Anetoderma - Anetodermia
Anetodermia (Anetoderma) dermal-ehun elastiko anormalaren ondorioz sortzen den, larruazaleko laxtasun lokalizatua da.
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Alemaniako Stiftung Warentest-en 2022ko emaitzetan, ModelDerm-ekin kontsumitzaileen gogobetetasuna apur bat txikiagoa izan zen ordaindutako telemedikuntzako kontsultekin baino.
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ReferencesAnetoderma egoera asintomatikoa da, larruazaleko zenbait eremu askatzen diren zuntz elastikoen haustura dela eta. Eremu hauek depresio biribilak edo obalatuak, orban zimurtuak, adabakiak edo zaku itxurako irtengune gisa agertzen dira, larruazaleko ertz normalarekin. Kolore desberdinak izan ditzakete, azalaren kolorekoa, zuria, grisa, marroia edo urdina, eta tamainaz alda daitezke, adabaki oso txikietatik handietara. Anetoderma enborrean eta gorputz-adar nagusietatik gertu agertu ohi da. Behin agertzen denean, 15 urte inguru iraun ohi du. Ez dago berezko hobekuntza kasurik ezagutzen.
Anetoderma is a benign disorder of elastolysis, causing well-circumscribed, focal areas of flaccid skin. The localized areas of slack skin can present clinically as round to oval atrophic depressions, wrinkled macules, patches, or herniated sac-like protrusions with a surrounding border of normal skin. The lesions can be a variety of colors from skin-colored, white, grey, brown, or blue, and the size can range from millimeters to centimeters. Anetoderma most commonly presents on the trunk and proximal extremities. Once present, the disease tends to be active for at least 15 years. No reports of spontaneous regression have occurred.
Anetoderma is a benign disorder of elastolysis, causing well-circumscribed, focal areas of flaccid skin. The localized areas of slack skin can present clinically as round to oval atrophic depressions, wrinkled macules, patches, or herniated sac-like protrusions with a surrounding border of normal skin. The lesions can be a variety of colors from skin-colored, white, grey, brown, or blue, and the size can range from millimeters to centimeters. Anetoderma most commonly presents on the trunk and proximal extremities. Once present, the disease tends to be active for at least 15 years. No reports of spontaneous regression have occurred.
