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1.
Korean Journal of Dermatology ; : 146-149, 1987.
Artículo en Coreano | WPRIM | ID: wpr-127383

RESUMEN

The coexistence of the variants of porokeratosis is very rare. We report a case of coexistence of linear porokeratosis with disseminated superficial actinic porokeratosis (DSAP). A 43-year-old wornan first noticed a brownish papule on the left side of groin in early infancy. She developed multiple discrete or confluent keratotic plaques in linear fashion on the left lower extrernity and trunk in childhood. These leaions became pruritic in summer. Two years ago, she developed multiple scattered small annular lesions on the face and forearms. Her family history showed no abnormalities. Biopsy specimene from the groin and trunk showed eornoid lamella.


Asunto(s)
Adulto , Humanos , Biopsia , Antebrazo , Ingle , Poroqueratosis
2.
Korean Journal of Dermatology ; : 254-258, 1986.
Artículo en Coreano | WPRIM | ID: wpr-14080

RESUMEN

Serologic tests for syphilis including VDRL and TPHA tests were carried out in 5,413 VISA applicants for emigration, from January, 1981 to December, l984 The results are summarized as follows: 1. In 5,413 VISA applicants, the reactive rate of VDRL test was 2,0% totally. The reactive rate of VDRL test of male was 2. 6%, and that of female was 1. 6% 2. The reactive rate of 1983 was 1.4% and that was the lowest in annual incidence, but there was no statistically significant differences in comparing the annual incidences. 3. The reactive rate increased with age, and males above the 5 th decade revealed an especially high reactive rate. 4. The biologic false positive rate of VDRL teet was 16. 5%, in gl VDRL reactive persons, using TPHA as standard. 5. The quantitative test of VDRL showed low titer below 1: 4 in 88. 4%, and high titer above 1: 8 in 11. 6% of the applicants.


Asunto(s)
Femenino , Humanos , Masculino , Emigración e Inmigración , Incidencia , Pruebas Serológicas , Sífilis
3.
Korean Journal of Dermatology ; : 100-104, 1985.
Artículo en Coreano | WPRIM | ID: wpr-13844

RESUMEN

We report a case of multiple leatiginea syndrome in an 8 year old boy. He had numeroua lentigines acattered over his face, trunk, buttock and thlghe, and eome larger black macular leeians on the trunk and thighs. Gn phyaiaal examinatlon, he wae well developed but he had ocular hyperteloriem. Chest roentgenogram showed hypertrophy of both ventricles. Electrocardiogram and audiogram revealed conduction defects and severe sensorineural deafness, reepectively. Blopsy af dark brown lesion from the back showed the histopathologlc pattern of lentigo.


Asunto(s)
Niño , Humanos , Masculino , Nalgas , Sordera , Electrocardiografía , Hipertrofia , Lentigo , Síndrome LEOPARD , Muslo , Tórax
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