1.The Clinical Observation in Kawasaik Disease.
Min Young PARK ; Gye Sik SHIN ; Sung Ho CHA ; Chang Il AHN
Journal of the Korean Pediatric Society 1994;37(2):167-173
One-hundred ninty five cases with Kawasaki disease who were diagnosed and treated at the Department of Pediatrics, Kyung Hee University Hospital from January 1985 to June 1993, were investigated for their clinical manifestations and laboratory findings, and cardiac complications. The results are as follows: 1) Most patients (92.8%) were under 5 years of the age. 2) Boys were more prevalent than girls, as a ratio of 2.3 : l 3) The incidence of principal symptoms and signs were fever over 5 days (89.8%), bilateral conjunctival injection (78.5%), changes of oral mucosa and lip (82.3%), skin eruption (72.8%), changes in extremities (58.5%), and cervical lymphadenopathy (47.2%). 4) The main laboratory findings observed were anemia (29.2%), leukocytosis (90.8%), thrombocytosis (89.7%), increased ESR (85.1%), positive CRP (100%), increased sGOT (33.3%), increased sGPT (34.9%), pyuria (41.5%), proteinuria (5.6%), microscopic hematuria (9.7%), and abnormalities of EKG (23.5%). 5) Abnormal findings of the heart were found in 27.2% by echocardiogram and coronary aneurysm and dilatation were present in 19.7%. 6) Among 147 cases assessed by echocardiogram, the abnormalities of coronary artery were present in 16 of 92 cases (17.4%) in the aspirin and intravenous gammaglobulin treated group, as compared with 13 of 55 cases (23.6%) in the aspirin treated group.
Alanine Transaminase
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Anemia
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Aspartate Aminotransferases
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Aspirin
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Coronary Aneurysm
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Coronary Vessels
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Dilatation
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Electrocardiography
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Extremities
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Female
;
Fever
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Heart
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Hematuria
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Humans
;
Incidence
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Leukocytosis
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Lip
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Lymphatic Diseases
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Mouth Mucosa
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Mucocutaneous Lymph Node Syndrome
;
Pediatrics
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Proteinuria
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Pyuria
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Skin
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Thrombocytosis
2.A Case of Dandy-Walker Syndrome Associated with Multiple Congenital Anomalies.
Gye Weon SHIN ; Chul Ho LEE ; Bo Kyung CHO ; Chung Sik CHUN ; Sung Hun CHO
Journal of the Korean Pediatric Society 1990;33(6):848-853
No abstract available.
Dandy-Walker Syndrome*
3.Manual Preparation of Donor Lenticule Using Artificial Anterior Chamber for Descemet's Membrane Stripping Endothelial Keratoplasty
Gye Jung KIM ; Min Chul SHIN ; Ho Sik HWANG
Journal of the Korean Ophthalmological Society 2020;61(2):209-213
PURPOSE: To report a patient with a pseudophakic bullous keratopathy (PBK) who underwent Descemet's membrane stripping endothelial keratoplasty (DSEK) with manual preparation of the donor corneal graft.CASE SUMMARY: A 61-year-old female presented with visual disturbance in her right eye. Five months prior, she was treated with phacoemulsification and intraocular lens exchange surgery of the right eye, and a very severe corneal edema was revealed by slit-lamp examination. We diagnosed PBK and planned DSEK with manual preparation of a donor corneal graft because of the non-availability of a microkeratome or a femtosecond laser. After making the corneal graft using an artificial anterior chamber, crescent knife and cornea dissector, the keratoplasty proceeded using the graft. Three months after surgery, her graft was well-maintained on the right eye. The patient's visual acuity was 0.3, and the corneal endothelial cell count was 1,844/mm².CONCLUSIONS: Manual preparation of the donor corneal graft for DSEK is suitable as a second choice treatment method when the availability of surgical devices is limited.
Anterior Chamber
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Cornea
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Corneal Edema
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Corneal Transplantation
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Descemet Membrane
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Endothelial Cells
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Female
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Humans
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Lenses, Intraocular
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Methods
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Middle Aged
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Phacoemulsification
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Tissue Donors
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Transplants
;
Visual Acuity
4.The Estimation of the Probable Cause and the Time of Cerebral Insult in Cerebral Palsy.
Jeong Lim MOON ; Young Wan MOON ; In Sik WHANG ; Joon Ho YEO ; Hyeon Bo SHIN ; Gye Yeon LIM
Journal of the Korean Academy of Rehabilitation Medicine 2002;26(5):508-513
OBJECTIVE: To estimate the probable cause and the time of cerebral insult in cerebral palsy (CP) based on MRI findings and risk factors. METHOD: The subjects comprised all sixty-seven patients with CP showing abnormal MRI findings between March 1999 and September 2001 at the Catholic University of Korea, St. Mary's Hospital. A detailed medical history was available for all patients including those not born in our hospital. They ranged in age from two months to five years. We analyzed the brain magnetic resonance (MR) findings of patients with CP to correlate the probable cause and the time of cerebral insult through the consideration of medical histories including prenatal, perinatal and postnatal histories. RESULTS: Of the 67 MRIs, abnormalities were the followings; periventricular leukomalacias (PVLs) in 49 cases, cortical or subcortical infarction in 4 cases, brain atrophy in 7 cases, neuronal migration disorder in 4 cases, and delayed myelination in 3 cases. Among the patients with PVL, perinatal risk factors were responsible for cerebral insult in preterm, but pre- and perinatal contribution were similar in patients born at full term. Among the patients with cerebral infarction, only one case with meningitis at 11 months was suspected for cerebral insult. These patients had no risk factor as a peri- or post-natal etiology. Four patients with neuronal migration disorder had no risk factor for peri- or postnatal etiology except for the one who was a twin. CONCLUSION: Review of brain MRI findings such as PVL, infarct, neuronal migration disorder and a detailed medical history including prenatal and perinatal etiology would be a useful method to estimate the probable cause and the time of cerebral insult in CP.
Atrophy
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Brain
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Cerebral Infarction
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Cerebral Palsy*
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Humans
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Infant, Newborn
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Korea
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Leukomalacia, Periventricular
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Magnetic Resonance Imaging
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Meningitis
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Myelin Sheath
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Neuronal Migration Disorders
;
Risk Factors
;
Twins
5.Clinical Features and Surgical Outcomes of Primary Rhegmatogenous Retinal Detachment according to Age.
Gye Jung KIM ; Min Chul SHIN ; Ho Sik HWANG ; So Young HAN ; Bum Joo CHO
Journal of the Korean Ophthalmological Society 2017;58(1):56-61
PURPOSE: To investigate the clinical features and surgical outcomes of rhegmatogenous retinal detachment (RRD) requiring surgery according to age. METHODS: Medical records of patients who underwent surgery for primary RRD between January 2008 and March 2016 were reviewed retrospectively. Patients were classified into two groups according to age at diagnosis: the under-40 group and the over-40 group. The two groups were compared in terms of demographic features, ocular manifestation, operating methods, primary anatomical success rate, and visual outcome. RESULTS: One hundred and forty-four eyes from 144 patients were included. Mean subject age was 48.6 ± 16.9 years old. The under-40 group involved 42 eyes from 42 patients, and the over-40 group included 102 eyes from 102 patients. Symptom duration was shorter in the under-40 group compared to the over-40 group (7.6 ± 10.7 days vs. 14.5 ± 24.4 days; p = 0.029). Proliferative vitreoretinopathy (PVR) occurred more frequently in the under-40 group (40.0% vs. 17.4%, p = 0.007) than in the over-40 group. The anatomical success rate of primary surgery was significantly different between the two groups; 78.6% in the under-40 group and 91.2% in the over-40 group (p = 0.038). Preoperative PVR increased the rate of anatomical failure (40.0% vs. 6.2%, p < 0.001). The visual outcomes were not significantly different between the two groups. CONCLUSIONS: RRD is combined with PVR more frequently in young patients than in old patients, which increases the failure rate of primary re-attachment surgery.
Diagnosis
;
Humans
;
Medical Records
;
Retinal Detachment*
;
Retinaldehyde*
;
Retrospective Studies
;
Scleral Buckling
;
Vitrectomy
;
Vitreoretinopathy, Proliferative