内科理论与实践 ›› 2023, Vol. 18 ›› Issue (04): 247-250.doi: 10.16138/j.1673-6087.2023.04.007
周薇薇, 郑思畅, 王卫庆(
)
收稿日期:2023-05-31
出版日期:2023-08-30
发布日期:2024-01-09
通讯作者:
王卫庆 E-mail: 基金资助:
ZHOU Weiwei, ZHENG Sichang, WANG Weiqing()
Received:2023-05-31
Online:2023-08-30
Published:2024-01-09
中图分类号:
周薇薇, 郑思畅, 王卫庆. 库欣病机制新认识[J]. 内科理论与实践, 2023, 18(04): 247-250.
ZHOU Weiwei, ZHENG Sichang, WANG Weiqing. New understanding of mechanism of Cushing’s disease[J]. Journal of Internal Medicine Concepts & Practice, 2023, 18(04): 247-250.
| [1] |
Molitch ME. Diagnosis and treatment of pituitary adenomas[J]. JAMA, 2017, 317(5): 516-524.
doi: 10.1001/jama.2016.19699 pmid: 28170483 |
| [2] |
Melmed S. Pituitary-tumor endocrinopathies[J]. N Engl J Med, 2020, 382(10): 937-950.
doi: 10.1056/NEJMra1810772 URL |
| [3] |
Fleseriu M, Auchus R, Bancos I, et al. Consensus on diagnosis and management of Cushing’s disease[J]. Lancet Diabetes Endocrinol, 2021, 9(12): 847-875.
doi: 10.1016/S2213-8587(21)00235-7 URL |
| [4] |
Reincke M, Sbiera S, Hayakawa A, et al. Mutations in the deubiquitinase gene USP8 cause Cushing’s disease[J]. Nat Genet, 2015, 47(1): 31-38.
doi: 10.1038/ng.3166 pmid: 25485838 |
| [5] |
Ma ZY, Song ZJ, Chen JH, et al. Recurrent gain-of-function USP8 mutations in Cushing’s disease[J]. Cell Res, 2015, 25(3): 306-317.
doi: 10.1038/cr.2015.20 |
| [6] |
Castellnou S, Vasiljevic A, Lapras V, et al. SST5 expression and USP8 mutation in functioning and silent corticotroph pituitary tumors[J]. Endocr Connect, 2020, 9(3): 243-253.
doi: 10.1530/EC-20-0035 URL |
| [7] | Chen J, Jian X, Deng S, et al. Identification of recurrent USP48 and BRAF mutations in Cushing’s disease[J]. NNat Commun, 2018, 9(1): 3171. |
| [8] |
Hernández-Ramírez LC, Gam R, Valdés N, et al. Loss-of-function mutations in the CABLES1 gene are a novel cause of Cushing’s disease[J]. Endocr Relat Cancer, 2017, 24(8): 379-392.
doi: 10.1530/ERC-17-0131 URL |
| [9] |
Schernthaner-Reiter MH, Trivellin G, Stratakis CA. MEN1, MEN4, and carney complex: pathology and molecular genetics[J]. Neuroendocrinology, 2016, 103(1): 18-31.
doi: 10.1159/000371819 pmid: 25592387 |
| [10] |
Chasseloup F, Pankratz N, Lane J, et al. Germline CDKN1B loss-of-function variants cause pediatric Cushing’s disease with or without an MEN4 phenotype[J]. J Clin Endocrinol Metab, 2020, 105(6): 1983-2005.
doi: 10.1210/clinem/dgaa160 URL |
| [11] |
Mete O, Lopes MB. Overview of the 2017 WHO classification of pituitary tumors[J]. Endocr Pathol, 2017, 28(3): 228-243.
doi: 10.1007/s12022-017-9498-z pmid: 28766057 |
| [12] |
Asa SL, Mete O, Perry A, et al. Overview of the 2022 WHO classification of pituitary tumors[J]. Endocr Pathol, 2022, 33(1): 6-26.
doi: 10.1007/s12022-022-09703-7 pmid: 35291028 |
| [13] | WHO Classification of Tumours Editorial Board. WHO classification of endocrine and neuroendocrine tumours[M]. Lyon: IARC Press, 2022. |
| [14] |
Reincke M, Theodoropoulou M. Genomics in Cushing’s disease: the dawn of a new era[J]. J Clin Endocrinol Metab, 2021, 106(6): e2455-e2456.
doi: 10.1210/clinem/dgaa969 pmid: 33524136 |
| [1] | 周薇薇, 王卫庆. 原发性双侧大结节样肾上腺增生症的认识变迁[J]. 内科理论与实践, 2023, 18(04): 239-241. |
| [2] | 张翠, 王卫庆. 异位促肾上腺皮质激素综合征[J]. 内科理论与实践, 2023, 18(04): 242-246. |
| [3] | 林纬, 陈刚,. 妊娠合并库欣综合征的现状与对策[J]. 内科理论与实践, 2019, 14(03): 144-148. |
| [4] | 迟婧, 宋琦,. ACTH非依赖性库欣综合征的影像学表现[J]. 诊断学理论与实践, 2013, 12(06): 649-653. |
| [5] | 毕宇芳. 异位促肾上腺皮质激素综合征的病因与诊断进展[J]. 诊断学理论与实践, 2003, 2(02): 72-74. |
| 阅读次数 | ||||||
|
全文 |
|
|||||
|
摘要 |
|
|||||
