{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,4,30]],"date-time":"2024-04-30T00:29:59Z","timestamp":1714436999771},"reference-count":10,"publisher":"Springer Science and Business Media LLC","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2024,4,29]]},"DOI":"10.7759\/cureus.59295","type":"journal-article","created":{"date-parts":[[2024,4,29]],"date-time":"2024-04-29T17:26:51Z","timestamp":1714411611000},"source":"Crossref","is-referenced-by-count":0,"title":["Hormonally Silent Multifocal Pheochromocytoma in the Setting of a Well-Differentiated Neuroendocrine Tumor of the Appendix: A Case Report"],"prefix":"10.7759","author":[{"given":"Patrick T","family":"Weldon","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Megan","family":"McNally","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"ref1","doi-asserted-by":"publisher","DOI":"10.1210\/jc.2014-1498","article-title":"Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline","volume":"99","author":"Lenders JW","year":"2014","unstructured":"Lenders JW, Duh QY, Eisenhofer G, et al.. Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline. J Clin Endocrinol Metab. 2014, 99:1915-42. 10.1210\/jc.2014-1498","journal-title":"J Clin Endocrinol Metab"},{"key":"ref2","doi-asserted-by":"publisher","DOI":"10.1001\/jamasurg.2022.3544","article-title":"American Association of Endocrine Surgeons guidelines for adrenalectomy: executive summary","volume":"157","author":"Yip L","year":"2022","unstructured":"Yip L, Duh QY, Wachtel H, et al.. American Association of Endocrine Surgeons guidelines for adrenalectomy: executive summary. JAMA Surg. 2022, 157:870-7. 10.1001\/jamasurg.2022.3544","journal-title":"JAMA Surg"},{"key":"ref3","doi-asserted-by":"publisher","DOI":"10.1097\/MED.0000000000000059","article-title":"Genetic testing in the clinical care of patients with pheochromocytoma and paraganglioma","volume":"21","author":"Rana HQ","year":"2014","unstructured":"Rana HQ, Rainville IR, Vaidya A. Genetic testing in the clinical care of patients with pheochromocytoma and paraganglioma. Curr Opin Endocrinol Diabetes Obes. 2014, 21:166-76. 10.1097\/MED.0000000000000059","journal-title":"Curr Opin Endocrinol Diabetes Obes"},{"key":"ref4","doi-asserted-by":"publisher","DOI":"10.1007\/s00441-017-2760-3","article-title":"Pheochromocytoma and paraganglioma: genotype versus anatomic location as determinants of tumor phenotype","volume":"372","author":"Fliedner SM","year":"2018","unstructured":"Fliedner SM, Brabant G, Lehnert H. Pheochromocytoma and paraganglioma: genotype versus anatomic location as determinants of tumor phenotype. Cell Tissue Res. 2018, 372:347-65. 10.1007\/s00441-017-2760-3","journal-title":"Cell Tissue Res"},{"key":"ref5","doi-asserted-by":"publisher","DOI":"10.1210\/jcem.86.5.7496","article-title":"Pheochromocytomas in von Hippel-Lindau syndrome and multiple endocrine neoplasia type 2 display distinct biochemical and clinical phenotypes","volume":"86","author":"Eisenhofer G","year":"2001","unstructured":"Eisenhofer G, Walther MM, Huynh TT, et al.. Pheochromocytomas in von Hippel-Lindau syndrome and multiple endocrine neoplasia type 2 display distinct biochemical and clinical phenotypes. J Clin Endocrinol Metab. 2001, 86:1999-2008. 10.1210\/jcem.86.5.7496","journal-title":"J Clin Endocrinol Metab"},{"key":"ref6","doi-asserted-by":"publisher","DOI":"10.1158\/1078-0432.CCR-14-2751","article-title":"Superiority of [68Ga]-DOTATATE PET\/CT to other functional imaging modalities in the localization of SDHB-associated metastatic pheochromocytoma and paraganglioma","volume":"21","author":"Janssen I","year":"2015","unstructured":"Janssen I, Blanchet EM, Adams K, et al.. Superiority of [68Ga]-DOTATATE PET\/CT to other functional imaging modalities in the localization of SDHB-associated metastatic pheochromocytoma and paraganglioma. Clin Cancer Res. 2015, 21:3888-95. 10.1158\/1078-0432.CCR-14-2751","journal-title":"Clin Cancer Res"},{"key":"ref7","doi-asserted-by":"publisher","DOI":"10.1530\/ERC-15-0175","article-title":"15 years of paraganglioma: imaging and imaging-based treatment of pheochromocytoma and paraganglioma","volume":"22","author":"Castinetti F","year":"2015","unstructured":"Castinetti F, Kroiss A, Kumar R, Pacak K, Taieb D. 15 years of paraganglioma: imaging and imaging-based treatment of pheochromocytoma and paraganglioma. Endocr Relat Cancer. 2015, 22:T135-45. 10.1530\/ERC-15-0175","journal-title":"Endocr Relat Cancer"},{"key":"ref8","doi-asserted-by":"publisher","DOI":"10.1016\/j.surg.2018.08.033","article-title":"Multifocal pheochromocytoma-paraganglioma in a 29-year-old woman with cyanotic congenital heart disease","volume":"165","author":"Wcislak SM","year":"2019","unstructured":"Wcislak SM, King WS, Waller BR 3rd, Goins N, Dickson PV. Multifocal pheochromocytoma-paraganglioma in a 29-year-old woman with cyanotic congenital heart disease. Surgery. 2019, 165:228-31. 10.1016\/j.surg.2018.08.033","journal-title":"Surgery"},{"key":"ref9","doi-asserted-by":"publisher","DOI":"10.1016\/j.ccell.2017.01.001","article-title":"Comprehensive molecular characterization of pheochromocytoma and paraganglioma","volume":"31","author":"Fishbein L","year":"2017","unstructured":"Fishbein L, Leshchiner I, Walter V, et al.. Comprehensive molecular characterization of pheochromocytoma and paraganglioma. Cancer Cell. 2017, 31:181-93. 10.1016\/j.ccell.2017.01.001","journal-title":"Cancer Cell"},{"key":"ref10","doi-asserted-by":"publisher","DOI":"10.1530\/ERC-15-0215","article-title":"15 years of paragangl\u0131oma: Metabolism and pheochromocytoma\/paraganglioma","volume":"22","author":"Mannelli M","year":"2015","unstructured":"Mannelli M, Rapizzi E, Fucci R, Canu L, Ercolino T, Luconi M, Young WF Jr. 15 years of paragangl\u0131oma: Metabolism and pheochromocytoma\/paraganglioma. Endocr Relat Cancer. 2015, 22:T83-90. 10.1530\/ERC-15-0215","journal-title":"Endocr Relat Cancer"}],"container-title":["Cureus"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.cureus.com\/articles\/240789-hormonally-silent-multifocal-pheochromocytoma-in-the-setting-of-a-well-differentiated-neuroendocrine-tumor-of-the-appendix-a-case-report","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,4,29]],"date-time":"2024-04-29T17:26:55Z","timestamp":1714411615000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.cureus.com\/articles\/240789-hormonally-silent-multifocal-pheochromocytoma-in-the-setting-of-a-well-differentiated-neuroendocrine-tumor-of-the-appendix-a-case-report"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2024,4,29]]},"references-count":10,"URL":"https:\/\/doi.org\/10.7759\/cureus.59295","relation":{},"ISSN":["2168-8184"],"issn-type":[{"value":"2168-8184","type":"print"}],"subject":[],"published":{"date-parts":[[2024,4,29]]}}}