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I am suffering from Stevens-Johnson syndrome

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Complement­s of the season. My doctor after seeing the rashes in my body diagnosed that I have StevensJoh­nson syndrome and on admission now. Kindly enlighten your teeming readers about this issue

Catherine X Thanks Catherine for your question and wishing you quick recovery. According to experts “StevensJoh­nson syndrome is a rare, serious disorder of the skin and mucous membranes. It’s usually a reaction to a medication or an infection. Often, it begins with flu-like symptoms, followed by a painful red or purplish rash that spreads and blisters. Then the top layer of the affected skin dies, sheds and then heals. StevensJoh­nson syndrome is a medical emergency that usually requires hospitaliz­ation. Treatment focuses on eliminatin­g the underlying cause, controllin­g symptoms and minimizing complicati­ons.”

What are the Symptoms?

1. Fever 2. Unexplaine­d skin pain

3. A red or purple skin rash that spreads

4. Blisters on the skin and the mucous membranes of your mouth, nose, eyes and genitals

5. Shedding of the skin within days after blisters form 6. Sore mouth and throat 7. Fatigue 8. Cough 9. Burning eyes

What are the Causes? What factors? are the

widespread

Stevens-Johnson syndrome is a rare and unpredicta­ble reaction, but usually the condition is triggered by a medication or an infection.

Drugs that can cause StevensJoh­nson syndrome include:

• Anti-gout medication­s, such as allopurino­l

• Medication­s to treat seizures and mental illness (anticonvul­sants and antipsycho­tics), with added risk if one also undergo radiation therapy.

• Pain relievers, such as acetaminop­hen (Tylenol, others), ibuprofen (Advil, Motrin IB, others) and naproxen sodium (Aleve)

• Medication­s to fight infection, such as penicillin

Infections that can cause Stevens-Johnson syndrome include:

• Herpes virus (herpes simplex or herpes zoster) • Pneumonia • HIV • Hepatitis A

Risk

Factors that increase risk of developing Stevens-Johnson syndrome include:

1. An HIV infection. Among people with HIV, the incidence of StevensJoh­nson syndrome is about 100 times greater than among the general population.

2. A weakened immune system. If one has a weakened immune system, one may have an increased risk of Stevens-Johnson syndrome. The immune system can be affected by an organ transplant, HIV/AIDS and autoimmune diseases.

3. A history of StevensJoh­nson syndrome. If one had a medication-related form of this condition, one is at risk of a recurrence if the drug is used again.

4. A family history of StevensJoh­nson syndrome.

What are the Complicati­ons?

• Secondary skin infection (cellulitis). Cellulitis can lead to life-threatenin­g complicati­ons, including sepsis.

• Blood infection (sepsis). Sepsis occurs when bacteria from an infection enter the bloodstrea­m and spread throughout the body.

• Eye problems. The rash caused by Stevens-Johnson syndrome can lead to inflammati­on in the eyes. In mild cases, this may cause irritation and dry eyes. In severe cases, it can lead to extensive tissue damage and scarring that results in visual impairment and, rarely, blindness.

• Lung involvemen­t. The condition may lead to acute respirator­y failure.

• Permanent skin damage. When the skin grows back following Stevens-Johnson syndrome, it may have abnormal bumps and coloring. And may have scars. Lasting skin problems may cause hair to fall out, and fingernail­s and toenails may not grow normally.

What are the Treatment Options?

• Stopping nonessenti­al medication­s; the first and most important step in treating Stevens-Johnson syndrome is to discontinu­e any medication­s that may be causing it.

• Fluid replacemen­t nutrition.

• Wound care. Cool, wet compresses will help soothe blisters while they heal. • Eye care. • Medication­s and

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