Eosinophilic cellulitis | |
---|---|
Other names | Wells' syndrome, recurrent granulomatous dermatitis with eosinophilia[1] |
Initial rash in eosinophilic cellulitis | |
Specialty | Dermatology |
Symptoms | Painful, red, raised, warm patches of skin, fever, joint pain[2] |
Usual onset | Sudden and recurrent[2] |
Duration | Few weeks[2] |
Causes | Unknown[2] |
Differential diagnosis | Vasculitis, cellulitis, anaphylaxis[2][1] |
Medication | Corticosteroids, antihistamines[2][1] |
Prognosis | Often goes away by itself[2] |
Frequency | ~200 documented cases[1] |
Eosinophilic cellulitis, also known as Wells' syndrome (not to be confused with Weil's disease), is a skin disease that presents with painful, red, raised, and warm patches of skin.[2] The rash comes on suddenly, lasts for a few weeks, and often repeatedly comes back.[2] Scar formation does not typically occur.[1]
Eosinophilic cellulitis is of unknown cause.[2] It is suspected to be an autoimmune disorder.[2] It may be triggered by bites from insects and arachnids such as spiders, fleas, or ticks, or from medications or surgery.[2] Diagnosis is made after other potential cases are ruled out.[1] Skin biopsy of the affected areas may show an increased number of eosinophils.[2] Other conditions that may appear similar include cellulitis, contact dermatitis, and severe allergic reactions such as anaphylaxis.[2]
Treatment is often with a corticosteroids.[2] Steroids applied as a cream is generally recommended over the use of steroids by mouth.[3] Antihistamines may be used to help with itchiness.[1] Many times the condition goes away after a few weeks without treatment.[2] The condition is uncommon.[1] It affects both sexes with the same frequency.[2] It was first described by George Crichton Wells in 1971.[1][4]
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