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CC BY-NC-ND 4.0 · Arq Neuropsiquiatr 2017; 75(12): 895
DOI: 10.1590/0004-282X20170154
Images in Neurology

Multiple sporadic cerebral cavernous malformations

Múltiplos cavernomas cerebrais esporádicos
Rodrigo Alencar e Silva
1   Hospital Monsenhor Walfredo Gurgel, Divisão de Neurologia, Natal RN, Brasil
,
Thadeu Alexandre Paulino de Souza
2   Hospital Monsenhor Walfredo Gurgel, Divisão de Radiologia, Natal RN, Brasil
,
Thiago Cardoso Vale
3   Universidade Federal de Juiz de Fora, Faculdade de Medicina, Hospital Universitário, Unidade de Distúrbios do Movimento, Serviço de Neurologia, Juiz de Fora MG, Brasil
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A 32-year-old previously healthy man presented with headache that progressively worsened during the day. He denied any previous history of headache and trauma. There was no family history of neurological diseases. Examination revealed nuchal rigidity. Cranial computed tomography disclosed a left frontal hemorrhage. Brain magnetic resonance imaging revealed multiple cerebral cavernous malformations (CCM). The patient received conservative treatment. Cerebral cavernous malformations are commonly described in the familial form and are frequently asymptomatic. When symptoms do occur, seizures are the most common followed by focal deficits and headache[1]. Several mutations in CCM genes have already been identified in patients with sporadic disease[2].

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Figure 1 Axial cranial CT scan: an oval-shaped hyperdense lesion in the left frontal lobe with perilesional vasogenic edema and a small focus of blood in the contralateral frontal lobe.
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Figure 2 Brain MRI in axial T1 (A), Axial-susceptibility-weighted (B) and multiplanar reconstruction (C) showing an heterogeneous lesion with a hyperintense signal associated with perilesional vasogenic edema suggestive of acute hematoma. Additionally, there are multiple nodules with hypointense signal throughout the parenchyma and a subarachnoid hemorrhage in the left Sylvian fissure.


Publikationsverlauf

Eingereicht: 25. Januar 2017

Angenommen: 05. September 2017

Artikel online veröffentlicht:
01. September 2023

© 2023. Academia Brasileira de Neurologia. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commecial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

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  • References

  • 1 Chahine LM, Berg MJ. Clinical reasoning: cerebral cavernous malformations. Neurology. 2009;73(9):e44-9. https://doi.org/10.1212/WNL.0b013e3181b59a5b
  • 2 Scimone C, Bramanti P, Alafaci C, Granata F, Piva F, Rinaldi C et al. Update on novel CCM gene mutations in patients with cerebral cavernous malformations. J Mol Neurosci. 2016;61(2):189-98. https://doi.org/10.1007/s12031-016-0863-z