Metaphyseal dysplasia associated with chronic facial nerve palsy

被引:1
|
作者
Christodoulou, Loucas [1 ]
Pavlidou, Efterpi [1 ]
Spyridou, Cristina [1 ]
Eccles, Simon [2 ]
Calder, Alistair [3 ]
Mankad, Kshitij [1 ,4 ]
Kinali, Maria [1 ]
机构
[1] Chelsea & Westminister Hosp, Pediat Neurol Dept, 369 Fulham Rd, London SW10 9NH, England
[2] Chelsea & Westminister Hosp, Dept Craniofacial Surg, London, England
[3] Great Ormond St Hosp Sick Children, Dept Radiol, London, England
[4] Chelsea & Westminister Hosp, Dept Radiol, London, England
关键词
Pyle disease; Metaphyseal dysplasia; Erlenmeyer flask sign; Facial nerve palsy; CRANIOMETAPHYSEAL DYSPLASIA; PYLE DISEASE;
D O I
10.1007/s00381-016-3021-6
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Metaphyseal dysplasia (Pyle disease) is a rare autosomal recessive disease with impressive and characteristic radiological findings but relatively mild clinical features. It is usually incidentally diagnosed, despite the impressive radiological findings of gross metaphyseal widening and thinning of cortical bone. Herein, we report an exceptionally unusual case of metaphyseal dysplasia in association with chronic facial nerve palsy. Chronic facial nerve palsy due to compression of the facial nerve in a patient with Pyle disease represents an unusual novelty. Furthermore, this case delineates the clinical spectrum and phenotype of such a rare clinical entity. To the best of our knowledge, this is the first time that such an association is being described.
引用
收藏
页码:1333 / 1336
页数:4
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