Skip Navigation
Skip to contents

JYMS : Journal of Yeungnam Medical Science

Indexed in: ESCI, Scopus, PubMed,
PubMed Central, CAS, DOAJ, KCI
FREE article processing charge
OPEN ACCESS
SEARCH
Search

Author index

Page Path
HOME > Browse Articles > Author index
Search
Han Won Jang 3 Articles
Bilateral Medial Medullary Infarction Demonstrated by Diffusion-Weighted Imaging: Case Report.
Han Won Jang, Woo Mok Byun
Yeungnam Univ J Med. 2009;26(1):70-73.   Published online June 30, 2009
DOI: https://doi.org/10.12701/yujm.2009.26.1.70
  • 1,402 View
  • 0 Download
  • 1 Crossref
AbstractAbstract PDF
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.

Citations

Citations to this article as recorded by  
  • 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-
Han Won Jang, Woo Mok Byun, Jae Kyo Lee, Jae Ho Cho, Kil Ho Cho, Mi Soo Hwang, Bok Hwan Park, Joon Hyuk Choi
Yeungnam Univ J Med. 2007;24(2 Suppl):S770-774.   Published online December 31, 2007
DOI: https://doi.org/10.12701/yujm.2007.24.2S.S770
  • 1,338 View
  • 1 Download
  • 4 Crossref
AbstractAbstract PDF
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.

Citations

Citations to this article as recorded by  
  • 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.
Han Won Jang, Woo Mok Byun, Kil Ho Cho, Mi Soo Hwang
Yeungnam Univ J Med. 1998;15(2):306-315.   Published online December 31, 1998
DOI: https://doi.org/10.12701/yujm.1998.15.2.306
  • 1,664 View
  • 16 Download
AbstractAbstract PDF
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.

JYMS : Journal of Yeungnam Medical Science