Imaging of advanced craniofacial fibrous dysplasia associated with McCune-Albright syndrome: A case report
نویسندگان
چکیده
منابع مشابه
A case of craniofacial fibrous dysplasia associated with McCune-Albright syndrome lost to follow-up.
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 ea...
متن کاملMcCune-Albright syndrome: Report of a case
A 29- year old female with bone pain and history of precocious puberty was referred for bone scintigraphy. On physical examination café au lait macular spots were noted on her neck, buttocks and left leg. Bone scan showed multiple areas of intense increased activity which was in favour of polyostotic fibrous dysplasia. Considering the presence of polyostotic fibrous...
متن کامل[A case of fibrous dysplasia (McCune Albright syndrome) associated with acromegaly].
We report a case of a 47-year-old woman with McCune-Albright syndrome associated with unusual growth-hormone and prolactin hypersecretion. Acromegaly was suspected on clinical examination, and she was referred to us. She had no history of precocious puberty or pathological fracture. She was 154cm tall, weighing 62kg with so-called acromegalic facies. There were two lumps, one of which was on he...
متن کاملMaxillary fibrous dysplasia associated with McCune-Albright syndrome. A case study
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.
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ژورنال
عنوان ژورنال: European Journal of Radiology Open
سال: 2020
ISSN: 2352-0477
DOI: 10.1016/j.ejro.2019.12.002