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Clinical features of polyarteritis nodosa in Korea

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dc.contributor.authorBae, Young Deok-
dc.contributor.authorChoi, Hyo Jin-
dc.contributor.authorLee, Jung Chan-
dc.contributor.authorPark, Jeong Jin-
dc.contributor.authorLee, Yun Jong-
dc.contributor.authorLee, Eun Bong-
dc.contributor.authorSong, Yeong Wook-
dc.date.accessioned2010-01-11T05:06:24Z-
dc.date.available2010-01-11T05:06:24Z-
dc.date.issued2006-08-08-
dc.identifier.citationJ Korean Med Sci. 2006 Aug;21(4):591-5.en
dc.identifier.issn1011-8934 (Print)-
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=16891798-
dc.identifier.urihttps://hdl.handle.net/10371/29313-
dc.description.abstractPolyarteritis nodosa (PAN) is a systemic vasculitis characterized by multi-organ involvement with protean manifestations. We evaluated the clinical features of PAN in Korea. Twenty-seven patients were diagnosed as PAN at Seoul National University Hospital between January 1990 and July 2003. The male-to-female ratio was 1.7:1 and mean age at onset (+/-SD) was 47.4+/-20 yr. Their presenting features at diagnosis were similar to those reported previously, i.e., myalgia, muscle weakness or leg tenderness (70%), fever (52%), weight loss >4 kg (44%), skin rash (44%), peripheral edema (33%), abdominal pain (33%), and arthralgia/arthritis (30%). However, the prevalence of testicular pain or tenderness was higher (24%) than reported previously and only three (11.5%) had HBsAg positivity without liver enzyme elevation. Nine patients (33%) had a five-factor score (FFS) of 2. Fourteen patients (52%) responded to treatment, 2 patients relapsed and 4 died within 1 yr of diagnosis. During a median follow-up of 55.5 months, three of the four PAN-related deaths had an initial FFS of 2. The clinical features of PAN were not significantly different from those reported previously. However, testicular pain or tenderness was more frequent and patients with a high FFS tended to have a poorer prognosis.en
dc.language.isoenen
dc.publisherKorean Academy of Medical Scienceen
dc.subjectAdolescenten
dc.subjectAdulten
dc.subjectExanthema/pathologyen
dc.subjectFemaleen
dc.subjectFever/pathologyen
dc.subjectHumansen
dc.subjectKoreaen
dc.subjectMaleen
dc.subjectMiddle Ageden
dc.subjectPolyarteritis Nodosa/ethnology/mortality/*pathologyen
dc.subjectSurvival Rateen
dc.subjectAsian Continental Ancestry Group-
dc.titleClinical features of polyarteritis nodosa in Koreaen
dc.typeArticleen
dc.contributor.AlternativeAuthor배영덕-
dc.contributor.AlternativeAuthor최효진-
dc.contributor.AlternativeAuthor이정찬-
dc.contributor.AlternativeAuthor박정진-
dc.contributor.AlternativeAuthor이윤종-
dc.contributor.AlternativeAuthor이은봉-
dc.contributor.AlternativeAuthor송영욱-
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