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McCune-Albright综合征伴甲状腺功能亢进1例报告及文献复习

McCune-Albright syndrome with hyperthyroidism: report of one case and review of literature
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摘要 Mc Cune-Albright综合征(MAS)是一种临床罕见的疾病,其典型三联征包括多骨性骨纤维异常增殖症、牛奶咖啡色斑及性早熟。本文报告1例伴有甲状腺功能亢进的Mc Cune-Albright综合征患者,并通过相关文献复习,阐述MAS的病因、临床表现、诊断及治疗等。 McCune-Albright Syndrome(MAS) is a rare disease characterized by triad of polyostotic fibrous dysplasia of bone(FD), precocious puberty, and café-au-lait skin pigmentation. This paper reported a case of McCune-Albright syndrome with hyperthyroidism, and discussed the pathogenesis, clinical manifestations, diagnosis and treatment of MAS.
作者 陈启铭 孟箭 CHEN Qi-ming;MENG Jian(Department of Stomatology,Central Hospital of Xuzhou City.Xuzhou 221009,Jiangsu Province,China)
出处 《上海口腔医学》 CAS CSCD 北大核心 2018年第4期445-448,共4页 Shanghai Journal of Stomatology
基金 江苏省卫生和计划生育委员会科研课题(H2017080) 徐州市科技项目(KC17196)
关键词 MCCUNE-ALBRIGHT综合征 甲状腺功能亢进 GNAS基因突变 McCune-Albright syndrome Hyperthyroidism GNAS mutation
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二级参考文献51

  • 1廖东.McCune-Albright综合征合并垂体肿瘤一例[J].中华儿科杂志,2005,43(3):224-225. 被引量:3
  • 2陈瑞敏,林祥泉,陈文茹.McCune-Albright Syndrome五例报道[J].中国优生与遗传杂志,2005,13(10):99-100. 被引量:5
  • 3梁立阳,孟哲,曾巧慧,李文益.McCune-Albright综合征[J].中国当代儿科杂志,2006,8(4):311-314. 被引量:14
  • 4Lumbroso S, Paris F, Sultan C, et al. Activating Gsα mutations: analysis of 113 patients with signs of McCune-Albright Syndrome-a European Collaborative Study[J]. J Clin Endocrinol Metab, 2004,89(5):2107-2113.
  • 5Alawi F.Benign fibro-osseous lesions of the maxillofacial bones:A review and differential diagnosis[J].Am J Clin Pathol,2002,118(Suppl 1):S50-S70.
  • 6Alsharif MJ,Sun ZJ,Chen XM,et al.Benign fibro-osseous lesions of the jaws:A study of 127 Chinese patients and review of the literature[J].Int J Surg Pathol,2009,17(2):122-134.
  • 7Nevilie BD,Damm DD,Allen CM,et al.Oral and Maxillofacial Pathology[M].2nd ed.Philadelphia:Saunders,2002:553-563.
  • 8Waldron CA.Fibro-osseous lesions of the jaws[J].J Oral Maxillofac Surg,1993,51(8):828-835.
  • 9Toyosawa S,Yuki M,Kishino M,et al.Ossifying fibroma vs fibrous dysplasia of the jaw:Molecular and immunological characterization[J].Mod Pathol,2007,20 (3):389-396.
  • 10Ringel MD,Schwindinger WF,Levine MA.Clinical implications of genetic defects in G proteins.The molecular basis of McCuneAlbright syndrome and Albright hereditary osteodystrophy[J].Medicine,1996,75(4):171-184.

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