Infantile papular acrodermatitis
Infantile Papular Acrodermatitis (IPA), also known as Gianotti-Crosti syndrome, is a benign skin condition that typically affects children between the ages of 3 months and 15 years. It is characterized by a symmetric, itchy, papular rash that predominantly affects the face, buttocks, and extremities. The condition is often associated with viral infections, particularly Hepatitis B, Epstein-Barr virus, and Enteroviruses, among others. Despite its alarming appearance, IPA is self-limiting and usually resolves without treatment within 2 to 8 weeks.
Etiology[edit | edit source]
The exact cause of Infantile Papular Acrodermatitis is not well understood, but it is believed to be a hypersensitivity reaction to various viral infections. The most commonly associated viruses include:
Symptoms[edit | edit source]
The primary symptom of IPA is a sudden onset of pink to red-brown papules, which may become confluent, forming plaques. These lesions are typically distributed symmetrically on the face, buttocks, and extensor surfaces of the arms and legs. Other symptoms may include:
- Mild itching
- Low-grade fever
- Lymphadenopathy (swollen lymph nodes)
- Hepatomegaly (enlarged liver) in some cases
Diagnosis[edit | edit source]
Diagnosis of Infantile Papular Acrodermatitis is primarily clinical, based on the characteristic appearance and distribution of the rash. Laboratory tests may be conducted to identify the underlying viral infection and to rule out other conditions with similar presentations. These tests may include:
- Complete blood count (CBC)
- Liver function tests
- Viral serologies
Treatment[edit | edit source]
Treatment of IPA is mainly supportive, as the condition is self-limiting and typically resolves on its own. Management may include:
- Use of emollients to soothe the skin
- Antihistamines to relieve itching
- Avoidance of scratching to prevent secondary infections
Prognosis[edit | edit source]
The prognosis for children with Infantile Papular Acrodermatitis is excellent. The rash usually resolves within 2 to 8 weeks without scarring or long-term complications. Recurrences are rare.
Prevention[edit | edit source]
There is no specific prevention for IPA, but minimizing exposure to known associated viruses can reduce risk. Ensuring up-to-date vaccinations, practicing good hygiene, and avoiding close contact with individuals who have viral infections can help prevent the spread of viruses linked to IPA.
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Contributors: Prab R. Tumpati, MD