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与McCune-Albright综合征相关的上颌骨纤维性发育不良。病例报告。

Maxillary fibrous dysplasia associated with McCune-Albright syndrome. A case study.

作者信息

Wójcik Sylwia, Koszowski Rafał, Drozdowska Bogna, Śmieszek-Wilczewska Joanna, Raczkowska-Siostrzonek Agnieszka

机构信息

Chair of Dental Surgery, Department of Cranio-Maxillofacial Surgery and Oral Surgery, School of Medicine with the Division of Dentistry in Zabrze, Medical University of Silesia in Katowice, Poland.

Chair of Pathomorphology, Medical University of Silesia in Katowice, Poland.

出版信息

Open Med (Wars). 2016 Nov 16;11(1):465-470. doi: 10.1515/med-2016-0082. eCollection 2016.

Abstract

McCune Albright syndrome (MCA) is a rare complication of genetic origin. The authors present a case study of a patient with MCA diagnosed with multifocal fibrous dysplasia in his limb and craniofacial bones. The symptoms of the disease in the patient's facial and oral tissue and the treatment administered have been described.

摘要

McCune-Albright综合征(MCA)是一种罕见的遗传性并发症。作者介绍了一例被诊断为四肢及颅面骨多灶性纤维发育不良的MCA患者的病例研究。描述了该患者面部和口腔组织的疾病症状及所采取的治疗措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f577/5329869/77ccd2e22f17/j_med-2016-0082_fig_001.jpg

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