Wallenberg syndrome caused by hemorrhage in medulla oblongata: a case report
Hong-Liang Zhang, Jiang Wu, Ping Liu, Jie Lei, Jia Liu
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DOI: 10.4236/health.2010.210180   PDF   HTML     6,955 Downloads   12,789 Views   Citations

Abstract

A previously healthy 19 year-old college student presented with abrupt onset of nausea, vomiting, dizziness and vertigo, and progressively worsened with hoarseness, and swallowing disturbance, imbalance, numbness of right face and left-side limbs and trunk. The diagnosis of Wallenberg syndrome was established by clinical manifestations and medullary hemorrhage by combination use of magnetic resonance imaging (MRI) with computed tomography (CT). Supportive treatment was given to the patient and there was considerable improvement in his neurologic status after 40 days treatment.

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Zhang, H. , Wu, J. , Liu, P. , Lei, J. and Liu, J. (2010) Wallenberg syndrome caused by hemorrhage in medulla oblongata: a case report. Health, 2, 1218-1220. doi: 10.4236/health.2010.210180.

Conflicts of Interest

The authors declare no conflicts of interest.

References

[1] Wallenberg, A. (1895) Akute bulb?raffektion (Embolie der arteria cerebelli post inf sinistra). Archives fur Psychiatry, 27(1), 504-540.
[2] Qiu, W., et al. (2009) Wallenberg syndrome caused by multiple sclerosis mimicking stroke. Journal of Clinical Neuroscience, 16(12), 1700-1702.
[3] Satoh, M., et al. (2005) Brain stem ischemia from intracranial dural arteriovenous fistula: Case report. Surgical Neurology, 64(4), 341-345.
[4] Nokura, K., et al. (2001) Intramedullary hemorrhage caused by arteriovenous malformation: a case of mixed lateral and medial medullary syndrome. Journal of Stroke and Cerebrovascular Diseases, 10(1), 30-33.

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