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Journals / Şişli Etfal Hastanesi Tıp Bülteni / 2009 / Cilt: 43 - Sayı: 4

Systemic capillary leak syndrome: Because of 3 cases

Sistemik kapiller kaçış sendromu: 3 olgu nedeni ile

Demet ALBAYRAK
BELGİN AKAN
Deniz ERDEM
İnan KILIÇ
Nermin GÖĞÜŞ
Pages
184–186
DOI
—
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AI Summary & Key Takeaways

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

In this report, we aimed to discuss 3 cases with systemic capillary leak syndrome.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Systemic capillary leak syndrome is a rare diseases was first described by Clarkson et al in 1960.
📊
Key Findings & Data:The syndrome is characterized by chronic recurrent episodes of a triad of hypotension, hypoalbuminemia and hemoconsentration.
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Conclusion & Impact:In this report, we aimed to discuss 3 cases with systemic capillary leak syndrome.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Orta yaşlı · Erkek · Kadın

Abstract

Systemic capillary leak syndrome is a rare diseases was first described by Clarkson et al in 1960. The syndrome is characterized by chronic recurrent episodes of a triad of hypotension, hypoalbuminemia and hemoconsentration. Supportive treatment is essential and prognosis is poor. In this report, we aimed to discuss 3 cases with systemic capillary leak syndrome.

Özet

Sistemik kapiller kaçış sendromu (SKKS), ilk kez 1960 yılında Clarkson ve arkadaşları tarafından tanımlanmış nadir görülen bir hastalıktır. Hipotansiyon, hipoalbüminemi ve hemokonsantrasyon kronik tekrarlayıcı epizodlardaki klasik triaddır. Tedavi destekleyicidir ve prognoz kötüdür. Biz bu derleme ile yoğun bakımda rastladığımız 3 kapiller kaçış sendromlu olguyu tartışmayı amaçladık.

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Cite This Article

ALBAYRAK, D., AKAN, B., ERDEM, D., KILIÇ, İ., GÖĞÜŞ, N. (2009). Systemic capillary leak syndrome: Because of 3 cases. Şişli Etfal Hastanesi Tıp Bülteni, Cilt: 43 - Sayı: 4, 184–186. https://ajindex.com/articles/356836

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References (1)

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