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Journal of the Polish Society of Internal Medicine founded by professor Władysław Antoni Gluziński
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IC Value for 2009: 7.80 pts,
MNiSW Value: 9 pts.
The journal receives funding from the Ministry of Science and Higher Education for promoting scientific research.
Polish Archives of Internal Medicine is an open-access journal and does not charge readers for access to the full texts of the articles.
Partner Polskiej Interny
Marcin Grzegorz Dębski, Katarzyna Życińska, Marek Czarkowski, Małgorzata Żukowska, Kazimierz A. Wardyn, Ewa Bar-Andziak
Abstract
57-year-old woman with a history of ischaemic heart disease, arterial hypertension and after
myocardial infarction was admitted to the uniwersity hospital because of progressive hearing loss and fever of
unknown origin. Shortly before hospitalization she developed cough, hameoptisisand conjunctivitis. On the basis
of clinical presentation Wegener’s granulomatosis was suspected. To confirm the diagnosis, CT scans of the
chest, sinuses and ears were performed and revealed massive lesions especially in tht tympanic cavity, mastoid
antrum and cells. Infiltrations were also observed in sinuses, especially maxillary, and typical granuloms were
found in the lungs. Moreover, the biopsy taken from the mucous membrane of the nose showed abnormalities
typical of Wegener’s granulomatosis. Antineutrophil cytoplasmatic antibodies (ANCA) were also examined. It is
of interest that c-ANCA (cytoplasmatic) were negative and p-ANCA (perinuclear) were positive which is rare in
this disease. The patient was treated with immunosuppressive drugs (intravenous methylprednisolon, oral
prednisolon and cyclophosphamide). Following therapy fever, hemoptisis and conjuctivitis subsided, while
inflamantory parameters normalized. This case report presents on unusual clinical manifestation of Wegener’s
granulomatosis with the leading sign of hearing loss.
Keywords
fever of unknown origin, hearing loss, Wegener’s granulomatosis
Pol Arch Med Wewn, 2007; 117 (5-6): 266-269
PMID: 18030878