1.Acute Arterial Occlusive Disease.
Journal of the Korean Medical Association 1998;41(6):584-593
No abstract available.
Arterial Occlusive Diseases*
2.Thirty Year-Old Korean Society for Vascular Surgery: Challenging Issues to Overcome.
Vascular Specialist International 2014;30(2):43-48
No abstract available.
3.Surgical Treatment of Primary Varicose Vein.
Journal of the Korean Society for Vascular Surgery 2001;17(1):136-144
No abstract available.
Varicose Veins*
4.Reoperations after Aortic Surgery.
Journal of the Korean Society for Vascular Surgery 2000;16(2):274-282
No abstract available.
5.Two Cases of Pigmented Bowen's Disease.
Seon Wook HWANG ; Seon Wook HWANG ; Jung Wook KIM ; Sung Wook PARK ; Han Young WANG
Annals of Dermatology 2002;14(2):127-129
Pigmented Bowen's disease (PBD) is a rare variant of Bowen's disease(BD). Most of the reported cases showed pigmented patches or thin plaques. Thus its clinical manifestations may simulated other various pigmented skin lesions. We experienced 2 cases of PBD in patients with multiple BD developed after taking Korean proprietary pills (KPP, "Hwan-Yak"), which were suspected to contain certain amount of arsenics. Both patients also showed arsenical keratosis on their palms and soles. The darker pigmentation of the PBL led us to differentiated them from melanoma.
Bowen's Disease*
;
Humans
;
Keratosis
;
Melanoma
;
Pigmentation
;
Skin
6.The Genetic and Clinical Study of Pseudoxanthoma Elasticum.
Sun Wook HWANG ; Young Gyun KIM
Korean Journal of Dermatology 1985;23(3):346-354
A genetic and clinical study was done on 20 index cases and their families who had lived in Chonnam province, visited Chonnam University Hospital from 1968 through 1983, and were diagnosed as peudoxanthoma elasticum based on clinical and histopathological findings. In Chonnam province, pseudoxanthoma elsticum occurred in a incidence of more thar, one per 125,000. The male to female ratio was 1: 1.25 (8: 10) with only the cases of familial occurrence although the sex ratio was 1: l. 85 (7: 13) among 20 index cases. Among 8 index cases showing familial occurrence, 6 showed autosomal recessive inheritance with 5 Type 1 and 1 Type 2 whereas 2 showed the autosomal dominant inheritance with both of thern Type 2 (Pope), pointing out the genetic heterogeneity in pseudoxanthorna elsticum. The age of patients ranged from 12 to 42 years old at the time of their first visit to our hospital, but the age that the patients first recognized the disease onset ranged from 9 to 22 years old. The duration of t he disease was also variable ranging from 11/2 to 30 years. The angioid streaks were observed in 38g of the cases whose disease duration ranged from 11/2 to 20 years. The sites of skin lesions were the neck, axillae and groin in the order of frequency.
Adult
;
Angioid Streaks
;
Axilla
;
Classification
;
Female
;
Genetic Heterogeneity
;
Groin
;
Humans
;
Incidence
;
Jeollanam-do
;
Male
;
Neck
;
Pseudoxanthoma Elasticum*
;
Sex Ratio
;
Skin
;
Wills
;
Young Adult
9.The study for weight of non-pregnant uterine tumor by ultrasonogram.
Korean Journal of Obstetrics and Gynecology 1993;36(7):1146-1157
No abstract available.
Ultrasonography*
10.Histiocytoma Papulosa Benigna Congenita: A Case Report.
Young Pio KIM ; Sun Wook HWANG
Korean Journal of Dermatology 1984;22(5):574-577
We herein described a female newborn baby who, on the day of birth, exhibited widespread discrete reddish purple colored, round and slightly hyperkeratotic papules measuring about 4 mm in size, the biopsy specimen of which showed the histologic findings of histiocytosis X. The skin lesions resolved spontaneously within a week. The following diseases were discussed as possible diagnoses; histiocytosis X, generalized eruptive histiocytoma, juvenile xanthogranuloma, congenital self-healing reticulohistiocytosis and xanthoma disseminaturn. Since the current case didn't fit well any of them, we proposed a new descriptive term for this : Histiocytoma Papulosa Benigna Congenita.
Biopsy
;
Diagnosis
;
Female
;
Histiocytoma*
;
Histiocytosis, Langerhans-Cell
;
Humans
;
Infant, Newborn
;
Parturition
;
Skin
;
Xanthogranuloma, Juvenile
;
Xanthomatosis