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Localized pagetoid reticulosis ( W oringer– K olopp disease) completely response to NB‐UVB combined with IFN
Author(s) -
Wang Tao,
Liu Yuehua,
Zheng Heyi
Publication year - 2014
Publication title -
dermatologic therapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.595
H-Index - 68
eISSN - 1529-8019
pISSN - 1396-0296
DOI - 10.1111/dth.12123
Subject(s) - medicine , pagetoid , dermatology , guideline , incidence (geometry) , pathology , disease , immunohistochemistry , physics , optics
A cutaneous lymphoproliferative disorder, localized pagetoid reticulosis ( LPR ), is rare but distinctive in its clinical and histopathological manifestations. Without an evidence‐based medicine treatment guideline because of extremely low incidence, LPR poses a therapeutic challenge. We describe a 67‐year‐old C hinese woman with LRP who showed complete response to narrow‐band ultraviolet B combined with intramuscular interferon alpha‐2b.