Cargando…
A Familial Poikiloderma-Like Cutaneous Amyloidosis
Familial poikiloderma-like cutaneous amyloidosis(FPLCA) is a rare, generalized but genetic dyschromic skin disorder characterized by amyloid deposits in dermis due to defective DNA repair secondary to sunlight damage. Clinically, it presents with diffuse brownish pigmentation with hypo-pigmented mac...
Autores principales: | Unni, Mahesh, Ankad, Balachandra, Naidu, Varna, Sudakar Rao, KM |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4248533/ https://www.ncbi.nlm.nih.gov/pubmed/25484425 http://dx.doi.org/10.4103/0019-5154.143581 |
Ejemplares similares
-
Recurrent and Diffuse Eczema with Severe Itch and Peripheral Eosinophilia in Healthy Middle Aged Woman
por: Unni, Mahesh, et al.
Publicado: (2015) -
Poikiloderma Vasculare Atrophicans: A Distinct Clinical Entity?
por: Mahajan, Vikram K, et al.
Publicado: (2015) -
Primary localized cutaneous amyloidosis with lichen and
poikiloderma-like lesions and an excellent response to systemic acitretin
por: MA, Han, et al.
Publicado: (2016) -
Successful Treatment of Poikiloderma-Like Cutaneous Amyloidosis: A Case Report and Literature Review
por: Lin, Yi-Liang, et al.
Publicado: (2021) -
Bullous Variant of Familial Biphasic Lichen Amyloidosis: A Unique Combination of Three Rare Presentations
por: Suranagi, Vijayalaxmi Veerabasappa, et al.
Publicado: (2015)