{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,8]],"date-time":"2026-09-08T09:44:14Z","timestamp":1788860654815,"version":"build-2803163510"},"reference-count":18,"publisher":"BMJ","content-domain":{"domain":["bmj.com"],"crossmark-restriction":true},"short-container-title":["BMJ Case Reports"],"accepted":{"date-parts":[[2014,12,6]]},"abstract":"<jats:p>Primary cutaneous lymphomas (PCLs) are exceedingly rare in children and adolescents, with mycosis fungoides (MF) being the most frequent PCL diagnosed in childhood. There are numerous unusual clinical variants of MF, including the hypopigmented type form (HMF). HMF is exceptional overall, but comparatively common among children. We present an 8-year-old boy with a 3-year history of progressive, generalised, scaly, hypopigmented round patches and few erythematous papules. He was first diagnosed with pityriasis alba (PA), and moisturisers were prescribed with no improvement. Skin biopsy showed typical features of MF, and the patient was successfully treated with narrowband ultraviolet B. HMF may simulate atopic dermatitis, PA, pityriasis lichenoides, tinea versicolour, vitiligo, postinflammatory hypopigmentation or leprosy. Therefore, persistent and unusual hypopigmented lesions should be biopsied to rule out this rare variant of MF.<\/jats:p>","DOI":"10.1136\/bcr-2014-208306","type":"journal-article","created":{"date-parts":[[2014,12,23]],"date-time":"2014-12-23T12:50:16Z","timestamp":1419339016000},"page":"bcr2014208306","update-policy":"https:\/\/doi.org\/10.1136\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":17,"title":["Childhood hypopigmented mycosis fungoides: a commonly delayed diagnosis"],"prefix":"10.1136","volume":"2014","author":[{"given":"Ana","family":"Gameiro","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Miguel","family":"Gouveia","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"\u00d3scar","family":"Tellechea","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ana","family":"Moreno","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"239","published-online":{"date-parts":[[2014,12,23]]},"reference":[{"key":"2025042707104584000_2014.dec23_1.bcr2014208306.1","doi-asserted-by":"publisher","DOI":"10.1111\/cup.12217"},{"key":"2025042707104584000_2014.dec23_1.bcr2014208306.2","doi-asserted-by":"publisher","DOI":"10.1111\/j.1525-1470.2006.00291.x"},{"key":"2025042707104584000_2014.dec23_1.bcr2014208306.3","doi-asserted-by":"publisher","DOI":"10.1111\/pde.12352"},{"key":"2025042707104584000_2014.dec23_1.bcr2014208306.4","doi-asserted-by":"publisher","DOI":"10.1016\/S0190-9622(00)90006-9"},{"key":"2025042707104584000_2014.dec23_1.bcr2014208306.5","doi-asserted-by":"publisher","DOI":"10.1200\/JCO.2009.27.7665"},{"key":"2025042707104584000_2014.dec23_1.bcr2014208306.6","first-page":"66","article-title":"Pityriasis alba revisited: perspectives on an enigmatic disorder of childhood","volume":"87","author":"Jadotte","year":"2011","journal-title":"Cutis"},{"key":"2025042707104584000_2014.dec23_1.bcr2014208306.7","doi-asserted-by":"publisher","DOI":"10.2165\/00128071-200708010-00004"},{"key":"2025042707104584000_2014.dec23_1.bcr2014208306.8","doi-asserted-by":"publisher","DOI":"10.1067\/S0190-9622(03)00907-1"},{"key":"2025042707104584000_2014.dec23_1.bcr2014208306.9","unstructured":"Willemze R , Hodak E , Zinzani PL , et al . Primary cutaneous lymphomas: ESMO clinical practice guidelines for diagnosis, treatment and follow-up, on behalf of the ESMO guidelines."},{"key":"2025042707104584000_2014.dec23_1.bcr2014208306.10","unstructured":"Willemze R , Jaffe ES , Burg G , et al . 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