1.Delayed Non-arteritic Anterior Ischemic Optic Neuropathy Following Acute Primary Angle Closure.
Kyoung Nam KIM ; Chang Sik KIM ; Sung Bok LEE ; Yeon Hee LEE
Korean Journal of Ophthalmology 2015;29(3):209-211
No abstract available.
Female
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Glaucoma, Angle-Closure/complications/surgery
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Humans
;
Middle Aged
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Optic Neuropathy, Ischemic/complications/*diagnosis
2.Delayed Non-arteritic Anterior Ischemic Optic Neuropathy Following Acute Primary Angle Closure.
Kyoung Nam KIM ; Chang Sik KIM ; Sung Bok LEE ; Yeon Hee LEE
Korean Journal of Ophthalmology 2015;29(3):209-211
No abstract available.
Female
;
Glaucoma, Angle-Closure/complications/surgery
;
Humans
;
Middle Aged
;
Optic Neuropathy, Ischemic/complications/*diagnosis
3.RE: Diffusion MR Imaging of Postoperative Bilateral Acute Ischemic Optic Neuropathy.
Anusha KANNAN ; Sivasubramanian SRINIVASAN
Korean Journal of Radiology 2012;13(5):664-664
No abstract available.
Diffusion Magnetic Resonance Imaging/*methods
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Female
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Humans
;
Optic Neuropathy, Ischemic/*diagnosis
;
Postoperative Complications/*diagnosis
4.Anterior Ischemic Optic Neuropathy in a Patient with Churg-Strauss Syndrome.
Ji Eun LEE ; Seung Uk LEE ; Soo Young KIM ; Tae Won JANG ; Sang Joon LEE
Korean Journal of Ophthalmology 2012;26(6):469-472
We describe a patient with Churg-Strauss syndrome who developed unilateral anterior ischemic optic neuropathy. A 54-year-old man with a history of bronchial asthma, allergic rhinitis, and sinusitis presented with sudden decreased visual acuity in his right eye that had begun 2 weeks previously. The visual acuity of his right eye was 20 / 50. Ophthalmoscopic examination revealed a diffusely swollen right optic disc and splinter hemorrhages at its margin. Goldmann perimetry showed central scotomas in the right eye and fluorescein angiography showed remarkable hyperfluorescence of the right optic nerve head. Marked peripheral eosinphilia, extravascular eosinophils in a bronchial biopsy specimen, and an increased sedimentation rate supported the diagnosis of Churg-Strauss syndrome. Therapy with methylprednisolone corrected the laboratory abnormalities, improved clinical features, and preserved vision, except for the right central visual field defect. Early recognition of this systemic disease by ophthalmologists may help in preventing severe ocular complications.
Biopsy
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Churg-Strauss Syndrome/*complications/diagnosis
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Diagnosis, Differential
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Fluorescein Angiography
;
Fundus Oculi
;
Humans
;
Male
;
Middle Aged
;
Ophthalmoscopy
;
Optic Neuropathy, Ischemic/diagnosis/*etiology
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Visual Acuity
;
Visual Field Tests
5.Silent Giant Cell Arteritis in an Elderly Korean Woman.
Dong Min CHA ; Taeseung LEE ; Gheeyoung CHOE ; Hee Kyung YANG ; Jeong Min HWANG
Korean Journal of Ophthalmology 2013;27(3):224-227
Giant cell arteritis (GCA) is a rare disease among Asians. Arteritic anterior ischemic optic neuropathy, which accompanies GCA, has not yet been reported in Koreans. Diagnosis of GCA is difficult if typical symptoms other than visual loss are absent. Here, we report a case of an 83-year-old Korean woman presenting with sudden visual loss in both eyes (oculus uterque, OU). Her visual acuities included perception of light in the right eye (oculus dexter, OD) and perception of hand motion in the left eye (oculus sinister, OS). The results of the Hardy-Rand-Rittler test and Ishihara test showed total dyschromatopsia OU. The Goldmann perimetry test revealed a total field defect OD and paracentral island OS. Fundus examination revealed chalky-white disc swelling OU. Other systemic symptoms and signs were unremarkable. The erythrocyte sedimentation rate, C-reactive protein and platelet count were highly elevated. Temporal artery biopsy revealed multiple lymphocytes and multinucleated giant cells in the arterial media layer. To our knowledge, this is the first report of GCA in a Korean that has been confirmed with temporal artery biopsy. In conclusion, silent GCA can occur in Koreans, and hence, elderly patients presenting with chalky-white disc swelling, and corresponding laboratory findings must be evaluated for GCA.
Aged, 80 and over
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*Asian Continental Ancestry Group
;
Female
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Giant Cell Arteritis/complications/*diagnosis
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Humans
;
Optic Neuropathy, Ischemic/*diagnosis/etiology
;
Vision Disorders/*diagnosis/etiology
6.Diffusion MR Imaging of Postoperative Bilateral Acute Ischemic Optic Neuropathy.
Ju Young PARK ; In Ho LEE ; Chang June SONG ; Hee Youn HWANG
Korean Journal of Radiology 2012;13(2):237-239
A 57-year-old woman experienced bilateral acute ischemic optic neuropathy after spine surgery. Routine MR imaging sequence, T2-weighted image, showed subtle high signal intensity on bilateral optic nerves. A contrast-enhanced T1 weighted image showed enhancement along the bilateral optic nerve sheath. Moreover, diffusion-weighted image (DWI) and an apparent diffusion coefficient map showed markedly restricted diffusion on bilateral optic nerves. Although MR findings of T2-weighted and contrast enhanced T1-weighted images may be nonspecific, the DWI finding of cytotoxic edema of bilateral optic nerves will be helpful for the diagnosis of acute ischemic optic neuropathy after spine surgery.
Contrast Media/diagnostic use
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Diffusion Magnetic Resonance Imaging/*methods
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Female
;
Humans
;
Intervertebral Disc Displacement/surgery
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Middle Aged
;
Optic Neuropathy, Ischemic/*diagnosis
;
Postoperative Complications/*diagnosis
;
Spinal Stenosis/surgery
7.Arteritic Anterior Ischemic Optic Neuropathy Associated with Giant Cell Arteritis in an Elderly Korean Man.
Yeon Soo KANG ; Sang Woo PARK ; Ho Kyun LEE ; Yoo Duk CHOI ; Hwan HEO
Korean Journal of Ophthalmology 2016;30(3):239-241
No abstract available.
Aged
;
Giant Cell Arteritis/*complications/diagnosis
;
Humans
;
Male
;
Optic Neuropathy, Ischemic/diagnosis/*etiology
;
Republic of Korea
;
Temporal Arteries/diagnostic imaging
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Ultrasonography
;
*Visual Acuity
8.A Case of Odontogenic Orbital Cellulitis Causing Blindness by Severe Tension Orbit.
Chang Hyun PARK ; Dong Hyun JEE ; Tae Yoon LA
Journal of Korean Medical Science 2013;28(2):340-343
We report a very rare case of odontogenic orbital cellulitis causing blindness by severe tension orbit. A 41-yr old male patient had visited the hospital due to severe periorbital swelling and nasal stuffiness while he was treated for a periodontal abscess. He was diagnosed with odontogenic sinusitis and orbital cellulitis, and treated with antibiotics. The symptoms were aggravated and emergency sinus drainage was performed. On the next day, a sudden decrease in vision occurred with findings of ischemic optic neuropathy and central retinal artery occlusion. Deformation of the eyeball posterior pole into a cone shape was found from the orbital CT. A high-dose steroid was administered immediately resulting in improvements of periorbital swelling, but the patient's vision had not recovered. Odontogenic orbital cellulitis is relatively rare, but can cause blindness via rapidly progressing tension orbit. Therefore even the simplest of dental problems requires careful attention.
Adult
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Anti-Bacterial Agents/adverse effects/therapeutic use
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Blindness/*diagnosis/etiology
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Drainage
;
Fluorescein Angiography
;
Humans
;
Male
;
Optic Neuropathy, Ischemic/complications
;
Orbit/*physiopathology
;
Orbital Cellulitis/*diagnosis
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Retinal Artery Occlusion/complications
;
Sinusitis/diagnosis/drug therapy
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Tomography, X-Ray Computed
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Tooth Root