{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,26]],"date-time":"2026-08-26T16:17:58Z","timestamp":1787761078516,"version":"build-2784847793"},"reference-count":20,"publisher":"Wiley","issue":"9","license":[{"start":{"date-parts":[[2026,7,21]],"date-time":"2026-07-21T00:00:00Z","timestamp":1784592000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/"},{"start":{"date-parts":[[2026,7,21]],"date-time":"2026-07-21T00:00:00Z","timestamp":1784592000000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Pediatric Blood &amp; Cancer"],"published-print":{"date-parts":[[2026,9]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:p>\n                    Primary cutaneous anaplastic large cell lymphoma (pcALCL) is a rare pediatric CD30\u2010positive T\u2010cell lymphoproliferative disorder with an excellent prognosis, but its genomic drivers are poorly defined. We report three children with skin\u2010limited disease demonstrating striking molecular heterogeneity, including\n                    <jats:italic>NPM<\/jats:italic>\n                    ::\n                    <jats:italic>ALK<\/jats:italic>\n                    ,\n                    <jats:italic>NUP214<\/jats:italic>\n                    ::\n                    <jats:italic>FRK<\/jats:italic>\n                    , and a novel\n                    <jats:italic>PICALM<\/jats:italic>\n                    ::\n                    <jats:italic>JAK2<\/jats:italic>\n                    fusion not previously described in pcALCL. Clinical courses ranged from spontaneous regression to systemic therapy, yet all achieved durable complete remission without progression over 31\u201350\u00a0months. These findings highlight previously unrecognized genomic diversity and expand the molecular landscape of pediatric pcALCL.\n                  <\/jats:p>","DOI":"10.1002\/1545-5017.70437","type":"journal-article","created":{"date-parts":[[2026,7,21]],"date-time":"2026-07-21T10:45:07Z","timestamp":1784630707000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Genomic Diversity and Clinical Variability in Pediatric Primary Cutaneous Anaplastic Large Cell Lymphoma: A Case Series"],"prefix":"10.1002","volume":"73","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-8308-2790","authenticated-orcid":false,"given":"Shoshana","family":"Greenberger","sequence":"first","affiliation":[{"name":"Pediatric Dermatology Unit, Department of Dermatology Sheba Medical Center  Ramat Gan Israel"},{"name":"Gray Faculty of Medical and Health Sciences Tel Aviv University  Tel Aviv 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