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Journals / Dicle Tıp Dergisi / 2010 / Cilt: 37 - Sayı: 4

Wegener granulomatosis presented with crescentic glomerulonephritis: Case report

Kresentik glomerülonefritle başvuran bir Wegener granülomatozu olgusu

Sebahat TÜLPAR
Funda BAŞTUĞ
M. Hakan POYRAZOĞLU
Zübeyde GÜNDÜZ
Hülya AKGÜN
Ali YIKILMAZ
Pages
413–417
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The patient has been still followed-up with stage 4 chronic kidney disease.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Wegener granulomatosis is a rare vasculitis in childhood and is associated with morbidity and mortality in untreated cases.
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Key Findings & Data:We reported a 10 year-old female who presented with pulmonary renal syndrome.
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Conclusion & Impact:The patient has been still followed-up with stage 4 chronic kidney disease.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Wegener granulomatosis is a rare vasculitis in childhood and is associated with morbidity and mortality in untreated cases. We reported a 10 year-old female who presented with pulmonary renal syndrome. Laboratory investigations revealed the diagnosis of Wegener granulomatosis, and immunosuppressive therapy was started. Renal biopsy was consistent with crescentic glomerulonephritis. The patient has been still followed-up with stage 4 chronic kidney disease.

Özet

Wegener granülomatozu çocukluk çağında nadir görülen, tedavi edilmediğinde morbidite ve mortalite ile seyredebilen bir vaskülittir. Başvurusunda pulmoner renal sendrom tablosunda olan 10 yaşındaki bir kız hasta sunuldu. Yapılan tetkikler sonucunda Wegener Granülomatozu tanısı konup immunosupresif tedavi başlandı. Böbrek biyopsisi kresentik glomerülonefrit ile uyumluydu. Hasta şu anda evre 4 kronik böbrek yetmezliği tanısı ile takip edilmektedir.

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Cite This Article

TÜLPAR, S., BAŞTUĞ, F., POYRAZOĞLU, M. H., GÜNDÜZ, Z., AKGÜN, H., YIKILMAZ, A. (2010). Wegener granulomatosis presented with crescentic glomerulonephritis: Case report. Dicle Tıp Dergisi, Cilt: 37 - Sayı: 4, 413–417. https://ajindex.com/articles/349205

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