Dyschromatosis Universalis Hereditaria

Dyschromatosis universalis hereditaria is a rare pigmentary disorder initially described in the Japanese literature. The pattern of inheritance is believed to be autosomal dominant, but many sporadic cases have been reported. We encountered a family in which dyschromatosis universalis hereditaria occurred in seventeen members of three generations. In the two members whom we observed, typical skin lesions were distributed all over the body except palrns and soles. By pedigree analysis, we found an autosomal dominant pattern of inheritance. The differential diagnosis of the other reticulate pigmentary disorders is discussed with a review of dyschromatosis reported in the Korean literature.

Serologic Tests for Syphilis in the General Entertainers and Prostitutes (1982) / 대한피부과학회지

We previously reported the result of the VDRL and TPHA tests among the general entertainers and prostitutes in the Youngdeungpo Ku, Chung Ku, Seoul and Paju area, Kyunggi province in 1979 The study resulted in an overall, VDRL reactive rate of 5 .6% in the 6, 666 subjects including general entertainers and prostitutes: 5 3% in the 5, 289 entertainers and 7.6% in the 837 prostitutes. 34.8% of VDRL reactive entertainers showed VDRL titers of 1: 8 or higher. In order to investigate the changing patterns of VDRL reactive rates in general entertainers and prostitutes, we compared the results of the present VDRL tests (1982) with those of our previous study (1979) Total 6, 808 subjects consisted of 2,931 residents who wanted to have medical certification from Jan. 4, 1982 to June 30, 1982 and 2, 562 general entertainers in the Youngdeungpo Ku and Chung Ku areas and 120 general entertainers and 1,195 prostitutes in the Paju area frorn Jan, 4, 1982 to Dec. 31, 1981. (countinued..)

A Case of Disseminate and Recurrent Infundibulo-folliculitis / 대한피부과학회지

Disseminate and recurrent infundibulo-folliculitis is a rare,but distinctive dermatosis characterized by pruritic papular follicular eruption over the trunk and proximal extremities with histologic findings of lymphocytic infiltrations and spongiosis confined to the infundibulum. Little is known about the cause. Resistance to treatment is one of the characteristics of this disease. We herein report a case with typical clinical and histological findings in a 22 year old male.