{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,1]],"date-time":"2026-06-01T21:36:13Z","timestamp":1780349773197,"version":"3.54.1"},"reference-count":13,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2012,12,14]],"date-time":"2012-12-14T00:00:00Z","timestamp":1355443200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Cutan Pathol"],"published-print":{"date-parts":[[2013,3]]},"abstract":"<jats:p>Mycosis fungoides (<jats:styled-content style=\"fixed-case\">MF<\/jats:styled-content>) represents the most common type of cutaneous lymphoma. <jats:styled-content style=\"fixed-case\">MF<\/jats:styled-content> shows varieties in both its clinical presentation and immunophenotype. We herein report one case of poikilodermatous <jats:styled-content style=\"fixed-case\">MF<\/jats:styled-content> with a <jats:styled-content style=\"fixed-case\">CD8<\/jats:styled-content>+ <jats:styled-content style=\"fixed-case\">CD56<\/jats:styled-content>+ immunophenotype and present a literature review. A 20\u2010year\u2010old Japanese woman presented with a 10\u2010year history of multiple poikilodermatous and reddish or brownish patches with mild pruritus on the chest, abdomen, back, buttock and thighs. Histopathologically, small\u2010 to medium\u2010sized atypical lymphocytes infiltrated into the epidermis, indicating epidermotropism, along the basal layer, and distributed in band\u2010like appearance in the papillary dermis. Immunohistochemically, atypical lymphocytes expressed <jats:styled-content style=\"fixed-case\">CD3<\/jats:styled-content>, <jats:styled-content style=\"fixed-case\">CD8<\/jats:styled-content>, <jats:styled-content style=\"fixed-case\">CD56<\/jats:styled-content>, T\u2010cell intracellular antigen (TIA)\u20101, granzyme B and beta <jats:styled-content style=\"fixed-case\">F1<\/jats:styled-content> but lacked expression of <jats:styled-content style=\"fixed-case\">CD4<\/jats:styled-content>, <jats:styled-content style=\"fixed-case\">CD20<\/jats:styled-content>, <jats:styled-content style=\"fixed-case\">CD30<\/jats:styled-content> and Epstein\u2010Barr virus (<jats:styled-content style=\"fixed-case\">EBV<\/jats:styled-content>) latent membrane protein 1. An <jats:styled-content style=\"fixed-case\">EBV<\/jats:styled-content>\u2010encoded small non\u2010polyadenylated <jats:styled-content style=\"fixed-case\">RNA<\/jats:styled-content>\u20101 (EBER\u20101) signal was not detected. On the basis of these findings, the diagnosis of <jats:styled-content style=\"fixed-case\">CD8<\/jats:styled-content>+ <jats:styled-content style=\"fixed-case\">CD56<\/jats:styled-content>+ <jats:styled-content style=\"fixed-case\">MF<\/jats:styled-content> was established. Poikilodermatous <jats:styled-content style=\"fixed-case\">MF<\/jats:styled-content> with a <jats:styled-content style=\"fixed-case\">CD8<\/jats:styled-content>+ <jats:styled-content style=\"fixed-case\">CD56<\/jats:styled-content>+ immunophenotype, as presented herein, is extremely rare. Although further investigation is needed to fully clarify the nature of this aberrant phenotype of <jats:styled-content style=\"fixed-case\">MF<\/jats:styled-content>, we stress that it is important to recognize this rare immunophenotype of <jats:styled-content style=\"fixed-case\">MF<\/jats:styled-content> to distinguish it from aggressive cytotoxic cutaneous lymphomas.<\/jats:p>","DOI":"10.1111\/cup.12067","type":"journal-article","created":{"date-parts":[[2012,11,28]],"date-time":"2012-11-28T23:33:06Z","timestamp":1354145586000},"page":"317-320","source":"Crossref","is-referenced-by-count":24,"title":["Poikilodermatous mycosis fungoides with a <scp>CD8<\/scp>+ <scp>CD56<\/scp>+ immunophenotype: a case report and literature review"],"prefix":"10.1111","volume":"40","author":[{"given":"Tatsushi","family":"Shiomi","sequence":"first","affiliation":[{"name":"Department of Pathology, Kawasaki Medical School Kawasaki Hospital  Okayama Japan"},{"name":"Department of Pathology Kawasaki Medical School  Kurashiki Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yasumasa","family":"Monobe","sequence":"additional","affiliation":[{"name":"Department of Pathology, Kawasaki Medical School Kawasaki Hospital  Okayama Japan"},{"name":"Department of Pathology Kawasaki Medical School  Kurashiki Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Chiaki","family":"Kuwabara","sequence":"additional","affiliation":[{"name":"Department of Dermatology, Kawasaki Medical School Kawasaki Hospital  Okayama Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Haruko","family":"Hayashi","sequence":"additional","affiliation":[{"name":"Department of Dermatology, Kawasaki Medical School Kawasaki Hospital  Okayama Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Takenobu","family":"Yamamoto","sequence":"additional","affiliation":[{"name":"Department of Dermatology, Kawasaki Medical School Kawasaki Hospital  Okayama Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yoshito","family":"Sadahira","sequence":"additional","affiliation":[{"name":"Department of Pathology Kawasaki Medical School  Kurashiki Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2012,12,14]]},"reference":[{"key":"e_1_2_6_2_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1365-2133.2009.09301.x"},{"key":"e_1_2_6_3_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.jaad.2005.01.133"},{"key":"e_1_2_6_4_1","doi-asserted-by":"crossref","first-page":"97","DOI":"10.1002\/9781444316742.ch6","volume-title":"Skin lymphoma. 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