Erasmus syndrome: A rare case report of silicosis and systemic sclerosis

Author:

Rauniyar Somee1ORCID,Thapa Biyas1,Gupta Prakash2ORCID,Subedi Rupak3,Baral Bishwodip4

Affiliation:

1. Rangpur Medical College Rangpur Bangladesh

2. Virgen Milagrosa University Foundation College of Medicine San Carlos City Philippines

3. Madan Bhandari Academy of Health Sciences Hetauda Nepal

4. Sukraraj Tropical and Infectious Disease Hospital Kathmandu Nepal

Abstract

AbstractPeople with silicosis may develop Erasmus syndrome, a condition characterized by the emergence of systemic sclerosis (SSc) after silica exposure. This case study emphasizes the significance of understanding the connection between occupational silica exposure, silicosis, and SSc. A 24‐year‐old male stonecutter got silicosis and a form of SSc following 8 years on his job as a stonecutter. The signs and symptoms the patient experienced were Raynaud's phenomenon, cutaneous fibrosis, arthralgia, digital pitting, and respiratory distress. High‐resolution computed tomography (HRCT) revealed interstitial lung disease and calcified mediastinal lymph nodes. This case study demonstrates the clinical importance of the relationship between occupational silica exposure, silicosis, SSc, and Erasmus syndrome. Healthcare providers need to be aware of the possible difficulties and issues that may result from silica exposure. They should prioritize quick detection and efficient treatment plans for those who have been exposed to silica while on the job.

Publisher

Wiley

Subject

General Medicine

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4. Prevalence of connective tissue disease in silicosis (1985-2006)-a report from the state of michigan surveillance system for silicosis

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