Dyschromia
Historical document, translated for reference. It reflects medical knowledge of the 1920s–30s and is not medical advice.
Summary
Dyschromia refers to a group of skin diseases characterized by persistent changes in skin color due to abnormal melanin levels, deposition of endogenous or exogenous pigments, or other factors. These changes can be diffuse, spotted, or reticulate and may result from various external and internal causes including physical agents, chemicals, infections, and systemic diseases.
Encyclopedia article (1928–1936)
DYSCHROMIA, dyschromia, a group of dermatoses characterized by more or less persistent changes in skin color due to a) thickening (hyperpigmentation) or loss (depigmentation) of the normal skin pigment melanin, or b) deposition in the skin of pigments not normally present there of endogenous origin (hemosiderin) or exogenous origin (tattooing, argyria, impregnations). Changes in color depending on the impregnation of the horny layer with dye and washable do not belong here. Often, areas of depigmentation are surrounded peripherally by zones of hyperpigmentation. Dyschromia can be diffuse, even universal (melanoderma), spotted, sometimes reticulate (reticulata); it arises either secondarily, after or during one or another dermatosis, or primarily, immediately as such. The causes of dyschromia are very numerous: 1) external, physical, such as friction, pressure, scratches, radiant energy, heat, etc.; chemical - flies, mustard plasters, tincture of iodine, especially chrysarobin, etc.; 2) internal - diseases of the central nervous system, organs of blood circulation and especially endocrine organs, from infections, especially chronic ones (syphilis, tbc, malaria, leprosy, etc.), intoxications or neoplasms.
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“Dyschromia.” Soviet Medical Encyclopedia. English translation of Bolshaya Meditsinskaya Entsiklopediya, 1st ed. (Moscow, 1928–1936), ed. N. A. Semashko. https://sovietmedicalencyclopedia.pages.dev/article/dyschromia/