Understanding Stevens-Johnson Syndrome: Causes, Symptoms, and Treatment

Stevens-Johnson Syndrome (SJS) is a rare but serious condition that primarily affects the skin and mucous membranes. It is usually triggered by a severe reaction to certain medications or, in some cases, infections. SJS causes the skin to blister and peel off, and can also affect the eyes, mouth, and other parts of the body.

Causes of Stevens-Johnson Syndrome

The most common cause (75-80% of cases) of SJS is a severe allergic reaction to certain medications, such as:

• Allopurinol (used to treat gout)

• Pain relievers (acetaminophen, ibuprofen, naproxen sodium)

• Sulfa antibiotics (used to treat infections)

• Anti-seizure or mental health medications

• Nevirapine (antiretroviral)

In rare cases, infections like Mycoplasma pneumonia, Cytomegalovirus (CMV), Epstein-Barr virus (EBV - the cause of mononucleosis), or the herpes virus can also trigger SJS. Other causes include malignancy-related, vaccines (very rare) and idiopathic (unknown). People with certain risk factors, such as HIV, lupus, or a history of SJS, are more likely to develop the condition.

Symptoms of Stevens-Johnson Syndrome

The initial symptoms of SJS may resemble the flu, including fever and general discomfort. After a few days, other symptoms appear:

• A painful, blistering rash that spreads and causes the skin to peel off

• Blisters on the mucous membranes (mouth, nose, genitals)

• Red, painful, watery eyes

Diagnosing Stevens-Johnson Syndrome

To diagnose SJS, your healthcare provider will review your medical history, examine your rash, and may perform additional tests such as:

• Skin biopsy

• Culture tests to rule out infections

• Lung imaging to check for pneumonia

• Blood tests to check for signs of infection

Treating Stevens-Johnson Syndrome

Treatment for SJS typically involves hospitalization, often in a burn center or intensive care unit. The primary goals of treatment are to:

1. Stop the medication or treat the infection that triggered SJS

2. Relieve symptoms and prevent complications

3. Support healing by replacing fluids and nutrients, wound care, and eye care

4. Medications (Corticosteroids, IVIG, Cyclosporin, Etanercept)

Recovery from SJS can take several weeks, and most people do recover. However, some may experience long-term effects, such as scarring, eye problems, or lung issues.

Preventing Stevens-Johnson Syndrome

While it's not always possible to prevent SJS, there are steps you can take to reduce your risk:

• Inform your doctors if you've had SJS in the past

• Wear a medical alert bracelet

• Avoid taking medications that have previously caused SJS or similar reactions

• Be aware of risk factors (like HLA-B*1502 in southeast Asians taking carbamazepine) or immunosuppression

If you suspect that you or someone you know has Stevens-Johnson Syndrome, seek emergency medical attention immediately. Early diagnosis and treatment are crucial for minimizing complications and ensuring the best possible outcome.

For more information on Stevens-Johnson Syndrome, visit the following reputable sources:

• Mayo Clinic: Stevens-Johnson Syndrome

• National Institute of Health: Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis

• American Academy of Dermatology: Stevens-Johnson Syndrome