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Progressive facial hemiatrophy with multiple benign tumors and hamartomas.

作者信息

Derex L, Isnard H, Revol M

机构信息

Service d'Explorations Neurologiques, Centre Hospitalier Lyon-Sud, Pierre-Bénite, France.

出版信息

Neuropediatrics. 1995 Dec;26(6):306-9. doi: 10.1055/s-2007-979779.

DOI:10.1055/s-2007-979779
PMID:8719745
Abstract

We report the unusual association of Progressive Facial Hemiatrophy (Parry-Romberg syndrome) with multiple benign tumors (orbital neurinoma, mandibular odontogenous fibroma) and hamartomas. The neurological clinical features were infantile hemiplegia, mild mental retardation and focal seizures. Brain CT-scan and MRI showed porencephaly and cerebral calcifications ipsilateral to hemifacial atrophy. Immunological investigations proved negative. The etiology of the disease and the bridging of this case to phakomatoses are discussed.

摘要

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The central nervous system manifestations of localized craniofacial scleroderma: a study of 10 cases and literature review.
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BMC Ophthalmol. 2015 Sep 5;15:119. doi: 10.1186/s12886-015-0093-0.
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A significant proportion of children with morphea en coup de sabre and Parry-Romberg syndrome have neuroimaging findings.患有剑击状硬斑病和帕里-罗默伯格综合征的儿童中有很大一部分有神经影像学检查结果。
Pediatr Dermatol. 2012 Nov-Dec;29(6):738-48. doi: 10.1111/pde.12001.
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Case Rep Neurol. 2010 Jun 1;2(2):57-62. doi: 10.1159/000314927.
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Giant intracranial aneurysm in a ten-year-old boy with parry romberg syndrome. A case report and literature review.一名患有帕里-龙贝格综合征的10岁男孩的巨大颅内动脉瘤。病例报告及文献综述。
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Difficulties in differentiation of Parry-Romberg syndrome, unilateral facial sclerodermia, and Rasmussen syndrome.鉴别帕里-罗默伯格综合征、单侧面部硬皮病和拉斯穆森综合征的困难。
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