Literature DB >> 12661936

Encephalofacial angiomatosis sparing the occipital lobe and without facial nevus: on the spectrum of Sturge-Weber syndrome variants?

Anne M Comi1, Richard Fischer, Eric H Kossoff.   

Abstract

We report two cases of leptomeningeal angiomatosis in atypical frontoparietotemporal locations without an associated facial port-wine stain. Evidence of a leptomeningeal angioma was found in each when they were evaluated for headaches and seizures. The diagnosis of a leptomeningeal angioma was suggested by calcifications noted on computed tomographic scan of the head and confirmed with contrast-enhanced magnetic resonance images of the brain. We hypothesize that given the lack of occipital involvement with the angioma, and therefore the noncontiguous nature of this lesion with the developing upper facial ectoderm, the failure to develop a facial angioma would be expected. We found that the useof an anticonvulsant along with a migraine prophylactic medication appeared to have the greatest efficacy in these two cases, whereas anticonvulsants alone were less helpful. This diagnosis should be considered in any child presenting with seizures or complicated migraines and intracranial calcifications.

Entities:  

Mesh:

Year:  2003        PMID: 12661936     DOI: 10.1177/08830738030180010601

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  8 in total

1.  Sturge-Weber syndrome with an unusual onset in the sixth decade: a case report.

Authors:  L Ferrari; E Coppi; F Caso; R Santangelo; L S Politi; V Martinelli; G Comi; G Magnani
Journal:  Neurol Sci       Date:  2011-10-22       Impact factor: 3.307

Review 2.  Presentation, diagnosis, pathophysiology, and treatment of the neurological features of Sturge-Weber syndrome.

Authors:  Anne M Comi
Journal:  Neurologist       Date:  2011-07       Impact factor: 1.398

Review 3.  Multifocal arteriovenous malformations and facial nevus without leptomeningeal angioma: a variant form of Sturge-Weber syndrome? A case report and review of the literatures.

Authors:  In-Seok Bae; Hyeong-Joong Yi; Young Jun Lee
Journal:  Childs Nerv Syst       Date:  2012-09-30       Impact factor: 1.475

4.  Sturge-Weber Syndrome without Facial Nevus.

Authors:  Anuradha Ganesh; Abdullah Al-Mujaini
Journal:  Sultan Qaboos Univ Med J       Date:  2014-04-07

5.  Reliability and Clinical Correlation of Transcranial Doppler Ultrasound in Sturge-Weber Syndrome.

Authors:  Elizabeth A Offermann; Aditya Sreenivasan; M Robert DeJong; Doris D M Lin; Charles E McCulloch; Melissa G Chung; Anne M Comi
Journal:  Pediatr Neurol       Date:  2017-05-08       Impact factor: 3.372

Review 6.  Killing two birds with one stone: successful opioid monotherapy in intractable migraine-triggered epilepsy, a case series.

Authors:  Iraj Derakhshan
Journal:  Ther Adv Chronic Dis       Date:  2017-01-18       Impact factor: 5.091

7.  Study protocol: retrospectively mining multisite clinical data to presymptomatically predict seizure onset for individual patients with Sturge-Weber.

Authors:  Pooja Vedmurthy; Anna L R Pinto; Doris D M Lin; Anne M Comi; Yangming Ou
Journal:  BMJ Open       Date:  2022-02-04       Impact factor: 2.692

8.  Isolated leptomeningeal angiomatosis in the sixth decade of life, an adulthood variant of Sturge Weber Syndrome (Type III): role of advanced Magnetic Resonance Imaging and Digital Subtraction Angiography in diagnosis.

Authors:  Vetrivel Muralidharan; Gaetano Failla; Mario Travali; Tiziana Liliana Cavallaro; Marco Angelo Politi
Journal:  BMC Neurol       Date:  2020-10-06       Impact factor: 2.474

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.