Dermatolysis

Dermatology & Venereology, Pathology, Biology & Genetics

Also known as: Cutis Laxa, Chaloderma, Loose Skin

Historical document, translated for reference. It reflects medical knowledge of the 1920s–30s and is not medical advice.

Summary

Dermatolysis is a rare congenital skin disease described by Alibert in 1835, characterized by exceptional skin elasticity and joint hypermobility. The condition presents either as loose, hanging skin folds or as skin that tightly covers underlying tissues, with histological findings primarily showing changes in the connective tissue.

Encyclopedia article (1928–1936)

DERMATOLYSIS (from Greek derma-skin and lysis-relaxation; synonyms: cutis laxa, chaloderma, loose skin), a name given by Alibert (1835) to the rare congenital disease of the skin that he described, which manifests as exceptional elasticity of the skin (and ligamentous apparatus). In such patients, the skin can be stretched very far (for example, from the sternum to the head), and movements in the joints occur in an abnormally large range ('rubber people'). The skin may hang in irregular folds (like a cape, etc., properly cutis laxa), but more often it evenly covers the underlying parts (cutis hyperelastica). It is usually somewhat doughy in consistency and sometimes appears particularly easily injured. Combinations of cutis laxa with molluscum fibrosum have been described. Histologically, changes are mainly found in the connective tissue of the skin. Du Mesnil discovered mucoid degeneration of it and, on this basis, believes that cutis laxa represents a developmental defect of the skin, as if it were arrested at an early stage of its embryonic state. The disease is congenital; its development after injuries in more mature age has also been described.

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“Dermatolysis.” Soviet Medical Encyclopedia. English translation of Bolshaya Meditsinskaya Entsiklopediya, 1st ed. (Moscow, 1928–1936), ed. N. A. Semashko. https://sovietmedicalencyclopedia.pages.dev/article/dermatolysis/