A case of craniofacial fibrous dysplasia associated with McCune-Albright syndrome lost to follow-up.
作者信息
Williams Robert Gareth Michael
机构信息
Department of Oral and Maxillofacial, Aintree University Hospital, Liverpool, UK.
出版信息
BMJ Case Rep. 2015 Feb 26;2015:bcr2014209011. doi: 10.1136/bcr-2014-209011.
Abstract
McCune-Albright syndrome is a rare fibro-osseous syndrome characterised by a classic triad of fibrous dysplasia (FD), café-au-lait macules and various underlying endocrinopathies. This case report describes how a patient was rediagnosed by a general dental practitioner following attendance for a routine dental examination. The patient had been previously diagnosed with the condition 28 years earlier but no follow-up or monitoring of her condition had taken place. As a result, she was found to have several undiagnosed and untreated complications of the disease including FD of the mandible, optic neuropathy and potential thyroid involvement.
摘要
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引用本文的文献
1
Craniofacial fibrous dysplasia associated with McCune-Albright syndrome: challenges in diagnosis and treatment: case reports.
BMC Oral Health. 2019 Aug 8;19(1):180. doi: 10.1186/s12903-019-0872-8.
本文引用的文献
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