Journals / Şişli Etfal Hastanesi Tıp Bülteni / 2005 / Cilt: 39 - Sayı: 3

Henoch-Schonlein purpura in childhood: Clinical experience

Henoch-Schonlein purpuralı olgularımızın değerlendirilmesi

Pages
27–31
DOI
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AI Summary & Key Takeaways

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

Other causes of vasculitis should also be included in the differential diagnosis.

📌 3 Key Takeaways

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Objective & Hypothesis:Objective: Henoch-Schönlein purpura (HSP) is a common le-ukocytoclastic vasculitis of childhood, characterized, by purpuric skin lesions, arthritis, gastrointestinal and renal involvement.
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Key Findings & Data:Study Design: 75 patients diagnosed as HSP who were hospitalized in our clinic between January 2002 and April. 2005 were retrospectively evaluated: Results: Mean age of the patients (55% boys and 45% girls) were 9.3 ±3.1.
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Conclusion & Impact:Other causes of vasculitis should also be included in the differential diagnosis.
🔬Design:Research Article
📍Scope:2002 Verileri
⚙️Variables:Geriyedönük çalışma · Çocuk · Purpura

Abstract

Objective: Henoch-Schönlein purpura (HSP) is a common le-ukocytoclastic vasculitis of childhood, characterized, by purpuric skin lesions, arthritis, gastrointestinal and renal involvement. Our aim was to evaluate the clinical findings of our patients with HSP. Study Design: 75 patients diagnosed as HSP who were hospitalized in our clinic between January 2002 and April. 2005 were retrospectively evaluated: Results: Mean age of the patients (55% boys and 45% girls) were 9.3 ±3.1. Hospitalization rates were lowest during summer seasons. All patients had palpable purpura, 78% had. GIS findings, 72% had. arthritis or arthralgia and 33% had renal involvement. Occult blood was present in 49%,,6.7% had. acute abdominal symptoms, scalp edema was present, in 5.3% and scrotal edema in 12%. Mean follow-up period for patients with renal involvement was 22.3 ± 15 months. Renal biopsy was performed in 13 patients with serios renal involvement. Conclusion: Although the most common finding in HSP is the purpura; arthritis, renal or gastrointestinal findings may be present previously or during the, follow-up. Other causes of vasculitis should also be included in the differential diagnosis.

Özet

Amaç: Henoch-Schönlein Purpurası (HSP), çocukluk çağında sık görülen lökositoklasük bir vaskülittir. Sıklıkla palpabl purpura, artralji-artrit, gastrointestinal ve renal bulgular ile karaklerize sistemik bir hastalıktır. Bu çalışmada HSP'li hastalarımızın klinik özelliklerinin değerlendirilmesi amaçlandı. Yöntem: Ocak 2002 - Nisan 2005 tarihleri arasında I. Çocuk Kliniğinde HSP tanısı alarak yatırılan 75 hastanın dosyaları retrospektif olarak incelendi. Bulgular: Olguların yas ortalaması 9.3 ± 3.1 yıldL Hastalarımızın %55'i. erkek, %45'i kız idi. Yaz aylarında başvuru oldukça nadirdi. Hastaların tamamında palpabl purpura,%78'inde GİS.tutulumu, %72'sinde artrit yada artralji, %33'ünde renal tutulum mevcuttu, %49 hastada dışkıda gizli kan pozitifliği, vardı. Akut batın tablosunda başvuran %6.7 hasta mevcuttu. Saçlı deride ödem %5.3 hastada, skrotal ödem %12 hastada saptandı. Böbrek tutulumu olan hastalarda ortalama izlem süresi 2-2.3 ± 75 aydı.Ağır böbrek tutulumu olan toplam 13 hastaya böbrek biyopsisi yapıldı. Yorum: HSP'nın en sık görülen bulgusu cilt döküntüsü olmakla beraber! daha önce veya takipte eklem tutulumu, renal ve gastrointestinal bulguların ortaya.çıkabileceği, diğer vaskülit tablolarına eşlik edebileceği akılda tutulmalı ve ayırıcı tanıda dikkatli olunmalıdır.

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Cite This Article

ARAPOĞLU, M., TELHAN, L., ÖZÇELİK, G., KEPEKÇİ, L., ERDEM, E., PALANDUZ, A. (2005). Henoch-Schonlein purpura in childhood: Clinical experience. Şişli Etfal Hastanesi Tıp Bülteni, Cilt: 39 - Sayı: 3, 27–31. https://ajindex.com/articles/363529

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