| 词条 | Pagetoid reticulosis |
| 释义 |
| name = Pagetoid reticulosis | synonyms = | image = | alt = | caption = | pronounce = | field = dermatology | symptoms = | complications = | onset = | duration = | types = | causes = | risks = | diagnosis = | differential = | prevention = | treatment = | medication = | prognosis = | frequency = | deaths = }} Pagetoid reticulosis (also known as "acral mycoses fungoides",[1] "localized epidermotropic reticulosis",[1] "mycosis fungoides palmaris et plantaris",[1] "unilesional mycosis fungoides",[1] and "Woringer–Kolopp disease"[1]) is a cutaneous condition, an uncommon lymphoproliferative disorder, sometimes considered a form of mycosis fungoides.[2]{{rp|734}} Symptoms and SignsLesions emerge as well-demarcated psoriasiform or hyperkeratotic patches and 36 plaques, with a central clearing and an elevated border[3]. Pagetoid reticulosis is a very slow progressive variant of mycosis fungoides and is usually localized unlike the latter [4]. Cause{{Empty section|date=June 2017}}Diagnosis{{Empty section|date=June 2017}}TreatmentThe most common method of treatment includes radiotherapy and/or surgical excision [5]. See also
References1. ^{{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 |pages= |isbn=978-1-4160-2999-1 |oclc= |doi= |accessdate=}} 2. ^1 2 3 4 {{cite book |author=James, William D. |author2=Berger, Timothy G.|title=Andrews' Diseases of the Skin: clinical Dermatology |publisher=Saunders Elsevier |location= |year=2006 |pages= |isbn=978-0-7216-2921-6 |oclc= |doi= |accessdate=|display-authors=etal}} 3. ^{{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}} 4. ^{{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|url=http://www.bloodjournal.org/content/105/10/3768|journal=Blood|language=en|volume=105|issue=10|pages=3768–3785|doi=10.1182/blood-2004-09-3502|issn=0006-4971|pmid=15692063}} 5. ^{{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}} External links{{Medical resources| DiseasesDB = | ICD10 = C84.0 | ICD9 = | ICDO = 9700/3 | OMIM = | MedlinePlus = | eMedicineSubj = | eMedicineTopic = | MeshID = D056267 | Orphanet = 178517 }}{{Medicine}}{{Cutaneous-condition-stub}} 1 : Lymphoid-related cutaneous conditions |
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