Scleroderma

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Scleroderma
Classification and external resources
MercMorphea.JPG
ICD-10L94.0-L94.1, M34
ICD-9701.0 710.1
MedlinePlus000429
 
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This article is about the disease. For the mushroom, see Scleroderma (fungus).
Not to be confused with scleredema.
Scleroderma
Classification and external resources
MercMorphea.JPG
ICD-10L94.0-L94.1, M34
ICD-9701.0 710.1
MedlinePlus000429

Scleroderma, also known as systemic sclerosis, is a chronic systemic autoimmune disease characterised by hardening (sclero) of the skin (derma). In the more severe form, it also affects internal organs.[1][2]

Limited scleroderma involves cutaneous manifestations that mainly affect the hands, arms and face. It was previously called CREST syndrome in reference to the following common manifestations:[3] calcinosis (the deposition of calcium nodules in the skin), raynaud's phenomenon (exaggerated vasoconstriction in the hands, with fingers undergoing white-blue-red color transitions in the cold), esophageal dysfunction (leading to difficulty swallowing), sclerodactyly (skin thickening on the fingers), and telangiectasias (dilated capillaries on the face, hands and mucous membranes).

Diffuse scleroderma is rapidly progressing and affects a large area of the skin and one or more internal organs, frequently the kidneys, esophagus, heart and/or lungs. This form of scleroderma can be quite disabling. There are no treatments for scleroderma itself, but individual organ system complications are treated.[4][5]

The prognosis is generally good for limited cutaneous scleroderma persons who escape pulmonary complications, but is worse for those with the diffuse cutaneous disease, particularly in older age and for males. Death occurs most often from pulmonary, heart and kidney complications. In diffuse cutaneous disease, five-year survival is 70% and 10-year survival is 55%.[6]

The cause of scleroderma is unknown.[1] It is an autoimmune condition, in which the body's immune system attacks healthy tissues.[1] Strong associations with certain mutations in the HLA gene have been identified.[7][8] Strong environment influences have also been implicated in the aetiology of scleroderma.[9][10]

Signs and symptoms[edit]

Left arm of a scleroderma sufferer, showing skin lesions

Potential signs and symptoms include:[2][3][6]

Cause[edit]

The exact cause is yet to be fully elucidated; although the available data does support a genetic and environmental component to the condition.[7][8][9][10] Mutations in the HLA gene seems to play a crucial role in the pathogenesis of some cases (but not all), likewise silica, aromatic and chlorinated solvents, ketones, trichloroethylene, welding fumes and white spirits exposure seems to contribute to the condition in a small proportion of affected persons.[7][8][9][10][11]

Pathophysiology[edit]

It is characterised by increased synthesis of collagen (leading to the sclerosis), damage to small blood vessels, activation of T lymphocytes and production of altered connective tissues.[12] Its proposed pathogenesis is the following:[13][14][15][16][17]

Vitamin D is also implicated in the pathophysiology of the disease, for one an inverse correlation between plasma levels of vitamin D and scleroderma severity has been noted and vitamin D is known to play a crucial role in regulating (usually suppressing) the actions of the immune system.[19]

Diagnosis[edit]

Typical scleroderma is classically defined as symmetrical skin thickening, with about 70% of cases also presenting with Raynaud's phenomenon, nail-fold capillary changes and antinuclear antibodies. Affected individuals may or may not experience systemic organ involvement. There is no single test for scleroderma that works all of the time and hence the diagnosis is often a matter of exclusion. Atypical scleroderma may show any variation of these changes without skin changes or with finger swelling only.[20]

Laboratory testing can show antitopoisomerase antibodies, like anti-scl70 (causing a diffuse systemic form), or anticentromere antibodies (causing a limited systemic form and the CREST syndrome). Other autoantibodies can be seen, such as anti-U3 or anti-RNA polymerase.[1]

Differential[edit]

Diseases that are often in the differential include:[21]

Classification[edit]

Scleroderma is characterised by the appearance of circumscribed or diffuse, hard, smooth, ivory-colored areas that are immobile and which give the appearance of hidebound skin, a disease occurring in both localised and systemic forms:[22]

Treatment[edit]

There is no cure available for scleroderma, although relief of symptoms is often achieved. These include:[2][23]

Systemic disease-modifying treatment with immunosuppressants is also often also used.[7][24][25][26][27][28] Immunosuppressants used in its treatment include: azathioprine, methotrexate, cyclophosphamide, mycophenolate, intravenous immunoglobulin, rituximab, sirolimus, alefacept and the tyrosine kinase inhibitors, imatinib, nilotinib and dasatinib.[7][23][24][25][26][27][28][29] Experimental therapies currently under investigation include endothelin receptor antagonsits, tyrosine kinase inhibitors, beta-glycan peptides, halofuginone, basiliximab, alemtuzumab, abatacept and haematopoietic stem cell transplantation.[30][31]

Prognosis[edit]

The 5-year survival rate for scleroderma is about 85%, whereas the 10-year survival rate is less than 70%.[35] This varies according to the subtype; for instance, persons with limited skin disease have a 10-year survival rate of 71%, whereas those with diffuse skin disease have a 10-year survival rate of just 21%.[1] The major causes of death in persons with scleroderma are: pulmonary hypertension, pulmonary fibrosis and scleroderma renal crisis.[1] People with scleroderma are also at a heightened risk for contracting cancers (especially liver, lung, haematologic and bladder cancers) and, perhaps, cardiovascular disease.[36][37][38][39][40]

Epidemiology[edit]

This disease is found worldwide and women are four to nine times more likely to develop scleroderma than men.[1] In the United States, prevalence is estimated at 240 per million and the annual incidence of scleroderma is 19 per one million.[1] Likewise in the US it is slightly more common in African Americans than in their white counterparts.[1] In Germany, on the other hand, the prevalence is 1-15/100,000 and the annual incidence is 0.3-2.8/100,000.[35] In South Australia the annual incidence is 22.8 per 1 million and the prevalence 233 per 1 million.[41] It most commonly first presents between the ages of 20 and 50 years, although any age group can be affected and is less common in the Asian population.[1][2][42]

Pregnancy[edit]

Scleroderma in pregnancy is a complex situation; it increases the risk to both mother and child.[43] Overall scleroderma is associated with reduced foetal weight for gestational age.[43] The treatment for scleroderma often includes known teratogens such as cyclophosphamide, methotrexate, mycophenolate, etc. and hence careful avoidance of such drugs during pregnancy is advised.[43] In these cases hydroxychloroquine and low-dose corticosteroids might be used for disease control.[43]

See also[edit]

References[edit]

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