1.A statistical analysis of dermatoses in west Gyeongsangnamdo area (1987-1990).
Korean Journal of Dermatology 1991;29(3):399-406
The authors reviewed 7,065 new outpatients who visited the dermatology clinic of Gyeongsang National University Hospital in Chinju from Jan. 1st, 1987 to Dee. 31st, 1990 to study the prevalence of common dermatoses in this region as compared to other regions in Korea, The results suggest that age, sex, monthly and yearly distribution patterns around Chinju are similar to those of other areas in Korea except for higher prevalences of vitiligo, psoriasis, alopecia, and for lower prevalences of scabies, insect bites, and syphilis.
Alopecia
;
Dermatology
;
Gyeongsangnam-do*
;
Humans
;
Insect Bites and Stings
;
Korea
;
Outpatients
;
Prevalence
;
Psoriasis
;
Scabies
;
Skin Diseases*
;
Syphilis
;
Vitiligo
2.Pharmacologic Management of Rheumatic Diseases.
Journal of the Korean Medical Association 2000;43(4):367-376
No abstract available.
Rheumatic Diseases*
3.Pharmacologic Management of Rheumatic Diseases.
Journal of the Korean Medical Association 2000;43(4):367-376
No abstract available.
Rheumatic Diseases*
4.A case of the lupus syndrome induced by hydralazine.
Beom Soo PARK ; Joong Gon KIM ; Yong Soo YUN
Journal of the Korean Pediatric Society 1991;34(5):736-739
No abstract available.
Hydralazine*
6.A case of grideofulvin-induced phototoxic reaction.
Jin Soo KANG ; Tae Heung KIM ; Ki Beom PARK
Korean Journal of Dermatology 1992;30(4):524-528
We report a case of a phototoxic reaction in a 48-year-old female induced by griseofulvin ingestion. The patient hac! erythematous papules, vesicles and patches on the sun-exposed areas. Phototest revealed a decreased minimal erythemal dose to UVA (10J/cm). Photopatch tests with 1%, 5%, 10% Griseofulvin ointment and vaseline as a control and photoingestion tests with Griseofulvin (50mg b.i.d.) were all negative. After the cessation of Griseofulvin, her skin lesions were markedly improved with complete loss of photosensitivity.
Eating
;
Female
;
Griseofulvin
;
Humans
;
Middle Aged
;
Petrolatum
;
Skin
7.Secondary erythromelagia associated with bronchial asthma.
Jin Soo KANG ; Tae Heung KIM ; Ki Beom PARK
Korean Journal of Dermatology 1992;30(4):519-523
Erythromelalgia is a rare disorder characterized by intense hun ing pain in the distal extremities associated with erythema and increased skin temperature. The patient was a 42- year-old woman with a 5 year history of burning pain, erythema, and warmth of the skin on both hands and feet. She had been suffering from bronchiali astalima since childhood. The onset of the symptoms were temporally related to the attacks of hei bronchial asthma. Physical examination revealed mottled dusky red patches on her both ha ids and feet, and purplish acrocyanosis on the finger and toe tips. We present a case of secondary erythromelalgia associated with bronchial asthma and acrocyanosis.
Asthma*
;
Burns
;
Erythema
;
Erythromelalgia
;
Extremities
;
Female
;
Fingers
;
Foot
;
Hand
;
Humans
;
Physical Examination
;
Skin
;
Skin Temperature
;
Toes
8.A case of porokeratosis induced by topical PUVA in a vitiligo patient.
Ho Seong LEE ; Jin Soo KANG ; Ki Beom PARK
Korean Journal of Dermatology 1992;30(1):131-134
A 20-year-old female, who had been treated with topical PUVA therapy for her vitiligo, developed characteristic skin lesions of disseminated superficial artiric porokeratosis(DSAP). All of her three sisters had vitiligo and had been treated with topica PUVA, hut only one developed DSAP lesion. Her mother had had DSAP lesions on expcsec areas for 20 years. DSAP shows an autosomal dominant mode of inheritance, and is charaterized by multiple ciark brownish keratotic papaules surrounded by slightly elevatied order. The exacerbation of the lesion by exposure t.o UV lignt indicates that the regulatingene for DSAP is related to sunlight. 1-lerein we reported a case of DSAP induced by topica] PUVA therapy in one patient during management of familial vitiligo in 3 sisters.
Female
;
Humans
;
Mothers
;
Porokeratosis*
;
PUVA Therapy
;
Siblings
;
Skin
;
Sunlight
;
Vitiligo*
;
Wills
;
Young Adult
9.Potter's Syndrome with Adult Polycystic Renal Disease: An autopsy case report.
Hwa Sook JEONG ; Beom Soo PARK ; Geon Kook LEE
Korean Journal of Pathology 1997;31(4):361-365
Potter's syndrome including bilateral renal agenesis or polycystic renal disease, bilateral pulmonary hypoplasia and characteristic face was first described in 1946. Although a great number of cases of Potter's syndrome was reported, Potter's syndrome with adult polycystic kidney disease(Potter type III) was very rarely found. In this report, we described an autopsy case of Potter's syndrome having adult polycystic kidneys disease, bilateral pulmonary hypoplasia and characteristic face in conjunction with multiple hepatic cysts, features of congenital hepatic fibrosis and a pancreatic cyst. Microscopically, all cysts were lined by cuboidal epithelial cells, showing positive for epithelial membrane antigen and cytokeratins.
Adult*
;
Autopsy*
;
Epithelial Cells
;
Fibrosis
;
Humans
;
Keratins
;
Mucin-1
;
Pancreatic Cyst
;
Polycystic Kidney Diseases*
10.Two cases of Darier's disease treated with etretinate.
Jin Soo KANG ; Tae Heung KIM ; Ki Beom PARK
Korean Journal of Dermatology 1992;30(5):705-709
We report two cases of Darier's disease improved with Etretmate in the 44-year-old father and his 18-year-old son. Clinically, multiple dirty brownish, verrucous, discrete or confluent papules and plaques were noted on their back, abdomen, and face. Histopathologically, both of them demonstrated hyperkeratosis, suprabasal acantholysis, acantholytic cells in the lacunae, corpsronds, grains, and dyskeratotic cells. Oral Etretinate 30mg daily was given in both cases with remakable improvement 3 weeks after treatment. Six months later, they showed almost total clearin, of their skin lesions. No specific adverse effect was noted. There has been no evidence of recurrence for 6 months follow up period.
Abdomen
;
Acantholysis
;
Acitretin*
;
Adolescent
;
Adult
;
Edible Grain
;
Darier Disease*
;
Etretinate*
;
Fathers
;
Follow-Up Studies
;
Humans
;
Recurrence
;
Skin