Egyszerű nézet

dc.contributor.author Szocs HI
dc.contributor.author Torma K
dc.contributor.author Petrovicz E
dc.contributor.author Hársing, Judit
dc.contributor.author Fekete, György
dc.contributor.author Kárpáti, Sarolta
dc.contributor.author Horváth, Attila
dc.date.accessioned 2018-10-16T07:07:17Z
dc.date.available 2018-10-16T07:07:17Z
dc.date.issued 2003
dc.identifier 0344013441
dc.identifier.citation pagination=898-902; journalVolume=42; journalIssueNumber=11; journalTitle=INTERNATIONAL JOURNAL OF DERMATOLOGY;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/4988
dc.identifier.uri doi:10.1046/j.1365-4362.2003.01924.x
dc.description.abstract A 59-year-old male patient developed a necrotizing ulceration on the right shin. Both clinical and histopathologic examinations suggested pyoderma gangrenosum. After temporary improvement of skin symptoms under peroral glucocorticoid treatment, a hemorrhagic-purulent discharge started from the nose, he began to have fever, malaise, cough, and a chest X-ray revealed inflammation in the lung. Cerebral CT and MRI disclosed midline bone loss within the nasal septum and granulomatosus tissue masses protruding into the right orbit. The c-ANCA test was positive, serum IgA was elevated, and he had microhaematuria and proteinuria. In this severe case of Wegener's granulomatosis prolonged methylprednisone and cyclophosphamide treatment was initiated. Both the skin symptoms and the granulomatosus infiltrations resolved.
dc.relation.ispartof urn:issn:0011-9059
dc.title Wegener's granulomatosis presenting as pyoderma gangrenosum
dc.type Journal Article
dc.date.updated 2018-02-22T13:08:18Z
dc.language.rfc3066 en
dc.identifier.mtmt 1267100
dc.identifier.wos 000186171200009
dc.identifier.pubmed 14636209
dc.contributor.department SE/AOK/K/Bőr-, Nemikórtani és Bőronkológiai Klinika
dc.contributor.institution Semmelweis Egyetem


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