{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,12,30]],"date-time":"2025-12-30T03:35:54Z","timestamp":1767065754538},"reference-count":14,"publisher":"Hindawi Limited","license":[{"start":{"date-parts":[[2014,1,1]],"date-time":"2014-01-01T00:00:00Z","timestamp":1388534400000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/3.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Surgery Research and Practice"],"published-print":{"date-parts":[[2014]]},"abstract":"<jats:p>Parathyroid carcinoma is a very rare malignancy. It has been associated with hyperparathyroidism-jaw tumour syndrome, familial isolated primary hyperparathyroidism, and multiple endocrine neoplasia type 1 (MEN-1) and 2A (MEN-2A) syndromes. We report a 54-year-old man with a MEN-2A which presents with a nonfunctional metastatic parathyroid carcinoma and a pheochromocytoma in the absence of medullary thyroid carcinoma. Only a few cases of parathyroid carcinoma have been reported in the literature associated with this syndrome.<\/jats:p>","DOI":"10.1155\/2014\/731481","type":"journal-article","created":{"date-parts":[[2014,2,26]],"date-time":"2014-02-26T06:12:32Z","timestamp":1393395152000},"page":"1-4","source":"Crossref","is-referenced-by-count":5,"title":["Nonfunctional Metastatic Parathyroid Carcinoma in the Setting of Multiple Endocrine Neoplasia Type 2A Syndrome"],"prefix":"10.1155","volume":"2014","author":[{"given":"Mar\u00eda","family":"Posada-Gonz\u00e1lez","sequence":"first","affiliation":[{"name":"Department of General and Gastrointestinal Surgery, La Princesa University Hospital, 62 Diego de Leon Street, 28006 Madrid, Spain"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Joaqu\u00edn","family":"G\u00f3mez-Ram\u00edrez","sequence":"additional","affiliation":[{"name":"Department of General and Gastrointestinal Surgery, Fundaci\u00f3n Jim\u00e9nez D\u00edaz Hospital, 2 Reyes 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