• Rev Assoc Med Bras (1992) · Oct 2020

    Case Reports

    Cerebellar infarction after sneezing.

    • Gustavo Bittencourt Camilo, Marco Antônio Riccio, Anna Luíza Machado Nogueira, Amanda Campos Querubino, Ana Luísa Dos Santos Maciel, Daniela Girardi Pereira Linhares Rodrigues, and Carlos Alberto Corrêa de Sá Júnior.
    • Departamento de Radiologia do Hospital e Maternidade Terezinha de Jesus - HMTJ e da Faculdade de Ciências Médicas e da Saúde de Juiz de Fora - SUPREMA, Juiz de Fora, MG, Brasil.
    • Rev Assoc Med Bras (1992). 2020 Oct 1; 66 (10): 1351-1354.

    AbstractVertebral Artery Dissection (VAD) is a rare condition that can be caused by a wide amplitude of neck movement, which injures the vessel wall and can cause ischemia in the cerebellum. We present a 37-year-old man with herniated lumbar disc and allergic rhinosinusitis, which caused sneezing spells. After one of these bouts with a ricochet of the head, he presented C3 misalignment with local pain. Twenty-one days later, affected by a new crisis, he presented left temporal headache, nystagmus, and vertigo. After 3 days, Magnetic Resonance Imaging (MRI) identified 2 regions of cerebellar ischemia and filling failure of the right vertebral artery. After 2 days, Computed Angiotomography (CT Angiography) was performed and showed right VAD with a local thrombus, without aneurysmal signs. Transcranial Doppler did not indicate an increase in blood flow from this artery. The suggested treatment involved administration of anticoagulant Apixabana 5mg, 12/12h, for 3 months, until the condition was reevaluated with new Angio CT and MRI. It was recommended that the patient was released from work for 1 month and forbidden from doing intense physical exercises for 3 months; however, due to setbacks, these deadlines were extended until a new appointment, 4 months after the first visit. The new tests showed no changes, indicating that the condition was stable. This case aims to indicate the possible investigations of the diagnosis and therapeutic options of the rare association between VAD with cerebellar infarction in a well-documented case.

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