Anetoderma
I- Anetoderma kukutyibilika kolusu okubangelwa kukungaqheleki kwe-dermal elastic tissue.
☆ Kwiziphumo zika-2022 ze-Stiftung Warentest ezivela eJamani, ukwaneliseka kwabathengi ngeModelDerm bekungaphantsi kancinci kunokubonisana nge-telemedicine ehlawulweyo.
References
Anetoderma yimeko engabonakaliyo apho iindawo ezithile zolusu zikhululeka ngenxa yokuqhekeka kwemicu ye-elastic. Ezi ndawo zinokubonakala njengengqukuva engqukuva okanye emile okwe-oval, amabala ashwabeneyo, amabala, okanye iprotrusions efana nesaka, enomda wesikhumba oqhelekileyo. Basenokuba nemibala eyahlukeneyo njengebala lolusu, elimhlophe, elingwevu, elimdaka, okanye elibhlowu, kwaye ziyahluka ngokobukhulu ukusuka kwezincinci ukuya kwezinkulu. Anetoderma idla ngokuvela esiqwini nakufutshane namalungu aphambili omzimba. Nje ukuba ibonakale, ikholisa ukuhlala malunga neminyaka eyi-15. Akukho ziganeko zaziwayo zokuphucula okuzenzekelayo.
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.
