1.A Case of Sturge-Weber Syndrome.
Soo Young KIM ; Hyang Sook KIM ; Myung Sook KIM ; So Young PARK ; Dong Hak SHIN
Journal of the Korean Pediatric Society 1981;24(11):1111-1115
No abstract available.
Sturge-Weber Syndrome*
2.A Case of Sturge-Weber Syndrome.
Jin Soo JO ; Moon Chung CHAO ; Doo Seong MOON ; Kyung Sook CHO ; Chong Dae CHO
Journal of the Korean Pediatric Society 1986;29(4):103-108
No abstract available.
Sturge-Weber Syndrome*
3.A Case of Sturge-Weber Syndrome.
Jun Taek PARK ; Geom Hyun JANG ; Jae Kyu LEE ; Kyu Eun LEE ; Jung Hyup OH
Journal of the Korean Pediatric Society 1983;26(8):823-828
No abstract available.
Sturge-Weber Syndrome*
4.A case of neonatal Sturge-Weber syndrome.
Bei-yian ZHUO ; Guang-jin LU ; Zheng-zhi YE ; Yukun HAN
Chinese Journal of Pediatrics 2004;42(12):944-944
5.Sturge-Weber syndrome: report of a case.
Xue-qin CHEN ; Ni CHEN ; Xiao-jie WANG ; Ping HUA ; Ji-min GU ; Qiao ZHOU
Chinese Journal of Pathology 2006;35(8):503-504
6.A Case of Sturge-Weber Syndrome.
Won Hyuck LEE ; Suk Jun OH ; Hae Dong JHO ; Yung Rak YOO ; Nam Kyu KIM ; Hwan Yung CHUNG
Journal of Korean Neurosurgical Society 1983;12(4):715-719
Sturge-Weber syndrome was rare. But reported from 1860. We present a typical case of Sturge-Weber syndrome in a child and discussed the symptoms, signs, and pathological finding of various examinations in neurosurgical field such as plain x-ray, 4-vessel angiography, CT scan, EEG, IQ test, exophthamometry, opthalmometry, and fundoscopy. We find marked abnormality and asymmetry in that examination.
Angiography
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Child
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Electroencephalography
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Humans
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Sturge-Weber Syndrome*
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Tomography, X-Ray Computed
7.One case of Sturge-Weber syndrome.
Chinese Journal of Pediatrics 2003;41(9):705-705
8.Sturge-Weber syndrome: a case report and review of literatures.
Jing ZHOU ; Nan-yun LI ; Xiao-jun ZHOU ; Jian-dong WANG ; Heng-hui MA ; Ru-song ZHANG
Chinese Medical Journal 2010;123(1):117-121
Adult
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Female
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Humans
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Male
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Sturge-Weber Syndrome
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diagnosis
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pathology
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Young Adult
9.Serous Retinal Detachment Following Trabeculectomy in a Case of Sturge-Weber Syndrome with Glaucoma.
Ji Hong BAE ; Heyon Deuck CHO ; Sung Chil WOO
Journal of the Korean Ophthalmological Society 1996;37(12):2150-2153
A trabeculectomy with mitomycin (0.2mg/ml, 5 minutes) was performed in a 28-year-old man with glaucoma associated with Sturge-Weber syndrome. Two prophylactic posterior sclerotomies were made in an attempt to prevent sudden uveal effusion. The surgery was uncomplicated. On the first postoperative day, however, the anterior chamber became shallow with hypotony (<4mmHg). A 360 degrees choroidal detachment with serous retinal detachment encroaching upon macula was recognized. On the third postoperative day, evacuation of the suprachoroidal space was performed. However, the eye remained hypotonus and choroidal expansion with overlying retinal detachment occured again. The bleb decreased in size with time and the intraocular pressures(IOPs) rose gradually (10-14mmHg). The choroidal and retinal detachment resolved spontaneously with the increased IOP in 40 days. Twenty seven monthes after trabeculectomy, he has a small localized. bleb. The IOP is maintained in the high-teens(15-20mmHg) without any medication.
Adult
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Anterior Chamber
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Blister
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Choroid
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Glaucoma*
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Humans
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Mitomycin
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Retinal Detachment*
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Retinaldehyde*
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Sturge-Weber Syndrome*
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Trabeculectomy*
10.MR Findings of Sturge-Weber Syndrome : Emphasis on Vascular Abnormality.
Ho Kil BAEK ; Tae Yon NO ; Jong Bu WON ; Seung Kuk BAIK ; Mi Jeong SHIN ; Bong Ki KIM ; Han Yong CHOI
Journal of the Korean Radiological Society 1997;37(3):409-414
PURPOSE: To observe MR findings of vascular abnormality in Sturge-Weber syndrome and to determine the value of MRI in diagnosis. MATERIALS AND METHODS: Ten patients with Sturge-Weber syndrome (age : 3 months-32 years)were evaluated by MR imaging ; in six and four cases, respectively, the results were correlated with those of CT and angiography. We retrospectively analysed changes in the cortical vein and deep venous system, including the medullary and subependymal vein, as well as an largement of the choroid plexus, leptomeningeal enhancement, and changes in diploic space. RESULTS: In all cases except one, in which non-contrast enhanced study had been performed, varying degrees of leptomeningeal enhancement were seen. In nine cases the cortical vein became smaller; enlargement of the choroid plexus was seen in eight cases, change in the diploic space in seven (including three in which there was angiomatous involvement), and enlargement of the deep venous system in seven. In younger patients, collateral pathways were less developed and leptomeningeal angiomatous changes were more pronounced than in those who were older. CONCLUSION: MRI is a useful modality for the evaluationn of vascular changes in Sturge-Weber syndrome. These changes vary according to a patient's age and the duration of the disease.
Angiography
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Choroid Plexus
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Diagnosis
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Humans
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Magnetic Resonance Imaging
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Retrospective Studies
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Sturge-Weber Syndrome*
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Veins