Pagetoid reticulosis (also known as "acral mycoses fungoides",[1] "localized epidermotropic reticulosis",[1] "mycosis fungoides palmaris et plantaris",[1] "unilesional mycosis fungoides",[2] and "Woringer–Kolopp disease"[1]) is a cutaneous condition, an uncommon lymphoproliferative disorder, sometimes considered a form of mycosis fungoides.[1]: 734
Pagetoid reticulosis | |
---|---|
Other names | Woringer-Kolopp disease |
Specialty | Dermatology |
Lesions emerge as well-demarcated psoriasiform or hyperkeratotic patches and 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]
The most common method of treatment includes radiotherapy and/or surgical excision.[5]