1.A Case of Fetal Supraventricular Tachycardia with Fetal Ascites Treated by Antiarrhythmic Agent.
Byoung Shick SHIN ; Yong CHO ; Eu Sun RO ; Dong Ook LEE ; Ki Suk MUN
Korean Journal of Obstetrics and Gynecology 2004;47(9):1794-1799
We experienced a case of fetal supraventricular tachycardia (SVT) with fetal ascites diagnosed at 29 weeks of gestation in 29 year-old primigravida woman. Transplacental fetal therapy with maternal oral antiarrhythmic agent (verapamil, diltiazem) resulted in restoration of normal fetal sinus rhythm and disappearance of fetal ascites. At birth, the infant did not show any cardiac arrhythmia and hydropic appearance.
Adult
;
Arrhythmias, Cardiac
;
Ascites*
;
Diltiazem
;
Female
;
Fetal Therapies
;
Humans
;
Hydrops Fetalis
;
Infant
;
Parturition
;
Pregnancy
;
Tachycardia, Supraventricular*
;
Verapamil
2.A Case of Immature Teratoma of the Ovary with Gliomatosis Peritonei.
Kyoung Hyun CHO ; Oh Sung CHOI ; Byoung Shick SHIN ; Dong Ook LEE ; Sung Won LEE ; Yong CHO ; Eu Sun RO ; Young Hee CHOI
Korean Journal of Obstetrics and Gynecology 2003;46(12):2496-2501
Immature teratoma is composed of varying quantities of immature differentiating among anyone or all three germ layer. The pure immature teratoma accounts for fewer than 1% of all ovarian cancer, but it is the second most common germ cell malignancy. About 50% of pure immature teratomas of the ovary occur in women between the ages of 10 and 20 years, and they rarely occur in postmenopausal women. The most frequent site of dissemination is the peritoneum, and much less commonly, the retroperitoneal lymph node. Among the tumors with embryonal elements, those containing neural tissues demonstrate most clearly the importance of the ability to mature. Gliomatosis peritonei is the most dramatic demonstration of the significance of maturation, because most patients with these tumors have survived, even with this disseminated disease. The purpose of this paper is to report on a immature ovarian teratoma with predominantly mature glial tissues in peritoneum which we have experienced in this hospital recently with brief review of the literature.
Female
;
Germ Cells
;
Germ Layers
;
Humans
;
Lymph Nodes
;
Ovarian Neoplasms
;
Ovary*
;
Peritoneum
;
Teratoma*
3.A Case of Edward Syndrome.
Yeon Hwa LA ; Byoung Shick SHIN ; Young Hwa PARK ; Hyung Yong KEUM ; Zong Chul KIM ; Dong Ook LEE ; Woo Chuel JUNG ; Sung Won LEE ; Yong CHO ; Eu Sun RO
Korean Journal of Obstetrics and Gynecology 2001;44(11):2155-2160
Trisomy 18, called Edward syndrome, occurs in about 3500-8000 births. It is much more common at conception, with about 95% of cases resulting in spontaneous abortion or stillbirth. Postnatal survival is poor, with the majority of patients dying in early infancy. Characteristic findings include cardiac malformations, mental retardation, growth retardation, a prominent occiput, micrognathia, clenched hands, and rocker-bottom feet, omphalocele. The prenatal sonographic findings of our case include delayed growth, omphalocele, wrist joint fixation, choroid plexus cyst, hydramnios and postnatal gross findings include growth retardation, omphalocele, wirst joint fixation, absence of radius, syndactyly, focal absence of phalanges and flexion deformities of fingers and toes. We report a case of prenatally diagnosed Edward syndrome, which is confirmed by chromosome analysis, with brief review of related literatures.
Abortion, Spontaneous
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Choroid Plexus
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Congenital Abnormalities
;
Female
;
Fertilization
;
Fingers
;
Foot
;
Hand
;
Hernia, Umbilical
;
Humans
;
Intellectual Disability
;
Joints
;
Parturition
;
Polyhydramnios
;
Pregnancy
;
Radius
;
Stillbirth
;
Syndactyly
;
Toes
;
Trisomy
;
Ultrasonography
;
Ultrasonography, Prenatal
;
Wrist Joint
4.Genomic gain and loss of cervical cancer using BAC Chip.
Guo Hua DING ; Su Mi BAE ; Sun Young KWAK ; Hyun Jin MIN ; Aery LEE ; Hee Jeong YU ; Jeong NAMKOONG ; Eun Kyeong OH ; Jae Eun SHIN ; Ji Hyang CHOE ; Seo Yun TONG ; Sung Jae SHIN ; Yong Wan KIM ; Jong Chul SHIN ; Byoung Don HAN ; Chong Kook KIM ; Woong Shick AHN
Korean Journal of Obstetrics and Gynecology 2006;49(9):1881-1891
OBJECTIVE: Cervical cancer has long been linked to the sexually transmitted human papillomavirus (HPV), and the oncoproteins E6 and E7 disrupt the functions of tumour suppressor genes, resulting in genetic alteration. It was shown that loss of heterozygosity at 6p is a common genetic alteration in cervical cancer. However, the molecular genetics of cancer have only recently been understood, and for the development of cervical cancer additional genetic alterations in host cell genes are required. The present study has identified the differential changes of the cervical cancer-associated genetic alterations by a genome-wide array based comparative genomic hybridization (array-CGH). METHODS: We analyzed 15 cases of cervical cancer from St. Mary's hospital of The paraffin-fixed tissue samples were microdissected under microscope and DNA was extracted by the procedures of proteinase K digestion and chloroform extraction. Array-based CGH and genomic PCR were carried out with statistical analyses such as hierarchical clustering and Gene Ontology. The BAC array used in this study consisted of 1,440 human BACs, the space among the clones were approximately 2.08 megabase (Macrogen, Seoul, Korea). RESULTS: All of 15 cases of cervical cancer showed specific gains and losses. The analysis limit of average gains and losses was 53%. A significant positive correlation was found between 1p36.32, 3p14.2, 3q27.1, 7p21.1, 8q24.3 and 11q13.1 changes through the cervical carcinogenesis. The high-level of gain regions, BAC clones encoded GSDMDC1, RECQL4, TP73, ABCF3, ALG3, HDAC9, ESRRA and RPS6KA4 genes. Frequently gained BAC clones encoded genes were PRSS8, FUS, COL18A1, PCOLN3, MAFG and ASPSCR1. The genes encoded by frequently lost BAC clones were PTPRG, GRM7, ZDHHC3, EXOSC7, LRP1B and NR3C2. Also, hierarchical clustering of the expression data readily distinguished genomic alterations in cervical cancer. A subset of cellular processes from each gene was clustered by Gene Ontology database. CONCLUSION: Using Array-CGH, genomic alterations related to cervical cancer were identified to determine whether induction of chromosomal imbalances occurs prior to carcinogenesis. The high resolution of array-CGH combined with human genome database would give a chance to find out possible target genes present in the gained or lost clones.
Carcinogenesis
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Chloroform
;
Clone Cells
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Comparative Genomic Hybridization
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Digestion
;
DNA
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Endopeptidase K
;
Gene Ontology
;
Genes, Suppressor
;
Genome, Human
;
Humans
;
Loss of Heterozygosity
;
Molecular Biology
;
Oncogene Proteins
;
Polymerase Chain Reaction
;
Seoul
;
Uterine Cervical Neoplasms*
5.Validity and Reliability of the Korean Version of the Hamilton Depression Rating Scale(K-HDRS).
Jung Seo YI ; Seung Oh BAE ; Yong Min AHN ; Doo Byoung PARK ; Kyung Sun NOH ; Hyun Kyun SHIN ; Haing Won WOO ; Hong Shick LEE ; Sang Ick HAN ; Yong Sik KIM
Journal of Korean Neuropsychiatric Association 2005;44(4):456-465
OBJECTIVES: The reliability and validity of the Korean version of Hamilton Depression Rating Scale (K-HDRS) were examined in Korean patients depressive symptoms. METHODS: 33 inpatients and 70 outpatients diagnosed as major depressive disorder or depressive episode of bipolar I disorder according to the DSM-IV criteria were assessed with K-HDRS, Clinical Global Impression score(CGI), Beck Depression Inventory (BDI) and Montgomery-Aberg Depression Rating Scale (MADRS). RESULTS: Internal consistency (Cronhach's alpha coefficeint=0.76) and interrater reliability (r=0.94, p<0.001) were statistically significant. Principal axis factoring analysis revealed 4 factors that accounted for 50.4% of the total variance. The correlations of K-HDRS with CGI, BDI and MADRS were 0.84, 0.54, 0.58 respectively. CONCLUSION: These results showed that the K-HDRS could be a reliable and valid tool for the assessment of depressive Korean patients. The K-HDRS will be a useful tool for assessing depressive symptoms in Korea.
Axis, Cervical Vertebra
;
Depression*
;
Depressive Disorder, Major
;
Diagnostic and Statistical Manual of Mental Disorders
;
Humans
;
Inpatients
;
Korea
;
Outpatients
;
Reproducibility of Results*