{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,4]],"date-time":"2026-05-04T10:24:40Z","timestamp":1777890280363,"version":"3.51.4"},"reference-count":20,"publisher":"SAGE Publications","issue":"1","license":[{"start":{"date-parts":[[2012,3,1]],"date-time":"2012-03-01T00:00:00Z","timestamp":1330560000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["Rare Tumors"],"published-print":{"date-parts":[[2012,3,20]]},"abstract":"<jats:p>Primary thyroid lymphoma is a rare malignancy, representing 2\u20138% of all thyroid malignancies and 1\u20132% of all extranodal lymphomas. The majority of cases concern non-Hodgkin's lymphoma of B cell origin, following by Hodgkin's disease, T cell lymphomas and rarely marginal zone B-cell mucosa-associated lymphoid tissue (MALT) lymphomas. MALT lymphomas have been associated with long-standing autoimmune Hashimoto's thyroiditis. We present the case of a 44-years-old woman with thyroid MALT lymphoma in the background of multinodular goiter of autoimmune origin.<\/jats:p>","DOI":"10.4081\/rt.2012.e2","type":"journal-article","created":{"date-parts":[[2012,1,31]],"date-time":"2012-01-31T04:50:48Z","timestamp":1327985448000},"page":"4-6","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":7,"title":["Primary Mucosa-Associated Lymphoid Tissue Thyroid Lymphoma: A Rare Thyroid Neoplasm of Extrathyroid Origin"],"prefix":"10.1177","volume":"4","author":[{"given":"Melpomeni","family":"Peppa","sequence":"first","affiliation":[{"name":"Endocrine Unit, Second Department of Internal Medicine-Propaedeutic, Research Institute and Diabetes Center, Athens University Medical School, Attikon University Hospital, Athens, 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