Search results for "Angiomatosis"

showing 7 items of 7 documents

Slow-growing angiomatous lesions on the limbs.

2014

MalePathologymedicine.medical_specialtyLegSkin Neoplasmsbusiness.industryMycobacterium Infections NontuberculousGeneral MedicineDiagnosis DifferentialNeoplasms Multiple PrimaryAngiomatosis BacillaryArmMedicineHumansbusinessSlow GrowingSarcoma KaposiAgedCleveland Clinic journal of medicine
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Sturge-Weber syndrome: a report of 14 cases

2013

Sturge-Weber-Krabe syndrome (SWS), also known as encephalotrigeminalangiomatosis and named the forthfacomatosis, recall the names of the authors who first describedit in its basic clinical, radiological andanatomopathological aspects. We report here 14 cases of Sturge-Weber disease. In 6 of these, despite what had been previously described in literature, an extension of the angioma has been noted in other parts of the body. The study of these subjects stresses not only the need for a pharmacological/neuropsychomotor intervention, but alsothe need of a psychotherapeutic approach, for the emotional and affective implications thatcould derive from this syndrome. The reported cases are similar …

Sturge-Weber syndrome encephalotrigeminalangiomatosis epilepsy neurocutaneous syndrome.Pediatricsmedicine.medical_specialtylcsh:RC435-571Sturge–Weber syndromelcsh:MedicineCase ReportSturge-Weber syndromeDiseaseAngiomaEpilepsyIntervention (counseling)lcsh:PsychiatrymedicineencephalotrigeminalangiomatosisRecallbusiness.industryNeurological statuslcsh:Rmedicine.diseaseSettore MED/39 - Neuropsichiatria InfantilePsychiatry and Mental healthSturge-Webersyndrome encephalotrigeminalangiomatosis epilepsy neurocutaneous syndromeepilepsyneurocutaneous syndromebusinessMental Illness
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Percutaneous osteoplasty in treatment of bone lymphangiomatosis

2013

Primary bone lymphangiomatosis is a disease of unknown etiology that can cause lytic lesions in long bones, the pelvis, the spinal column and the cranium. We are presenting the case of a woman with localized bone lymphangiomatosis in the left knee. The authors believe this is the first case in which percutaneous osteoplasty was used in long bones for the treatment of bone lesions resulting from this disease showing good clinical results.

medicine.medical_specialtyOsteoplastyPercutaneouskneeCase Reportosteoplastylymphangiomatosislcsh:Orthopedic surgerymedicineOrthopedics and Sports MedicineBoneLymphangiomatosisPelvisbusiness.industrymedicine.diseaseSpinal columnSurgerylcsh:RD701-811Primary bonemedicine.anatomical_structurepercutaneousOrthopedic surgeryPercutaneous OsteoplastyRadiologybusiness
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Comprehensive three‐dimensional morphology of neoangiogenesis in pulmonary veno‐occlusive disease and pulmonary capillary hemangiomatosis

2019

Abstract Pulmonary veno‐occlusive disease (PVOD) is a rare lung disease characterized by fibrotic narrowing of pulmonary veins leading to pulmonary hypertension (PH) and finally to death by right heart failure. PVOD is often accompanied by pulmonary capillary hemangiomatosis (PCH), a marked abnormal proliferation of pulmonary capillaries. Both morphological patterns often occur together and are thought to be distinct manifestations of the same disease process and accordingly are classified together in group 1′ of the Nice classification of PH. The underlying mechanisms of these aberrant remodeling processes remain poorly understood. In this study, we investigated the three‐dimensional struc…

Pathologymedicine.medical_specialtyLung NeoplasmsHypertension Pulmonarypulmonary veno‐occlusive diseasePulmonary capillary hemangiomatosis030204 cardiovascular system & hematologypulmonary capillary hemangiomatosisPathology and Forensic Medicine03 medical and health sciencesThree dimensional morphology0302 clinical medicineRight heart failurepulmonary hypertensionmedicinelcsh:PathologyHumansHemangioma CapillaryLungNeovascularization Pathologicbusiness.industryBrief Definitive Reportintussusceptive neoangiogenesismedicine.diseasePulmonary hypertension3. Good healthmedicine.anatomical_structurePulmonary VeinsLung disease030220 oncology & carcinogenesisPulmonary Veno-Occlusive DiseaseImmunohistochemistryPulmonary Veno-Occlusive Diseasebusinesspulmonary vascular remodelinglcsh:RB1-214The Journal of Pathology: Clinical Research
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Splenic lymphangiomatosis showing rapid growth during lactation: a case report.

2010

Splenic lymphangiomatosis is a very rare condition that, from 1990 to date, has been described only nine times. In the present report, we describe the first case of splenic lymphangiomatosis with rapid growth during lactation in a 35-year-old woman. We also underline the difficultly in making an accurate preoperative diagnosis, despite more modern imaging techniques. Total splenectomy was considered to be the treatment needed, both to make a definitive diagnosis and to exclude the presence of malignancy.

Adultmedicine.medical_specialtymedicine.medical_treatmentBiopsySplenectomySplenic NeoplasmCase ReportMalignancyPredictive Value of TestsLactationLymphangiomaBiopsyLymphangiomatosiMedicineHumansLactationLymphangiomatosismedicine.diagnostic_testLymphangiomabusiness.industrySplenic NeoplasmsGastroenterologyGeneral Medicinemedicine.diseaseSurgerymedicine.anatomical_structureTreatment OutcomePredictive value of testsDisease ProgressionSplenectomyFemalebusinessTomography X-Ray ComputedSpleen
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Blood pressure variability and cardiovascular risk in 9 eastern european countries: data from the BP-Care study

2015

Methods: Total 327 patients were enrolled from 2008 to 2011 in the Korean registry program. They met the criteria of PAH and we investigated the clinical data, the medication prescribed and survival status et al. Results: Their mean age was 40.8 15.8years with female /male patient ratio of 2.7:1. The patients in WHO I/II were 32.4% and WHO III/IV were 67.6%. The peak/mean pulmonary arterial pressure was 86.3/ 56.6 mmHg. Idiopathic PAH (22%), connective tissue disease (24%) and congenital heart disease (46%) were predominant. Small number of patients with familial PAH, portal hypertension, HIV infection, pulmonary capillary hemangiomatosis (PCH) existed. The patients described bosentan were …

medicine.medical_specialtyHeart diseasebusiness.industrySildenafilPulmonary capillary hemangiomatosismedicine.diseaseBosentanEastern europeanchemistry.chemical_compoundBlood pressurechemistryInternal medicineInternal MedicinemedicineCardiology and Cardiovascular MedicinebusinessSurvival ratemedicine.drugCohort studyJournal of the American Society of Hypertension
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Intravitreal ranibizumab treatment of retinal angiomatous proliferation

2010

. Purpose:  To determine the efficacy of intravitreal injections of ranibizumab in the treatment of retinal angiomatous proliferation (RAP) in neovascular age-related macular degeneration. Methods:  Retrospective, consecutive case series of 26 eyes (26 patients) treated with intravitreal injections of 0.5 mg ranibizumab for RAP. Patients received intravitreal injections at monthly intervals during upload phase for a 3-month period. Results:  Mean visual acuity before treatment was 0.75 ± 0.38logMAR (mean ± SD, n = 26). In the upload phase, mean visual acuity improved 4 weeks after the initial injection to 0.6 ± 0.37logMAR (n = 26) and to 0.53 ± 0.34logMAR (n = 26) 4 weeks after the third mo…

MaleAngiomatosismedicine.medical_specialtyVisual acuitygenetic structuresVisual AcuityAngiogenesis InhibitorsFoveal thicknessRetinal NeovascularizationAntibodies Monoclonal Humanizedchemistry.chemical_compoundOpticsRanibizumabOphthalmologymedicineHumansMaintenance phaseAgedRetrospective StudiesAged 80 and overbusiness.industryRetinalGeneral MedicineMiddle AgedMacular degenerationmedicine.diseaseeye diseasesOphthalmologyTreatment OutcomechemistryIntravitreal InjectionsRetreatmentWet Macular DegenerationFemalesense organsRanibizumabIntravitreal ranibizumabmedicine.symptombusinessTomography Optical Coherencemedicine.drugActa Ophthalmologica
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