斜坡及枕骨多发纤维结构不良1例并文献复习
Multiple Fibrous Dysplasia of the Clivus and Occipital Bone: A Case Report and Literature Review
DOI: 10.12677/ACM.2022.122116, PDF,   
作者: 刘文卿*, 辛 涛#:山东大学附属山东省千佛山医院神经外科,山东 济南;丁 锋:山东第一医科大学附属省立医院神经外科,山东 济南
关键词: 多发纤维结构不良颅骨诊断治疗Multiple Fibrous Dysplasia Occipital Bone Diagnosis Treatment
摘要: 颅骨纤维结构不良(Fibrous dysplasia, FD)又称骨纤维异常增殖症,是一类罕见的良性骨病,多发于四肢长骨、肋骨及上颌骨,其临床症状多变,多与颅骨病变位置相关。对于其治疗应结合病变特点及临床表现实行个体化方案。本文报告本院收住的1例斜坡、枕骨多发纤维结构不良并Chairi畸形病例,参考国内外文献,分析此类病例的临床表现、影像学特点、治疗方式及管理。
Abstract: Fibrous dysplasia (FD) is a rare benign bone disease. It mostly occurs in long bones of limbs, ribs and maxilla. Its clinical symptoms are changeable and mostly related to the location of skull lesions. The treatment should be individualized according to the characteristics and clinical manifestations of the disease. This paper reports a case of multiple fibrous dysplasia of clivus and occipital bone with chairi malformation in our hospital. Referring to the literature at home and abroad, this paper analyzes the clinical manifestations, imaging characteristics, treatment and management of this kind of case.
文章引用:刘文卿, 丁锋, 辛涛. 斜坡及枕骨多发纤维结构不良1例并文献复习[J]. 临床医学进展, 2022, 12(2): 798-803. https://doi.org/10.12677/ACM.2022.122116

参考文献

[1] Valentini, V., Cassoni, A., Terenzi, V., et al. (2017) Our Experience in the Surgical Management of Craniofacial Fibrous Dysplasia: What Has Changed in the Last 10 Years? Acta Otorhinolaryngologica Italica, 37, 436-443. [Google Scholar] [CrossRef
[2] Lee, J.S., Fitzgibbon, E.J., Chen, Y.R., et al. (2012) Clinical Guidelines for the Management of Craniofacial Fibrous Dysplasia. Orphanet Journal of Rare Diseases, 7, Article No. S2. [Google Scholar] [CrossRef
[3] Chanson, P., Salenave, S. and Orcel, P. (2007) McCune-Albright Syndrome in Adulthood. Pediatric Endocrinology Reviews: PER, 4, 453-462.
[4] 汤其华, 张剑宁. 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, 25(9): 639-641. [Google Scholar] [CrossRef
[5] Zreik, R.T., Littrell, L.A., Jin, L., et al. (2017) Malignant Transformation of Polyostotic Fibrous Dysplasia with Aberrant Keratin Expression. Human Pathology, 62, 170-174. [Google Scholar] [CrossRef] [PubMed]
[6] Li, Z., Raynald, Wang, Z., et al. (2020) Malignant Transformation of Craniofacial Fibrous Dysplasia: A Systematic Review of Overall Survival. Neurosurgical Review, 43, 911-921. [Google Scholar] [CrossRef] [PubMed]
[7] Glorieux, F.H. and Rauch, F. (2006) Medical Therapy of Children with Fibrous Dysplasia. Journal of Bone and Mineral Research, 21, 110-113. [Google Scholar] [CrossRef] [PubMed]
[8] Yap, F.H.X., Amanuel, B., Van Vliet, C., et al. (2021) Malignant Transformation of Fibrous Dysplasia into Osteosarcoma Confirmed with TP53 Somatic Mutation and Mutational Analysis of GNAS Gene. Pathology, 53, 652-654. [Google Scholar] [CrossRef] [PubMed]
[9] 王忠, 冯勇, 张晓军, 张仲. 颅骨纤维结构不良合并多发脑膜瘤1例并文献复习[J]. 临床神经外科杂志, 2013, 10(5): 289-290.
[10] Pan, K.S., Heiss, J.D., Brown, S.M., et al. (2018) Chiari I Malformation and Basilar Invagination in Fibrous Dysplasia: Prevalence, Mechanisms, and Clinical Implications. Journal of Bone and Mineral Research, 33, 1990-1998. [Google Scholar] [CrossRef] [PubMed]
[11] Chen, Y.R., Wong, F.H., Hsueh, C., et al. (2002) Computed Tomography Characteristics of Non-Syndromic Craniofacial Fibrous Dysplasia. Chang Gung Medical Journal, 25, 1-8.
[12] 蔡明俊, 舒凯, 郭东生, 雷霆, 李龄. 颅骨骨纤维结构不良的诊断和治疗[J]. 中国临床神经外科杂志, 2009, 14(3): 137-139.
[13] Heman-Ackah, S.E., Boyer, H. and Odland, R. (2014) Clival Fibrous Dysplasia: Case Series and Review of the Literature. Ear, Nose, & Throat Journal, 93, E4-E9. [Google Scholar] [CrossRef] [PubMed]
[14] 吕新文, 张鹏, 宋建荣, 周小龙, 朱峰, 蔡珂, 张超, 何蓓. 手术治疗颅骨纤维异常增生症1例报告[J]. 中华神经外科疾病研究杂志, 2017, 16(6): 562-564.