Clinical aspects of epidermodysplasia verruciformis and review of the literature

@article{Gl2007ClinicalAO,
  title={Clinical aspects of epidermodysplasia verruciformis and review of the literature},
  author={{\"U}lker G{\"u}l and Arzu Şen Kılıç and M{\"u}zeyyen G{\"o}n{\"u}l and Seray Cakmak and Seçil Soylu Bayis},
  journal={International Journal of Dermatology},
  year={2007},
  volume={46}
}
Background  Epidermodysplasia verruciformis (EV), is an unusual genodermatosis characterized by persistent human papilloma virus infection with an autosomal recessive inheritance pattern. Clinically, it is characterized by flat wart‐like lesions, scaly hypo‐ and hyperpigmented macules and/or patches, which resemble pityriasis versicolor, and development of early beginning nonmelanoma cutaneous carcinomas. 
Epidermodysplasia verruciformis: clinical presentation with varied forms of lesions.
TLDR
A case of epidermodysplasia verruciformis with a variety of lesions such as multiple plane warts, pityriasis versicolor-like lesions and aggressive squamous cell carcinoma on the face is presented.
A sporadic case of epidermodysplasia verruciformis in a young boy
TLDR
A case of 7 year boy with complaints of asymptomatic hypopigmented macular lesions over the face, neck, and forearms, suggestive of Epidermodysplasia verruciformis is presented.
Epidermodysplasia Verruciformis: A Rare Case Report
TLDR
A 36-year-old female with complaints of asymptomatic, multiform lesions over the face, neck, chest, and upper arms is presented with suspectedEpidermodysplasia verruciformis.
Epidermodisplasia verruciforme: apresentação clínica com variadas formas de lesões
TLDR
A case of epidermodysplasia verruciformis with a variety of lesions such as multiple plane warts, pityriasis versicolor-like lesions and aggressive squamous cell carcinoma on the face is presented.
Epidermodysplasia verruciformis: an unusual malignant transformation.
TLDR
The association of EV with SEC in a 29-year-old male is reported and it is concluded that EV is an extremely invasive, rare, locally destructive, slowly growing adnexal tumor.
Epidermodysplasia Verruciformis acquired in an HIV-positive patient
TLDR
With the increased survival of immunosuppressed patients, especially with AIDS, a form of the disease called epidermodysplasia verruciformis acquired from a clinician similar to the genetic disease has been reduced, but challenging to manage, since an antiretroviral therapy leads to a cutaneous one, making patients more resistant to any treatment modality.
Multifocal leiomyosarcomatosis in a 6-year-old child with epidermodysplasia verruciformis and immune defect.
TLDR
A 6-year-old girl, who has had multifocal leiomyosarcomatosis after the previous diagnoses of epidermodysplasia verruciformis and immune defect, represents an interesting association of these features.
An ANKRD26 nonsense somatic mutation in a female with epidermodysplasia verruciformis (Tree Man Syndrome)
TLDR
The first female severe EV case in Bangladesh is reported, a 10‐year‐old girl with a nonsense somatic mutation impacting ANKRD26 gene, which is an abnormal susceptibility to the human papilloma virus.
Epidermodysplasia verruciform-like Lesions in an HIV patient.
TLDR
A 42-year-old HIV-positive man who presented with hypo- and hyperpigmented papules and plaques on the upper trunk, head, and neck, with histopathologic findings of epidermodysplasia verruciformis is described.
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References

SHOWING 1-10 OF 18 REFERENCES
Epidermodysplasia verruciformis with neurological manifestations
Background Epidermodysplasia verruciformis (EV) is a rare, inherited disorder in which there is widespread and persistent infection by multiple subtypes of human papilloma virus, tinea
Epidermodysplasia verruciformis-like lesions in a patient with systemic lupus erythematosus.
TLDR
A patient with systemic lupus erythematosus (SLE) and EV-like lesions associated with HPV-17 and HPV-20 is presented and lesions similar to those present in EV are presented.
Treatment of epidermodysplasia verruciformis with a combination of acitretin and interferon alfa-2a.
TLDR
This work presents a case of EV that was treated with a combination of acitretin and interferon alfa-2a and found it to be of value in the treatment of EV.
Cimetidine therapy for epidermodysplasia verruciformis.
TLDR
A 16-year-old boy with an 8-year history of multiple slightly keratotic papules on his face, trunk, and limbs, is described and a diagnosis of epidermodysplasia verruciformis was made.
Epidermodysplasia verruciformis: association with isolated IgM deficiency and response to treatment with acitretin
  • Iraji, Faghihi
  • Medicine
    Clinical and experimental dermatology
  • 2000
TLDR
A 25‐year-old woman, who had extensive, large viral warts consistent with epidermodysplasia verruciformis (EV) since she was 6‐year‐old, is described, who has an isolated IgM‐deficiency but the patient demonstrated no other abnormalities.
Clinical aspects of epidermodysplasia verruciformis
TLDR
Epidermodysplasia verruciformis is a rare genodermatosis characterized by a generalized infection with a specific group of human papilloma virus and a propensity for developing skin malignant tumours in 30%−50% of patients.
Treatment of localized epidermodysplasia verruciformis with tacalcitol ointment
A 69‐year‐old Japanese woman presented with multiple, erythematous, keratotic plaques distributed on her right breast, right shoulder, and left cubital fossa. The lesions varied in size from 5 mm to
Epidermodysplasia verruciformis: 14 members of a pedigree with an intriguing squamous cell carcinoma transformation
TLDR
A 38‐year‐old farmer was apparently well until 5 years of age, when his mother found mildly itchy, raised eruptions over the scalp during combing of the scalp hair, which in due course ulcerated and was diagnosed as squamous cell carcinoma, for which liquid nitrogen cryosurgery was performed.
Epidermodysplasia verruciformis: what's new?
TLDR
Characteristic features of epidermodysplasia verruciformis patients underline characteristic features of this genetic, life-long disease: polymorphic cutaneous lesions and development of nonmelanoma skin cancers in over 60% of cases.
Why epidermodysplasia verruciformis – a rare genetic disease – has raised such great interest
has created considerable interest, as it affected 14 individuals from three generations of one family. This genetic disease often runs in families and the mode of inheritance is usually, with a few
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