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Published on: March 24, 2017
Sclerosing skin disorders in association with multiple sclerosis. Coincidence, underlying autoimmune pathology or
T Hügle1, S Gratzl, T Daikeler
1Felix Platter Spital, Basel University Department of Rheumatology, Switzerland.
Objectives:
To describe and analyse the manifestation of sclerosing skin disorders in patients with multiple sclerosis (MS).
Case Reports:
We describe three patients with relapsing-remitting MS who developed skin sclerosis while receiving interferon (IFN)-beta treatment and review nine further cases of systemic sclerosis (SSc) in MS from the literature. Of all 12 patients reported, eight had limited cutaneous SSc, three had diffuse cutaneous SSc and one patient had an antisynthetase syndrome. Localised scleroderma such as morphoea was not described. The mean age at diagnosis was 25.2 years for MS (range 12 to 51) and 38.3 years for SSc (range 16 to 66). Eleven patients developed SSc after the onset of MS and manifested with skin sclerosis after a mean of 14.9 years (range 1 to 45). In five patients IFN-beta was commenced before the development of skin sclerosis (mean 4.6 years, range 1 to 8 years). There was no relationship between the onset of skin sclerosis and MS activity. With the exception of one individual, all patients had antinuclear antibodies.
Conclusions:
Sclerosing skin disorders may develop in the course of MS. The relatively early age of SSc onset in patients with MS suggests a genetic predisposition and/or an IFN-associated trigger.
Insights
Sclerosing skin disorders, like systemic sclerosis (SSc), can occur in patients with multiple sclerosis (MS). Interferon beta treatment may be a trigger for SSc in MS patients.
Area of Science:
- Dermatology and Neurology
- Autoimmune Disorders
Background:
- Multiple sclerosis (MS) is a chronic autoimmune disease affecting the central nervous system.
- Sclerosing skin disorders, particularly systemic sclerosis (SSc), are characterized by skin hardening and connective tissue abnormalities.
Observation:
- Three patients with relapsing-remitting MS developed skin sclerosis during interferon (IFN)-beta therapy.
- A literature review identified nine additional cases of SSc in MS patients, totaling 12 cases.
- The majority of SSc cases were limited cutaneous SSc (8/12), with three diffuse cutaneous SSc and one antisynthetase syndrome.
Findings:
- Systemic sclerosis (SSc) onset in MS patients occurred at a mean age of 38.3 years, significantly after MS diagnosis (mean age 25.2 years).
- In five patients, IFN-beta treatment preceded SSc development by a mean of 4.6 years.
- No correlation was found between SSc onset and MS disease activity; most patients (11/12) tested positive for antinuclear antibodies.
Implications:
- The early onset of SSc in MS patients suggests a potential genetic predisposition or an IFN-beta-associated trigger.
- These findings highlight the importance of monitoring for sclerosing skin disorders in MS patients, especially those on IFN-beta therapy.
- Further research is warranted to elucidate the mechanisms linking MS, SSc, and IFN-beta treatment.
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