1.A case of preoperative angiographic uterine artery embolization for the conservative treatment of cervical pregnancy.
Ki Young RYU ; Young Gyu LEE ; Soon Young SONG ; Ja Hong KOO ; Hwa Eun OH
Korean Journal of Obstetrics and Gynecology 2000;43(5):936-940
A 35 year old woman, gravid 5, multiparous, was admitted to our department at 6 weeks and 5 days of gestation after being diagnosed with cervical pregnancy. Before the evacuation, the uterine arteries were embolized using angiographic techniques. As a result, dilatation and curettage were performed with minimal hemorrhage. We report one case of cervical pregnancy managed, successfully with preoperative uterine artery embolization and evacuation.
Adult
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Dilatation and Curettage
;
Female
;
Hemorrhage
;
Humans
;
Pregnancy*
;
Uterine Artery Embolization*
;
Uterine Artery*
2.Spinal pseudoarthrosis with paraplegia in ankylosing spondylitis: a case report.
Hyung Seok KIM ; Ki Do HONG ; Sung Sik HA ; Young Hwa HONG
The Journal of the Korean Orthopaedic Association 1991;26(4):1346-1349
No abstract available.
Paraplegia*
;
Pseudarthrosis*
;
Spondylitis, Ankylosing*
3.A Case of Darier - White Disease on the Sun Exposed Areas.
Hong Jig KIM ; Young Keun KIM ; Sung Hwa KIM ; Young Man PARK
Korean Journal of Dermatology 1986;24(3):455-459
We deacribe herein a case of Darier-White disease occurring to a 50-year-old man who had a characteristic lesions limited to the sun exposed area and no skin lesion in the sun protected area for 40 years. The akin lesions recurred in summer time and aggravated after sun exposure and disappeared spontaneously in winter time. Histologic findings from the neck lesions revealed hyperkeratosis, parakeratosis, supirabasal lacunae, acantholytic cells, villi, corps ronds and grains.
Edible Grain
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Darier Disease
;
Humans
;
Middle Aged
;
Neck
;
Parakeratosis
;
Skin
;
Solar System*
4.A Case of Renal Teratoma.
Tae Yung JEONG ; Hei Young SHIM ; Ja Hong KOO ; Soon Young SONG ; Hwa Eun OH
Korean Journal of Urology 2000;41(7):904-906
No abstract available.
Teratoma*
6.Clinical observations of drug intoxication.
Dae Hong MIN ; Young Mi KIM ; Sang Hwa LEE ; Dong Young CHO
Journal of the Korean Academy of Family Medicine 1991;12(4):8-16
No abstract available.
7.A clinicostatistical Study of Congenital Intestinal Obstruction.
Min Young LEE ; Young Sook HONG ; Se Jin KANG ; Soon Kyum KIM ; Pyung Hwa CHOE
Journal of the Korean Pediatric Society 1990;33(4):456-462
No abstract available.
Intestinal Obstruction*
8.CT and MR Findings of Persistent Hyperplastic Primary Vitreous(PH PV).
Byung Gil CHOI ; Hong Jun CHUNG ; Ok Hwa KIM ; Bo Young AHN ; Sung Kun CHUNG
Journal of the Korean Radiological Society 1994;30(6):1141-1146
PURPOSE: The purpose of this paper is to discuss the characteristic CT and MR findings in persistent hyperplastic primary vitreous(PHPV) and to compare the detectability of those findings in each modality. MATERIALS AND METHODS: We retrospectively evaluated CT and MR findings in 32 patients with PHPV. Twenty-five patients had CT, 13 patients had MR, and 6 patients had both CT and MR. RESULTS: Major findings of PHPV in 32 patients on both imaging modalities were lens deformity(78%), shallow anterior chamber(72%), heterogeneous vitreous opacity(72%), enhancing hyaloid artery or remnant of fibrotic hand(69%), and microophthalmos(67%). Minor findings were retinal detachment(22%), and vitreous hemorrhage(6%). In MRI, lens deformity(92%) and shallow anterior chamber(85%) were detected most commonly whereas in CT, opaque vitreous(80%) was the most common finding. Findings of enhancing hyaloid vessel or remnant of fibrotic band, considered characteristic of PHPV, were more commonly detectable in MR (85%) than CT(52%). CONCLUSION: Characteristic MR and CT findings of PHPV were lena deformity, shallow anterior chanber, heterogeneons vitreons opacity, enhanciny hgalind artery or remnant fibrotic band, and microphthalmos. MR seemed to be more useful than CT in detecting Globe pathology.
Arteries
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Congenital Abnormalities
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Humans
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Magnetic Resonance Imaging
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Microphthalmos
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Pathology
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Retinaldehyde
;
Retrospective Studies
9.Detection of canine distemper virus (CDV) through one step RT-PCR combined with nested PCR.
Yong Hwan KIM ; Kyu Woan CHO ; Hwa Young YOUN ; Han Sang YOO ; Hong Ryul HAN
Journal of Veterinary Science 2001;2(1):59-63
A one step reverse transcription PCR (RT-PCR) combined nested PCR was set up to increase efficiency in the diagnosis of canine distemper virus (CDV) infection after developement of nested PCR. Two PCR primer sets were designed based on the sequence of nucleocapsid gene of CDV Onderstepoort strain. One-step RT-PCR with the outer primer pair was revealed to detect 10(2) PFU/ml. The sensitivity was increased hundredfold using the one-step RT-PCR combined with the nested PCR. Specificity of the PCR was also confirmed using other related canine virus and peripheral blood mononuclear cells (PBMC) and body secretes of healthy dogs. Of the 51 blood samples from dogs clinically suspected of CD, 45 samples were revealed as positive by one-step RT-PCR combined with nested PCR. However, only 15 samples were identified as positive with a single one step RT-PCR. Therefore approximately 60% increase in the efficiency of the diagnosis was observed by the combined method. These results suggested that one step RT-PCR combined with nested PCR could be a sensitive, specific, and practical method for diagnosis of CDV infection.
Animals
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Distemper Virus, Canine/genetics/*isolation & purification
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Dogs
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Polymerase Chain Reaction/*methods/*veterinary
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RNA, Viral/genetics/isolation & purification
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Reverse Transcriptase Polymerase Chain Reaction
;
Vaccines, Attenuated
;
Viral Vaccines
10.Congenital Adrenal Hyperplasia with 21-hydroxylase Deficiencies in Twins.
Young Don KIM ; Jeong Hwa CHOI ; Jae Hong PARK ; Hee Ju PARK ; Seong Suk JEON
Journal of the Korean Pediatric Society 1994;37(10):1469-1473
Congenital adrenal hyperplasia is inherited disorder of adrenal steroidogenesis. 21-hydroxylase deficiency is the most commone enzymatic defect and is divided into classic and late-onset or nonclassic forms. Both classic non-classic 21-hydrozylase deficiencies are inherited in a recessive manner as allelic variants. But it is rare that happened in twin infants. Chief complaints of affected twins in our case were ambiguous genitalia, hyperpigmentation and dehydrations. They were revealed into hyponatremia, hyperkalemia and increased amount of serum progesterone, 17-hydroxyprogesterone and urinary 17-ketosteroid excretion and were administered with DOCA, 9alpha-fluorohydrocortisone, hydrocortisone to control the electrolyte imbalance. And now, both of them are going to normal ratio of weight gain and body growth.
17-alpha-Hydroxyprogesterone
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Adrenal Hyperplasia, Congenital*
;
Desoxycorticosterone Acetate
;
Disorders of Sex Development
;
Humans
;
Hydrocortisone
;
Hyperkalemia
;
Hyperpigmentation
;
Hyponatremia
;
Infant
;
Progesterone
;
Steroid 21-Hydroxylase*
;
Twins*
;
Weight Gain