Acrodermatitis

From WikiMD's Wellness Encyclopedia

Other names[edit | edit source]

Gianotti-Crosti syndrome

Clinical features[edit | edit source]

Gianotti Crosti syndrome (GCS) is a rare childhood skin condition characterized by a papular rash with blisters on the skin of the legs, buttocks, and arms.

Age of onset[edit | edit source]

It typically affects children between 9 months and 9 years of age.

Signs and symptoms[edit | edit source]

  • Skin lesions typically last at least 10 days and often last for several weeks.
  • The lesions are usually preceded by an underlying infection (usually a virus), which may cause associated symptoms such as low-grade fever, sore throat, or symptoms of an upper respiratory infection.
  • When GCS is associated with hepatitis B, Epstein-Barr, or cytomegalovirus (CMV) infection, acute hepatitis may also occur.
  • GCS is thought to be a hypersensitive response to the underlying infection.

Cause[edit | edit source]

  • While in many countries the underlying cause is hepatitis B, this is rarely the cause in North America.
  • In Italian children, Gianotti-Crosti syndrome is seen frequently with hepatitis B. But this link is rarely seen in the United States.
  • Epstein-Barr virus (EBV, mononucleosis) is the virus most often associated with acrodermatitis.

Pathophysiology[edit | edit source]

  • Gianotti Crosti syndrome (GCS) is thought to be due to a hypersensitive response to a previous infection.
  • The underlying infection tends to correlate with the infectious agent endemic to a specific geographic region.
  • For example, in Japan and Mediterranean countries, GCS is more commonly associated with hepatitis B virus infection.
  • Since there is more universal use of hepatitis B immunization, Epstein-Barr virus is now the most common associated infection worldwide.
  • GCS may also occur after coxsackievirus, infectious mononucleosis, cytomegalovirus, enterovirus infections, ECHO viruses, respiratory syncytial virus, or after vaccination with a live virus serum.
  • In most cases, no laboratory tests are needed when a person is diagnosed with GCS.

Treatment[edit | edit source]

  • GCS typically does not require treatment and goes away on its own within 1 to 3 months.
  • In some cases, a mild topical steroid cream may be prescribed to relieve itching.
  • Infections linked with this condition, such as hepatitis B and Epstein-Barr, are treated.
  • Cortisone creams and oral antihistamines may help with itching and irritation.

Prognosis[edit | edit source]

The rash usually disappears on its own in about 3 to 8 weeks without treatment or complication. Associated conditions must be watched carefully.

Complications[edit | edit source]

Complications occur as a result of associated conditions, rather than as a result of the rash.

Other names[edit | edit source]

  • Papular acrodermatitis of childhood;
  • Infantile acrodermatitis;
  • Acrodermatitis - infantile lichenoid;
  • Acrodermatitis - papular infantile;
  • Papulovesicular acro-located syndrome


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Contributors: Prab R. Tumpati, MD