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Journals / Journal of Clinical and Analytical Medicine / 2016 / Cilt: 7 - Sayı: 4

Nadir Görülen Klinik Bir Durum; Erasmus Sendromu

A Rare Clinical Condition: Erasmus Syndrome

Atalay DOGRU
Yunus UGAN
Sevket Ercan TUNC
Mehmet SAHİN
Pages
554–556
Publication Date
2022-10-18
DOI
—
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AI Summary & Key Takeaways

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

Here, we report on a 30-year-old patient working in denim sandblasting who developed SS while being followed for 6 years due to silicosis.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Systemic sclerosis (SS) is a systemic autoimmune disease progressing with fibrosis of the skin and internal organs, the cause of which cannot be precisely explained.
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Key Findings & Data:The disease is known to be associated with environmental factors.
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Conclusion & Impact:Here, we report on a 30-year-old patient working in denim sandblasting who developed SS while being followed for 6 years due to silicosis.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Systemic sclerosis (SS) is a systemic autoimmune disease progressing with fibrosis of the skin and internal organs, the cause of which cannot be precisely explained. The disease is known to be associated with environmental factors. In particular, exposure to silica powders is believed to have a part in the pathogenesis of the disease by the triggering of a number of immune reactions. Silicosis and SS association is defined as Erasmus Syndrome (ES). Here, we report on a 30-year-old patient working in denim sandblasting who developed SS while being followed for 6 years due to silicosis.

Özet

Sistemik Skleroz (SS), cildin ve iç organların fibrozisi ile giden, sebebi tam olarak aydınlatılamayan sistemik otoimmün bir hastalıktır. Hastalığın çevresel faktörlerle ilişkisi olduğu bilinmektedir. Özellikle silica tozlarıyla maruziyetin bir takım immun reaksiyonların tetiklenmesiyle hastalığın patogenezinde rol aldığı düşünülmektedir. Silikozis ve SS birlikteliği Erasmus Sendromu (ES) olarak tanımlanmaktadır. Burada 6 yıldır silikozis nedeniyle takipli, kotlama işçisi olarak çalışan 30 yaşında sistemik sklerozlu bir olgu sunulmaktadır.

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Cite This Article

DOGRU, A., UGAN, Y., TUNC, S. E., SAHİN, M. (2022). Nadir Görülen Klinik Bir Durum; Erasmus Sendromu. Journal of Clinical and Analytical Medicine, Cilt: 7 - Sayı: 4, 554–556. https://ajindex.com/articles/560870

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References (8)

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