1.A Case of Kaposi's Varicelliform Eruption Occuring in Pemphigus Foliaceus.
Su Hee OH ; Jong Seok HWANG ; Sang Lip CHUNG
Korean Journal of Dermatology 1984;22(6):635-638
This report presents a case of a 17-year-old-girl who developed a, Kaposis varicelliforrn eruption(eczema herpeticum) during oral prednisolone therapy in order to control pemphigus foliaceus. Diagnosis was made by the history, clinical feature and histologic examination. Within 24 hours after the initiation of therapy with ribavirin(Viramid), new lesions had ceased to develop.
Diagnosis
;
Kaposi Varicelliform Eruption*
;
Pemphigus*
;
Prednisolone
2.Risk Factors Contributing to Extrauterine Growth Restriction in Very Low Birth Weight Infants
Neonatal Medicine 2024;31(2):31-37
Purpose:
Despite advances in neonatal care, extrauterine growth restriction (EUGR) remains common in preterm infants. This retrospective single-center study aimed to determine the incidence and risk factors of EUGR in very low birth weight (VLBW) infants.
Methods:
Data were collected concerning VLBW infants with gestational age (GA) <32 weeks between 2011 and 2020. EUGR was defined as a decline in weight z-score >1.2 from birth to discharge, using Fenton growth charts.
Results:
Among 331 eligible preterm infants, the prevalence of EUGR at discharge was 71.6%. Infants with EUGR had lower GA and birth weight than those without EUGR. They also underwent prolonged durations of parenteral nutrition, invasive ventilation, and hospitalization. Neonatal morbidities, such as bronchopulmonary dysplasia, patent ductus arteriosus, necrotizing enterocolitis, gastrointestinal surgery, sepsis, and parenteral nutrition-associated cholestasis were more prevalent in the EUGR group. Multivariate analysis identified lower GA and longer time to reach full enteral feeding as independent risk factors, whereas maternal use of antenatal steroids and history of gestational diabetes mellitus were independent protective factors for EUGR.
Conclusion
As VLBW infants are at a high risk of EUGR, continuous attention and efforts to achieve early full enteral nutrition are required to decrease the incidence of EUGR.
3.The Prevalence of Transfusion-Transmitted Virus Infection in Children.
Ju Young CHUNG ; Tae Hee HAN ; Eung Su HWANG
Korean Journal of Pediatrics 2004;47(2):183-186
PURPOSE: Transfusion-transmitted virus(TTV) is an newly described nonenveloped human virus, with a circular, negative stranded DNA genome. Although a high prevalence of TTV infection in the normal population has been demonstrated, there is a still possibility of association with hepatitis according to the genotype of TTV. The aim of this study is to investigate the prevalence of TTV infection in Korean children. METHODS: Nested polymerase chain reaction(PCR) using priner sets generated from the noncoding region(NCR) of the viral genome was done in 105 children without liver disease, aged 0-15 years. We performed a second set of PCR using N22 primer in 88 children after the first set of PCR. RESULTS: The TTV DNA was detectable in 36(34%) of 105 children without hepatitis by 5'NCR primer. The prevalence of TTV varied with age:<1 y,16%(4/25); 1-3 y, 44%(15/31); 4-6 y, 31%(5/ 16); 7-9 y, 25%(3/12); 10-15 y, 14%(3/21). By using N22 primers, the prevalence of TTV DNA in children without hepatitis was 11.3%(11/88):<1 y 8%(2/25); 1-3 y, 13.7%(4/29); 4-6 y, 6.2%(1/16); 7-9 y, 33.3%(2/6); 10-14 y, 8.2%(1/12). CONCLUSION: Our result showed a high prevalence of TTV infection, varying with age, in Korean children. Further evaluation of genotypes of TTV in patients with hepatitis and normal children is needed.
Child*
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DNA
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Genome
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Genome, Viral
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Genotype
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Hepatitis
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Humans
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Liver Diseases
;
Polymerase Chain Reaction
;
Prevalence*
;
Torque teno virus*
4.Esophageal reconstruction with isoperistaltic interposition of left colon.
Si Chan SUNG ; Si Young HAM ; Jong Su WOO ; Sam Ryul RYU ; Hwang Kiw CHUNG ; Soo Keun WANG
The Korean Journal of Thoracic and Cardiovascular Surgery 1991;24(9):895-902
No abstract available.
Colon*
5.Treatment of Obsessive Symptoms in Schizophrenic Patient with a Risperidone-Fluoxetine Combination.
Myong Su CHOI ; Sang Keun CHUNG ; Ik Keun HWANG
Korean Journal of Psychopharmacology 2002;13(1):62-67
Recent studies have reported that obsessive-compulsive (OC) symptoms are highly prevalent in schizophrenia, and schizophrenic patients with OC symptoms have a poorer clinical course compared to those without OC symptoms. In spite of many previous case reports, treatment of OC symptoms in schizophrenia has not been systematically studied. We report a patient with chronic schizophrenia who had obsessive symptoms such as bizarre, stereotyped behaviors. Treatment with olanzapine and risperidone, resulted in partial response for his psychotic symptoms, respectively. The obsessive symptoms, however, persisted and fluoxetine was added to the risperidone regimen. After 4 weeks of combination treatment, fluoxetine was titrated up to 80 mg/day and his obsessive symptoms became less in frequency and intensity. After 7 weeks on combination treatment of risperidone and fluoxetine, obsessive symptoms resulted in a significant reduction. On the 20 months of following, he remained in a recovered state and had been treated with risperidone 4 mg/day, and fluoxetine 20 mg/day.
Fluoxetine
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Humans
;
Risperidone
;
Schizophrenia
;
Stereotyped Behavior
6.The molecular pathophysiology of vascular anomalies: Genomic research
Jong Seong KIM ; Su-Kyeong HWANG ; Ho Yun CHUNG
Archives of Plastic Surgery 2020;47(3):203-208
Vascular anomalies are congenital localized abnormalities that result from improper development and maintenance of the vasculature. The lesions of vascular anomalies vary in location, type, and clinical severity of the phenotype, and the current treatment options are often unsatisfactory. Most vascular anomalies are sporadic, but patterns of inheritance have been noted in some cases, making genetic analysis relevant. Developments in the field of genomics, including next-generation sequencing, have provided novel insights into the genetic and molecular pathophysiological mechanisms underlying vascular anomalies. These insights may pave the way for new approaches to molecular diagnosis and potential disease-specific therapies. This article provides an introduction to genetic testing for vascular anomalies and presents a brief summary of the etiology and genetics of vascular anomalies.
7.Comparison of Lacrimal Scintigraphy and Contrast Dacryocystography in Epiphora.
Young Min HAN ; Ki Chul CHOI ; Chong Soo KIM ; Gyung Ho CHUNG ; Myung Hee SOHN ; Eui Il HWANG ; Su Hyun JEONG ; Chun Su RYU ; Hyo Suk AN
Journal of the Korean Radiological Society 1995;32(4):563-569
PURPOSE: Conventional contrast dacryocystography(C-DCG) has been used mainly for anatomical assessment of the lacrimal drainage apparatus, due to its limited information on the dynamics of the lacrimal system, and thus correlation role in epiphora. The purpose of study was to improve the diagnostic value in epiphora by utilizing RI dacryocystography(RI-DCG) with quantitative criteria. MATERIALS AND METHODS: The patient for RI dacryocystography set erect with the head fixed in front of gamma camera fitted with a standard 6 mm pinhole collimater. Both eyes of 85 patients(170 eyes) were scanned with 99rnTc-pertechnetate followed by conventional dacryocystography. The data from gamma camera were recorded simultaneously on a computer system for subsequent quantitative analysis. RESULTS: In 94 of 96 eyes without epiphora, RI-DCG was correlated with normal C-DCG and % of emptying was at least over 50%. In 58 of 74 eyes with epiphora, RI-DCG was correlated with abnormal C-DCG and % of emptying was at most below 50%. In 16 eyes with functional block, quantitative RI-DCG showed abnormal % of emptying. CONCLUSION: Nuclear DCG with quantitation had higher diagnostic yield in functional block and correlated higher with epiphora. Thus nuclear DCG with quantitation would be a valuable functional test after postprocedures such as dacryocystoplasty.
Computer Systems
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Drainage
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Gamma Cameras
;
Head
;
Humans
;
Lacrimal Apparatus Diseases*
;
Radionuclide Imaging*
8.Delayed-onset Wernicke Encephalopathy in a Patient with Gastrectomy.
Byung Su KIM ; Chi Hun KIM ; Woo Sub HWANG ; Chin Sang CHUNG ; Dae Won SEO
Journal of the Korean Neurological Association 2008;26(1):59-62
A 62-year-old man was transferred to our emergency room because of acute encephalopathy. He was a nondrinker with history of a gastrectomy nineteen years ago. Two weeks before his visit, he had experienced transient poor oral intake due to gastroesophageal reflux (GER). His brain MRI showed definite lesions compatible with Wernicke Encephalopathy (WE). A trivial event like GER can complicate the marginal equilibrium of thiamine and, after a long latent interval following a gastrectomy, may induce delayed-onset WE.
Brain
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Emergencies
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Gastrectomy
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Gastroesophageal Reflux
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Humans
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Middle Aged
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Thiamine
;
Wernicke Encephalopathy
9.A Case of Trichosporon beigelii Pneumonia in a Boy with Normal Immunological Status.
Hyun Hee KIM ; Hai Lee CHUNG ; Jin Bok HWANG ; Cheol Woo KO ; Si Eun LEE ; Su Jin LEE
Journal of the Korean Pediatric Society 2000;43(2):300-305
Invasive diseases caused by Trichosporon beigelii are rare, usually fatal, opportunistic infections that occur exclusively in immunocompromised patients. This fungus has been known to produce cutaneous involvement in immunocompetent hosts, and is rarely reported to cause systemic disease in patients with cardiac valve replacement. In this report, we described a case of invasive Trichosporon beigelii pneumonia in a 9-year-old boy who presented with persistent cough and dyspnea for 1 week. He showed no abnormality in immunologic function tests and had no predisposing factors. Trichosporon beigelii was isolated from the bronchoalveolar lavage culture.
Bronchoalveolar Lavage
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Causality
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Child
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Cough
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Dyspnea
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Fungi
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Heart Valves
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Humans
;
Immunocompromised Host
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Male*
;
Opportunistic Infections
;
Pneumonia*
;
Trichosporon*
10.Bypass of Superior Vena Cava with Spiral Vein Graft.
Su Hee HWANG ; Byoung Jun KIM ; Sung Woon CHUNG ; Jong Won KIM
The Korean Journal of Thoracic and Cardiovascular Surgery 1997;30(3):344-347
A 49-year-old female patient who had obstruction of superior vena cava(SVC) with SVC syndrome was successfully managed by bypass operation of superior vena cava with spiral vein graft. A composite spiral vein graft was placed between the right innominate vein and the right atrium to bypass the occluded SVC. The graft was constructed from the patient's own saphenous vein, which was split longitudinally and wrapped around a stent in spiral fashion and the edges of the vein were sutured together to form a large autogenous conduit. The patient was relieved of SVC obstructive symtoms and signs and discharged 21 days postoperatively without any complication.
Brachiocephalic Veins
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Female
;
Heart Atria
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Humans
;
Middle Aged
;
Saphenous Vein
;
Stents
;
Superior Vena Cava Syndrome
;
Transplants*
;
Veins*
;
Vena Cava, Superior*