{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,10,16]],"date-time":"2023-10-16T08:43:31Z","timestamp":1697445811771},"reference-count":44,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2012,6,20]],"date-time":"2012-06-20T00:00:00Z","timestamp":1340150400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Histopathology"],"published-print":{"date-parts":[[2012,8]]},"abstract":"<jats:p>McKelvie P A, Thompson P A &amp; Tam C S \u2028(2012) <jats:italic>Histopathology<\/jats:italic>\u00a0<jats:bold>61,<\/jats:bold> 212\u2013233<\/jats:p><jats:p><jats:bold>Peripheral T cell and natural killer (NK)\u2003T cell lymphomas: a clinicopathological study from a single Australian centre<\/jats:bold><\/jats:p><jats:p><jats:bold>Aims:\u2002<\/jats:bold> Using pathological and clinical review, to identify all cases diagnosed as peripheral T cell and natural killer (NK)\u2003T cell lymphoma over 10\u2003years from one metropolitan Australian hospital.<\/jats:p><jats:p><jats:bold>Methods and results:\u2002<\/jats:bold> Subtyping was performed using World Health Organization (WHO) 2008 criteria and a comprehensive immunohistochemical panel. Clinical data including follow\u2010up were obtained. There were 47 cases, including 11 peripheral T cell lymphomas, not otherwise specified (NOS), nine extranodal NK\u2003T cell lymphomas, nasal type (eight nasal), eight primary cutaneous anaplastic large cell lymphomas, seven angioimmunoblastic T cell lymphomas, three anaplastic lymphoma kinase (ALK)\u2010positive anaplastic large cell lymphomas, four ALK\u2010negative anaplastic large cell lymphomas, three enteropathic T cell lymphomas and two subcutaneous panniculitis\u2010like T cell lymphomas. Follow\u2010up of 46 of 47 cases (median time 45\u2003months) revealed that 50% (23 of 46) of patients died. Five\u2010year survival rates were: peripheral T cell lymphoma, NOS 39%; angioimmunoblastic T cell, 43%; nasal NK\u2003T 67%; ALK\u2010negative anaplastic large cell lymphoma 67% (at 2\u2003years); ALK<jats:sup>+<\/jats:sup> anaplastic large cell lymphoma 33%; subcutaneous panniculitis\u2010like T cell lymphomas 100%; primary cutaneous anaplastic large cell lymphoma 86%; and enteropathic T cell lymphoma 33% (at 1\u2003year). One patient with Lennert lymphoma suffered four late cutaneous relapses.<\/jats:p><jats:p><jats:bold>Conclusions:\u2002<\/jats:bold> This first Australian clinicopathological series of peripheral T cell and NK\u2003T cell lymphoma shows epidemiological and survival data similar to those for Europe and North America.<\/jats:p>","DOI":"10.1111\/j.1365-2559.2012.04238.x","type":"journal-article","created":{"date-parts":[[2012,6,21]],"date-time":"2012-06-21T12:15:31Z","timestamp":1340280931000},"page":"212-223","update-policy":"http:\/\/dx.doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":2,"title":["Peripheral T cell and natural killer (NK)\u2003T cell lymphomas: a clinicopathological study from a single Australian centre"],"prefix":"10.1111","volume":"61","author":[{"given":"Penelope A","family":"McKelvie","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Philip A","family":"Thompson","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Constantine S","family":"Tam","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2012,6,20]]},"reference":[{"key":"e_1_2_8_2_2","doi-asserted-by":"publisher","DOI":"10.1200\/JCO.2008.16.4558"},{"key":"e_1_2_8_3_2","doi-asserted-by":"publisher","DOI":"10.3109\/10428190903552104"},{"key":"e_1_2_8_4_2","doi-asserted-by":"publisher","DOI":"10.1080\/003130202760120463"},{"key":"e_1_2_8_5_2","volume-title":"WHO classification of tumours of the haematopoietic and lymphoid tissues","author":"Swerdlow SH","year":"2008"},{"key":"e_1_2_8_6_2","doi-asserted-by":"publisher","DOI":"10.1002\/(SICI)1096-9896(199603)178:3<303::AID-PATH475>3.0.CO;2-I"},{"key":"e_1_2_8_7_2","doi-asserted-by":"publisher","DOI":"10.1038\/sj.leu.2404481"},{"key":"e_1_2_8_8_2","doi-asserted-by":"publisher","DOI":"10.1111\/j.1365-2559.2007.02632.x"},{"key":"e_1_2_8_9_2","first-page":"306","volume-title":"WHO classification of tumours of the haematopoietic and lymphoid tissues","author":"Pileri SA","year":"2008"},{"key":"e_1_2_8_10_2","doi-asserted-by":"publisher","DOI":"10.1097\/PAS.0b013e31817f123e"},{"key":"e_1_2_8_11_2","doi-asserted-by":"publisher","DOI":"10.1182\/blood-2010-09-310342"},{"key":"e_1_2_8_12_2","doi-asserted-by":"publisher","DOI":"10.1097\/PAS.0b013e31802d68e9"},{"key":"e_1_2_8_13_2","first-page":"309","volume-title":"WHO classification of tumours of the haematopoietic and lymphoid tissues","author":"Dogan A","year":"2008"},{"key":"e_1_2_8_14_2","doi-asserted-by":"publisher","DOI":"10.3109\/10428191003777971"},{"key":"e_1_2_8_15_2","doi-asserted-by":"publisher","DOI":"10.1182\/blood-2008-10-185256"},{"key":"e_1_2_8_16_2","first-page":"285","volume-title":"WHO classification of tumours of the haematopoietic and lymphoid tissues","author":"Chan JKC","year":"2008"},{"key":"e_1_2_8_17_2","first-page":"312","volume-title":"WHO classification of tumours of the haematopoietic and lymphoid tissues","author":"Delsol G","year":"2008"},{"key":"e_1_2_8_18_2","first-page":"317","volume-title":"WHO classification of tumours of the haematopoietic and lymphoid tissues","author":"Mason DY","year":"2008"},{"key":"e_1_2_8_19_2","doi-asserted-by":"publisher","DOI":"10.1182\/blood-2008-01-134270"},{"key":"e_1_2_8_20_2","first-page":"100","article-title":"Epstein\u2013Barr virus positive anaplastic large cell lymphoma: myth or reality?","volume":"4","author":"Ma Y","year":"2011","journal-title":"Int. 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