The diagnosis of Sweet syndrome often starts with a physical examination. The doctor, usually a dermatologist, will closely examine the affected area. In addition, the doctor may ask for the patient’s medical history, experienced symptoms and a few tests prior making a conclusive diagnosis. The required tests include:
The treatment for Sweet syndrome depends on the underlying cause of the condition. In some cases, it may resolve on its own without any medical intervention, although it may take longer. Medications such as corticosteroids can potentially expedite the process. These drugs diminish inflammation and suppress immune system function. Corticosteroids protect tissue by reducing amounts of white blood cells and other immune system components that fight infections.
The most common medications are:
In order to prevent relapse, the medication must be taken for a few weeks. Alternatives to corticosteroids include dapsone, potassium iodide, and colchicine. This is generally prescribed to those who have issues with long-term corticosteroid use.
Most people with Sweet syndrome rash and skin lesions recover without scars. Skin discoloration may continue for a few months after the symptoms have subsided. To avoid recurrence of Sweet syndrome, medication must be taken regularly as advised by the doctor.