cardiovascular Medicinebusiness
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AN ATYPICAL CASE OF GIANT CELL ARTERITIS (HORTON'S DISEASE) ASSOCIATED WITH FACIAL SWELLING, CONFUSION, AND PERICARDITIS IN AN ELDERLY WOMAN

2010

Pathologymedicine.medical_specialtySystemic diseaseFacial swellingHeart diseaseVascular diseasebusiness.industryDiseasemedicine.diseasePericarditisGiant cell arteritismedicineGeriatrics and GerontologyVasculitisbusinessJournal of the American Geriatrics Society
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Changes in crevicular cytokines after application of melatonin in patients with periodontal disease

2017

Background A clinical trial was designed to evaluate the effects of topical application of melatonin on the crevicular fluid levels of interleukins and prostaglandins and to evaluate changes in clinical parameters. Material and methods A consecutive sample of 90 patients were recruited from the Health Centre of Pinos Puente in Granada, Spain and divided into 3 groups: 30 patients with diabetes and periodontal disease, who were given melatonin; 30 patients with diabetes and periodontal disease, who were given a placebo, and 30 healthy individuals with no history of systemic disease or clinical signs of periodontal disease, who were also given a placebo. The 30 patients with diabetes and peri…

Periodontitismedicine.medical_specialtySystemic diseasebusiness.industryResearchInterleukin030206 dentistrymedicine.diseasePlacebo:CIENCIAS MÉDICAS [UNESCO]GastroenterologyMelatoninClinical trial03 medical and health sciences0302 clinical medicineDiabetes mellitusInternal medicineUNESCO::CIENCIAS MÉDICASmedicinePeriodontologyProstaglandin E2businessGeneral Dentistry030217 neurology & neurosurgerymedicine.drug
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