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While its biological course is typically marked by spontaneous regression, the histopathological findings of LyP are consistent with cutaneous T\u2010cell lymphoma. Provided patients do no develop a secondary lymphoma, they exhibit unusually high 10\u2010year survival rates (&gt; 90\u00a0%), which is a typical feature of LyP. To date, the etiology and pathogenesis of LyP have not been elucidated. One particular subtype of LyP is known to be associated with chromosome 6p25.3 rearrangement (DUSP22\u2010IRF4 translocation).<\/jats:p><jats:p>Treatment is guided by the clinical presentation. In addition to a wait\u2010and\u2010see approach, recommended options include topical corticosteroids and PUVA therapy.<\/jats:p>","DOI":"10.1111\/ddg.14041","type":"journal-article","created":{"date-parts":[[2020,2,26]],"date-time":"2020-02-26T13:04:17Z","timestamp":1582722257000},"page":"199-205","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":5,"title":["Lymphomatoid papulosis"],"prefix":"10.1111","volume":"18","author":[{"given":"Gunnar","family":"Wagner","sequence":"first","affiliation":[{"name":"Skin Cancer Center Department of Dermatology Allergology and Phlebology Bremerhaven Reinkenheide Medical Center  Bremerhaven Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Christian","family":"Rose","sequence":"additional","affiliation":[{"name":"Dermatopathology Laboratory  L\u00fcbeck 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