- Bilateral Medial Medullary Infarction Demonstrated by Diffusion-Weighted Imaging: Case Report.
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Han Won Jang, Woo Mok Byun
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Yeungnam Univ J Med. 2009;26(1):70-73. Published online June 30, 2009
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DOI: https://doi.org/10.12701/yujm.2009.26.1.70
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- A 78-year-old woman presented with weakness of the extremities, dysarthria, dizziness, and sensory impairment. Magnetic resonance imaging showed acute bilateral medial medullary infarction. Contrast enhanced magnetic resonance angiography demonstrated stenosis or occlusion of both intracranial vertebral arteries. We present a rare case of bilateral medullary infarction seen on diffusion-weighted imaging.
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- Bilateral Medial Medullary Infarction (Dejerene Syndrome) Patient Suffering from Quadriplegia Treated by Korean Traditional Medicine: a Case Report
Yoo-na Lee, Yu-min An, Kyungmin Baek, Woo-seok Jang The Journal of Internal Korean Medicine.2020; 41(5): 902. CrossRef
- Supratentorial Leptomeningeal Hemangioblstoma -Case Report-
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Han Won Jang, Woo Mok Byun, Jae Kyo Lee, Jae Ho Cho, Kil Ho Cho, Mi Soo Hwang, Bok Hwan Park, Joon Hyuk Choi
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Yeungnam Univ J Med. 2007;24(2 Suppl):S770-774. Published online December 31, 2007
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DOI: https://doi.org/10.12701/yujm.2007.24.2S.S770
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- Hemangioblastoma is a benign tumor that most commonly occurs in the cerebellum and associated with von Hippel-Lindau (VHL) disease. Supratentorial hemanigoblastomas are exceptionally rare. We describe the magnetic resonance imaging (MRI) and histopathologic findings of a supratentorial leptomeningeal hemangioblastoma.
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- Sporadic supratentorial hemangioblastoma with meningeal affection: A case report and literature review
Juan Francisco Sánchez-Ortega, Marta Claramonte, Mónica Martín, Juan Calatayud-Pérez Surgical Neurology International.2021; 12: 394. CrossRef - Supratentorial hemangioblastomas in von Hippel–Lindau wild-type patients – case series and literature review
Luís Rocha, Carolina Noronha, Ricardo Taipa, Joaquim Reis, Mário Gomes, Ernesto Carvalho International Journal of Neuroscience.2018; 128(3): 295. CrossRef - Meningeal Supratentorial Hemangioblastoma in a Patient with Von Hippel-Lindau Disease Mimicking Angioblastic Menigioma
Hoon Kim, Ik-Seong Park, Kwang Wook Jo Journal of Korean Neurosurgical Society.2013; 54(5): 415. CrossRef - Supratentorial hemangioblastoma: clinical features, prognosis, and predictive value of location for von Hippel-Lindau disease
S. A. Mills, M. C. Oh, M. J. Rutkowski, M. E. Sughrue, I. J. Barani, A. T. Parsa Neuro-Oncology.2012; 14(8): 1097. CrossRef
- MRI Findings of Neuro-Behcet' Disease.
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Han Won Jang, Woo Mok Byun, Kil Ho Cho, Mi Soo Hwang
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Yeungnam Univ J Med. 1998;15(2):306-315. Published online December 31, 1998
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DOI: https://doi.org/10.12701/yujm.1998.15.2.306
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- MR findings in nine patients(three female, six male) with neuroBehcet's disease were retrospectively analyzed. NeuroBehcet's disease was diagnosed on the basis of typical clinical symptoms. Involved site, pattern, signal intensity, and contrast enhancement pattern on MRI were evaluated. In addition, follow up MR imaging was performed in four patients. The midbrain(7/9), internal capsule(7/9), pons(6/9), thalamus(6/9), basal ganglia(5/9), middle cerebella peduncle(4/9), medulla oblongata(2/9), and subcortical white matter(2/9) are involved on MRI. The size of lesions were 1cm to 3cm and their margin was ill-defined and patchy. Inhomogeneous high signal intensity on the T2-weighted images and low signal intensity on T1-weighted images was seen respectvely. In four of nine cases, there was focal enhancement. On follow up MR imaging, improvement or recurrance of the lesions was found. Also in two cases of follow up cases there was artophy in brainstem and/or middle cerebellar peduncles. In conclusion, MR imaging with systemic clinical symptoms is useful for diagnosing neuro-Behcet's disease.
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