Literature DB >> 14563334

Parry-Romberg syndrome: intracranial MRI appearances.

Sheree Bernadette Moko1, Yezdi Mistry, Tristan Maurice Blandin de Chalain.   

Abstract

AIM: To gain further insight into the pathogenesis of Parry-Romberg syndrome, a sporadic disease of unknown aetiology characterized by progressive wasting of one side of the face.
METHOD: Cranial MRI was performed in 10 patients with Parry-Romberg syndrome. The central nervous system findings are correlated to clinical findings and a review of the literature.
RESULTS: Three patients with a history of migraine had abnormal brain findings confined to the cerebral hemisphere ipsilateral to the facial hemiatrophy. Two patients without CNS symptoms had intracranial changes, one ipsilateral, the other both ipsilateral and contralateral to the facial hemiatrophy, on MRI. These changes consisted of either intracerebral atrophy or white matter hyperintensity. Five patients without CNS symptoms had no pathological intracranial MRI appearances.
CONCLUSION: A significant number of patients with Parry-Romberg syndrome may have underlying brain involvement. These findings are consistent with previous reports.

Entities:  

Mesh:

Year:  2003        PMID: 14563334     DOI: 10.1016/s1010-5182(03)00028-3

Source DB:  PubMed          Journal:  J Craniomaxillofac Surg        ISSN: 1010-5182            Impact factor:   2.078


  19 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.  Diffusion tensor imaging and fiber tractography in Parry-Romberg syndrome.

Authors:  W J Moon; H J Kim; H G Roh; J Oh; S H Han
Journal:  AJNR Am J Neuroradiol       Date:  2008-01-17       Impact factor: 3.825

3.  Parry-Romberg syndrome: conventional and advanced MRI follow-up in a boy.

Authors:  Paolo Rigamonti; Silvia Squarza; Marco Politi; Roberto Sangermani; Maurizio Cariati; Carla Uggetti
Journal:  Neuroradiol J       Date:  2017-03-01

Review 4.  Parry Romberg Syndrome: 7 Cases and Literature Review.

Authors:  M Wong; C D Phillips; M Hagiwara; D R Shatzkes
Journal:  AJNR Am J Neuroradiol       Date:  2015-06-11       Impact factor: 3.825

5.  Parry-Romberg syndrome with ipsilateral hemipons involvement presenting as monoplegic ataxia.

Authors:  Yun-Jin Lee; Kee-Yang Chung; Hoon-Chul Kang; Heung Dong Kim; Joon Soo Lee
Journal:  Korean J Pediatr       Date:  2015-09-21

6.  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

7.  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

Review 8.  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

9.  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

10.  A significant proportion of children with morphea en coup de sabre and Parry-Romberg syndrome have neuroimaging findings.

Authors:  Yvonne E Chiu; Sheetal Vora; Eun-Kyung M Kwon; Mohit Maheshwari
Journal:  Pediatr Dermatol       Date:  2012 Nov-Dec       Impact factor: 1.588

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