線維性異形成症部に生じた下顎骨骨折の治療を行った1例
Fibrous dysplasia is a benign bone disease characterized by fibro-osseous lesions consisting of metaplastic fibrous tissue with immature bone remodeling. It is now thought to be caused by Gs α somatic mutation leading to abnormal development of the osteogenic mesenchymal tissue. In fibrous dysplasia...
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Published in | 日本口腔外科学会雑誌 Vol. 60; no. 4; pp. 209 - 213 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | Japanese |
Published |
社団法人 日本口腔外科学会
20.04.2014
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ISSN | 0021-5163 2186-1579 |
DOI | 10.5794/jjoms.60.209 |
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Abstract | Fibrous dysplasia is a benign bone disease characterized by fibro-osseous lesions consisting of metaplastic fibrous tissue with immature bone remodeling. It is now thought to be caused by Gs α somatic mutation leading to abnormal development of the osteogenic mesenchymal tissue. In fibrous dysplasia, a majority of fractures occur in femur and tibia, and mandibular fracture is extremely rare. We report a case of mandibular fracture in fibrous dysplasia arising in a 19-year-old man. The patient underwent open reduction and fixation of the mandibular fracture. He had a good functional occlusion after surgery. |
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AbstractList | Fibrous dysplasia is a benign bone disease characterized by fibro-osseous lesions consisting of metaplastic fibrous tissue with immature bone remodeling. It is now thought to be caused by Gs α somatic mutation leading to abnormal development of the osteogenic mesenchymal tissue. In fibrous dysplasia, a majority of fractures occur in femur and tibia, and mandibular fracture is extremely rare. We report a case of mandibular fracture in fibrous dysplasia arising in a 19-year-old man. The patient underwent open reduction and fixation of the mandibular fracture. He had a good functional occlusion after surgery. |
Author | 別所, 和久 北本, 幸恵 池野, 正幸 高橋, 克 三島, 清香 磯部, 悠 |
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References | 4) 坂本昭夫,岩本幸之:GNAS1遺伝子変異の有無による線維性異形成と骨線維性異形成の鑑別.骨・関節・靭帯 15: 65-68, 2002. 6) Rosai J and Ackerman L : Surgical Pathology, Ninth Edition, mosby Co, St. Louis, 2192-2194, 2004. 13) 古屋光太郎:Fibrous dysplasiaとその類似疾患.日整会誌 43: 151-174, 1969. 21) Robert PS, Ernesto I, et al : The surgical management of fibrous dysplasia of bone. Orphanet Journal of Rare Diseases 7, 2012. 17) 波利井清紀:形成外科ADVANCE シリーズI - 5 頭蓋顔面外科.最新の進歩.第2版, 克誠堂出版, 東京,2007, 297-406頁 9) Riminucci M, Robey PG, et al : Skeletal progenitors and the GNAS Gene:fibrous dysplasia of bone read throught stem cells. J Mol Endocrinol 45: 335-634, 2010. 1) Weinstein LS, Shenker A, et al : Activating Mutations of the Stimulatory G Protein in the McCune-Albright Syndrome. N Engl J Med 325: 1688-1695, 1991. 2) Cohen M and Howell R : Etiology of fibrous dysplasia and McCune-Albright syndrome. Int J Oral Maxillofac Surg 28: 366-371, 1999. 12) 林 輝嘉,赤松栄之,他:68歳女性で下顎骨線維性骨異形成症と診断された1例.日口診誌 23: 79-84, 2010. 16) Chen Y and Moordhoof M : Treatment of cranio maxilla facial fibous dysplasia : How early and how extensive?. Plast Reconstr Surg 86: 835-844, 1990. 20) Matthew R and William F : Fibrous Dysplasia. Pathophysiology, Evaluation, and Treatment. J Bone Joint Surg 87: 1848-1864, 2005. 22) Al-Mouazzen L, Rajakulendran K, et al : Fibrous dysplasia, shepherd's crook deformity and an intracapsular femoral neck fracture 8: 187-191, 2013. 24) 伊藤雄也,吉原愛雄,他:大腿骨頭下に病的骨折を生じたMc-Cune-Albright症候群の手術例.関東整災外会誌 41: 317-322, 2010. 3) Lichtenstein L : Polyostotic fibrous dysplasia. Arch Surg 36: 874-898, 1938. 23) 片桐 聡,熊本久大,他:大腿骨転子下骨折を伴い内反股が進行したMcCune-Albright症候群の一例. 昭和医会誌 69: 194-197, 2009. 15) Barnes L, Verbin R, et al : Disease of the bones and joints.Surgical pathology of head and neck, Mercel Dekker, New York-Basel 17: 920-926, 1985. 11) Sakata T, Takahashi K, et al : Repeated surgical reduction of the mandible over a 19-year period due to fibrous dysplasia : A case report.Asian Journal of Oral and Maxillofacial Surgery 22: 33-36, 2010. 8) Weinstein LS, Chen M, et al : Gs (alpha) mutations and imprinting defects in human disease. Ann NY Acad Sci 968: 173-197, 2002. 5) 山本威久,大薗恵一:Gs α遺伝子の活性型変異とMcCune-Albright症候群の骨病変.医学のあゆみ 192: 662-666, 2000. 18) Conejero J, Babbitt R, et al : Management of incidental fibrous dysplasia of the maxilla in a patient with facial fractures.J Craniofac Surg 18: 1463-1464, 2007. 19) Leet AI, Chebli C, et al : Fracture incidence in polyostotic fibro. J Bone Miner Res 19: 571-577, 2003. 7) Bianco P, Riminucci M, et al : Mutations of the GNAS1 Gene, Stromal Cell Dysfunction, and Osteomalacic Changes in Non-McCune-Albright Fibrous Dysplasia of Bone. J Bone Miner Res 15: 120-128, 2000. 10) 平田 功,別所和久,他:抗BMP-2抗体を用いて免疫組織化学的検索を行った線維性骨異形成症の1例.日口外誌 45: 712-714, 1999. 14) Jundt G : Fibrous dysplasia.In Barnes L, Eveson JW, eds; WHO Classification of Tumours. Pathology and Genetics of Head and Neck Tumours. IARC Press, Lyon, 2005, p321-322. |
References_xml | – reference: 14) Jundt G : Fibrous dysplasia.In Barnes L, Eveson JW, eds; WHO Classification of Tumours. Pathology and Genetics of Head and Neck Tumours. IARC Press, Lyon, 2005, p321-322. – reference: 19) Leet AI, Chebli C, et al : Fracture incidence in polyostotic fibro. J Bone Miner Res 19: 571-577, 2003. – reference: 18) Conejero J, Babbitt R, et al : Management of incidental fibrous dysplasia of the maxilla in a patient with facial fractures.J Craniofac Surg 18: 1463-1464, 2007. – reference: 16) Chen Y and Moordhoof M : Treatment of cranio maxilla facial fibous dysplasia : How early and how extensive?. Plast Reconstr Surg 86: 835-844, 1990. – reference: 1) Weinstein LS, Shenker A, et al : Activating Mutations of the Stimulatory G Protein in the McCune-Albright Syndrome. N Engl J Med 325: 1688-1695, 1991. – reference: 7) Bianco P, Riminucci M, et al : Mutations of the GNAS1 Gene, Stromal Cell Dysfunction, and Osteomalacic Changes in Non-McCune-Albright Fibrous Dysplasia of Bone. J Bone Miner Res 15: 120-128, 2000. – reference: 8) Weinstein LS, Chen M, et al : Gs (alpha) mutations and imprinting defects in human disease. Ann NY Acad Sci 968: 173-197, 2002. – reference: 4) 坂本昭夫,岩本幸之:GNAS1遺伝子変異の有無による線維性異形成と骨線維性異形成の鑑別.骨・関節・靭帯 15: 65-68, 2002. – reference: 6) Rosai J and Ackerman L : Surgical Pathology, Ninth Edition, mosby Co, St. Louis, 2192-2194, 2004. – reference: 10) 平田 功,別所和久,他:抗BMP-2抗体を用いて免疫組織化学的検索を行った線維性骨異形成症の1例.日口外誌 45: 712-714, 1999. – reference: 2) Cohen M and Howell R : Etiology of fibrous dysplasia and McCune-Albright syndrome. Int J Oral Maxillofac Surg 28: 366-371, 1999. – reference: 21) Robert PS, Ernesto I, et al : The surgical management of fibrous dysplasia of bone. Orphanet Journal of Rare Diseases 7, 2012. – reference: 11) Sakata T, Takahashi K, et al : Repeated surgical reduction of the mandible over a 19-year period due to fibrous dysplasia : A case report.Asian Journal of Oral and Maxillofacial Surgery 22: 33-36, 2010. – reference: 3) Lichtenstein L : Polyostotic fibrous dysplasia. Arch Surg 36: 874-898, 1938. – reference: 15) Barnes L, Verbin R, et al : Disease of the bones and joints.Surgical pathology of head and neck, Mercel Dekker, New York-Basel 17: 920-926, 1985. – reference: 17) 波利井清紀:形成外科ADVANCE シリーズI - 5 頭蓋顔面外科.最新の進歩.第2版, 克誠堂出版, 東京,2007, 297-406頁. – reference: 9) Riminucci M, Robey PG, et al : Skeletal progenitors and the GNAS Gene:fibrous dysplasia of bone read throught stem cells. J Mol Endocrinol 45: 335-634, 2010. – reference: 20) Matthew R and William F : Fibrous Dysplasia. Pathophysiology, Evaluation, and Treatment. J Bone Joint Surg 87: 1848-1864, 2005. – reference: 5) 山本威久,大薗恵一:Gs α遺伝子の活性型変異とMcCune-Albright症候群の骨病変.医学のあゆみ 192: 662-666, 2000. – reference: 24) 伊藤雄也,吉原愛雄,他:大腿骨頭下に病的骨折を生じたMc-Cune-Albright症候群の手術例.関東整災外会誌 41: 317-322, 2010. – reference: 12) 林 輝嘉,赤松栄之,他:68歳女性で下顎骨線維性骨異形成症と診断された1例.日口診誌 23: 79-84, 2010. – reference: 13) 古屋光太郎:Fibrous dysplasiaとその類似疾患.日整会誌 43: 151-174, 1969. – reference: 22) Al-Mouazzen L, Rajakulendran K, et al : Fibrous dysplasia, shepherd's crook deformity and an intracapsular femoral neck fracture 8: 187-191, 2013. – reference: 23) 片桐 聡,熊本久大,他:大腿骨転子下骨折を伴い内反股が進行したMcCune-Albright症候群の一例. 昭和医会誌 69: 194-197, 2009. |
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SubjectTerms | 線維性異形成症 骨折 |
Title | 線維性異形成症部に生じた下顎骨骨折の治療を行った1例 |
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