Erasmus syndrome: systemic sclerosis and silicosis co‐occurrence

Sürmeli, Zühre Sari; Oruçoğlu, Nurdan

doi:10.1111/1756-185x.13296

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2024

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Cited by 6 publications

(2 citation statements)

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“…The treatment of ES is no different to that for idiopathic forms of SSc. Case reports of ES describe the use of methylprednisolone, mycophenate, azathioprine, cyclophosphamide, acetylsalicylic acid, methotrexate, endothelin receptor antagonists, amlodipine, and nifedipine for treatment ( 20 - 23 ). In our case, after diagnosis, the patient was treated with methylprednisolone.…”

Section: Discussionmentioning

confidence: 99%

Erasmus syndrome: case description of a rare entity

Gao,

Yang,

Tong

et al. 2024

Quant Imaging Med Surg

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Section: Discussionmentioning

confidence: 99%

Erasmus syndrome: case description of a rare entity

Gao,

Yang,

Tong

et al. 2024

Quant Imaging Med Surg

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“…Parenteral cyclophosphamide, mycophenolate mofetil, and azathioprine and the combination of these two agents with systemic steroids are among the most frequently used agents in interstitial lung disease. [ 9 10 ]…”

Section: Discussionmentioning

confidence: 99%

Erasmus Syndrome

Manav¹,

Avcı²,

Erdem³

et al. 2022

Indian Journal of Dermatology

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Erasmus syndrome is a rare syndrome accompanied by interstitial lung disease and scleroderma caused by silica exposure. There are a limited number of case reports in the literature. Awareness of this rare syndrome is important and occupational exposure should be questioned in patients presenting with scleroderma in our country, silica exposure is quite frequent and it should be kept in mind. Here, we report a case of a 41-year-old male patient presenting with interstitial lung disease, scleroderma, and serpiginous supravenous hypermelanosis caused by silica exposure who worked in the denim grinding for a short period of three months.

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