<?xml version="1.0"?><rdf:RDF xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:edm="http://www.europeana.eu/schemas/edm/" xmlns:wgs84_pos="http://www.w3.org/2003/01/geo/wgs84_pos" xmlns:foaf="http://xmlns.com/foaf/0.1/" xmlns:rdaGr2="http://rdvocab.info/ElementsGr2" xmlns:oai="http://www.openarchives.org/OAI/2.0/" xmlns:owl="http://www.w3.org/2002/07/owl#" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:ore="http://www.openarchives.org/ore/terms/" xmlns:skos="http://www.w3.org/2004/02/skos/core#" xmlns:dcterms="http://purl.org/dc/terms/"><edm:WebResource rdf:about="http://www.dlib.si/stream/URN:NBN:SI:DOC-MLMGUWVC/a43f1376-c8bd-4900-a2b8-75075cae764c/HTML"><dcterms:extent>46 KB</dcterms:extent></edm:WebResource><edm:WebResource rdf:about="http://www.dlib.si/stream/URN:NBN:SI:DOC-MLMGUWVC/8dc9ba15-0a5f-4d66-be52-0e7529cd34c7/PDF"><dcterms:extent>142 KB</dcterms:extent></edm:WebResource><edm:WebResource rdf:about="http://www.dlib.si/stream/URN:NBN:SI:DOC-MLMGUWVC/6a3a72e5-688e-46bd-9599-6a48d749760b/TEXT"><dcterms:extent>43 KB</dcterms:extent></edm:WebResource><edm:TimeSpan rdf:about="1929-2026"><edm:begin xml:lang="en">1929</edm:begin><edm:end xml:lang="en">2026</edm:end></edm:TimeSpan><edm:ProvidedCHO rdf:about="URN:NBN:SI:DOC-MLMGUWVC"><dcterms:isPartOf rdf:resource="https://www.dlib.si/details/urn:nbn:si:spr-a30mfzkp" /><dcterms:issued>2009</dcterms:issued><dc:creator>Hočevar, Alojzija</dc:creator><dc:creator>Jurčić, Vesna</dc:creator><dc:creator>Vizjak, Alenka</dc:creator><dc:format xml:lang="sl">številka:6/7</dc:format><dc:format xml:lang="sl">letnik:78</dc:format><dc:format xml:lang="sl">str. 329-336</dc:format><dc:identifier>ISSN:1318-0347</dc:identifier><dc:identifier>COBISSID:25803737</dc:identifier><dc:identifier>URN:URN:NBN:SI:doc-MLMGUWVC</dc:identifier><dc:language>sl</dc:language><dc:publisher xml:lang="sl">Slovensko zdravniško društvo</dc:publisher><dcterms:isPartOf xml:lang="sl">Zdravniški vestnik</dcterms:isPartOf><dc:subject xml:lang="en">Antibodies, Antineutrophil Cytoplasmic</dc:subject><dc:subject xml:lang="sl">Biopsija</dc:subject><dc:subject xml:lang="en">Biopsy</dc:subject><dc:subject xml:lang="en">Cryoglobulinemia</dc:subject><dc:subject xml:lang="en">Diagnosis</dc:subject><dc:subject xml:lang="sl">histopatologija</dc:subject><dc:subject xml:lang="sl">Kožne bolezni žil</dc:subject><dc:subject xml:lang="sl">kožne spremembe</dc:subject><dc:subject xml:lang="sl">Krioglubulinemija</dc:subject><dc:subject xml:lang="en">Pathology</dc:subject><dc:subject xml:lang="sl">Poliarteritis nodozni</dc:subject><dc:subject xml:lang="en">Polyarteritis Nodosa</dc:subject><dc:subject xml:lang="sl">Protitelesa antinevtrofilna, citoplazemska</dc:subject><dc:subject xml:lang="sl">Purpura Schoenlein-Henochova</dc:subject><dc:subject xml:lang="en">Purpura, Schoenlein-Henoch</dc:subject><dc:subject xml:lang="sl">sistemski vaskulitis</dc:subject><dc:subject xml:lang="en">Skin Diseases, Vascular</dc:subject><dc:subject xml:lang="en">Urticaria</dc:subject><dc:subject xml:lang="sl">Urtikarija</dc:subject><dc:subject xml:lang="en">Vasculitis</dc:subject><dc:subject xml:lang="sl">Vaskulitis</dc:subject><dcterms:temporal rdf:resource="1929-2026" /><dc:title xml:lang="sl">Kožni vaskulitisi in kožni pojavi pri sistemskih vaskulitisih| Cutaneous vasculitides and cutaneous manifestations of systemic vasculitides|</dc:title><dc:description xml:lang="sl">Cutaneous vasculitis may be limited to the skin or may appear as part of systemic vasculitides. The type and intensity of changes depend on vessel sizeand the severity of involvement. The most common manifestation of small vesel vasculitis is palpable purpura, while vasculitis of medium-sized and large vessels usually express as livide noduses and ulcers. Cutaneous vasculitis may also manifest as bruises, erythema multiforme, papules, pustules, livedo and vesiculo-bullous lesions. The diagnostic procedure, in addition to clinical and laboratory investigations, frequently includes skin biopsy. Evaluation of tissue specimen includes standard histological examination of formalin fixed tissue and direct immunofluorescence of non-fixed fresh samples. The commonest histologic type of skin vasculitis is leukocytoclastic, which involves venules and capillaries and is a consequence of deposition of immune complexes with complement activation. Typical representatives are Henoch-Schönlein purpura, cryoglobulinemic vasculitis and vasculitis in systemic lupus erythematosus. Necrotizing arteriolitis and arteritis of small arteries are usually found in ANCA positive vasculitides. Medium-sized arteries can be involved in both ANCA positive vasculitides and polyarteritis nodosa. Conclusions This article presents the clinical picture, histopathologic characteristics, pathogenetic mechanisms and treatment of someclinicopathologic entities of vasculitides, such as Henoch-Schönlein purpura, urticarial vasculitis, cryoglobulinemic vasculitis, microscopic polyangiitis, Wegener's granulomatosis, Churg-Strauss syndrome and polyarteritis nodosa</dc:description><edm:type>TEXT</edm:type><dc:type xml:lang="sl">znanstveno časopisje</dc:type><dc:type xml:lang="en">journals</dc:type><dc:type rdf:resource="http://www.wikidata.org/entity/Q361785" /></edm:ProvidedCHO><ore:Aggregation rdf:about="http://www.dlib.si/?URN=URN:NBN:SI:DOC-MLMGUWVC"><edm:aggregatedCHO rdf:resource="URN:NBN:SI:DOC-MLMGUWVC" /><edm:isShownBy rdf:resource="http://www.dlib.si/stream/URN:NBN:SI:DOC-MLMGUWVC/8dc9ba15-0a5f-4d66-be52-0e7529cd34c7/PDF" /><edm:rights rdf:resource="http://creativecommons.org/licenses/by-nc/4.0/" /><edm:provider>Slovenian National E-content Aggregator</edm:provider><edm:intermediateProvider xml:lang="en">National and University Library of Slovenia</edm:intermediateProvider><edm:dataProvider xml:lang="sl">Slovensko zdravniško društvo</edm:dataProvider><edm:object rdf:resource="http://www.dlib.si/streamdb/URN:NBN:SI:DOC-MLMGUWVC/maxi/edm" /><edm:isShownAt rdf:resource="http://www.dlib.si/details/URN:NBN:SI:DOC-MLMGUWVC" /></ore:Aggregation></rdf:RDF>