[1]汤其华 综述 张剑宁 审校.颅骨纤维结构不良研究新进展[J].中国临床神经外科杂志,2020,(09):639-641.[doi:10.13798/j.issn.1009-153X.2020.09.023]
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颅骨纤维结构不良研究新进展()
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《中国临床神经外科杂志》[ISSN:1009-153X/CN:42-1603/TN]

卷:
期数:
2020年09期
页码:
639-641
栏目:
综述
出版日期:
2020-09-20

文章信息/Info

文章编号:
1009-153X(2020)09-0639-03
作者:
汤其华 综述 张剑宁 审校
100048 北京,解放军总医院第一医学中心神经外科医学部(汤其华、张剑宁)
关键词:
颅骨纤维结构不良发病机制病理治疗
分类号:
B
DOI:
10.13798/j.issn.1009-153X.2020.09.023
文献标志码:
R 681.1

参考文献/References:

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[3] Menon S, Venkatswamy S, Ramu V, et al. Craniofacial dys- plasia: surgery and literature review [J]. Ann Maxillofac Surg, 2013, 3(1): 66-71.
[4] Sirvanci M, Karaman K, Onat L, et al. Monostotic fibrous dysplasia of the clivus: MRI and CT findings [J]. Neuro- radiology, 2002, 44(9): 847-850.
[5] Okamotos S, Hisaoka M, Meis JM, et al. Juxta-articular myxoma and. intramuscular myxoma are two distinct entities activating Gsα mutation at Arg 201 codon does not occur in juxta articular myxoma [J]. Virchows Arch, 2002, 440(1): 12-15.
[6] Candeliere GA, Roughley PJ, Glorieux FH, et al. Polymerase chain reaction-based technique for the selective enrich- ment and analysis of mosaic arg201 mutations in G alpha s from patients with fibrous dysplasia of bone [J]. Bone, 1997, 21(2): 201-206.
[7] Pollandt K, Engels C, Kaiser E, et al. Gsα gene mutations in monostotic fibrous dysplasia of bone and fibrous dysplasia- like low-grade central osteosarcoma [J]. Virchows Arch, 2001, 439(2): 170-175.
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[10] Weinstein LS, Shenker A, Gejman PV, et al. Activating mutations of the stimulatory G protein in the McCune- Albright syndrome [J]. N Engl J Med, 1991, 325(24): 1688- 1695.
[11] Bianco P, Kuznetsov SA, Riminucci M, et al. Reproduction of human fibrous dysplasia of bone in immunocompromised mice by transplanted mosaics of normal and Gsalpha- mutated skeletal progenitor cells [J]. Clin Invest, 1998, 101 (8): 1737-1744.
[12] Dal Cin P, Sciot R, Brys P, et al. Recurrent chromosome aberrations in fibrous dysplasia of the bone: a report of the CHAMP study group: chromosomes and morphology [J]. Cancer Genet Cytogenet, 2000, 122(1): 30-32.
[13] Riminucci M, Kuznetsov SA, Cherman N, et al. Osteoclasto- genesis in fibrous dysplasia of bone: in situ and in vitro analysis of IL-6 expression [J]. Bone, 2003, 33(3): 434-442.
[14] Riminucci M, Saggío I, Robey GP, et al. Fibrous dysplasia as a stem cell disease [J]. J Bone Miner Res, 2006, 21 Suppl 2: 125-131.
[15] Kumta SM, Huang L,Cheng YY, et al. Expression of VEGF and MMP-9 in giant cell tumor of bone and other osteolytic lesions [J]. Life Sci, 2003, 73(11): 1427-1436.
[16] Yasuoka T, Takagi N. Fibrous dysplasia in the maxilla: possible mechanism of bone remodeling by calcitonin treatment [J]. Oral Oncol, 2003, 39(39): 301-305.
[17] 赵继宗. 颅脑肿瘤外科学[M]. 北京:人民卫生出版社, 2003. 625-626.
[18] 王忠诚. 神经外科学[M]. 武汉:湖北科学技术出版社, 2008. 897.
[19] 方 燕,刘鹏程,高文清,等. 颅面骨骨纤维结构不良与骨 化性纤维瘤的CT鉴别[J]. 中国临床医学影像杂志, 2003,14(2):119-121.
[20] Hanifi B, Samil KS, Yasar C, et al. Craniofacial fibrous dys- plasia [J]. Clin Imaging, 2013, 37(6): 1109-1115.
[21] Chapurlat RD, Delmas PD, Liens D, et al. Long term effects of intravenous pamidronate in fibrous dysplasia of bone [J]. J Bone Miner Res, 1997, 12(2): 1746-1752.
[22] Lala R, Matarazzo P, Bertelloni S, et al. Pamidronste treat- ment of bone fibrous dysplasia in nice children with McCune-Albright syndrome [J]. Acta Paediatr, 2000, 89(2): 188-193.
[23] 傅继弟,赵景武,殷大力,等. 神经导航技术外科治疗颅骨 纤维异常增生[J]. 中华医学杂志,2004,84(10):808-812.
[24] Sammut SJ, Kandasamy J, Newman W, et al. Relief of severe retroorbital pain and vision improvement after optic nerve decompression in polyostotic fibrous dysplasia: case report and review of the literature [J]. Childs Nerv Syst, 2008, 24(4): 515-520.
[25] Tan YC, Yu CC, Chang CN, et al. Optic nerve compression in craniofacial fibrous dysplasia: the role and indications for decompression [J]. Plast Reconstr Surg, 2007, 120(7): 1957-1962.
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[27] 申璐敏,胡莹莹,李 鑫,等. 颅骨多发骨纤维异常增生症 1例报告及文献复习[M]. 中国口腔颌面外科杂志,2016, 14(4):381-384
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备注/Memo

备注/Memo:
(2020-04-26收稿,2020-05-23修回)通讯作者:张剑宁,E-mail:jnzhang2018@163.com
更新日期/Last Update: 2020-09-20