| Pityriasis lichenoides et varioliformis acuta | |
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| Classification and external resources | |
| ICD-10 | L41.0 |
| ICD-9 | 696.2 |
| eMedicine | derm/334 |
Pityriasis lichenoides et varioliformis acuta (also known as "Acute guttate parapsoriasis," "Acute parapsoriasis," "Acute pityriasis lichenoides," "Mucha-Habermann disease," "Parapsoriasis acuta," "Parapsoriasis lichenoides et varioliformis acuta," and "Parapsoriasis varioliformis"[1]:456[2]:736) is a disease of the immune system. It is the more severe version of Pityriasis lichenoides chronica. The disease is characterized by rashes and small lesions on the skin. The disease is most common in females and usually occurs in young adulthood, although it has been seen in every age group and every race. It is possible for the disease to go into remission for short periods of time or forever.
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It is commonly misdiagnosed as chickenpox or rosacea. Pleva is also often misidentified as a form of Staph. The most accurate way to diagnose is by biopsy. This disease has not been known to be life threatening. However, there may be mutations of the disease that can cause ulcers on the exterior.
There is no known cause of this disease;[3] however, many links from viruses, vaccines, and other illnesses have been made. There is some evidence associating it with Parvovirus B19.[4]
It is not contagious and currently there is no cure for the disease, although the lesions can be treated with ultraviolet therapy as well as topical steroids and antibiotics.
Treatment often involves multiple therapies that address the immune system and bacterial, viral, or dermatological causes.
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