1.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
2.Sister chromatid exchange(SCE) and chromosome abberrations inFanconi's anemia..
Yong Wook JUNG ; Sung Ik CHANG ; Chang Gu HU
Korean Journal of Physical Anthropology 1991;4(2):137-144
No abstract available.
Anemia*
;
Chromatids*
;
Humans
;
Siblings*
3.A clinical evaluation and follow up results of the surgical management on 172 patients with perforated peptic ulcer.
Rae Gyun KANG ; Sung Yoon JUN ; Jung Wook SUH
Journal of the Korean Surgical Society 1992;42(3):292-303
No abstract available.
Follow-Up Studies*
;
Humans
;
Peptic Ulcer*
4.Extracorporeal Membrane Oxygenation for the Support of a Potential Organ Donor with a Fatal Brain Injury before Brain Death Determination.
Sung Wook CHANG ; Sun HAN ; Jung Ho KO ; Jae Wook RYU
Korean Journal of Critical Care Medicine 2016;31(2):169-172
The shortage of available organ donors is a significant problem and various efforts have been made to avoid the loss of organ donors. Among these, extracorporeal membrane oxygenation (ECMO) has been introduced to help support and manage potential donors. Many traumatic brain injury patients have healthy organs that might be eligible for donation for transplantation. However, the condition of a donor with a fatal brain injury may rapidly deteriorate prior to brain death determination; this frequently results in the loss of eligible donors. Here, we report the use of venoarterial ECMO to support a potential donor with a fatal brain injury before brain death determination, and thereby preserve donor organs. The patient successfully donated his liver and kidneys after brain death determination.
Brain Death*
;
Brain Injuries*
;
Brain*
;
Extracorporeal Membrane Oxygenation*
;
Humans
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Kidney
;
Liver
;
Tissue and Organ Procurement
;
Tissue Donors*
5.Two Cases of Occupational Radiodermatitis.
Sung Wook PARK ; Jung Wook KIM ; Seon Wook HWANG ; Han Young WANG
Korean Journal of Dermatology 2000;38(10):1409-1410
We observed 2 cases of occupational radiodermatitis which occurred during the radioisotope transpierce test. Patient 1, a 40-year-old man, noticed swelling, erythema, and stiffness on his left 2nd, 3rd, 4th, and 5th fingers 5 days after the exposure to about 2700 rem. Patient 2, a 32-year-old man, noticed painful swelling, erythema, bullae and necrosis on his right palm and thumb 1 week after the exposure to about 5500 rem. Clinicopathologically, patient 1 and 2 came under 2 and 3 burns respectively. The symptoms have been improving after treatment with systemic and topical corticosteroids and antibiotics.
Adrenal Cortex Hormones
;
Adult
;
Anti-Bacterial Agents
;
Burns
;
Erythema
;
Fingers
;
Humans
;
Necrosis
;
Radiodermatitis*
;
Thumb
6.A Case of Hereditary Epidermolytic Palmoplantar Keratoderma in Four Consecutive Generations.
Sung Wook PARK ; Seon Wook HWANG ; Jung Wook KIM ; Han Young WANG
Korean Journal of Dermatology 2001;39(2):231-234
We observed a family with 12 members in four consecutive generations affected by hereditary epidermolytic palmoplantar keratoderma(HEPPK). The affected family members demonstrated not only autosomal dominant inheritance, but also a high penetrance and constant expression. The lesion of all affected person had developed at birth or within the first few weeks of life. The lesions of three members(the proband, her sister and mother) were biopsed, and all of them showed the characteristic features of epidermolytic hyperkeratosis. Two of family members(the proband, her nephew-not affected by HEPPK) had vitiligo, but we concluded that this coexistance was accidental.
Family Characteristics*
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Humans
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Hyperkeratosis, Epidermolytic
;
Keratoderma, Palmoplantar, Epidermolytic*
;
Parturition
;
Penetrance
;
Siblings
;
Vitiligo
;
Wills
7.Complex Method for Correction of Inverted Nipple.
Ki Tae KIM ; Sung Hoon JUNG ; Sung Ho YUN ; Dong Il KIM ; Jae Wook OH
Journal of the Korean Society of Aesthetic Plastic Surgery 1998;4(1):66-71
The inverted nipple presents many problems including both cosmetic and functional aspects and impairment in breast feeding. the histopathologic characters of inverted nipple are that inverted nipple has less fibromuscular tissue than normal nipple and has short lactiferous duct and dense fibrous tissue. Many surgical and non-surgical techniques have been designed for correction of the inverted nipple. But most of these techniques have produced unsatisfactory problems. especially undesirable recurrence is most important problem. We experienced 19 inverted nipples in 12 patients between March 1995 and January 1998. We combined modified Teimourian method, purse-string suture and Z-plasty. and had good result for 3weeks to 30months follow up. This method was effective for correction of the inverted nipple with low recurrence rate and simple techniques.
Breast Feeding
;
Follow-Up Studies
;
Humans
;
Nipples*
;
Recurrence
;
Sutures
9.Family Function and Children of Alcoholics Screening Test Score in High School Students .
In Wook JUNG ; Jong Sung KIM ; Jin Gyu JUNG ; Keun Bae KIM ; Chan Il PARK ; Won Ki HONG ; Sung Soo KIM
Journal of the Korean Academy of Family Medicine 2007;28(6):436-441
BACKGROUND: Parent's alcohol drinking not only influences their health but also their children. This research was designed to assess the family function of children who were affected by parent's alcohol drinking. METHODS: Questionnaire survey was performed on 208 high school students (129 males and 79 females) in Daejeon from March to April, 2005. We defined the students whose CAST (Children of Alcoholics Screening Test) score was 6 or more as children of alcoholics (COA) group. Then, we evaluated the family function by family APGAR score between the COA group and the control group. RESULTS: Among the total, 36 (27.9%) male and 27 (34.1%) female students were in COA group. There was a significant (P<0.01) negative correlation between the CAST score and the family APGAR score in all students. In boys, there was no significant correlation between the CAST score and the family APGAR score, but in girls, there was significant negative correlation (P<0.01). Mean family APGAR score of the COA group was significantly (P<0.05) lower than that of the control group in all students. In boys, there was no significant difference, but in girls, the COA group's family APGAR score was significantly lower than the control group's score (P<0.05). CONCLUSION: The high school students, especially girl students, who were affected by parent's alcohol drinking showed a lower family APGAR score. Therefore, family physicians need to evaluate the family function when encountering students similar to COA group.
Alcohol Drinking
;
Alcoholics*
;
Apgar Score
;
Child*
;
Female
;
Humans
;
Male
;
Mass Screening*
;
Physicians, Family
;
Surveys and Questionnaires
10.Nail Abnormalities in Alopecia Areata.
Jung Wook PARK ; Sung Wook KIM ; Han Young WANG
Korean Journal of Dermatology 2003;41(2):152-157
BACKGROUND: Nail abnormalities may be associated with alopecia areata and nail abnormalities in alopecia areata are reported to range from 10%-66%. OBJECTIVES: This study investigates the clinical characteristics of nail abnormalities in alopecia areata, such as prevalence depending on sex, age and severities of hair loss. METHODS: Prospective analysis was undertaken by examining the finger nails of 424 alopecia areata patients and the nails of 465 non-alopecic patients were examined as controls. RESULTS: The number of the patients was 424(214 males, 210 females) and their mean age was 28.6 years (range 1-69). Nail abnormalities were noted in 98 (23.1%) out of 424 patients and in 24 (5.1%) out of 465 controls. According to age group, the prevalence of nail abnormalities was high at age under 9(31.7%) and at age of 10-19 (31.6%). The incidence according to severity of hair loss was 20.8% in below 50% of hair loss on scalp, 27.8% in 51%-100% of hair loss on scalp and 41.5% in 51%-100% of hair loss on the scalp and also involving body hair. The Frequent nail abnormalities were leukonychia punctata (8.5%) and pitting nail(8.0%). The other minor nail abnormalities were onychorrhexis, transverse ridging, trachyonychia, melanonychia, abnormality of lunula, onycholysis and koilonychia. CONCLUSIONS: The incidence of nail abnormalities in alopecia areata was significantly higher than in controls and the nail abnormalities were more common in children. The more severe was the degree of alopecia, the higher was the prevalence of nail abnormalities. Leukonychia punctata and pitting nail were frequently found in alopeica areata in Korea. The examination of nail in alopecia areata patients may be helpful in expectation of prognosis.
Alopecia Areata*
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Alopecia*
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Child
;
Fingers
;
Hair
;
Humans
;
Incidence
;
Korea
;
Male
;
Nails, Malformed*
;
Onycholysis
;
Prevalence
;
Prognosis
;
Prospective Studies
;
Scalp