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Review
. 2024 Jun 3:15:1351675.
doi: 10.3389/fimmu.2024.1351675. eCollection 2024.

Scleroderma and scleroderma-like syndromes

Affiliations
Review

Scleroderma and scleroderma-like syndromes

Katarzyna Romanowska-Próchnicka et al. Front Immunol. .

Erratum in

  • Corrigendum: Scleroderma and Scleroderma-like syndromes.
    Romanowska-Próchnicka K, Dziewit M, Lesiak A, Reich A, Olesińska M. Romanowska-Próchnicka K, et al. Front Immunol. 2024 Jul 22;15:1456067. doi: 10.3389/fimmu.2024.1456067. eCollection 2024. Front Immunol. 2024. PMID: 39104532 Free PMC article.

Abstract

Systemic sclerosis is a systemic connective tissue disease whose main pathophysiological mechanism is a progressive fibrosis of internal organs and skin leading to thickening and induration. Blood vessels may also be involved. However, systemic scleroderma is not the only disease causing cutaneous sclerosis. There is a group of diseases that mimic scleroderma in their clinical presentation - these are scleroderma-like syndromes. A distinction can be made between syndromes of inflammatory/autoimmune, genetic, metabolic, toxic, drug-induced, occupational, paraneoplastic and syndromes caused by deposition disorders. In the following paper, we have reviewed the literature on scleroderma-like syndromes. We have outlined the factors predisposing to the development of each disease, its pathogenesis, clinical presentation, diagnostic and treatment process and the differences between each syndrome and systemic scleroderma.

Keywords: genetic; morphea; scleroderma; scleroderma-like syndromes; syndromes of inflammatory/autoimmune; systemic sclerosis; toxic.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
Scleroderma-like disorders.
Figure 2
Figure 2
Dominant areas of affected skin.

References

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