{"id":58787,"date":"2016-10-26T14:52:16","date_gmt":"2016-10-26T18:52:16","guid":{"rendered":"https:\/\/rarediseases.org\/nord-publishes-physician-guide-to-cutaneous-t-cell-lymphoma\/"},"modified":"2022-12-01T11:59:01","modified_gmt":"2022-12-01T16:59:01","slug":"nord-publishes-physician-guide-to-cutaneous-t-cell-lymphoma","status":"publish","type":"post","link":"https:\/\/rarediseases.org\/es\/nord-publishes-physician-guide-to-cutaneous-t-cell-lymphoma\/","title":{"rendered":"NORD Publishes Physician Guide to Cutaneous T-Cell Lymphoma"},"content":{"rendered":"<p><strong>Washington, D.C., October 26, 2016<\/strong>\u2014As part of its ongoing series to promote physician awareness of rare diseases, the National Organization for Rare Disorders has published <em>The NORD Physician Guide to Cutaneous T-Cell Lymphoma (CTCL)<\/em>. This new resource is available free online to medical professionals around the world.<\/p>\n<p>As the primary advocacy organization in the U.S. for people who have rare diseases, NORD provides educational resources for patients, caregivers and medical professionals. The NORD physician guides are developed in collaboration with medical experts and can be accessed at <a href=\"https:\/\/rarediseases.org\" target=\"_blank\" rel=\"noopener\">rarediseases.org<\/a> or <a href=\"https:\/\/nordphysicianguides.org\" target=\"_blank\" rel=\"noopener nofollow\">NORDPhysicianGuides.org<\/a>.<\/p>\n<p>\u201cPeople who have rare diseases often go for many years without a diagnosis,\u201d said Marsha Lanes, MS, CGC, a genetic counselor in NORD\u2019s Educational Initiatives Department. \u201cThe purpose of NORD\u2019s free online physician guides is to reduce the time to diagnosis and encourage optimal treatment for patients with little-known and little-understood rare diseases.\u201d<\/p>\n<p>The <em>NORD Physician Guide to Cutaneous T-Cell Lymphoma (CTCL) <\/em>was developed in collaboration with Oleg E. Akilov, MD, PhD, assistant professor of dermatology and director of the Cutaneous Lymphoma Program at the University of Pittsburgh School of Medicine. CTCLs are a group of rare disorders characterized by abnormal accumulation of malignant T-cells in the skin, potentially resulting in the development of rashes, plaques and tumors.<\/p>\n<p>\u201cEczema and even some cases of psoriasis may look very similar to mycosis fungoides, the most common type of cutaneous T-cell lymphomas,\u201d Dr. Akilov said. \u201cIt is important to be aware of these similarities and to be ready to think about cutaneous lymphoma when a patient with \u2018common dermatosis\u2019 does not respond to regular treatments.\u201d<\/p>\n<p>In addition to information about the disease, the new guide includes information about resources for physicians and patients such as the <a href=\"https:\/\/www.clfoundation.org\/\" target=\"_blank\" rel=\"noopener nofollow\">Cutaneous Lymphoma Foundation<\/a>, which is one of NORD\u2019s 250 member organizations.<\/p>\n<p>NORD established its physician guide series as part of a broader strategic initiative to promote earlier diagnosis and state-of-the-art care for all people with rare diseases. Each online guide is written or reviewed by a medical professional with expertise on the topic. The guides cover signs and symptoms, diagnosis, treatment, investigational therapies, standard therapies, and related topics.<\/p>\n<p>Other recent guides in the series include <a href=\"https:\/\/nordphysicianguides.org\/mitochondrial-myopathies-mm\/\" target=\"_blank\" rel=\"noopener nofollow\"><em>The NORD Physician Guide to Mitochondrial Myopathies<\/em><\/a><em>, <\/em><a href=\"https:\/\/nordphysicianguides.org\/paroxysmal-nocturnal-hemoglobinuria-pnh\/\" target=\"_blank\" rel=\"noopener nofollow\"><em>The NORD Physician Guide to Paroxysmal Nocturnal Hemoglobinuria (PNH),<\/em><\/a> <em>The NORD Physician Guide to Atypical Hemolytic Uremic Syndrome (aHUS)<\/em> and <a href=\"https:\/\/nordphysicianguides.org\/nontuberculous-mycobacterial-lung-disease-ntm\/\" target=\"_blank\" rel=\"noopener nofollow\"><em>The NORD Physician Guide to Nontuberculous Mycobacterial Lung Disease<\/em><\/a><em>.\u00a0\u00a0 <\/em><\/p>\n<p><em>The NORD Physician Guide to Cutaneous T-Cell Lymphoma <\/em>was made possible by an educational grant from Therakos, now a part of Mallinckrodt Pharmaceuticals.<\/p>\n<p style=\"text-align: center;\"><em>NORD\u2019s team of medical writers works closely with medical professionals and disease-specific organizations to provide accurate and detailed disease information. By raising awareness of rare diseases among physicians and other medical professionals, NORD strives to help patients obtain earlier diagnosis and appropriate treatment. Search our online <a href=\"https:\/\/rarediseases.org\/for-clinicians-and-researchers\/resources\/rare-disease-information\/?utm_source=press_release_physician_guide_CTCL&amp;utm_medium=email\" target=\"_blank\" rel=\"noopener\">resources<\/a>.<\/em><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Washington, D.C., October 26, 2016\u2014As part of its ongoing series to promote physician awareness of rare diseases, the National Organization for Rare Disorders has published The NORD Physician Guide to &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/rarediseases.org\/es\/nord-publishes-physician-guide-to-cutaneous-t-cell-lymphoma\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;NORD Publishes Physician Guide to Cutaneous T-Cell Lymphoma&#8221;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"_relevanssi_hide_post":"","_relevanssi_hide_content":"","_relevanssi_pin_for_all":"","_relevanssi_pin_keywords":"","_relevanssi_unpin_keywords":"","_relevanssi_related_keywords":"","_relevanssi_related_include_ids":"","_relevanssi_related_exclude_ids":"","_relevanssi_related_no_append":"","_relevanssi_related_not_related":"","_relevanssi_related_posts":"","_relevanssi_noindex_reason":"","_price":"","_stock":"","_tribe_ticket_header":"","_tribe_default_ticket_provider":"","_tribe_ticket_capacity":"","_ticket_start_date":"","_ticket_end_date":"","_tribe_ticket_show_description":"","_tribe_ticket_show_not_going":false,"_tribe_ticket_use_global_stock":"","_tribe_ticket_global_stock_level":"","_global_stock_mode":"","_global_stock_cap":"","_tribe_rsvp_for_event":"","_tribe_ticket_going_count":"","_tribe_ticket_not_going_count":"","_tribe_tickets_list":"[]","_tribe_ticket_has_attendee_info_fields":false,"footnotes":""},"categories":[191,504],"tags":[1293,1296,1299,1298,208,1297,814,1294],"class_list":["post-58787","post","type-post","status-publish","format-standard","hentry","category-medical","category-press-releases","tag-card9-deficiency","tag-dr-donald-c-vinh","tag-high-risk-pool","tag-icer","tag-marsha-lanes","tag-melanie-langelier-rn","tag-nord-physician-guides","tag-rare-disease-reports"],"acf":[],"_links":{"self":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/58787","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/comments?post=58787"}],"version-history":[{"count":0,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/58787\/revisions"}],"wp:attachment":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/media?parent=58787"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/categories?post=58787"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/tags?post=58787"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}