Pityriasis Lichenoides Et Varioliformis Acuta (PLEVA) is a rare skin condition characterized by the development of red, scaly patches and pustules on the skin. Saunders Elsevier. ISBN 0-7216-2921-0.

Understanding the Context

^ "PLEVA, or Mucha-Habermann disease - MayoClinic.com". Archived from the original on 2007-07-15. Retrieved 2007-11-18. ^ Tomasini D, Tomasini CF, Cerri A, et al.

Pleva | Pitiyriasis Lichenoides Et Variolaformis Acuta Pleva

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Key Insights

(2004). "Pityriasis lichenoides: a cytotoxic T-cell-mediated skin disorder. Evidence of human parvovirus B19 DNA in nine cases". J. Cutan.

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Final Thoughts

Pityriasis lichenoides et varioliformis acuta (PLEVA), also known as Mucha-Habermann disease, is a rare inflammatory skin disorder characterized by the sudden eruption of small, red-brown papules that may evolve into vesicles, pustules, or necrotic ulcers. PLEVA and PLC are uncommon, distinctive skin eruptions of unknown cause. PLEVA and PLC are usually mild, but unfortunately, can linger, even with proper treatment. PLEVA and PLC are non-contagious skin diseases. They can occur at any age but are more common in young people. PLEVA is seen most commonly in children and is rarely associated with fever and malaise.

The skin lesions can be in various stages: vesicular, pustular, and crusted. The acute form, pityriasis lichenoides et varioliformis acuta (PLEVA), and the chronic form, pityriasis lichenoides chronica (PLC), sit at either end of a disease spectrum with many patients showing overlapping features. There are two types of pityriasis lichenoides: an acute (more sudden onset and less persistent) form known as pityriasis lichenoides et varioliformis acuta (PLEVA), and a milder, more persistent form known as pityriasis lichenoides chronica (PLC). Pityriasis lichenoides et varioliformis acuta (PLEVA), otherwise known as Mucha-Habermann disease, is an uncommon cutaneous inflammatory disorder that most frequently affects young adults and children.