{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,30]],"date-time":"2026-09-30T00:10:07Z","timestamp":1790727007012,"version":"4.1.0"},"reference-count":29,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[1982,7,1]],"date-time":"1982-07-01T00:00:00Z","timestamp":394329600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["World j. surg."],"published-print":{"date-parts":[[1982,7]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p><jats:bold>Pheochromocytoma is a rare malignancy. The opportunity to gain experience with persistent and recurrent pheochromocytoma is extremely limited. We have, therefore, reviewed our experience with 8 patients with persistent and recurrent pheochromocytoma treated during the last 6 years. In patients with multiple endocrine neoplasia, the recurrent or persistent adrenal tumor is usually situated in the contralateral adrenal, whereas in other patients the tumor is usually situated in an ectopic position or is due to recognized or unrecognized malignant disease<\/jats:bold>.<\/jats:p><jats:p><jats:bold>Survival from diagnosis ranged from 1.5 to 23 years in these patients. Because long\u2010term survival may occur following removal of both benign and malignant pheochromocytomas, an aggressive surgical approach is recommended<\/jats:bold>.<\/jats:p>","DOI":"10.1007\/bf01657665","type":"journal-article","created":{"date-parts":[[2005,5,8]],"date-time":"2005-05-08T12:11:34Z","timestamp":1115554294000},"page":"397-401","source":"Crossref","is-referenced-by-count":31,"title":["Persistent and recurrent pheochromocytoma: The role of surgery"],"prefix":"10.1002","volume":"6","author":[{"given":"Murray F.","family":"Brennan","sequence":"first","affiliation":[{"name":"Surgery Branch National Cancer Institute USA"},{"name":"Hypertension\u2010Endocrine Branch National Heart Lung and Blood Institute USA"},{"name":"Gastric and Mixed Tumor Service Memorial Sloan\u2010Kettering Cancer Center 1275 York Avenue 10021 New York New York USA"},{"name":"National Institutes of Health Bethesda Maryland USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Harry R.","family":"Kaiser","sequence":"additional","affiliation":[{"name":"Surgery Branch National Cancer Institute USA"},{"name":"Hypertension\u2010Endocrine Branch National Heart Lung and Blood Institute USA"},{"name":"National Institutes of Health Bethesda Maryland USA"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[1982,7]]},"reference":[{"key":"e_1_2_1_2_1","volume-title":"Principles and Practice of Oncology","author":"Brennan M.F.","year":"1981"},{"key":"e_1_2_1_3_1","doi-asserted-by":"publisher","DOI":"10.1097\/00000658-197605000-00016"},{"key":"e_1_2_1_4_1","doi-asserted-by":"publisher","DOI":"10.1097\/00000658-197405000-00029"},{"key":"e_1_2_1_5_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0022-5347(17)57951-3"},{"key":"e_1_2_1_6_1","doi-asserted-by":"publisher","DOI":"10.1097\/00000658-197605000-00015"},{"key":"e_1_2_1_7_1","first-page":"140","article-title":"Pheochromocytoma","volume":"137","author":"Sander S.","year":"1971","journal-title":"Acta Chir. 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