Search results for "VASCULITIS"

showing 8 items of 118 documents

Risk factors for refractory Kawasaki disease: clinical records of the paediatric clinic of palermo

2014

Kawasaki disease (KD) is an acute, self-limited febrile illness that mainly affecting small- to medium-sized vessels and occurs in early childhood. The etiology is currently unknown, however it likely results from an immunologic response triggered by microbial agents, with documented genetic susceptibility. Intravenous administration of immunoglobulin (IVIG) is the gold standard therapy for coronary arteritis in the acute phase of KD; some patients do not respond to IVIG and coronary aneurysms continue to develop in 5%. The most serious complications are coronary vasculitis and aneurysms. 15% of these patients do not respond to IVIG (Refractory KD:RMK) and have a higher risk of aneurysms.

medicine.medical_specialtyPediatricsbiologybusiness.industryGold standardmedicine.diseaseRheumatologySettore MED/38 - Pediatria Generale E SpecialisticaRefractoryRheumatologyhemic and lymphatic diseasesInternal medicinePoster PresentationPediatrics Perinatology and Child HealthmedicineGenetic predispositionEtiologybiology.proteinImmunology and AllergyKawasaki diseaseKawasaki disease risk factorsPediatrics Perinatology and Child HealthAntibodyVasculitisbusinessPediatric Rheumatology
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Utility of post mortem MRI in definition of thrombus in aneurismatic coronary arteries due to incomplete Kawasaki Disease in infants

2016

Abstract Kawasaki disease (KD) is an acute, self-limited vasculitis of unknown etiology that primarily affects the coronary artery (CA) and presents in childhood. The characteristic coronary arterial lesion is an aneurysm, which may lead to thrombosis, dilatation, stenosis, and occlusion. Such an aneurysm is typically calcified and generally develops five or more years after the onset of acute KD. It becomes more noticeable after ten years. KD is sometimes difficult to diagnose because of the limited clinical features, especially in infants younger than 6 months old, where the clinical presentations often do not fulfill the diagnostic criteria for KD. We report a case of Incomplete Kawasaki…

medicine.medical_specialtyRadiology Nuclear Medicine and Imaging2734Aneurismatic coronary arterieAutopsy030204 cardiovascular system & hematology030218 nuclear medicine & medical imagingPathology and Forensic MedicineForensic pathology03 medical and health sciences0302 clinical medicineAneurysmIncomplete Kawasaki diseaseInternal medicinemedicinePost-mortem MRIThrombusbusiness.industrymedicine.diseaseThrombosisCoronary arteriesStenosismedicine.anatomical_structureSudden infant deathThrombosiCardiologyKawasaki diseasebusinessVasculitis
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Reducing the initial number of rituximab maintenance-therapy infusions for ANCA-associated vasculitides: randomized-trial post-hoc analysis

2020

AbstractObjectiveThe randomized, controlled MAINRITSAN2 trial was designed to compare the capacity of an individually tailored therapy [randomization day 0 (D0)], with reinfusion only when CD19+ lymphocytes or ANCA had reappeared, or if the latter’s titre rose markedly, with that of five fixed-schedule 500-mg rituximab infusions [D0 + D14, then months (M) 6, 12 and 18] to maintain ANCA-associated vasculitis (AAV) remissions. Relapse rates did not differ at M28. This ancillary study was undertaken to evaluate the effect of omitting the D14 rituximab infusion on AAV relapse rates at M12.MethodsMAINRITSAN2 trial data were subjected to post-hoc analyses of M3, M6, M9 and M12 relapse-free surviv…

medicine.medical_specialtyRandomizationAntigens CD19Anti-Neutrophil Cytoplasmic Antibody-Associated VasculitisGastroenterologyDisease-Free SurvivalDrug Administration ScheduleAntibodies Antineutrophil CytoplasmicMaintenance Chemotherapylaw.invention03 medical and health sciences0302 clinical medicineRheumatologyMaintenance therapyRandomized controlled triallawInternal medicinePost-hoc analysismedicineHumansPharmacology (medical)030212 general & internal medicineSurvival rate030203 arthritis & rheumatologybusiness.industrymedicine.diseaseAntirheumatic AgentsRituximabRituximabMicroscopic polyangiitisGranulomatosis with polyangiitisbusinessmedicine.drugRheumatology
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Morbus Eales – 10 Jahre Erfahrung mit einem seltenen Krankheitsbild

2009

BACKGROUND: Eales’ disease is an uncommon vasoproliferative retinal disease affecting otherwise healthy young men. We report on our treatment results in a large patients group with long-term follow-up. PATIENTS AND METHODS: The treatment results in 50 eyes (35 patients) with Eales’ disease, that were cosecutively treated from May 1995 to August 2005, were analysed retrospectively. Recorded data included age, sex, race, association of systemic disease, medications, laboratory evaluation and the surgical treatment. Mean follow-up was 5.8 years (minimum: 3.2, maximum: 8.6 years). RESULTS: Systemic and laboratory evaluations detected a factor V Leiden mutation (4 × ), vestibuloauditory problems…

medicine.medical_specialtySystemic diseaseVisual acuitygenetic structuresbusiness.industrymedicine.medical_treatmentVitrectomyRetinalmedicine.diseaseeye diseasesSurgeryOphthalmologychemistry.chemical_compoundchemistryEales diseasemedicineCoagulopathyFactor V Leidenmedicine.symptomVasculitisbusinessKlinische Monatsblätter für Augenheilkunde
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Hautknoten und Ulzera der Extremitäten bei einem Patienten mit rheumatoider Arthritis

2002

CASE HISTORY: While being treated with corticosteroids and methotrexate for rheumatoid arthritis, a 63-year-old man developed livid nodules on his lower arms, hands and feet, as well as fever, necrotizing skin ulcers and rupture of a finger extensor tendon. INVESTIGATIONS: No vasculitis was found in a biopsy of one of the nodules on the lower arm. Fast growing mycobacteria, classified as M. marinum by PCR, were cultured from wound swabs. TREATMENT AND COURSE: The lesions healed on administration of ciprofloxacin, ethambutol and clarithromycin as well as local treatment. CONCLUSION: Cutaneous lesions of an atypical mycobacterial infection are often misdiagnosed. This is especially so in immu…

medicine.medical_specialtybiologymedicine.diagnostic_testbusiness.industryGeneral MedicineSkin ulcerbacterial infections and mycosesmedicine.diseasebiology.organism_classificationDermatologyRheumatoid arthritisBiopsyPrednisolonemedicineDifferential diagnosismedicine.symptombusinessVasculitisMycobacterium marinumEthambutolmedicine.drugDMW - Deutsche Medizinische Wochenschrift
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Cocaine-related oronasal communication and hard palate destruction

2011

Four cases of midpalatal perforation in cocaine abusers are presented. Other potential etiological processes are discussed to establish an adequate differential diagnosis. These patients were treated at our department, due to the drawback promoted by the establishment of oronasal communication that was provided after an accurate diagnosis. Histopathological evaluation of the lesion margins were conducted in two of the four cases, and yielded no evidence of vasculitis or active cocaine abuse. Therapeutic approach consisted of reconstructive surgeries and/or sealing prostheses. Histological assessment of oronasal communication margins could be useful in establishing the persistence of active …

medicine.medical_specialtybusiness.industryAddictionmedia_common.quotation_subjectPerforation (oil well)DentistryGeneral Medicinemedicine.diseaseSurgeryLesionTherapeutic approachmedicine.anatomical_structuremedicineEtiologyHard palatemedicine.symptomDifferential diagnosisVasculitisbusinessmedia_commonJournal of Investigative and Clinical Dentistry
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Extrahepatic Manifestations of Chronic HCV

2011

A number of extrahepatic manifestations have been reported in patients infected with HCV. The most prominent of theme are MC vasculitis, lymphoproliferative malignancies, renal disease, polyarthritis, thyroid and glucose disorders. Although these conditions might have a substantial impact on morbidity, patient management, and prognosis, for most of them the exact mechanisms underlying their development require further elucidation.

medicine.medical_specialtybusiness.industryThyroidDiseasemedicine.diseaseDermatologyNon-Hodgkin's lymphomaPatient managementmedicine.anatomical_structuremedicinePolyarthritisIn patientVasculitisbusinessB cell
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Is prolonged febrile syndrome associated with reactive thrombocytosis a possible association in the diagnosis of Takayasu’s arteritis? A case report

2021

Takayasu’s arteritis is a rare, systemic, inflammatory vasculitis of large blood vessels with an unknown aetiology that more frequently affects women of childbearing age with progression to stenosis, fibrosis or thrombogenesis. Clinical manifestations are associated either with inflammation of the vascular wall (including fever, myalgia, arthralgia, weight loss) or the development of aneurysms and extensive vascular lesions, which creates challenges for a differential diagnosis. This current report presents the case of a female Caucasian patient, aged 23 years, that presented herself repetitively at the hospital reporting symptoms including fever, productive cough, myalgia associated with …

medicine.medical_specialtyfibrin monomersMedicine (General)case presentationUnknown aetiologyTakayasu's arteritisCase ReportsConstriction PathologicBiochemistryFebrile syndromeDiagnosis DifferentialR5-920Reactive thrombocytosismedicineHumansArteritisThrombocytosisThrombocytosisbusiness.industryBiochemistry (medical)Takayasu’s arteritisCell BiologyGeneral Medicinemedicine.diseaseDermatologyTakayasu Arteritisprolonged febrile syndromeChildbearing ageFemalebusinessVasculitisJournal of International Medical Research
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