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 |
|