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《南非单中心 60 例嗜铬细胞瘤手术治疗回顾》。

Surgery for Pheochromocytoma: A Single-Center Review of 60 Cases from South Africa.

机构信息

Division of General Surgery, Groote Schuur Hospital and University of Cape Town, Cape Town, South Africa.

Division of Nuclear Medicine, Groote Schuur Hospital and University of Cape Town, Cape Town, South Africa.

出版信息

World J Surg. 2020 Jun;44(6):1918-1924. doi: 10.1007/s00268-020-05420-6.

DOI:10.1007/s00268-020-05420-6
PMID:32055970
Abstract

BACKGROUND

There is a paucity of data on the presentation and surgical management of pheochromocytoma in developing nations, particularly in Africa.

METHODS

This study was a retrospective review, which included all patients managed by the Groote Schuur Hospital/University of Cape Town Endocrine Surgery unit for pheochromocytoma and abdominal paragangliomas, from January 2002 to June 2019.

RESULTS

Sixty patients were included in the study, of which 33% were male and 67% female. The mean age was 47 years (range 14-81). The median tumor size was 6 cm, with 45% larger than 6 cm. 92% were located in the adrenal gland (87% unilateral, 5% bilateral), and 8% were extra-adrenal. The conversion rate for laparoscopic cases was 20%, with 55% of cases overall completed laparoscopically. Eleven patients with tumors > 6 cm were initially attempted laparoscopically, of which 3 were converted to open, without any associated increased morbidity. A major adverse event was recorded for 5 cases (8%), including 1 mortality. Overall morbidity, blood loss, operating time and hospital stay were all significantly reduced in the laparoscopic group. There were 5 patients with malignant disease (8%).

CONCLUSION

This large series, from an established academic endocrine surgery unit in Africa, can serve as a benchmark for units with similar settings and resource limitations, to compare their surgical management and perioperative outcomes.

摘要

背景

发展中国家,尤其是非洲,有关嗜铬细胞瘤的临床表现和外科治疗的数据十分有限。

方法

本研究为回顾性研究,纳入了 2002 年 1 月至 2019 年 6 月期间在开普敦大学格罗特舒尔医院/内分泌外科接受治疗的嗜铬细胞瘤和腹部副神经节瘤患者。

结果

研究共纳入 60 例患者,其中 33%为男性,67%为女性。平均年龄为 47 岁(14-81 岁)。肿瘤中位数大小为 6cm,45%的肿瘤大于 6cm。92%的肿瘤位于肾上腺(87%为单侧,5%为双侧),8%为肾上腺外肿瘤。腹腔镜手术的转化率为 20%,总体 55%的病例可通过腹腔镜完成。11 例肿瘤>6cm 的患者最初尝试腹腔镜手术,其中 3 例转为开放手术,无任何相关的发病率增加。有 5 例(8%)发生了重大不良事件,包括 1 例死亡。总体而言,腹腔镜组的发病率、出血量、手术时间和住院时间均显著降低。有 5 例(8%)患者患有恶性疾病。

结论

这项来自非洲一家成熟的学术内分泌外科的大型系列研究,可以为具有类似设置和资源限制的单位提供基准,以比较他们的手术管理和围手术期结果。

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Surgery for Pheochromocytoma: A Single-Center Review of 60 Cases from South Africa.《南非单中心 60 例嗜铬细胞瘤手术治疗回顾》。
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Retroperitoneoscopic adrenalectomy without previous control of adrenal vein is feasible and safe for pheochromocytoma.对于嗜铬细胞瘤,不预先控制肾上腺静脉的后腹腔镜肾上腺切除术是可行且安全的。
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A Study of Paraganglioma Cases With Non-European Ancestry.一项针对非欧洲血统副神经节瘤病例的研究。
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本文引用的文献

1
Surgical therapy of adrenal tumors: guidelines from the German Association of Endocrine Surgeons (CAEK).肾上腺肿瘤的外科治疗:德国内分泌外科学会(CAEK)指南。
Langenbecks Arch Surg. 2019 Jun;404(4):385-401. doi: 10.1007/s00423-019-01768-z. Epub 2019 Apr 1.
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European Society of Endocrinology Clinical Practice Guideline for long-term follow-up of patients operated on for a phaeochromocytoma or a paraganglioma.欧洲内分泌学会嗜铬细胞瘤或副神经节瘤手术患者长期随访临床实践指南
Eur J Endocrinol. 2016 May;174(5):G1-G10. doi: 10.1530/EJE-16-0033.
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Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline.
南非嗜铬细胞瘤-副神经节瘤患者中荷兰始祖型SDHB基因第3外显子缺失情况
Endocr Connect. 2022 Jan 31;11(1):e210560. doi: 10.1530/EC-21-0560.
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SDHB-Associated Paraganglioma Syndrome in Africa-A Need for Greater Genetic Testing.非洲与琥珀酸脱氢酶B亚基相关的副神经节瘤综合征——加强基因检测的必要性
J Endocr Soc. 2021 Jun 15;5(10):bvab111. doi: 10.1210/jendso/bvab111. eCollection 2021 Oct 1.
嗜铬细胞瘤和副神经节瘤:内分泌学会临床实践指南
J Clin Endocrinol Metab. 2014 Jun;99(6):1915-42. doi: 10.1210/jc.2014-1498.
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Current concepts of pheochromocytoma.当前的嗜铬细胞瘤概念。
Int J Surg. 2014;12(5):469-74. doi: 10.1016/j.ijsu.2014.04.001. Epub 2014 Apr 12.
5
Diagnosis and management of pheochromocytoma.嗜铬细胞瘤的诊断与管理
Curr Probl Surg. 2014 Apr;51(4):151-87. doi: 10.1067/j.cpsurg.2013.12.001. Epub 2014 Jan 23.
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Clinical experience with pheochromocytoma in a single centre over 16 years.16年间单中心嗜铬细胞瘤的临床经验。
High Blood Press Cardiovasc Prev. 2009 Dec;16(4):183-93. doi: 10.2165/11530430-000000000-00000. Epub 2013 Jan 3.
7
Surgical management of organ-contained unilateral pheochromocytoma: comparative outcomes of laparoscopic and conventional open surgical procedures in a large single-institution series.含器官单侧嗜铬细胞瘤的外科治疗:大型单机构系列中腹腔镜与传统开放手术的比较结果。
Langenbecks Arch Surg. 2012 Oct;397(7):1109-16. doi: 10.1007/s00423-011-0879-3. Epub 2011 Nov 26.
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Phaeochromocytoma in black South Africans - a 30-year audit.南非黑人嗜铬细胞瘤——30 年回顾性研究。
S Afr Med J. 2011 Mar 1;101(3):184-8. doi: 10.7196/samj.4320.
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One hundred two patients with pheochromocytoma treated at a single institution since the introduction of laparoscopic adrenalectomy.自开展腹腔镜肾上腺切除术以来,在单一机构接受治疗的102例嗜铬细胞瘤患者。
Arch Surg. 2010 Sep;145(9):893-7. doi: 10.1001/archsurg.2010.159.
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Size of the tumor and pheochromocytoma of the adrenal gland scaled score (PASS): can they predict malignancy?肿瘤大小和肾上腺嗜铬细胞瘤分级评分(PASS):它们能否预测恶性肿瘤?
World J Surg. 2010 Dec;34(12):3022-8. doi: 10.1007/s00268-010-0744-5.