Pityriasis lichenoides et varioliformis acuta

Common Name(s)

Pityriasis lichenoides et varioliformis acuta

Pityriasis lichenoides et varioliformis acuta (PLEVA) is a rare skin disorder that is characterized as a more severe form of pityriasis lichenoides. Signs and symptoms usually begin with itchy, burning skin lesions that ulcerate, breakdown, form open sores, then form a red-brown crust. Individuals with PLEVA may also experience a low-grade fever, headache, malaise (a vague feeling of bodily discomfort), and arthralgias (severe joint pain); these symptoms may occasionally precede or accompany the skin findings. The underlying cause of pityriasis lichenoides and PLEVA is unknown. Febrile ulceronecrotic Mucha-Habermann disease (FUMHD) is a rare and severe form of PLEVA.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Pityriasis lichenoides et varioliformis acuta" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Pityriasis lichenoides et varioliformis acuta" returned 5 free, full-text research articles on human participants. First 3 results:

Pityriasis lichenoides with ulceronecrosis and hyperthermia: a rare variant of pityriasis lichenoides et varioliformis acuta.
 

Author(s): Sarvjit Kaur Virdi, Amrinder Jit Kanwar, Uma Nahar Saikia

Journal: Indian J Dermatol Venereol Leprol. ;76(2):172-5.

 

Pityriasis lichenoides with ulceronecrosis and hyperthermia (PLUH) is a severe variant of pityriasis lichenoides et varioliformis acuta that is characterized by high fever and papulo-necrotic skin lesions. We report the case of a 49-year-old male with typical features of PLUH along ...

Last Updated: 15 Mar 2010

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[Pityriasis lichenoides et varioliformis acuta (Mucha-Habermann disease)].
 

Author(s): Ma T Bordel Gómez, J C Santos Durán, J Sánchez Estella, M Yuste Chaves, Ma T Alonso San Pablo

Journal: An Pediatr (Barc). 2007 Jan;66(1):98-100.

 

Last Updated: 1 Feb 2007

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Immunohistochemical distinction of lymphomatoid papulosis and pityriasis lichenoides et varioliformis acuta.
 

Author(s): F J Varga, E C Vonderheid, S M Olbricht, M E Kadin

Journal: Am. J. Pathol.. 1990 Apr;136(4):979-87.

 

Lymphomatoid papulosis (LyP) and pityriasis lichenoides et varioliformis acuta (PLEVA) are benign self-healing cutaneous eruptions that may be clinically and histologically similar. However LyP has a 5% to 20% risk of associated lymphoid malignancy, whereas PLEVA does not. To determine ...

Last Updated: 23 May 1990

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Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Pityriasis lichenoides et varioliformis acuta" returned 0 free, full-text review articles on human participants.

 
 
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Symptoms, Diagnosis, and Treatment

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Clinical Trial Information This information is provided by ClinicalTrials.gov

There are currently no open clinical trials for this condition.