{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,22]],"date-time":"2026-09-22T14:04:28Z","timestamp":1790085868491,"version":"4.0.1"},"reference-count":17,"publisher":"AOSIS","issue":"1","license":[{"start":{"date-parts":[[2024,7,31]],"date-time":"2024-07-31T00:00:00Z","timestamp":1722384000000},"content-version":"unspecified","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"abstract":"<jats:p>Thyroid gland vascular proliferations pose a challenge to pathologists, radiologists and surgeons. This is illustrated in the case of a 36-year-old woman who underwent a diagnostic thyroid lobectomy for a suspected follicular neoplasm according to cytology. Histological diagnosis confirmed a follicular adenoma as well as a cavernous haemangioma or venous malformation.\n\nContribution:\u00a0Thyroid vascular lesions are rare. Evolving nomenclature and application of the International Society for the Study of Vascular Anomalies classification are discussed. Pertinent radiological clues are highlighted to pre-empt the diagnosis and avoid potential surgical complications.<\/jats:p>","DOI":"10.4102\/sajr.v28i1.2863","type":"journal-article","created":{"date-parts":[[2024,7,31]],"date-time":"2024-07-31T07:31:26Z","timestamp":1722411086000},"update-policy":"https:\/\/doi.org\/10.4102\/crossmark-policy","source":"Crossref","is-referenced-by-count":1,"title":["Description of a concurrent thyroid haemangioma and a follicular adenoma"],"prefix":"10.4102","volume":"28","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-3743-6345","authenticated-orcid":false,"given":"Liezel","family":"Coetzee","sequence":"first","affiliation":[{"id":[{"id":"https:\/\/ror.org\/05bk57929","id-type":"ROR","asserted-by":"publisher"}],"name":"Stellenbosch University"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-9220-331X","authenticated-orcid":false,"given":"Wilhelmina","family":"Conradie","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/05bk57929","id-type":"ROR","asserted-by":"publisher"}],"name":"Stellenbosch University"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-5071-5424","authenticated-orcid":false,"given":"Razaan","family":"Davis","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/05bk57929","id-type":"ROR","asserted-by":"publisher"}],"name":"Stellenbosch University"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-2981-4724","authenticated-orcid":false,"given":"Rubina","family":"Razack","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/05bk57929","id-type":"ROR","asserted-by":"publisher"}],"name":"Stellenbosch University"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"2580","published-online":{"date-parts":[[2024,7,31]]},"reference":[{"key":"ref0","doi-asserted-by":"crossref","unstructured":"Papotti M, Arrondini M, Tavaglione V, Veltri A, Volante M. 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J Oral Maxillofac Pathol. 2014;18(5):117\u2013120. https:\/\/doi.org\/10.4103\/0973-029X.141321","DOI":"10.4103\/0973-029X.141321"},{"key":"ref13","doi-asserted-by":"crossref","unstructured":"Steele L, Zbeidy S, Thomson J, Flohr C. How is the term haemangioma used in the literature? An evaluation against the revised ISSVA classification. Pediatr Dermatol. 2019;36(5):628\u2013633. https:\/\/doi.org\/10.1111\/pde.13885","DOI":"10.1111\/pde.13885"},{"key":"ref14","doi-asserted-by":"crossref","unstructured":"Behr GG, Johnson CM. Vascular anomalies: Hemangiomas and beyond \u2013 Part 2, slow-flow lesions. Am J Roentgenol. 2013;200(2):423\u2013436. https:\/\/doi.org\/10.2214\/AJR.11.7853","DOI":"10.2214\/AJR.11.7853"},{"key":"ref15","doi-asserted-by":"crossref","unstructured":"Colletti G, Deganello A. Cavernous hemangioma: A term to be canceled. 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