Two cases of dyschromatosis universalis.
- Author:
Yong Joo KIM
;
Chang Nam OH
;
Byoung Soo CHUNG
;
Kyu Chul CHOI
- Publication Type:Original Article
- Keywords:
Dyschromatosis universalis
- MeSH:
Adult;
Coloring Agents;
Extremities;
Humans;
Japan;
Middle Aged;
Weights and Measures
- From:Korean Journal of Dermatology
1992;30(6):928-931
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Dyschromatosis universalis hereditaria was reported in 1933 by Ichikawa and Hiraga in Japan. This disease is characterized by small pigmented and depigmented mottled macules on the trunk and extremities. We report two cases of dyschromatosis universalis. Case one is a 47-year-old man presented with hypoand hyperpigmented spots on the trunk and extrexities. At about 30 years of age, he started to show pigmentary changes on the back, which became progressively spread to the other parts of the trunk and extremities. Case two is a 27-year-old man with numerous mottled hypo-and hyperpigmented spots on the trunk and extremities. He started to show pigmentary changes on the back about 12 years ago. This pigmentary changes also became progressively spread to the other part of the trunk and extrimities. There were no family history of similar disease. On physical exminations, both patients had hrown rice-grain sized pigmented and depigmented macules without scales and atropy on the trunk and extremites. Fontana-Masson stains revealed decreased and increased melar in granules in the basal cell layers in the hypopigrnented and hyperpigmented lesions respectively.
