{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,5,14]],"date-time":"2025-05-14T02:54:24Z","timestamp":1747191264423,"version":"3.40.5"},"reference-count":25,"publisher":"Wiley","license":[{"start":{"date-parts":[[2024,4,26]],"date-time":"2024-04-26T00:00:00Z","timestamp":1714089600000},"content-version":"unspecified","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Case Reports in Oncological Medicine"],"published-print":{"date-parts":[[2024,4,26]]},"abstract":"<jats:p>Paragangliomas are rare neuroendocrine tumors that arise from the paraganglia, which are clusters of neuroendocrine cells associated with the autonomic nervous system. These tumors are commonly found in the adrenal medulla but can also occur in other locations outside the adrenal gland. Here, we present a case report of a slow-growing paraganglioma in the left neck with spinal metastasis in a 60-year-old man. This case highlights the importance of considering paraganglion tumors in the differential diagnosis of neck masses and the need for early diagnosis and management to prevent potential complications. Importantly, both the clinical picture and anatomical location of these tumors is important when determining treatment plans.<\/jats:p>","DOI":"10.1155\/2024\/2025115","type":"journal-article","created":{"date-parts":[[2024,4,26]],"date-time":"2024-04-26T22:35:07Z","timestamp":1714170907000},"page":"1-5","source":"Crossref","is-referenced-by-count":0,"title":["Paraganglioma of the Neck: A Rare Case With Spinal Metastasis"],"prefix":"10.1155","volume":"2024","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-8368-0467","authenticated-orcid":true,"given":"Sean","family":"McCormack","sequence":"first","affiliation":[{"name":"Saint James School of Medicine, Cane Hall Road, Arnos Vale, Saint Vincent and the Grenadines"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Eyad","family":"Hamad","sequence":"additional","affiliation":[{"name":"Northwestern School of Medicine, Chicago, Illinois, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Amar","family":"Hamad","sequence":"additional","affiliation":[{"name":"Department of Hemetology\/Oncology, Advocate Christ Hospital, Oak Lawn, Illinois, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","reference":[{"key":"1","doi-asserted-by":"publisher","DOI":"10.1055\/s-2004-814466"},{"key":"2","doi-asserted-by":"publisher","DOI":"10.3390\/cancers11081070"},{"key":"3","doi-asserted-by":"publisher","DOI":"10.1056\/nejmra1806651"},{"key":"4","first-page":"183","article-title":"Phaechromocytoma","volume-title":"WHO Classification of Tumours of Endocrine Organs","author":"A. 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