Please use this identifier to cite or link to this item: http://hdl.handle.net/11607/2055
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dc.contributor.authorCandemir, Maşallah
dc.contributor.authorHalis, Hülya
dc.contributor.authorPolat, Aziz
dc.contributor.authorErgin, Hacer
dc.contributor.authorKılıç, İlknur
dc.contributor.authorSemiz, Serap
dc.contributor.authorCinbiş, Mine
dc.date.accessioned2016-02-24T13:27:23Z
dc.date.available2016-02-24T13:27:23Z
dc.date.issued2006
dc.identifier.citationCandemir, M., Halis, H., Polat, A., Ergin, H., Kılıç, İ., Semiz, S., Cinbiş, M. (2006) Henoch-Schonlein purpuralı hastaların analizi.Adnan Menderes Üniversitesi Tıp Fakültesi Dergisi, 7(3)39-43.tr_TR
dc.identifier.issn2149-9063
dc.identifier.urihttp://meandrosmedicaljournal.org/article_9499/Analysis-Of-Patients-With-Henoch-schonlein-Purpura
dc.identifier.urihttp://hdl.handle.net/11607/2055
dc.description.abstractAmaç: HSP'li hastalarımızın epidemiyolojik ve klinik özellikleri, laboratuar bulguları ve hastalıgın seyrinin incelenmesi amaçlandı. Yöntem: 2000-2006 yılları arasında, hastanemiz Çocuk Saglıgı ve Hastalıkları Klinigi'nde Henoch-Schonlein Purpurası tanısı alan ve izlenen 45 hasta retrospektif olarak incelendi. Bulgular: Hastaların 27 (%60,0)'si kız, 18 (%40,0)'i erkek, kız / erkek oranı 1.5 idi.Yas ortalaması 6 yas 9 ay (8 ay-14 yas) olarak saptandı. Basvuru sikayetleri sıklık sırasına göre döküntü (%100), yürüyememe ve/veya eklem agrısı (%71,1) ve karın agrısı (%40,0) idi. Hastaların % 57,7'inde ortalama 12 gün önce geçirilmis enfeksiyon öyküsü tespit edildi. Fizik muayenede purpurik döküntü (alt ekstremite ve gluteal bölgede %100, yaygın %11,1), artrit (32 hastada, %71,1, en sık ayak bilegi ve diz eklemlerinde), ates (9 hastada, %20,0) bulundu. Laboratuar bulguları anemi (8/45 hasta, %17,7), lökositoz (6/45 hasta, %13,3), trombositoz (16/45 hasta, %35,5), sedimentasyon yüksekligi (16/25 hasta, %64,0), CRP pozitifligi (33/34 hasta, %97,0), hematüri (4/45 hasta, %8,8), proteinüri (2/45 hasta, %,4,4), gaitada gizli kan pozitifligi (14/42 hasta, %33,3) bulundu. Hematüri ve proteinüri devam etmedigi için hiçbir hastada böbrek biyopsisine gerek duyulmadı. Gastrointestinal sistem tutulumu oldugu düsünülen 17 hastaya steroid tedavisi baslandı ve ortalama 9.1 gün kullanıldı. Perforasyon, invaginasyon gözlenmedi. Ortalama 15. günde 9 hastada relaps görüldü. Santral sinir sistemi tutulumu hiçbir hastada yoktu. Sonuç: Henoch-Schonlein Purpurası çocukluk çagında sık görülen benign karakterli bir hastalık olup komplikasyon ve sekel oranı oldukça düsüktür.tr_TR
dc.description.abstractAim: The aim of this study was to investigate the clinical and epidemiologic features, laboratory finding and outcome of disease in our patients with Henoch-Schönlein purpura. Methods: Fourty-five patients with Henoch-Schönlein purpura who were diagnosed and observed in our department of pediatrics between 2000-2006 were retrospectively evaluated. Results: Twentyseven (60.0%) of the patients were female and 18 (40.0%) were male, female to male ratio was1.5. Mean age of the patients was 6 year 9 months (8 months-14 years). İnitial symptoms and findings in the time of admission with decreasing frequency were purpura (100%), disability to walk and/or arthralgia (71.1%) ve stomachache (40.0%). An infection history was present in 57.7% of the patients in the last 12 days. In physical examination, purpura (lower extremity and hips 100%, diffuse 11.1%), arhtritis (32 patients, 71.1%, mostly diffused on ankle and knee), fever (9 patients, 20,0%) were discovered. Anaemia (8/45 patients, 17.7%), leukocytosis (6/45 patients, 13.3%), trombocytosis (16/45 patients, 35.5%), increased erythrocyte sedimentation rate (16/25 patients, 64.0%), positive CRP (33/34 patients, 97.0%), hematuria (4/45 patients, 8.8%), proteinuria (2/45 patients, 4.4%), positive fecal blood tests (14/42 patients, 33.3%) were determined. Renal biopsy was not needed as there was no persistant hematuria and proteinuria. 17 patients who had gastrointestinal involvement were treated with steroid therapy for a mean period of 9.1 days. Perforation and invagination was not observed. Relapse was seen in 9 patients. (mean duration 15th day). There was no nervous system involvement in any patients. Conclusion: Henoch-Schonlein Purpura is a frequent benign disease of childhood. Complicatios and sequeles are infrequent.tr_TR
dc.language.isoturtr_TR
dc.rightsinfo:eu-repo/semantics/openAccesstr_TR
dc.subjectHenoch-Schönlein Purpurasıtr_TR
dc.subjectVaskülittr_TR
dc.subjectHenoch-Schönlein Purpuratr_TR
dc.subjectVasculitistr_TR
dc.titleHenoch-Schonlein purpuralı hastaların analizitr_TR
dc.typearticletr_TR
dc.relation.journalAdnan Menderes Üniversitesi Tıp Fakültesi Dergisitr_TR
dc.contributor.authorIDTR3317tr_TR
dc.contributor.authorIDTR50070tr_TR
dc.contributor.authorIDTR202204tr_TR
dc.contributor.authorIDTR109529tr_TR
dc.contributor.authorIDTR159916tr_TR
dc.contributor.departmentPamukkale Üniversitesi, Tıp Fakültesi, Çocuk Sağlığı ve Hastalıkları Anabilim Dalıtr_TR
dc.identifier.volume7tr_TR
dc.identifier.issue3tr_TR
dc.identifier.startpage39tr_TR
dc.identifier.endpage43tr_TR
Appears in Collections:2006 Cilt 7 Sayı 3

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