Eosinophilic fasciitis: Difference between revisions

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{{Infobox medical condition
| name            = Eosinophilic fasciitis
| synonyms        = Shulman's syndrome
| field          = [[Rheumatology]]
| symptoms        = [[Swelling]], [[pain]], [[stiffness]] of the skin and [[fascia]]
| complications  = [[Contracture (medicine)|Contractures]], [[peripheral neuropathy]]
| onset          = Typically [[middle age]]
| duration        = [[Chronic (medicine)|Chronic]]
| causes          = Unknown, possibly [[autoimmune disease]]
| risks          = [[Strenuous exercise]], [[trauma (medicine)|trauma]]
| diagnosis      = [[Clinical diagnosis]], [[skin biopsy]]
| differential    = [[Scleroderma]], [[eosinophilia-myalgia syndrome]]
| treatment      = [[Corticosteroids]], [[immunosuppressive drug]]s
| prognosis      = Generally good with treatment
| frequency      = Rare
}}
'''Other Names:''' Shulman syndrome; EF
'''Other Names:''' Shulman syndrome; EF
Eosinophilic fasciitis is a very rare condition in which muscle tissue underneath the skin, called [[fascia]], becomes swollen and thick.
Eosinophilic fasciitis is a very rare condition in which muscle tissue underneath the skin, called [[fascia]], becomes swollen and thick.
Rapid swelling can occur in the hands, arms, legs, and feet. People with this condition have a buildup of [[eosinophils]], a type of [[white blood cell]], in the affected [[fascia]] and [[muscles]].  
Rapid swelling can occur in the hands, arms, legs, and feet. People with this condition have a buildup of [[eosinophils]], a type of [[white blood cell]], in the affected [[fascia]] and [[muscles]].  
Eosinophilic fasciitis is similar in appearance to [[scleroderma]]. However, in contrast with [[systemic sclerosis]],  internal organ involvement in eosinophilic fasciitis is generally absent. Some researchers believe that eosinophilic fasciitis may be a variant of [[morphea]] (localized scleroderma).
Eosinophilic fasciitis is similar in appearance to [[scleroderma]]. However, in contrast with [[systemic sclerosis]],  internal organ involvement in eosinophilic fasciitis is generally absent. Some researchers believe that eosinophilic fasciitis may be a variant of [[morphea]] (localized scleroderma).
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== '''Cause''' ==
== '''Cause''' ==
The cause of EF is unknown. Rare cases have occurred after taking [[L-tryptophan]] supplements. In people with this condition, [[white blood cells]], called [[eosinophils]], build up in the muscles and tissues. Eosinophils are linked to allergic reactions. The syndrome is more common in people ages 30 to 60.
The cause of EF is unknown. Rare cases have occurred after taking [[L-tryptophan]] supplements. In people with this condition, [[white blood cells]], called [[eosinophils]], build up in the muscles and tissues. Eosinophils are linked to allergic reactions. The syndrome is more common in people ages 30 to 60.
== '''Signs and symptoms''' ==
== '''Signs and symptoms''' ==
Symptoms may include:
Symptoms may include:
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* Muscle pain
* Muscle pain
* Thickened skin that looks puckered
* Thickened skin that looks puckered
For most diseases, symptoms will vary from person to person. People with the same disease may not have all the symptoms listed.
For most diseases, symptoms will vary from person to person. People with the same disease may not have all the symptoms listed.
80%-99% of people have these symptoms
80%-99% of people have these symptoms
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* Myalgia(Muscle ache)
* Myalgia(Muscle ache)
* Subcutaneous nodule(Firm lump under the skin)
* Subcutaneous nodule(Firm lump under the skin)
30%-79% of people have these symptoms
30%-79% of people have these symptoms
* [[Arthralgia]](Joint pain)
* [[Arthralgia]](Joint pain)
* [[Arthritis]](Joint inflammation)
* [[Arthritis]](Joint inflammation)
5%-29% of people have these symptoms
5%-29% of people have these symptoms
* [[Fasciitis]](Inflammation of the fascia)
* [[Fasciitis]](Inflammation of the fascia)
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* [[Paresthesia]](Pins and needles feeling)
* [[Paresthesia]](Pins and needles feeling)
* Weight loss
* Weight loss
== '''Diagnosis''' ==
== '''Diagnosis''' ==
Tests that may be done include:
Tests that may be done include:
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* Muscle [[biopsy]]
* Muscle [[biopsy]]
* Skin biopsy (the biopsy needs to include the deep tissue of the fascia)
* Skin biopsy (the biopsy needs to include the deep tissue of the fascia)
== '''Treatment''' ==
== '''Treatment''' ==
About 10-20% of people with eosinophilic fasciitis recover spontaneously without treatment.  For those who do not, [[glucocorticoids]] (0.5–1 mg/kg/d), such as '''[[prednisone]]''', are the mainstay therapy. Even with treatment, improvement in symptoms can take weeks or months. Glucocorticoids are successful in treating eosionophilic fasciitis in over 70% of cases.
About 10-20% of people with eosinophilic fasciitis recover spontaneously without treatment.  For those who do not, [[glucocorticoids]] (0.5‚Äì1 mg/kg/d), such as '''[[prednisone]]''', are the mainstay therapy. Even with treatment, improvement in symptoms can take weeks or months. Glucocorticoids are successful in treating eosionophilic fasciitis in over 70% of cases.
 
If glucocorticoids are unsuccessful, '''[[methotrexate]]''' at low doses (15‚Äì25 mg once weekly) is probably the most favored second-line treatment, especially in people with reddish to purpleish (morphea-like) skin [[lesions]].  Other treatment options include [[NSAIDs]], [[D-penicillamine]], [[chloroquine]], [[cimetidine]], [[azathioprine]], [[cyclosporin A]], [[infliximab]], [[UVA-1]], and bath [[PUVA]]. Physical therapy may help improve joint mobility and decrease contractures. Surgical release has been used in some severe cases to manage significant joint [[contractures]].
If glucocorticoids are unsuccessful, '''[[methotrexate]]''' at low doses (15–25 mg once weekly) is probably the most favored second-line treatment, especially in people with reddish to purpleish (morphea-like) skin [[lesions]].  Other treatment options include [[NSAIDs]], [[D-penicillamine]], [[chloroquine]], [[cimetidine]], [[azathioprine]], [[cyclosporin A]], [[infliximab]], [[UVA-1]], and bath [[PUVA]]. Physical therapy may help improve joint mobility and decrease contractures. Surgical release has been used in some severe cases to manage significant joint [[contractures]].
 
== '''Prognosis''' ==
== '''Prognosis''' ==
In most cases, the condition goes away within 1 to 3 years. However, symptoms may last longer or come back.
In most cases, the condition goes away within 1 to 3 years. However, symptoms may last longer or come back.
'''Possible Complications'''
'''Possible Complications'''
[[Arthritis]] is a rare complication of EF. Some people may develop very serious blood disorders or blood-related cancers, such as [[aplastic anemia]] or leukemia. The outlook is much worse if blood diseases occur.
[[Arthritis]] is a rare complication of EF. Some people may develop very serious blood disorders or blood-related cancers, such as [[aplastic anemia]] or leukemia. The outlook is much worse if blood diseases occur.
{{Systemic connective tissue disorders}}
{{Systemic connective tissue disorders}}
{{Soft tissue disorders}}
{{Soft tissue disorders}}
[[Category:Disorders of fascia]]
[[Category:Disorders of fascia]]
[[Category:Eosinophilic cutaneous conditions]]
[[Category:Eosinophilic cutaneous conditions]]

Latest revision as of 02:10, 4 April 2025


Eosinophilic fasciitis
Synonyms Shulman's syndrome
Pronounce N/A
Specialty N/A
Symptoms Swelling, pain, stiffness of the skin and fascia
Complications Contractures, peripheral neuropathy
Onset Typically middle age
Duration Chronic
Types N/A
Causes Unknown, possibly autoimmune disease
Risks Strenuous exercise, trauma
Diagnosis Clinical diagnosis, skin biopsy
Differential diagnosis Scleroderma, eosinophilia-myalgia syndrome
Prevention N/A
Treatment Corticosteroids, immunosuppressive drugs
Medication N/A
Prognosis Generally good with treatment
Frequency Rare
Deaths N/A


Other Names: Shulman syndrome; EF Eosinophilic fasciitis is a very rare condition in which muscle tissue underneath the skin, called fascia, becomes swollen and thick. Rapid swelling can occur in the hands, arms, legs, and feet. People with this condition have a buildup of eosinophils, a type of white blood cell, in the affected fascia and muscles. Eosinophilic fasciitis is similar in appearance to scleroderma. However, in contrast with systemic sclerosis, internal organ involvement in eosinophilic fasciitis is generally absent. Some researchers believe that eosinophilic fasciitis may be a variant of morphea (localized scleroderma).

Cause[edit]

The cause of EF is unknown. Rare cases have occurred after taking L-tryptophan supplements. In people with this condition, white blood cells, called eosinophils, build up in the muscles and tissues. Eosinophils are linked to allergic reactions. The syndrome is more common in people ages 30 to 60.

Signs and symptoms[edit]

Symptoms may include:

  • Tenderness and swelling of the skin on the arms, legs, or sometimes the joints (most often on both sides of the body)
  • Arthritis
  • Carpal tunnel syndrome
  • Muscle pain
  • Thickened skin that looks puckered

For most diseases, symptoms will vary from person to person. People with the same disease may not have all the symptoms listed. 80%-99% of people have these symptoms

  • Acrocyanosis(Persistent blue color of hands, feet, or parts of face)
  • Cellulitis(Bacterial infection of skin)
  • Eosinophilia(High blood eosinophil count)
  • Fatigue(Tired)
  • Macule(Flat, discolored area of skin)
  • Muscular edema
  • Myalgia(Muscle ache)
  • Subcutaneous nodule(Firm lump under the skin)

30%-79% of people have these symptoms

5%-29% of people have these symptoms

  • Fasciitis(Inflammation of the fascia)
  • Myositis(Muscle inflammation)
  • Paresthesia(Pins and needles feeling)
  • Weight loss

Diagnosis[edit]

Tests that may be done include:

Treatment[edit]

About 10-20% of people with eosinophilic fasciitis recover spontaneously without treatment. For those who do not, glucocorticoids (0.5–1 mg/kg/d), such as prednisone, are the mainstay therapy. Even with treatment, improvement in symptoms can take weeks or months. Glucocorticoids are successful in treating eosionophilic fasciitis in over 70% of cases. If glucocorticoids are unsuccessful, methotrexate at low doses (15–25 mg once weekly) is probably the most favored second-line treatment, especially in people with reddish to purpleish (morphea-like) skin lesions. Other treatment options include NSAIDs, D-penicillamine, chloroquine, cimetidine, azathioprine, cyclosporin A, infliximab, UVA-1, and bath PUVA. Physical therapy may help improve joint mobility and decrease contractures. Surgical release has been used in some severe cases to manage significant joint contractures.

Prognosis[edit]

In most cases, the condition goes away within 1 to 3 years. However, symptoms may last longer or come back. Possible Complications Arthritis is a rare complication of EF. Some people may develop very serious blood disorders or blood-related cancers, such as aplastic anemia or leukemia. The outlook is much worse if blood diseases occur.


NIH genetic and rare disease info[edit]

Eosinophilic fasciitis is a rare disease.


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