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基底细胞痣综合征的临床影像分析 被引量:1

Clinical Imaging Analysis of Basal Cell Nevus Syndrome
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摘要 基底细胞痣综合征(basal cell nevus syndrome,BCNS)又称痣样基底细胞癌综合征(nevoid basal cell carcinoma syndrome,NBCCS)或Gorlin-Goltz综合征(Gorlin-Goltz syndrome),是一种罕见的常染色体显性遗传性疾病,与人类同源PTCH基因和融合抑制子SUFU基因突变密切相关,偶有散发病例。基底细胞痣综合征累及人体多个系统,主要临床特征包括多种先天发育异常(如肋骨和脊柱发育异常、皮质骨缺损、颅内钙化、掌跖皮肤凹陷、唇腭裂等)和肿瘤易感性增加(如颌骨牙源性角化囊性瘤、多发基底细胞痣/癌和表皮囊肿、卵巢纤维瘤、髓母细胞瘤、胎儿横纹肌肉瘤等)[1]。
作者 吴晓蕾 律冉 Wu Xiaolei;Lu Ran(Department of Stomatology,Tongji Hospital,Tongji Medical College,Huaxhong University of Science and Technology,Wuhan 430030,China;Department of Rad iology,Tongji Hospital,Tongji Medical College,Huaxhong University of Science and Technology,Wuhan 430030,China;School of Stomatology,Tongji Medical College,Huazhong University of Science and Technology,Wuhan 430030,China)
出处 《华中科技大学学报(医学版)》 CAS CSCD 北大核心 2023年第3期388-392,共5页 Acta Medicinae Universitatis Scientiae et Technologiae Huazhong
基金 国家自然科学基金青年基金项目(No.81800981)。
关键词 基底细胞痣综合征 痣样基底细胞癌综合征 Gorlin-Goltz综合征 牙源性角化囊肿 影像学 nevoid basal cell carcinoma syndrome basal cell nevus syndrome Gorlin-Goltz syndrome odontogenic keratocyst imaging
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  • 1邱蔚六,吕燕,陈万涛.重视和加强对口腔遗传性疾病的研究[J].上海口腔医学,2005,14(3):205-209. 被引量:4
  • 2Koch CA, Chrousos GP, Chandra R, et al. Two-hit model for tumorigenesis of nevoid basal cell carcinoma (Gorlin) syndromeassociated hepatic mesenchymal tumor [J].Am J Med Genet,2002,109(1):74-76.
  • 3Reifenberger J, Arnold N, Kiechle M, et al. Coincident PTCH and BRCA1 gerrnline mutations in a patient with nevoid basal cell carcinoma syndrome and familial breast cancer [J].J Invest Dermatol,2001,116(3):472-474.
  • 4Boutet N, Bignon YJ, Drouin-Garraud V, et al. Spectrum of PTCH1 mutations in French patients with Gorlin Syndrome [J]. J Invest Dermatol,2003,121 (3):478-481.
  • 5Nagao K, Fujii K, Yamada M, et al. Identification of a novel polymorphism involving a CGG repeat in the PTCH gene and a genome-wide screening of CGG-containing genes[J].J Hum Genet,2004,49:97 - 101.
  • 6Cohen M. The Hedgehog signaling network[J]. Am J Med Genet,2003,123A:5 -28.
  • 7Savino M, dApolito M, Formica V, et al. Spectrum of PTCH mutations in Italian nevoid basal cell-carcinoma syndrome patients: identification of thirteen novel alleles [J].Hum Mutat,2004,24(5):441-447.
  • 8Zedan W, Robinson PA, High AS. A novel polymorphism in the PTC gene allows easy identification of allelic loss in basal cell nevus syndrome lesions[J]. Diagn Mol Pathol,2001,10(1):41-45.
  • 9Tate G, Li M, Suzuki T, et al. A new germline mutation of the PTCH gene in a Japanese patient with nevoid basal cell carcinoma syndrome associated with meningioma [J]. Jpn J Clin Oncol, 2003,33(1):47-50.
  • 10Zedan W, Robinson PA, Markham AF, et al. Expression of the Sonic Hedgehog receptor "PATCHED" in basal cell carcinomas and odontogenic keratocysts[J]. J Pathol,2001,194(4):473-477.

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