1.A Case of Child with Obstructive Sleep Apnea Syndrome Recurred after Adenotonsillectomy.
Curie KIM ; Dong Soon KIM ; Hyun Joo SEO ; Hong Beom SHIN ; Eui Joong KIM ; Hyun Joon SHIM ; Young Min AHN
Sleep Medicine and Psychophysiology 2008;15(2):94-99
The most common cause of obstructive sleep apnea syndrome (OSAS) in childhood is adenotonsillar hypertrophy. Adenotonsillectomy improves the symptoms quite well in most cases. However, some patients could experience the OSAS again after adenotonsillectomy, who might have several risk factors such as incomplete operation, misdiagnosis, combined anatomical malformation, sinusitis or chronic allergic rhinitis, obesity, initial severe OSAS, and early onset OSAS. We report a case of 11-year-old obese boy who presented with snoring for several years. He was obese with body mass index (BMI) of 26.3 kg/m2 and also found to have fatty liver by ultrasonogram. Initial polysomnography (PSG) showed that he met the criteria of severe OSAS with the apnea-hypopnea index (AHI) of 70.5. He underwent adenotonsillectomy and symptoms improved immediately. Four months later symptoms were relieved with AHI of 0, but 1 year after the adenotonsillectomy he started to complain snoring again and the subsequent PSG results showed that OSAS has relapsed with AHI of 43. Paranasal sinus X-ray and physical examination showed sinusitis and re-growth of adenoid. Obesity was proved not to be a contributing factor because his BMI decreased to normal range (23.1 kg/m2) after diet control and regular exercise. Also, liver transaminase was normalized and fatty liver was disappeared on follow-up abdominal ultrasonogram. After treatment of sinusitis, symptoms were relieved with decreased AHI (8.5). This case suggests that simple adenotonsillectomy might not be the end of OSAS treatment in childhood. Patients who had adenotonsillectomy should be followed by subsequent PSG if symptoms recur. It is also important to be aware of risk factors in the recurrent OSAS for the proper intervention according to the cause.
Adenoids
;
Body Mass Index
;
Child
;
Diagnostic Errors
;
Diet
;
Fatty Liver
;
Follow-Up Studies
;
Humans
;
Hypertrophy
;
Liver
;
Obesity
;
Physical Examination
;
Polysomnography
;
Reference Values
;
Rhinitis
;
Rhinitis, Allergic, Perennial
;
Risk Factors
;
Sinusitis
;
Sleep Apnea, Obstructive
;
Snoring
2.A Case of Constrictive Pericarditis due to Immunoglobulin G4-Related Disease.
Jiwon SEO ; In Ji SONG ; Sak LEE ; Hyeon Joo JEONG ; Hye Min KIM ; Beom Seok KOH ; Sung Ha PARK
Korean Circulation Journal 2015;45(2):161-164
Immunoglobulin G4-related disease (IgG4-RD) can involve any organ. The majority of reported cases involve IgG4-RD of the biliary tract or pancreas, while only two cases of pericarditis have been reported. A 58-year-old man visited the outpatient clinic of our institution with a seven-day history of progressive dyspnea. Based on his transthoracic echocardiogram and transesophageal echocardiogram, he was diagnosed with constrictive pericarditis. The histopathology of his pericardiectomy revealed the cause of constrictive pericarditis to be IgG4-RD. Prednisolone (40 mg) was initiated after the pericardiectomy. As the patient's symptoms resolved, he was discharged and followed-up on an outpatient basis. This is the first case report of constrictive pericarditis caused by IgG4-RD in Korea.
Ambulatory Care Facilities
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Biliary Tract
;
Dyspnea
;
Humans
;
Immunoglobulin G
;
Immunoglobulins*
;
Inflammation
;
Korea
;
Middle Aged
;
Outpatients
;
Pancreas
;
Pericardiectomy
;
Pericarditis
;
Pericarditis, Constrictive*
;
Prednisolone
3.Discrimination between obstructive sleep apnea syndrome and primary snoring in children : comparison of clinical parameters and behavioral disturbance.
Hyun Joo SEO ; Jae Suk LEE ; Hong Beom SHIN ; Eui Joong KIM ; Hyun Joon SHIM ; Young Min AHN
Korean Journal of Pediatrics 2008;51(3):267-275
PURPOSE: To determine whether primary snoring could be distinguished from obstructive sleep apnea syndrome (OSAS) by clinical evaluation and symptom scores. METHODS: 56 snoring and 20 asymptomatic subjects were recruited and polysomnography was used to confirm that there were 39 OSAS, 17 primary snoring, and 20 control subjects. We evaluated the size of the childrens adenoids and tonsils. Parents completed sleep disordered breathing scale (SDBS) and obstructive sleep apnea 18 (OSA-18) questionnaires for use as symptom scores, as well as an attention deficit hyperactivity disorder rating scale-IV (ADHD RS-IV). RESULTS: There were no differences between primary snoring and OSAS in terms of tonsil and adenoid size, SDBS (9.4+/-4.6 vs 10.8+/-4.5), and OSA-18 score (61.1+/-25.1 vs 71.2+/-8.4). The patients with OSAS (15.8+/-7.9) and PS (22.2+/-9.4) had a higher ADHD RS-IV score than the control subjects (2.9+/-3.3). There was no difference in the ADHD RS-IV scores of patients with primary snoring and OSAS. CONCLUSION: We confirmed that clinical evaluation could not distinguish OSAS and primary snoring. In addition, our study suggests that primary snoring as well as OSAS is associated with attention deficit hyperactivity disorder.
Adenoids
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Attention Deficit Disorder with Hyperactivity
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Child
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Discrimination (Psychology)
;
Humans
;
Palatine Tonsil
;
Parents
;
Polysomnography
;
Surveys and Questionnaires
;
Sleep Apnea Syndromes
;
Sleep Apnea, Obstructive
;
Snoring
4.Erratum: The biofilm removal effect of MnO2-diatom microbubbler fromthe dental prosthetic surfaces: In vitro study
Eun-Hyuk LEE ; Yongbeom SEO ; Ho‐Beom KWON ; Young‐Jun LIM ; Hyunjoon KONG ; Myung-Joo KIM
The Journal of Korean Academy of Prosthodontics 2020;58(2):176-
The article ‘The biofilm removal effect of MnO2-diatom microbubbler from the dental prosthetic surfaces: In vitro study’ authored by Eun-Hyuk Lee,Yongbeom Seo, Ho-Bum Kwon, Young-Jun Yim, Hyunjoon Kong, Myung-Joo Kim, published in April issue [Vol 58, No 1] of The Journal of KoreanAcademy of Prosthodontics (2020), has an erratum.The author names were mistakenly given as Ho-Bum Kwon, Young-Jun Yim. It should be corrected as Ho‐Beom Kwon, Young‐Jun Lim. The Journal ofKorean Academy of Prosthodontics apologizes to the readers for this error.
5.Association of Antipsychotic-Induced QTc Prolongation with 5-HTTLPR.
Beom Joo SEO ; Jung Goo RHEE ; Sung Woo PARK ; Bo Geum KONG ; Do Oun CHUNG ; Young Hoon KIM
Journal of the Korean Society of Biological Psychiatry 2004;11(1):49-53
OBJECTIVE: A Comparison of QTc prolongation for various antipsychotics and an analysis of QTc prolongation for the various types of serotonin transporter polymorphism were performed. METHOD: EKG was checked, followed by QTc measurement as Bazett's correction, and the serotonin transporter polymorphism was examined in 110 chronic schizophrenia patients were performed EKG before 24 weeks ago. We defiened QTc prolongation as over 450ms. The risk factor of sudden cardiac death were defiend as QTc prolongation and or 60ms in delta value. RESULT: The prevalence of QTc prolongation in this study was 7.3%, and the prevalence of over 60ms was 4.5%. Patients who had the risk factors were 10(9.1%). 6/52 who prescribed atypical antipsychotics and 2/58 who prescribed haloperidol showed QTc prolongation. The prevalence who had the risk factor of sudden cardiac death were 16% in atypical antipsychotics group, 3.4% in haloperidol group. QTc prolongation were observed more frequently in l/l type than s/s type. l allele frequency were 50% in QTc prolongated group, 19% in not prolongated group. l allele had an association with QTc prolongation(p<0.01). CONCLUSION: The prevalence of QTc prolongatin was frequent in chronic schizophrenia patients who were prescribed atypical antipsychotics. It has strong association with l allele of 5-HTTLPR.
Alleles
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Antipsychotic Agents
;
Death, Sudden, Cardiac
;
Electrocardiography
;
Gene Frequency
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Haloperidol
;
Humans
;
Prevalence
;
Risk Factors
;
Schizophrenia
;
Serotonin Plasma Membrane Transport Proteins
6.The Relationship between Language Ability and Cognitive Function in Patients with Schizophrenia.
Sung Jin KIM ; Joo Cheol SHIM ; Bo Geum KONG ; Je Wook KANG ; Jung Joon MOON ; Dong Wook JEON ; Sung Soo JUNG ; Beom Joo SEO ; Do Un JUNG
Clinical Psychopharmacology and Neuroscience 2015;13(3):288-295
OBJECTIVE: Cognitive dysfunction is common in people with schizophrenia, and language disability is one of the most notable cognitive deficits. This study assessed the use and comprehension ability of the Korean language in patients with schizophrenia and the correlations between language ability and cognitive function. METHODS: Eighty-six patients with schizophrenia and a group of 29 healthy controls were recruited. We assessed both clinical symptoms and cognitive functions including Korean language ability. For clinical symptoms, the Positive and Negative Syndrome Scale, Clinical Global Impression-Schizophrenia Scale, and Social and Occupational Functioning Assessment Scale were used. For the Korean language ability assessment, a portion of the Korean Broadcasting System (KBS) Korean Language Test was used. The Short-form of Korean-Wechsler Adult Intelligence Scale, the Korean version of the University of California San Diego (UCSD) Performance-based Skills Assessment (K-UPSA), and the Wisconsin Card Sorting Test (WCST) were used to assess cognitive functions. RESULTS: Schizophrenic patients had significantly lower scores in the language and cognitive function tests both in the total and subscale scores. Various clinical scores had negative correlations with reading comprehension ability of the KBS Korean Language Test. The WCST and a part of the K-UPSA had positive correlations with multiple domains of the language test. CONCLUSION: A significant difference was found between schizophrenic patients and controls in language ability. Correlations between Korean language ability and several clinical symptoms and cognitive functions were demonstrated in patients with schizophrenia. Tests of cognitive function had positive correlations with different aspects of language ability.
Adult
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California
;
Cognition
;
Comprehension
;
Humans
;
Intelligence
;
Language Tests
;
Language*
;
Schizophrenia*
;
Wisconsin
7.A case of mixed prolactin and growth hormone-secreting pituitary microadenoma presenting galactorrhea.
Myoung Beom KOH ; Jae Han PARK ; Yong Wan PARK ; Sang Ah CHANG ; Ki Ouk MIN ; Eun Joo SEO ; Ho Young SON
Korean Journal of Medicine 2003;64(6):690-694
We report a case of galactorrhea with acromegaly from the mixed prolactin and GH secreting pituitary microadenoma managed with a successful surgical complete removal. A 31-year-old woman visited our hospital complaining galactorrhea for more than 6 months after delivery. The physical findings of the patient were a prominent galactorrhea and mild acromegalic features of face and extremities. The laboratory findings of hematology and blood chemistry were normal. In addition, the basal levels of prolactin and GH were slightly elevated. The thyroid is in euthyroid state. The results of the combined anterior pituitary hormone-stimulation tests were that the prolactin and GH responses were stimulated exaggeratedly and the other hormonal ones were normal responses. The oral glucose loading test for acromegaly revealed non-responder results. The sellar MRI showed the 6 X 5 mm-sized pituitary microadenoma. She was operated for surgical removal of the lesions of which the immunohistochemistry findings were consistent with the positive findings for both prolactin and GH. She discharged without post-operative complication and has done well with normalized hormonal levels at outpatient department.
Acromegaly
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Adult
;
Chemistry
;
Extremities
;
Female
;
Galactorrhea*
;
Glucose
;
Hematology
;
Humans
;
Immunohistochemistry
;
Magnetic Resonance Imaging
;
Outpatients
;
Pituitary Neoplasms
;
Pregnancy
;
Prolactin*
;
Thyroid Gland
8.A Clinical Manifestation of Meckel's Diverticulum.
Jin Beom LEE ; Yong Soon LEE ; Eun Sun YOO ; Hae Soon KIM ; Se Jeong SON ; Eun Ae PARK ; Seung Joo LEE ; Sun Hee SUNG ; Jeong Wan SEO
Journal of the Korean Pediatric Society 2002;45(4):466-472
PURPOSE: The diagnosis of Meckel's diverticulum is difficult and delayed because it presents with various clinical symptoms. We evaluated clinical, imaging and pathologic findings of Meckel's diverticulum to facilitate detection of Meckel's diverticulum in children. METHODS: Review of clinical, imaging, surgical and pathological findings in 10 children aged 7 days to 14 years with Meckel's diverticulum during an 8-year period, 1993-2001, at Ewha Womans University Hospital was undertaken. RESULTS: The male to female ratio was 2.3 : 1. The chief complaint was painless lower gastrointestinal(GI) bleeding; others were abdominal pain, abdominal distention and vomiting, in order of frequency. The diagonsis before surgery were Meckel's diverticulum in 5 patients, non-reducible intussusception in 3 patients and intestinal obstruction in 2 patients. The diverticulum was located between 35 cm to 70 cm proximal to the ileocecal valve. The length of the diverticulum ranged from 4 cm to 12 cm and 80% of it was within 5 cm. A Meckel scan(99mTc-pertechnetate scintigraphy) after cimetidine administration was done in 6 cases. All 5 cases that presented with lower GI bleeding had ectopic gastric mucosa confirmed on pathology. Out of 5 cases of ectopic gastric mucosa, only 4 cases were positive on the Meckel's scan. CONCLUSION: In cases of unexplained GI bleeding, obstruction, or inflammation diagnostic workup should be carried out to rule out Meckel's diverticulum. Laparoscopy, high resolution ultrasonography and computed tomography of the abdomen may be indicated in the assessment of pediatric patient with lower GI bleeding, especially in patients with suspected bleeding from Meckel's diverticulum showing negative Meckel's scan.
Abdomen
;
Abdominal Pain
;
Child
;
Cimetidine
;
Diagnosis
;
Diverticulum
;
Female
;
Gastric Mucosa
;
Hemorrhage
;
Humans
;
Ileocecal Valve
;
Inflammation
;
Intestinal Obstruction
;
Intussusception
;
Laparoscopy
;
Male
;
Meckel Diverticulum*
;
Pathology
;
Ultrasonography
;
Vomiting
9.Genotype and Phenotype Analysis in Pediatric Patients with Cystinuria.
Ji Hyun KIM ; Eujin PARK ; Hye Sun HYUN ; Beom Hee LEE ; Gu Hwan KIM ; Joo Hoon LEE ; Young Seo PARK ; Hee Gyung KANG ; Il Soo HA ; Hae Il CHEONG
Journal of Korean Medical Science 2017;32(2):310-314
Cystinuria is an inherited disorder characterized by defective renal reabsorption of cystine and dibasic amino acids leading to nephrolithiasis. This study was conducted to analyze the genotypes and phenotypes of pediatric patients with cystinuria. Eight children from Seoul National University Hospital and Asan Medical Center presenting with cystinuria from January 2003 to June 2016 were retrospectively analyzed. Mutational studies were performed by direct sequencing. Two of the 8 were male and 6 were female. The median ages at onset and diagnosis were 1.5 (range, 0.3–13.6) and 2.6 (range, 0.7–16.7) years, respectively. The median followed up was 7.7 (range, 3.4–14.0) years. Mutational analyses were performed in 7 patients and revealed biallelic SLC3A1 mutations (AA genotype) in 4 patients, a single heterozygous SLC3A1 mutation (A- genotype) in 1 patient, biallelic SLC7A9 mutations (BB genotype) in 1 patient, and a single heterozygous SLC7A9 mutation (B- genotype) in 1 patient. Two of the mutations were novel. No genotype-phenotype correlations were observed, except for earlier onset age in patients with non-AA genotypes than in patients with the AA genotype. All patients suffered from recurrent attacks of symptomatic nephrolithiasis, which lead to urologic interventions. At the last follow-up, 3 patients had a mild-to-moderate degree of renal dysfunction. This is the first study of genotypic and phenotypic analyses of patients with cystinuria in Korea.
Age of Onset
;
Amino Acids, Diamino
;
Child
;
Chungcheongnam-do
;
Cystine
;
Cystinuria*
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Diagnosis
;
Female
;
Follow-Up Studies
;
Genetic Association Studies
;
Genotype*
;
Humans
;
Korea
;
Male
;
Nephrolithiasis
;
Phenotype*
;
Renal Reabsorption
;
Retrospective Studies
;
Seoul
10.Skill training in internal medicine student clerkship at a university hospital.
Wan Beom PARK ; Min HUR ; Ah Reum KIM ; Mi Sung SEO ; Joo Sung KIM ; Sung Tack KWON ; Yoon Seong LEE ; Jwa Seop SHIN
Korean Journal of Medicine 2009;76(4):451-458
BACKGROUND/AIMS: This study evaluated medical students' experience performing basic clinical skills with real patients in a tertiary hospital and their response to clinical skill training in the Skills Center during their clerkship in internal medicine. METHODS: We surveyed 169 third-year students at the end of the internal medicine clerkship. The questionnaire included questions on their experience sampling blood and inserting intravenous (IV) catheters with real patients, success with their first patient, and the usefulness of the Skills Center during the clinical clerkship. RESULTS: Of the 169 students, 145 (86%) answered the questionnaire. Two (5%) of 39 students had not sampled blood and 22 (56%) had not inserted an IV catheter during the 8 weeks of the internal medicine clerkship. Two (6%) of 35 students had not sampled blood and 8 (23%) had not inserted an IV catheter during 32 weeks of the 3rd-year clinical clerkships. The partial or complete success rate for performing the skills with real patients was 93% for blood sampling and 79% for IV catheter insertion. Ninety (62%) students stated that skill training in the Skills Center during the clinical clerkship improved their basic clinical skills and 62 (43%) agreed that it increased their confidence to perform those skills on real patients. CONCLUSIONS: A significant number of medical students do not experience basic clinical skills with real patients during the clinical clerkship in a university hospital, although they had relatively high success rates performing those skills.
Catheters
;
Clinical Clerkship
;
Clinical Competence
;
Humans
;
Internal Medicine
;
Students, Medical
;
Tertiary Care Centers
;
Surveys and Questionnaires