2.A Case of Microscopic Polyangiitis with Acute Myocardial Infarction.
Kyeong Han YOON ; Dae Hwan KIM ; Kyeong Han YOON ; Eun So LEE ; You Chan KIM
Annals of Dermatology 2002;14(3):181-185
Microscopic polyangiitis is a systemic small-vessel vasculitis, which may involve multiple organs, but cardiac involvement is relatively rare. We report a case of microscopic polyangiitis with multiple organ involvement, in which myocardial infarction was the early manifestation of the disease. A 53-year-old man presented with sudden papulovesicular eruptions and swellings on the face, posterior neck, dorsa of both hands and fingers, and with diffuse erythematous patches on the back. He had suffered from renal dysfunction, arthralgia, and hypertension for more than 8 years. He had been admitted to the department of cardiology for acute myocardial infarction and had suffered from recurrent gastrointestinal bleeding, renal failure, acute pancreatitis and sepsis during the admission. Histopathologically, small-vessel leukocytoclastic vasculitis with out granuloma was seen. Direct immunofluorescence showed no immune deposite. A high serum level of P-ANCA was detected by ELISA.
Acute Kidney Injury
;
Antibodies, Antineutrophil Cytoplasmic
;
Arthralgia
;
Cardiology
;
Enzyme-Linked Immunosorbent Assay
;
Fingers
;
Fluorescent Antibody Technique, Direct
;
Granuloma
;
Hand
;
Hemorrhage
;
Humans
;
Hypertension
;
Microscopic Polyangiitis*
;
Middle Aged
;
Myocardial Infarction*
;
Neck
;
Pancreatitis
;
Sepsis
;
Vasculitis
3.Keratosis Lichenoides Chronica with Pachyonychia Congenita-like Nail Changes.
Myung Soo CHA ; Kyeong Han YOON ; Soo Chan KIM
Annals of Dermatology 1996;8(2):164-167
A 26-year-old man presented with a 7-month history of hyperkeratotic skin lesions on both elbows and heels. He also had marked subungal hyperkeratosis and splinter hemorrhage on the finger and toe nails. A biopsy specimen from the elbow revealed lichenoid re-actions with areas of epidermal atrophy with alternating acanthosis and foci of parakeratosis. We made a diagnosis of keratosis lichenoides chronica based on the characteristic clinicopathologic findings. We have treated the patient with etretinate, but only the skin lesions on the elbows and heels responded to treatment.
Acitretin
;
Adult
;
Atrophy
;
Biopsy
;
Diagnosis
;
Elbow
;
Etretinate
;
Fingers
;
Heel
;
Hemorrhage
;
Humans
;
Keratosis*
;
Nails, Malformed*
;
Parakeratosis
;
Skin
;
Toes
4.Mammaplasty by the periareolar "round block" technique.
Kyeong Sook CHO ; Chin Ho YOON ; Han Joong KIM
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1993;20(5):1064-1071
No abstract available.
Female
;
Mammaplasty*
5.Molecular Typing of the Methicillin-Resistant Determinant (mec) and Coagulase Typing as Epidemiologic Markers for Study of Nosocomial Infections Caused by Methicillin-Resistant Staphylococcus aureus.
Jung Man KIM ; A Seong KIM ; Kyeong Hee KIM ; Tae Gyeom KIM ; Jin Yeong HAN ; In Hoo KIM
Korean Journal of Clinical Pathology 1997;17(4):588-597
BACKGROUND: Methicillin-resistant Staphylococcus aureus(MRSA) is an increasingly common cause of nosocomial infections worldwide. Epidemiologic investigation of MRSA outbreaks and identification of pathways of nosocomial MRSA spread require the ability to distinguish individual MRSA strains. We applied molecular tap ing of the methicillin-resistant determinant (mec) and coagulase typing in the investigation of a nosocomial MRSA infections. METHODS: We randomly selected 79 strains of mecA positive MRSA isolated from patients who visited Dong-A university Hospital from Dec. 1995 to Oct. 1996. Molecular typing of MRSA was performed by comparing the size of the mac-associated hypervariable region amplified by the polymerase chain reaction (PCR). Coagulase typing with type I-VIII antisera was also used for classification of MRSA based on its phenotype. Each isolates were classified by the combination of molecular analyses and coagulase type. RESULTS: The 79 MRSA isolates were grouped Into sin hypervariable legion (HVR) genotypes on the basis of the size of the PGR products. In coagulase typing, the most predominant type was II(46.8%) and type V was not found. Nine strains were not typable. The combination of HVR genotypes and coagulase types showed 23 different types in 79 MRSA Isolates. The strains which were repeatedly isolated from the same patients showed the same HYR genotypes and coagulate types. CONCLUSION: The combination of HVR genotypes and coagulase types is thought to be useful in epidemiolgical Investigation of nosocomial infections caused by MRSA ,because of its simplicity and reproducibility.
Classification
;
Coagulase*
;
Cross Infection*
;
Disease Outbreaks
;
Genotype
;
Humans
;
Immune Sera
;
Methicillin Resistance*
;
Methicillin-Resistant Staphylococcus aureus*
;
Molecular Typing*
;
Phenotype
;
Polymerase Chain Reaction
;
Staphylococcus
6.Identification of an i(21q) by Using Dinucleotide Repeat Polymorphisms.
Kyeong Hee KIM ; Tae Gyeom KIM ; Jin Yeong HAN ; Jung Man KIM ; Joo In PARK ; In Hoo KIM
Korean Journal of Clinical Pathology 1997;17(1):183-189
BACKGROUND: Recent DNA polymorphism analysis using numerous DNA markers has been used to determine the parental origin of the extra chromosome 21 in Down syndrome. In this study we used seven dinucleotide repeat polymorphisms on chromosome 21 to characterize a case of rea(21q21q) and to know whether it is consistent with an isochromosome or a true Robertsonian translocation. METHODS: Cytogenetic investigation was done by conventional G banding DNA was extracted from whole blood of a proband and her parents and was amplified by PCR using seven sets of (GT)n repeat dinucleotide markers located on the long arm of chromosome 21 After electrophoresis of the PCR product in polyacrylamide gel and silver staining the parental origin and number of DNA copy were determined by visual comparison of the band intensities within and between individuals. RESULTS: Conventional cytogenetics showed that the proband had a 46.XX.re(21q21q) chromosome pattern. Parental chromosome studies were normal, therefore, the rearrangement was a de novo event. All seven DNA markers showed one or two alleles, demonstrating rea(21q21q) to be an isochromosome. For D21S215 and D21S156 markers both parents were heterozygous and the proband inherited one copy of paternal allele and two copies of maternal allele which both parents did not share. This finding was consistent with a maternally derided isochromosome. CONCLUSION: Use of dinucleotide repeat DNA polymorphisms after PCR amplification will be very useful to detect the parental origin of additional chromosome 21 or rearrangement of chromosome 21 in Down syndrome. Besides employing siltier staining of a PCR product we will be able to avoid using of radioisotopes and apply to clinical laboratory diagnosis.
Alleles
;
Arm
;
Chromosomes, Human, Pair 21
;
Clinical Laboratory Techniques
;
Cytogenetics
;
Dinucleotide Repeats*
;
DNA
;
Down Syndrome
;
Electrophoresis
;
Genetic Markers
;
Humans
;
Isochromosomes
;
Parents
;
Polymerase Chain Reaction
;
Radioisotopes
;
Silver Staining
7.General Anesthesia for Patient with Broncho-gastric Fistula: A case report.
Kyeong Ah KIM ; Sang Wook HAN ; Chang Weon KIM ; Il Yeong JUNG ; Ho Jo JANG
Korean Journal of Anesthesiology 1997;33(5):988-992
Broncho-gastric fistula caused by benign gastric ulcer perforation after esophagectomy is very rare. In general anesthesia of a patient with broncho-gastric fistula, in spite of hyperventilation, leakage of the anesthetic gases through fistula may make the patient hypercapneic, and positive pressure ventilation may increase the risk of the pulmanary aspiration by the regurgitation of gastric fluid by stomach distension. For that reason, in this patient, denitrogenation was performed during patient's voluntary respiration with 100% oxygen for 5 minutes, and induction was performed without positive pressure ventilation, and one lung ventilation was carried out. Hypoxemia was followed by one lung ventilation because his pulmonary function was moderate obstructive type and his lung was damaged by aspiration of gastric fluid via broncho-gastric fistula. A low level of continuous positive airway pressure (CPAP) has no significant hemodynamic effect and can maintain the patency of nonventilated lung, so hypoxemia induced by one lung ventilation may be reduced. Thus we carried out one lung ventilation with CPAP (10 cmH2O) in nonventilated lung and blocked broncho-gastric fistula with a bronchial blocker for prevention of both regurgitation of gastric fluid and leakage of anesthetic gases. One lung anesthesia was performed without any problem in this case.
Anesthesia
;
Anesthesia, General*
;
Anesthetics, Inhalation
;
Anoxia
;
Continuous Positive Airway Pressure
;
Esophagectomy
;
Fistula*
;
Hemodynamics
;
Humans
;
Hyperventilation
;
Lung
;
One-Lung Ventilation
;
Oxygen
;
Positive-Pressure Respiration
;
Respiration
;
Stomach
;
Stomach Ulcer
8.A Case of 9p-Syndrome due to a Balanced Maternal Translocation t(9;16) (p22;p13.2).
Kyeong Hee KIM ; Sang Dong SIN ; Jin Yeong HAN ; Jung Man KIM ; Lisa G SHAFFER
Korean Journal of Clinical Pathology 1997;17(4):676-680
The deletion 9p syndrome is a well characterized syndrome with about one hundred cases having been reported. Most patients have dysmorphic facial features, cardiac anomalies, and mental retardation. We report on a female infant with micrognathia, corneal opacity, cleft palace, cardiac anomaly, left polycystic kidney, and deletion 9p. Chromosome analysis and fluorescence in situ hybridization (FISH) showed her to have a derived chromosome 9 inherited from a maternal t(9;16) (p22;p13.2) by adjacent I segregation There are few reports of this particular chromosome rearrangement. We review deletion Sp syndrome.
Chromosomes, Human, Pair 9
;
Corneal Opacity
;
Female
;
Fluorescence
;
Humans
;
In Situ Hybridization
;
Infant
;
Intellectual Disability
;
Polycystic Kidney Diseases
9.A Case of Group 0 without Anti-B.
Jung Man KIM ; Kyou Sup HAN ; Ah Seong KIM ; Kyeong Hi KIM ; Jae Ho WEE ; Jin Yeong HAN
Korean Journal of Blood Transfusion 1995;6(1):63-67
An ABO discrepancy was encountered in a 29-year-old woman with a pregnancy of 36 weeks. The patient's red cell was typed as group O and her serum had only anti-A antibody. Absence of B antigen on patient's RBC was confirmed by adsorption-elution test, B substance was not demonstrated in the saliva and serum. B-transferase activity was not detected in the serum. Patient's serum Ig level was within normal range. The patient's father and son had normal O phenotype and no additional abnormalities were detected among the family members studied.
Adult
;
Fathers
;
Female
;
Humans
;
Phenotype
;
Pregnancy
;
Reference Values
;
Saliva
10.Two Cases of Bullous Pemphigoid Showing the Characteristics of Herpes Gestationis Autoantibodies.
Kyeong Han YOON ; Mi Ra YOON ; Il Joo LEE ; Soo Chan KIM
Korean Journal of Dermatology 1998;36(3):451-455
Bullous pemphigoid(BP) and herpes gestationis(HG) are subepidermal bullous diseases which show clinical and immunological similarities. Both diseases show immune deposits along the basement membrane zone and their autoantibodies bind a common antigenic site within the non-collagenous stretch of the 180 kDa BPAG2 ectodomain. Besides its association with pregnancy, HG has some characteristic features that distinguish it from BP. The serum of patients with HG often contains an IgG that avidly fixes complement, and showes IgG1 subclass predominance. We report here two cases of non-pregnant young women presenting clinical and histological features of bullous pemphigoid or herpes gestationis. The immunopathology, IgG subtyping and immunoblotting studies showed that the autoantibodies in the patients were the characteristic ones of herpes gestationis. The patients might be a subtype of BP that have characteristics of autoantibodies of HG patients.
Autoantibodies*
;
Basement Membrane
;
Complement System Proteins
;
Female
;
Humans
;
Immunoblotting
;
Immunoglobulin G
;
Pemphigoid Gestationis*
;
Pemphigoid, Bullous*
;
Pregnancy