Anetoderma
Anetoderma wani yanki ne na laxity na fata wanda aka samo asali daga nama na roba na dermal.
☆ A cikin sakamakon Stiftung Warentest na 2022 daga Jamus, gamsuwar mabukaci tare da ModelDerm ya ɗan yi ƙasa kaɗan fiye da biyan shawarwarin telemedicine.
References
Anetoderma wani yanayi ne na asymptomatic inda wasu wurare na fata suka zama sako-sako saboda rugujewar fiber na roba. Waɗannan wuraren suna iya bayyana azaman ɓacin rai mai siffar zagaye ko oval, tabo masu lanƙwasa, faci, ko fitowar jaka, tare da iyakar fata ta al'ada. Suna iya samun launuka daban-daban kamar masu launin fata, fari, launin toka, launin ruwan kasa, ko shuɗi, kuma sun bambanta da girma daga ƙananan ƙananan zuwa manyan faci. Anetoderma yawanci yana nunawa akan gangar jikin kuma kusa da manyan gaɓoɓin jiki. Da zarar ya bayyana, yana kula da zama na kusan shekaru 15. Babu wasu abubuwan da aka sani na inganta ba zato ba tsammani.
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.
