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Editorial: Recent advances in pheochromocytoma and paraganglioma: molecular pathogenesis, clinical impacts, and therapeutic perspective, volume II.

作者信息

Abe Ichiro, Islam Farhadul, Pillai Suja

机构信息

Department of Endocrinology and Diabetes Mellitus, Fukuoka University Chikushi Hospital, Chikushino, Fukuoka, Japan.

Department of Biochemistry and Molecular Biology, University of Rajshahi, Rajshahi, Bangladesh.

出版信息

Front Endocrinol (Lausanne). 2025 May 2;16:1605189. doi: 10.3389/fendo.2025.1605189. eCollection 2025.

DOI:10.3389/fendo.2025.1605189
PMID:40385357
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12081245/
Abstract
摘要

相似文献

1
Editorial: Recent advances in pheochromocytoma and paraganglioma: molecular pathogenesis, clinical impacts, and therapeutic perspective, volume II.社论：嗜铬细胞瘤和副神经节瘤的最新进展：分子发病机制、临床影响及治疗前景，第二卷
Front Endocrinol (Lausanne). 2025 May 2;16:1605189. doi: 10.3389/fendo.2025.1605189. eCollection 2025.
2
Editorial: Recent Advances in Pheochromocytoma and Paraganglioma: Molecular Pathogenesis, Clinical Impacts, and Therapeutic Perspective.社论：嗜铬细胞瘤和副神经节瘤的最新进展：分子发病机制、临床影响及治疗前景
Front Endocrinol (Lausanne). 2021 Aug 23;12:720983. doi: 10.3389/fendo.2021.720983. eCollection 2021.
3
Malignant pheochromocytoma and paraganglioma: management options.恶性嗜铬细胞瘤和副神经节瘤：治疗选择。
Curr Opin Oncol. 2020 Jan;32(1):20-26. doi: 10.1097/CCO.0000000000000589.
4
Update on Pheochromocytoma and Paraganglioma from the SSO Endocrine/Head and Neck Disease-Site Work Group. Part 1 of 2: Advances in Pathogenesis and Diagnosis of Pheochromocytoma and Paraganglioma.来自 SSO 内分泌/头颈部疾病工作组的嗜铬细胞瘤和副神经节瘤更新。第 1 部分，共 2 部分：嗜铬细胞瘤和副神经节瘤发病机制和诊断的进展。
Ann Surg Oncol. 2020 May;27(5):1329-1337. doi: 10.1245/s10434-020-08220-3. Epub 2020 Feb 28.
5
Somatostatin Receptors and Analogs in Pheochromocytoma and Paraganglioma: Old Players in a New Precision Medicine World.生长抑素受体及其类似物在嗜铬细胞瘤和副神经节瘤中的作用：精准医学世界中的老牌选手。
Front Endocrinol (Lausanne). 2021 Mar 29;12:625312. doi: 10.3389/fendo.2021.625312. eCollection 2021.
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15 YEARS OF PARAGANGLIOMA: Metabolism and pheochromocytoma/paraganglioma.副神经节瘤的15年研究：代谢与嗜铬细胞瘤/副神经节瘤
Endocr Relat Cancer. 2015 Aug;22(4):T83-90. doi: 10.1530/ERC-15-0215. Epub 2015 Jun 25.
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15 YEARS OF PARAGANGLIOMA: Pheochromocytoma, paraganglioma and genetic syndromes: a historical perspective.副神经节瘤的15年：嗜铬细胞瘤、副神经节瘤与遗传综合征：历史视角
Endocr Relat Cancer. 2015 Aug;22(4):T147-59. doi: 10.1530/ERC-15-0221.
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A decade (2001-2010) of genetic testing for pheochromocytoma and paraganglioma.十余年来的嗜铬细胞瘤和副神经节瘤的基因检测。
Horm Metab Res. 2012 May;44(5):359-66. doi: 10.1055/s-0032-1304594. Epub 2012 Apr 19.
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Recent advances in the management of malignant pheochromocytoma and paraganglioma: focus on tyrosine kinase and hypoxia-inducible factor inhibitors.恶性嗜铬细胞瘤和副神经节瘤治疗的最新进展：聚焦于酪氨酸激酶和缺氧诱导因子抑制剂
F1000Res. 2018 Jul 30;7. doi: 10.12688/f1000research.13995.1. eCollection 2018.
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Endocr Relat Cancer. 2020 Dec;27(12):R433-R450. doi: 10.1530/ERC-19-0434.

本文引用的文献

1
Ectopic ACTH-secreting pheochromocytoma without typical signs of Cushing syndrome.无库欣综合征典型体征的异位促肾上腺皮质激素分泌性嗜铬细胞瘤。
Oxf Med Case Reports. 2025 Mar 28;2025(4):omaf005. doi: 10.1093/omcr/omaf005. eCollection 2025 Apr.
2
Cushing syndrome from an ACTH-producing pheochromocytoma or paraganglioma: structured review of 94 cases.由 ACTH 分泌性嗜铬细胞瘤或副神经节瘤引起的库欣综合征：94 例病例的结构化综述。
Endocr Relat Cancer. 2024 Oct 14;31(11). doi: 10.1530/ERC-24-0029. Print 2024 Nov 1.
3
VEGF-A/VEGF-B/VEGF-C expressions in non-hereditary, non-metastatic phaeochromocytoma.非遗传性、非转移性嗜铬细胞瘤中VEGF-A/VEGF-B/VEGF-C的表达情况
Histol Histopathol. 2021 Jun;36(6):645-652. doi: 10.14670/HH-18-329. Epub 2021 Mar 18.
4
Pheochromocytoma and Paraganglioma: From Clinical Findings to Diagnosis.嗜铬细胞瘤和副神经节瘤：从临床发现到诊断
Sisli Etfal Hastan Tip Bul. 2020 Sep 8;54(3):271-280. doi: 10.14744/SEMB.2020.14826. eCollection 2020.
5
Identification of Novel Mutations and Expressions of in Phaeochromocytomas and Paragangliomas.在嗜铬细胞瘤和副神经节瘤中鉴定新的突变和表达。
Genes (Basel). 2020 Oct 24;11(11):1254. doi: 10.3390/genes11111254.
6
Continued Tumor Reduction of Metastatic Pheochromocytoma/Paraganglioma Harboring Succinate Dehydrogenase Subunit B Mutations with Cyclical Chemotherapy.循环化疗治疗携带琥珀酸脱氢酶亚单位 B 突变的转移性嗜铬细胞瘤/副神经节瘤的肿瘤持续缩小。
Cell Mol Neurobiol. 2018 Jul;38(5):1099-1106. doi: 10.1007/s10571-018-0579-4. Epub 2018 Apr 5.
7
Updates on the genetics and the clinical impacts on phaeochromocytoma and paraganglioma in the new era.新时代中嗜铬细胞瘤和副神经节瘤的遗传学及临床影响的最新进展。
Crit Rev Oncol Hematol. 2016 Apr;100:190-208. doi: 10.1016/j.critrevonc.2016.01.022. Epub 2016 Jan 24.
8
Pheochromocytoma and paraganglioma pathogenesis: learning from genetic heterogeneity.嗜铬细胞瘤和副神经节瘤的发病机制：从遗传异质性中学习。
Nat Rev Cancer. 2014 Feb;14(2):108-19. doi: 10.1038/nrc3648. Epub 2014 Jan 20.
9
Pheochromocytoma crisis caused by Campylobacter fetus.由胎儿弯曲杆菌引起的嗜铬细胞瘤危象。
Int J Urol. 2012 May;19(5):465-7. doi: 10.1111/j.1442-2042.2011.02950.x. Epub 2012 Jan 6.