Literature DB >> 8141046

MR of brain involvement in progressive facial hemiatrophy (Romberg disease): reconsideration of a syndrome.

K Terstegge1, B Kunath, S Felber, J G Speciali, H Henkes, N Hosten.   

Abstract

PURPOSE: To gain further insight into the pathogenesis of progressive facial hemiatrophy, a sporadic disease of unclear etiology characterized by shrinking and deformation of one side of the face.
METHODS: We investigated possible brain involvement. MR of the head and face was performed in three female patients with progressive facial hemiatrophy. The central-nervous-system findings were correlated to a clinical protocol and a review of the literature.
RESULTS: One patient with epilepsy had abnormal brain findings confined to the cerebral hemisphere homolateral to the facial hemiatrophy. These consisted of monoventricular enlargement, meningocortical dysmorphia, and white-matter changes.
CONCLUSIONS: These MR findings, and corresponding neuroradiologic data disclosed by the review, indicate that homolateral hemiatrophy occasionally occurs in a subgroup of patients with progressive facial hemiatrophy. The MR features do not seem consistent with an underlying simple or nutritive atrophic process. We propose chronic localized meningoencephalitis with vascular involvement as a possible underlying cause of the occasional brain involvement in progressive facial hemiatrophy.

Entities:  

Mesh:

Year:  1994        PMID: 8141046      PMCID: PMC8332106     

Source DB:  PubMed          Journal:  AJNR Am J Neuroradiol        ISSN: 0195-6108            Impact factor:   3.825


  13 in total

1.  Parry-Romberg syndrome with a clinically silent white matter lesion.

Authors:  A Okumura; T Ikuta; T Tsuji; T Kato; H Fukatsu; S Naganawa; K Kato; K Watanabe
Journal:  AJNR Am J Neuroradiol       Date:  2006-09       Impact factor: 3.825

2.  Patient with Parry-Romberg syndrome complicated by Coats' syndrome.

Authors:  Dong Ho Park; In Taek Kim
Journal:  Jpn J Ophthalmol       Date:  2008-12-17       Impact factor: 2.447

3.  Hemifacial atrophy: a neurocutaneous disorder with coup de sabre deformity, telangiectatic naevus, aneurysmatic malformation of the internal carotid artery and crossed hemiatrophy.

Authors:  H Strenge; P Cordes; M Sticherling; J Brossmann
Journal:  J Neurol       Date:  1996-09       Impact factor: 4.849

4.  Frontal linear scleroderma en coup de sabre associated with epileptic seizure.

Authors:  Rahime Inci; Mehmet Fatih Inci; Fuat Ozkan; Perihan Oztürk
Journal:  BMJ Case Rep       Date:  2012-12-10

5.  Brain cavernomas associated with en coup de sabre linear scleroderma: Two case reports.

Authors:  Emily T Fain; Melissa Mannion; Elena Pope; Daniel W Young; Ronald M Laxer; Randy Q Cron
Journal:  Pediatr Rheumatol Online J       Date:  2011-07-29       Impact factor: 3.054

6.  Progressive hemifacial atrophy. A natural history study.

Authors:  M T Miller; M A Spencer
Journal:  Trans Am Ophthalmol Soc       Date:  1995

7.  Difficulties in differentiation of Parry-Romberg syndrome, unilateral facial sclerodermia, and Rasmussen syndrome.

Authors:  Justyna Paprocka; Ewa Jamroz; Dariusz Adamek; Elzbieta Marszal; Marek Mandera
Journal:  Childs Nerv Syst       Date:  2005-10-25       Impact factor: 1.475

8.  Parry-romberg syndrome: a rare entity.

Authors:  Hiren Patel; Chintan Thakkar; Kajal Patel
Journal:  J Maxillofac Oral Surg       Date:  2010-11-27

Review 9.  The central nervous system manifestations of localized craniofacial scleroderma: a study of 10 cases and literature review.

Authors:  Ezekiel Maloney; Sarah J Menashe; Ramesh S Iyer; Sarah Ringold; Amit K Chakraborty; Gisele E Ishak
Journal:  Pediatr Radiol       Date:  2018-07-03

10.  Giant intracranial aneurysm in a ten-year-old boy with parry romberg syndrome. A case report and literature review.

Authors:  T Bosman; J Van Bei Jnum; M A A Van Walderveen; P A Brouwer
Journal:  Interv Neuroradiol       Date:  2009-09-01       Impact factor: 1.610

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.