{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,6]],"date-time":"2026-05-06T15:24:27Z","timestamp":1778081067922,"version":"3.51.4"},"reference-count":20,"publisher":"Korean Cleft Palate-Craniofacial Association","issue":"5","license":[{"start":{"date-parts":[[2022,10,20]],"date-time":"2022-10-20T00:00:00Z","timestamp":1666224000000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/"}],"content-domain":{"domain":["e-acfs.org"],"crossmark-restriction":true},"short-container-title":["Arch Craniofac Surg"],"published-print":{"date-parts":[[2022,10,20]]},"abstract":"<jats:p>Cervical chondrocutaneous branchial remnants are very rare congenital lesions of the lateral neck; thus, our knowledge of this condition derives almost entirely from occasional case reports in the literature. They are thought to originate from the branchial arches and, therefore, can be found anywhere on the pathway along which those branchial arches migrate during embryogenesis. We report the case of a 5-year-old girl presenting with a cervical chondrocutaneous branchial remnant on the right lateral neck that had existed since birth, with no other anomalies.<\/jats:p>","DOI":"10.7181\/acfs.2022.00920","type":"journal-article","created":{"date-parts":[[2022,10,28]],"date-time":"2022-10-28T04:52:46Z","timestamp":1666932766000},"page":"241-245","update-policy":"https:\/\/doi.org\/10.7181\/crossmark_policy","source":"Crossref","is-referenced-by-count":5,"title":["Cervical chondrocutaneous remnant: a case report"],"prefix":"10.7181","volume":"23","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-9671-6510","authenticated-orcid":true,"given":"Dae Hwan","family":"Park","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-5343-2806","authenticated-orcid":true,"given":"June 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