{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,19]],"date-time":"2026-09-19T09:39:19Z","timestamp":1789810759784,"version":"4.0.1"},"reference-count":41,"publisher":"Wiley","issue":"7","license":[{"start":{"date-parts":[[2014,5,8]],"date-time":"2014-05-08T00:00:00Z","timestamp":1399507200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["The Journal of Dermatology"],"published-print":{"date-parts":[[2014,7]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>\n                    Hypopigmentation in cutaneous T\u2010cell lymphoproliferative disease should not always be equated with hypopigmented mycosis fungoides (\n                    <jats:styled-content style=\"fixed-case\">MF<\/jats:styled-content>\n                    ). A form of hypopigmented pre\u2010lymphomatous T\u2010cell dyscrasia falling under the designation of the so\u2010called hypopigmented interface variant of T\u2010cell dyscrasia has recently been proposed. The aim of the present study was to establish hypopigmented interface T\u2010cell dyscrasia as its own entity apart from other T\u2010cell dyscrasias and\n                    <jats:styled-content style=\"fixed-case\">MF<\/jats:styled-content>\n                    using a patient case series. Twenty four cases of hypopigmented interface T\u2010cell dyscrasia were identified in the dermatopathology database of Weill Medical College of Cornell University. There were 17 females and seven males (mean age, 36\u00a0years). In children and adolescents, the patients were most commonly of African American extraction. Truncal photo\u2010protected areas manifesting as large solitary patches or multiple smaller macules were characteristic; disease progression to\n                    <jats:styled-content style=\"fixed-case\">MF<\/jats:styled-content>\n                    occurred in only one patient. The lesions responded to topical steroids and light therapy. The pathology was defined by a cell poor interface associated with degeneration of keratinocytes and melanocytes, and by lymphocytes whose nuclei showed low\u2010grade cerebriform atypia, and which expressed a significant reduction in\n                    <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>\n                    7 and\n                    <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>\n                    62L expression. In 50% of the cases, the implicated cell type was of the\n                    <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>\n                    8 subset. Clonality was not identified. Hypopigmented interface T\u2010cell dyscrasia is a distinct entity separate from and rarely progressive to\n                    <jats:styled-content style=\"fixed-case\">MF<\/jats:styled-content>\n                    .\n                  <\/jats:p>","DOI":"10.1111\/1346-8138.12458","type":"journal-article","created":{"date-parts":[[2014,5,8]],"date-time":"2014-05-08T02:44:48Z","timestamp":1399517088000},"page":"609-617","source":"Crossref","is-referenced-by-count":19,"title":["Hypopigmented interface T\u2010cell dyscrasia: A form of cutaneous T\u2010cell dyscrasia distinct from hypopigmented mycosis fungoides"],"prefix":"10.1111","volume":"41","author":[{"given":"Cynthia M.","family":"Magro","sequence":"first","affiliation":[{"name":"Department of Pathology and Laboratory Medicine Weill Medical College of Cornell University New York New York USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Joshua 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