<?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-LFRK5ZRK/3096d3c2-e3d9-4fc0-920e-fb32186c4903/HTML"><dcterms:extent>27 KB</dcterms:extent></edm:WebResource><edm:WebResource rdf:about="http://www.dlib.si/stream/URN:NBN:SI:doc-LFRK5ZRK/7d716974-b9a2-4742-88d9-7c8549c7fa2e/PDF"><dcterms:extent>490 KB</dcterms:extent></edm:WebResource><edm:WebResource rdf:about="http://www.dlib.si/stream/URN:NBN:SI:doc-LFRK5ZRK/41bddb7a-3249-47bc-a00f-a8d39c91c94d/TEXT"><dcterms:extent>25 KB</dcterms:extent></edm:WebResource><edm:TimeSpan rdf:about="1992-2025"><edm:begin xml:lang="en">1992</edm:begin><edm:end xml:lang="en">2025</edm:end></edm:TimeSpan><edm:ProvidedCHO rdf:about="URN:NBN:SI:doc-LFRK5ZRK"><dcterms:isPartOf rdf:resource="https://www.dlib.si/details/URN:NBN:SI:SPR-WQVGMCSC" /><dcterms:issued>2009</dcterms:issued><dc:creator>Ben Osman, Amel</dc:creator><dc:creator>Cheikh Rouhou, Rim</dc:creator><dc:creator>El Euch, Dalenda</dc:creator><dc:creator>Hadid, Rym Ben</dc:creator><dc:creator>Mebazaa, Amel</dc:creator><dc:creator>Mokni, Mourad</dc:creator><dc:creator>Trojjet, Sondes</dc:creator><dc:creator>Zitouna, Moncef</dc:creator><dc:format xml:lang="sl">letnik:18</dc:format><dc:format xml:lang="sl">številka:4</dc:format><dc:format xml:lang="sl">str. 165-172</dc:format><dc:identifier>ISSN:1318-4458</dc:identifier><dc:identifier>COBISSID:26873049</dc:identifier><dc:identifier>URN:URN:NBN:SI:doc-LFRK5ZRK</dc:identifier><dc:language>en</dc:language><dc:publisher xml:lang="sl">Slovene Welding Society</dc:publisher><dcterms:isPartOf xml:lang="sl">Acta dermatovenerologica Alpina, Pannonica et Adriatica</dcterms:isPartOf><dc:subject xml:lang="en">Adult</dc:subject><dc:subject xml:lang="sl">akne</dc:subject><dc:subject xml:lang="sl">dermatologija</dc:subject><dc:subject xml:lang="en">Epidemiology</dc:subject><dc:subject xml:lang="sl">hidradenitis</dc:subject><dc:subject xml:lang="sl">Hidradenitis gnojni</dc:subject><dc:subject xml:lang="en">Hidradenitis Suppurativa</dc:subject><dc:subject xml:lang="sl">Odrasli</dc:subject><dc:subject xml:lang="en">Pathology</dc:subject><dc:subject xml:lang="en">Retrospective Studies</dc:subject><dc:subject xml:lang="sl">Retrospektivne študije</dc:subject><dc:subject xml:lang="en">Tunisia</dc:subject><dc:subject xml:lang="sl">Tunizija</dc:subject><dcterms:temporal rdf:resource="1992-2025" /><dc:title xml:lang="sl">Hidradenitis suppurativa: a disease with male predominance in Tunisia|</dc:title><dc:description xml:lang="sl">BACKGROUND: hidradenitis suppurativa (HS) is a chronic inflammatory, suppurating, fistulizing, and scar-producing disease of apocrine gland-bearingskin. The diagnosis is primarily clinical, based on the presence of both sinus tracts and abscesses with a characteristic distribution. OBJECTIVE: Review of epidemiological, clinical, and prognostic characteristicsof HS and discussion of the etiopathogenic aspects of this chronic problem. PATIENTS AND METHODS: We retrospectively report all cases of HS followed at the Department of Dermatology between January 1985 and December 2008. RESULTS: Eleven patients (10 male and 1 female), with a mean age of 35.2 years (range 21 dash, vertical53 years) at HS diagnosis were followed for HS. The average age of disease onset was 23.9 years. The median delay between onset of symptoms and diagnosis was 144 months (range 1 dash, vertical408 months). Clinical features showed inflamed discharging papules ornodules, painful tender erythematous nodules, and double-ended comedones. The disease mainly affected the axillary, anal, perineal, and genital areas. Histologically, dermal features showed active folliculitis or abscess, sinus tract formation, fibrosis, and granuloma formation. Pathological associations (Darier's disease and Down syndrome) were noted in two patients. Treatment consisted of antibiotics in eight patients, retinoids (1 mg/kg/ day) in three patients, and surgery in three patients. The mean follow-up was 13 months (range 2 dash, vertical30 months). Recurrence of lesions was observed in all patients approximately 1 month after treatment withdrawal. The Down syndrome patient developed vaginal hydrocele of the testis as a complication of his staphylococcic ulcers. In all cases healing occurred with substantial scarring. 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