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
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]
^ abcdeJames, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN978-0-7216-2921-6.
^Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN978-1-4160-2999-1.
^Beigi, Pooya Khan Mohammad (2017). "Variants of Mycosis Fungoides". Clinician's Guide to Mycosis Fungoides. Springer International Publishing. pp. 35–36. doi:10.1007/978-3-319-47907-1_7. ISBN9783319479064.
Sedghizadeh, Parish.P; Allen, Carl M.; Kalmar, John R.; Magro, Cynthia M. (2003). "Pagetoid reticulosis: A case report and review of the literature". Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology. 95 (3). Elsevier BV: 318–323. doi:10.1067/moe.2003.3. ISSN1079-2104.
