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Pagetoid reticulosis

FieldValue
namePagetoid reticulosis
synonymsWoringer-Kolopp disease
imageSkinTumors-PC181140.jpg
fieldDermatology

Pagetoid reticulosis (also known as "acral mycoses fungoides", "localized epidermotropic reticulosis", "mycosis fungoides palmaris et plantaris", "unilesional mycosis fungoides", and "Woringer–Kolopp disease") is a cutaneous condition, an uncommon lymphoproliferative disorder, sometimes considered a form of mycosis fungoides.

Symptoms and signs

Lesions emerge as well-demarcated psoriasiform or hyperkeratotic patches and plaques, with a central clearing and an elevated border. Pagetoid reticulosis is a very slow progressive variant of mycosis fungoides and is usually localized unlike the latter.

Treatment

The most common method of treatment includes radiotherapy and/or surgical excision.

References

References

  1. Rapini, Ronald P.. (2007). "Dermatology: 2-Volume Set". Mosby.
  2. James, William D.. (2006). "Andrews' Diseases of the Skin: clinical Dermatology". Saunders Elsevier.
  3. Harvey, Nathan T.. (2015-12-01). "'Could it be mycosis fungoides?': an approach to diagnosing patch stage mycosis fungoides". Journal of Hematopathology.
  4. Willemze, Rein. (2005-05-15). "WHO-EORTC classification for cutaneous lymphomas". Blood.
  5. Beigi, Pooya Khan Mohammad. (2017). "Clinician's Guide to Mycosis Fungoides". Springer International Publishing.
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This article was imported from Wikipedia and is available under the Creative Commons Attribution-ShareAlike 4.0 License. Content has been adapted to SurfDoc format. Original contributors can be found on the article history page.

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