Henri, French dermatologist, 1881-1955. See: Gougerot and Blum disease, Gougerot-Sjögren disease, Gougerot-Carteaud syndrome.
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Gougerot disease is an autoimmune disorder characterized by the lymphoid infiltration of salivary and lachrymal glands easily accessible favoring the diagnostic, and it could be primary or more often associated with another autoimmune disease (1).
Other differential diagnoses include maculopapular mastocytosis, postinflammatory hyperpigmentation, morphea, pityriasis rosea, Addison disease, hemochromatosis, arsenism, contact dermatitis, multiple fixed drug eruption, confluent and reticulated papillomatosis of Gougerot and Carteaud, tuberculoid leprosy, and pinta.
Confluent and reticulated papillomatosis (CARP) of Gougerot and Carteaud, also known as Gougerot-Carteaud syndrome, is an uncommon skin disorder of young individuals characterized by hyperkeratotic or verrucous brown papules or plaques that coalesce centrally and by a reticulated pattern peripherally.
Reticulate pigmentation, which is characterized by a mottled appearance and variation in the size and pigmentary content of lesions [3], is seen in reticulate acropigmentation of Kitamura, confluent and reticulated papillomatosis of Gougerot, and Carteaud and other rare dermatoses.
Gougerot and Carteaud papillomatosis: multiple hyperpigmented papules, brownish, 4-5 cm in size, hyperkeratosic, with the tendency of central confluation and peripheral reticular disposition, localized on the presternal area, interscapular area and upper abdomen.
adolescente no corte da cana- 2001; 26(97/98):9-27 de-acucar Suplemento cultural da 2003 Gougerot e nos Revista da APM.
The observation of nevi recurring in the scar of previously destroyed nevi led Gougerot (32) to propose seeding during removal as the mechanism for their recurrence, a concept that led some European physicians (33,34) to use high doses of irradiation before removal of pigmented lesions to prevent growth of theoretically seeded cells.
During the early 1900s in France, sporotrichosis was a common disease and scientists such as Beurmann, Ramond, and Gougerot described the fungus and its clinical signs.
The distribution and morphology of our patient's cutaneous eruption was highly suggestive of confluent and reticulated papillomatosis (CARP) of Gougerot and Carteaud, a rare dermatologic disorder characterized by epidermal changes (hyperkeratosis, scaling) and hyperpigmentation.
Confluent and reticulated papillomatosis of Gougerot and Carteaud (CRP) is a rare skin disorder characterized by benign blue-gray or brown hyperpigmented hyperkeratotic papules and plaques.