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Perioperative outcomes of syndromic paraganglioma and pheochromocytoma resection in patients with von Hippel‐Lindau disease, multiple endocrine neoplasia type 2, or neurofibromatosis type 1

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Background. Pheochromocytoma and/or paraganglioma associated with neurofibromatosis type 1, multiple endocrine neoplasia type 2A, and von Hippel‐Lindau disease have different catecholamine biochemical phenotypes. We examined perioperative outcomes of pheochromocytoma/paraganglioma resection… Click to show full abstract

Background. Pheochromocytoma and/or paraganglioma associated with neurofibromatosis type 1, multiple endocrine neoplasia type 2A, and von Hippel‐Lindau disease have different catecholamine biochemical phenotypes. We examined perioperative outcomes of pheochromocytoma/paraganglioma resection in 3 syndromic forms. Methods. Retrospective review of patients undergoing resection of syndromic pheochromocytoma/paraganglioma from 2000 through 2016. Results. Eighty‐one patients underwent pheochromocytoma/paraganglioma resection (multiple endocrine neoplasia type 2A, n = 36; neurofibromatosis type 1, n = 26; von Hippel‐Lindau disease, n = 19). Tumor size differed across groups; patients with neurofibromatosis type 1 and von Hippel‐Lindau disease had the largest tumors (P = .017). Larger tumor volumes correlated with higher urine 24‐hour total metanephrine (r = 0.94, P < .001; r = 0.67, P = .033; and r = 0.89, P < .001 for multiple endocrine neoplasia type 2A, von Hippel‐Lindau disease, and neurofibromatosis type 1, respectively). High adrenergic secretion (24‐hour urine metanepinephrine) was found in neurofibromatosis type 1 (median, 861 &mgr;g/24 h), similar to that found in multiple endocrine neoplasia type 2A (median, 809 &mgr;g/24 h). The highest noradrenergic secretion (24‐hour urine normetanephrine) occurred with von Hippel‐Lindau disease (median, 4,598 &mgr;g/24 h), followed by neurofibromatosis type 1 and multiple endocrine neoplasia type 2A (median, 1,607 and 923 &mgr;g/24 h, respectively). The highest graded complications occurred among patients with neurofibromatosis type 1 (P = .036). However, when comparing postoperative outcomes across 3 groups in those who had laparoscopic resection, there was no significant difference (P = .955). Conclusion. Patients with neurofibromatosis type 1 had the most volatile intraoperative hemodynamic course and more severe postoperative complications. These complications are related to large tumors associated with abundant catecholamine secretion and the fact that a high proportion underwent open resection. Among only patients who underwent laparoscopic procedures, there were no differences in postoperative outcomes across syndromic groups.

Keywords: neoplasia type; multiple endocrine; von hippel; endocrine neoplasia; neurofibromatosis type; type

Journal Title: Surgery
Year Published: 2017

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