{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,2]],"date-time":"2026-05-02T04:14:10Z","timestamp":1777695250785,"version":"3.51.4"},"reference-count":15,"publisher":"Walter de Gruyter GmbH","issue":"7","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2024,7,26]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:sec id=\"j_jpem-2024-0033_abs_001\">\n                  <jats:title>Objectives<\/jats:title>\n                  <jats:p>Pheochromocytomas (PHEO) are neuroendocrine tumors rarely diagnosed in children. We are reporting on the management challenges of three adolescent patients who present with hereditary PHEO.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec id=\"j_jpem-2024-0033_abs_002\">\n                  <jats:title>Case presentation<\/jats:title>\n                  <jats:p>The index patient and his male sibling presented with bilateral PHEO, while a third patient presented with a unilateral PHEO, all associated with von Hippel\u2013Lindau (VHL) syndrome. The patients were treated with computed tomography (CT)-guided percutaneous cryoablation (CRA) of the adrenal lesions, with varying degrees of success.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec id=\"j_jpem-2024-0033_abs_003\">\n                  <jats:title>Conclusions<\/jats:title>\n                  <jats:p>CT-guided percutaneous CRA of hereditary PHEO has not been reported in the pediatric population and may represent a novel treatment strategy that reduces the risk of intraprocedural complications and adrenal insufficiency (AI).<\/jats:p>\n               <\/jats:sec>","DOI":"10.1515\/jpem-2024-0033","type":"journal-article","created":{"date-parts":[[2024,5,29]],"date-time":"2024-05-29T06:40:37Z","timestamp":1716964837000},"page":"657-662","source":"Crossref","is-referenced-by-count":2,"title":["Computed tomography\u2013guided percutaneous cryoablation of hereditary adrenal pheochromocytoma in three patients"],"prefix":"10.1515","volume":"37","author":[{"given":"Emily","family":"Griffing","sequence":"first","affiliation":[{"name":"Division of Pediatric Endocrinology and Diabetes , Children\u2019s Mercy Hospital , Kansas City , MO , USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Brenton","family":"Reading","sequence":"additional","affiliation":[{"name":"Division of Radiology , Children\u2019s Mercy Hospital , Kansas City , MO , USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Francesco","family":"De Luca","sequence":"additional","affiliation":[{"name":"Division of Pediatric Endocrinology and Diabetes , Children\u2019s Mercy Hospital , Kansas City , MO , USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Daniel","family":"Agne","sequence":"additional","affiliation":[{"name":"Division of Anesthesiology , Children\u2019s Mercy Hospital , Kansas City , MO , USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"David","family":"Juang","sequence":"additional","affiliation":[{"name":"Division of Surgery , Children\u2019s Mercy Hospital , Kansas City , MO , USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-3884-2305","authenticated-orcid":false,"given":"Kelsee","family":"Halpin","sequence":"additional","affiliation":[{"name":"Division of Pediatric Endocrinology and Diabetes , Children\u2019s Mercy Hospital , Kansas City , MO , USA"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"374","published-online":{"date-parts":[[2024,5,30]]},"reference":[{"key":"2024071118565853619_j_jpem-2024-0033_ref_001","doi-asserted-by":"crossref","unstructured":"Lenders, JW, Duh, QY, Eisenhofer, G, Gimenez-Roqueplo, AP, Grebe, SK, Murad, MH, et al.. 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