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患有冯·希佩尔-林道病、2型多发性内分泌腺瘤病或1型神经纤维瘤病的患者,其综合征性副神经节瘤和嗜铬细胞瘤切除术后的围手术期结局。

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

作者信息

Butz James J, Yan Qi, McKenzie Travis J, Weingarten Toby N, Cavalcante Alexandre N, Bancos Irina, Young William F, Schroeder Darrell R, Martin David P, Sprung Juraj

机构信息

Department of Surgery, Mayo Clinic, Rochester, MN.

Department of Anesthesiology and Perioperative Medicine, Mayo Clinic, Rochester, MN.

出版信息

Surgery. 2017 Dec;162(6):1259-1269. doi: 10.1016/j.surg.2017.08.002. Epub 2017 Sep 14.

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 μg/24 h), similar to that found in multiple endocrine neoplasia type 2A (median, 809 μg/24 h). The highest noradrenergic secretion (24-hour urine normetanephrine) occurred with von Hippel-Lindau disease (median, 4,598 μg/24 h), followed by neurofibromatosis type 1 and multiple endocrine neoplasia type 2A (median, 1,607 and 923 μg/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.

摘要

背景

与1型神经纤维瘤病、2A型多发性内分泌腺瘤病及冯·希佩尔-林道病相关的嗜铬细胞瘤和/或副神经节瘤具有不同的儿茶酚胺生化表型。我们研究了3种综合征形式的嗜铬细胞瘤/副神经节瘤切除术的围手术期结局。

方法

回顾性分析2000年至2016年接受综合征性嗜铬细胞瘤/副神经节瘤切除术的患者。

结果

81例患者接受了嗜铬细胞瘤/副神经节瘤切除术(2A型多发性内分泌腺瘤病36例;1型神经纤维瘤病26例;冯·希佩尔-林道病19例)。各组肿瘤大小不同;1型神经纤维瘤病和冯·希佩尔-林道病患者的肿瘤最大(P = 0.017)。肿瘤体积越大,24小时尿总甲氧基肾上腺素越高(2A型多发性内分泌腺瘤病、冯·希佩尔-林道病和1型神经纤维瘤病的r分别为0.94,P < 0.001;r = 0.67,P = 0.033;r = 0.89,P < 0.001)。1型神经纤维瘤病患者肾上腺素分泌高(24小时尿甲氧基肾上腺素)(中位数为每24小时861μg),与2A型多发性内分泌腺瘤病患者相似(中位数为每24小时809μg)。去甲肾上腺素分泌最高(24小时尿去甲氧基肾上腺素)发生在冯·希佩尔-林道病患者中(中位数为每24小时4598μg),其次是1型神经纤维瘤病和2A型多发性内分泌腺瘤病患者(中位数分别为每24小时1607μg和923μg)。1型神经纤维瘤病患者发生的并发症分级最高(P = 0.036)。然而,比较接受腹腔镜切除术的3组患者的术后结局时,无显著差异(P = 0.955)。

结论

1型神经纤维瘤病患者术中血流动力学过程最不稳定,术后并发症更严重。这些并发症与儿茶酚胺分泌丰富的大肿瘤以及高比例患者接受开放性切除术有关。在仅接受腹腔镜手术的患者中,各综合征组的术后结局无差异。

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