Pagetoid reticulosis
| Pagetoid reticulosis | |
|---|---|
| Other names | Woringer-Kolopp disease |
 | |
| Specialty | Dermatology |
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
Symptoms and signs
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]
Treatment
The most common method of treatment includes radiotherapy and/or surgical excision.[5]
See also
- Pagetoid
- Cutaneous T-cell lymphoma
- List of cutaneous conditions
References
- ^ ISBN 978-0-7216-2921-6.
- ISBN 978-1-4160-2999-1.
- ISSN 1868-9256.
- PMID 15692063.
- ISBN 9783319479064.
Further reading
- Larson, Krista; Wick, Mark R. (2016-03-04). "Pagetoid Reticulosis: Report of Two Cases and Review of the Literature". Dermatopathology. 3 (1). MDPI AG: 8–12. PMC 4868934.
- 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. ISSN 1079-2104.