Poikiloderma - 시바트 다형피부증
시바트 다형피부증 (Poikiloderma)은 색소침착 저하증, 색소 과다 침착증, 모세혈관 확장증, 위축증 등으로 나타나는 피부 질환입니다. 시바트 다형피부증 (poikiloderma)은 주로 가슴이나 목에 발생하며, 일반적으로 햇빛 손상과 관련된 붉은 색소가 특징입니다.
relevance score : -100.0%
ReferencesPoikiloderma of Civatte은 주로 목과 얼굴에 나타나는 흔한 피부 질환으로, 특히 피부가 하얀 폐경기 여성에게 더욱 흔합니다. 붉은 선, 검은 반점, 얇은 피부가 혼합된 형태로 나타납니다. 일반적으로 얼굴, 목, 가슴 등 햇빛에 노출되는 부위에 영향을 주지만 그늘진 부위에는 영향을 미치지 않습니다. Poikiloderma of Civatte는 주요 특징에 따라 붉은기, 검은 반점 또는 두 가지가 혼합된 형태로 분류될 수 있습니다. 정확한 원인은 완전히 밝혀지지 않았지만 햇빛 노출, 호르몬 변화, 향수나 화장품에 대한 반응, 노화 등이 중요한 역할을 하는 것으로 생각됩니다. Poikiloderma of Civatte는 시간이 지나면서 서서히 악화되는 경향이 있습니다.
Poikiloderma of Civatte (PC) is a rather common benign dermatosis of the neck and face, mainly affecting fair-skinned individuals, especially postmenopausal females. It is characterized by a combination of a reticular pattern of linear telangiectasia, mottled hyperpigmentation and superficial atrophy. Clinically, it involves symmetrically sun-exposed areas of the face, the neck, and the V-shaped area of the chest, invariably sparing the anatomically shaded areas. Depending on the prevalent clinical feature, PC can be classified into erythemato-telangiectatic, pigmented, and mixed clinical types. The etiopathogenesis of PC is incompletely understood. Exposure to ultraviolet radiation, hormonal changes of menopause, contact sensitization to perfumes and cosmetics, and normal ageing have been incriminated. The diagnosis is usually clinical and can be confirmed by histology, which is characteristic, but not pathognomonic. The course is slowly progressive and irreversible, often causing significant cosmetic disfigurement.
Poikiloderma of Civatte (PC) is a rather common benign dermatosis of the neck and face, mainly affecting fair-skinned individuals, especially postmenopausal females. It is characterized by a combination of a reticular pattern of linear telangiectasia, mottled hyperpigmentation and superficial atrophy. Clinically, it involves symmetrically sun-exposed areas of the face, the neck, and the V-shaped area of the chest, invariably sparing the anatomically shaded areas. Depending on the prevalent clinical feature, PC can be classified into erythemato-telangiectatic, pigmented, and mixed clinical types. The etiopathogenesis of PC is incompletely understood. Exposure to ultraviolet radiation, hormonal changes of menopause, contact sensitization to perfumes and cosmetics, and normal ageing have been incriminated. The diagnosis is usually clinical and can be confirmed by histology, which is characteristic, but not pathognomonic. The course is slowly progressive and irreversible, often causing significant cosmetic disfigurement.
