Anetoderma
Anetoderma ndi kufooka kwa phokoso komwe kumachitika chifukwa cha minyela yotuluka pa phokoso.
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Muzotsatira za 2022 Stiftung Warentest zochokera ku Germany, kukhutitsidwa kwa ogula ndi ModelDerm kunali kotsika pang'ono kusiyana ndi kuyankhulana kwa telemedicine komwe kulipiridwa.
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ReferencesAnetoderma ndi vuto lomwe madera ena a khungu amamasuka chifukwa cha kuwonongeka kwa ulusi wotanuka. Maderawa amatha kuwoneka ngati zozungulira, oval, mawanga okwinya, zigamba, kapena thumba, ndipo amakhala ndi malire a khungu. Zitha kukhala zamitundu yosiyanasiyana monga zakhungu, zoyera, zotuwa, zofiirira, kapena zabuluu, ndipo zimakhala zosiyanasiyana pa kukula, kuyambira zazing'ono mpaka zazikulu. Anetoderma nthawi zambiri imawonekera pa thupi, makamaka pa thunthu komanso pafupi ndi miyendo yayikulu. Akawonekera, amatha kukhala pafupifupi zaka 15. Palibe zochitika zodziwika zakusintha kodzidzimutsa.
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.
