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颈部副神经节瘤、心脏副神经节瘤、肾上腺嗜铬细胞瘤:一场与高儿茶酚胺血症的较量

孙娟 刘剑州 文进 李汉忠 纪志刚 董德鑫 叶子兴 苗齐 童安莉 黄宇光 隆云

孙娟, 刘剑州, 文进, 李汉忠, 纪志刚, 董德鑫, 叶子兴, 苗齐, 童安莉, 黄宇光, 隆云. 颈部副神经节瘤、心脏副神经节瘤、肾上腺嗜铬细胞瘤:一场与高儿茶酚胺血症的较量[J]. 协和医学杂志. doi: 10.12290/xhyxzz.2021-0134
引用本文: 孙娟, 刘剑州, 文进, 李汉忠, 纪志刚, 董德鑫, 叶子兴, 苗齐, 童安莉, 黄宇光, 隆云. 颈部副神经节瘤、心脏副神经节瘤、肾上腺嗜铬细胞瘤:一场与高儿茶酚胺血症的较量[J]. 协和医学杂志. doi: 10.12290/xhyxzz.2021-0134
SUN Juan, LIU Jianzhou, WEN Jin, LI Hanzhong, JI Zhigang, DONG Dexin, YE Zixing, MIAO Qi, TONG Anli, HUANG Yuguang, LONG Yun. Carotid Body Tumor, Cardiac Paraganglioma, Adrenal Pheochromocytoma: A Contest with Hypercatecholamineemia[J]. Medical Journal of Peking Union Medical College Hospital. doi: 10.12290/xhyxzz.2021-0134
Citation: SUN Juan, LIU Jianzhou, WEN Jin, LI Hanzhong, JI Zhigang, DONG Dexin, YE Zixing, MIAO Qi, TONG Anli, HUANG Yuguang, LONG Yun. Carotid Body Tumor, Cardiac Paraganglioma, Adrenal Pheochromocytoma: A Contest with Hypercatecholamineemia[J]. Medical Journal of Peking Union Medical College Hospital. doi: 10.12290/xhyxzz.2021-0134

颈部副神经节瘤、心脏副神经节瘤、肾上腺嗜铬细胞瘤:一场与高儿茶酚胺血症的较量

doi: 10.12290/xhyxzz.2021-0134
基金项目: 

中国医学科学院中央级公益性科研院所基本科研业务费临床与转化医学研究基金(2019XK320027);外国文教专家项目管理基金(G20190001645)

详细信息
    通讯作者:

    文进,电话:010-69152511,E-mail:wjpumch@163.com

  • 中图分类号: R732.2+1;R732.1;R730.4

Carotid Body Tumor, Cardiac Paraganglioma, Adrenal Pheochromocytoma: A Contest with Hypercatecholamineemia

Funds: 

Non-profit Central Research Institute Fund of Chinese Academy of Medical Sciences (2019XK320027)

  • 摘要: 一例老年男性患者,同时合并左颈部副神经节瘤、心脏副神经节瘤及右肾上腺嗜铬细胞瘤,病例罕见,病情复杂,诊治难度大,经两次多学科团队共同讨论,我院先后为患者切除心脏及右肾上腺病灶,术后患者顺利出院,获得了良好的治疗效果。该患者的诊治过程体现了多学科协作在疑难重症诊疗过程中的重要作用。
  • [1] 嗜铬细胞瘤和副神经节瘤诊断治疗专家共识(2020版)[J].中华内分泌代谢杂志, 2020, 36:737-750.
    [2] Beard CM,Sheps SG,Kurland LT,et al.Occurrence of pheochromocytoma in Rochester, Minnesota, 1950 through 1979[J]. Mayo Clin Proc, 1983, 58:802-804.
    [3] McNeil AR, Blok BH, Koelmeyer TD,et al.Phaeochromocytomas discovered during coronial autopsies in Sydney, Melbourne and Auckland[J].Aust N Z J Med,2000, 30:648-652.
    [4] Sutton MG, Sheps SG, Lie JT.Prevalence of clinically unsuspected pheochromocytoma. Review of a 50-year autopsy series[J]. Mayo Clin Proc, 1981, 56:354-360.
    [5] Scoazec JY, Couvelard A; Réseau TENpath. Classification of pancreatic neuroendocrine tumours:Changes made in the 2017 WHO classification of tumours of endocrine organs and perspectives for the future[J].Ann Pathol, 2017, 37:444-456.
    [6] Abdelhady K, Durgam S, Orza D, et al. Left Atrial and Carotid Body Paraganglioma[J]. Ann Thorac Surg, 2017, 103:e323-e325.
    [7] Erickson D, Kudva YC, Ebersold MJ, et al. Benign paragangliomas:clinical presentation and treatment outcomes in 236 patients[J]. J Clin Endocrinol Metab, 2001, 86:5210-5216.
    [8] Al-Harthy M, Al-Harthy S, Al-Otieschan A, et al. Comparison of pheochromocytomas and abdominal and pelvic paragangliomas with head and neck paragangliomas[J]. Endocr Pract, 2009, 15:194-202.
    [9] Eisenhofer G, Tischler AS, de Krijger RR. Diagnostic tests and biomarkers for pheochromocytoma and extra-adrenal paraganglioma:from routine laboratory methods to disease stratification[J]. Endocr Pathol, 2012, 23:4-14.
    [10] Kimura N, Watanabe T, Noshiro T,et al. Histological grading of adrenal and extra-adrenal pheochromocytomas and relationship to prognosis:a clinicopathological analysis of 116 adrenal pheochromocytomas and 30 extra-adrenal sympathetic paragangliomas including 38 malignant tumors[J]. Endocr Pathol, 2005, 16:23-32.
    [11] Thompson LD. Pheochromocytoma of the Adrenal gland Scaled Score (PASS) to separate benign from malignant neoplasms:a clinicopathologic and immunophenotypic study of 100 cases[J]. Am J Surg Pathol, 2002, 26:551-566.
    [12] Strong VE, Kennedy T, Al-Ahmadie H, et al. Prognostic indicators of malignancy in adrenal pheochromocytomas:clinical, histopathologic, and cell cycle/apoptosis gene expression analysis[J]. Surgery, 2008, 143:759-768.
    [13] de Wailly P, Oragano L, Radé F, et al. Malignant pheochromocytoma:new malignancy criteria[J]. Langenbecks Arch Surg, 2012, 397:239-246.
    [14] Agarwal A, Mehrotra PK, Jain M, et al. Size of the tumor and pheochromocytoma of the adrenal gland scaled score (PASS):can they predict malignancy?[J]. World J Surg, 2010, 34:3022-3028.
    [15] Chen H, Sippel RS, O'Dorisio MS, et al. The North American Neuroendocrine Tumor Society consensus guideline for the diagnosis and management of neuroendocrine tumors:pheochromocytoma, paraganglioma, and medullary thyroid cancer[J]. Pancreas, 2010, 39:775-783.
    [16] Boedeker CC, Neumann HP, Offergeld C, et al. Clinical features of paraganglioma syndromes[J].Skull Base, 2009, 19:17-25.
    [17] Shen WT, Grogan R, Vriens M, et al. One Hundred Two Patients With Pheochromocytoma Treated at a Single Institution Since the Introduction of Laparoscopic Adrenalectomy[J]. Arch Surg, 2010, 145:893-897.
    [18] Pacak K, Eisenhofer G, Ahlman H, et al. Pheochromocytoma:recommendations for clinical practice from the First International Symposium. October 2005[J]. Nat Clin Pract Endocrinol Metab, 2007, 3:92-102.
    [19] Strajina V, Dy BM, Farley DR, et al. Surgical Treatment of Malignant Pheochromocytoma and Paraganglioma:Retrospective Case Series[J]. Ann Surg Oncol, 2017, 24:1546-1550.
    [20] Ellis RJ, Patel D, Prodanov T, et al. Response after surgical resection of metastatic pheochromocytoma and paraganglioma:can postoperative biochemical remission be predicted?[J]. J Am Coll Surg, 2013, 217:489-496.
    [21] Huang KH, Chung SD, Chen SC, et al. Clinical and pathological data of 10 malignant pheochromocytomas:long-term follow up in a single institute[J]. Int J Urol, 2007, 14:181-185.
    [22] Jain A, Baracco R, Kapur G. Pheochromocytoma and paraganglioma-an update on diagnosis, evaluation, and management[J]. Pediatr Nephrol, 2020, 35:581-594.
    [23] Bholah R, Bunchman TE. Review of Pediatric Pheochromocytoma and Paraganglioma[J]. Front Pediatr, 2017, 5:155.
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出版历程
  • 收稿日期:  2021-01-29
  • 网络出版日期:  2021-09-03

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