Pagetoid reticulosis
{{Infobox medical condition (new)
| name = Pagetoid reticulosis
| synonyms = Woringer-Kolopp disease
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| field = Dermatology
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Pagetoid reticulosis (also known as "acral mycoses fungoides", "localized epidermotropic reticulosis", "mycosis fungoides palmaris et plantaris", "unilesional mycosis fungoides",{{cite book |author=Rapini, Ronald P. |author2=Bolognia, Jean L. |author3=Jorizzo, Joseph L. |title=Dermatology: 2-Volume Set |publisher=Mosby |location=St. Louis |year=2007 |isbn=978-1-4160-2999-1 }} and "Woringer–Kolopp disease") is a cutaneous condition, an uncommon lymphoproliferative disorder, sometimes considered a form of mycosis fungoides.{{cite book |author=James, William D. |author2=Berger, Timothy G.|title=Andrews' Diseases of the Skin: clinical Dermatology |publisher=Saunders Elsevier |year=2006 |isbn=978-0-7216-2921-6 |display-authors=etal}}{{rp|734}}
Symptoms and signs
Lesions emerge as well-demarcated psoriasiform or hyperkeratotic patches and plaques, with a central clearing and an elevated border.{{Cite journal|last=Harvey|first=Nathan T.|last2=Spagnolo|first2=Dominic V.|last3=Wood|first3=Benjamin A.|date=2015-12-01|title='Could it be mycosis fungoides?': an approach to diagnosing patch stage mycosis fungoides|journal=Journal of Hematopathology|language=en|volume=8|issue=4|pages=209–223|doi=10.1007/s12308-015-0247-2|issn=1868-9256|doi-access=free}} Pagetoid reticulosis is a very slow progressive variant of mycosis fungoides and is usually localized unlike the latter.{{Cite journal|last=Willemze|first=Rein|last2=Jaffe|first2=Elaine S.|last3=Burg|first3=Günter|last4=Cerroni|first4=Lorenzo|last5=Berti|first5=Emilio|last6=Swerdlow|first6=Steven H.|last7=Ralfkiaer|first7=Elisabeth|last8=Chimenti|first8=Sergio|last9=Diaz-Perez|first9=José L.|date=2005-05-15|title=WHO-EORTC classification for cutaneous lymphomas|journal=Blood|language=en|volume=105|issue=10|pages=3768–3785|doi=10.1182/blood-2004-09-3502|issn=0006-4971|pmid=15692063|url=https://air.unimi.it/bitstream/2434/566817/2/3768.full.pdf|hdl=2434/566817|hdl-access=free}}
Treatment
The most common method of treatment includes radiotherapy and/or surgical excision.{{Cite book|title=Clinician's Guide to Mycosis Fungoides|last=Beigi|first=Pooya Khan Mohammad|date=2017|publisher=Springer International Publishing|isbn=9783319479064|pages=35–36|language=en|doi=10.1007/978-3-319-47907-1_7|chapter = Variants of Mycosis Fungoides}}
See also
References
{{reflist}}
Further reading
- {{cite journal | last=Larson | first=Krista | last2=Wick | first2=Mark R. | title=Pagetoid Reticulosis: Report of Two Cases and Review of the Literature | journal=Dermatopathology | publisher=MDPI AG | volume=3 | issue=1 | date=2016-03-04 | issn=2296-3529 | doi=10.1159/000444660 | pages=8–12 | ref=none| pmc=4868934 }}
- {{cite journal | last=Sedghizadeh | first=Parish.P | last2=Allen | first2=Carl M. | last3=Kalmar | first3=John R. | last4=Magro | first4=Cynthia M. | title=Pagetoid reticulosis: A case report and review of the literature | journal=Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology | publisher=Elsevier BV | volume=95 | issue=3 | year=2003 | issn=1079-2104 | doi=10.1067/moe.2003.3 | pages=318–323 | ref=none}}
External links
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| ICD11 = {{ICD11|2B01}}
| ICD10 = {{ICD10|C84.0}}
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