Coexistence of porokeratosis of Mibelli with Gardner's syndrome: A rare case report

Porokeratosis represents a heterogeneous group of disorders characterized clinically by a distinctive ridge-like border and histologically by cornoid lamellae. Gardner's syndrome, a variant of familial adenomatous polyposis (FAP), is an autosomal dominant disease characterized by colorectal pol...

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Detalles Bibliográficos
Autores principales: Ali, Syed Yousuf, Prabhat, Shivangi, Ramanamurty, Ch. V., Salma, Mahjabeen, Hussain, Shamshad, Murtaza, Ahmed Syed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications Pvt Ltd 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3481819/
https://www.ncbi.nlm.nih.gov/pubmed/23130235
http://dx.doi.org/10.4103/2229-5178.86001
Descripción
Sumario:Porokeratosis represents a heterogeneous group of disorders characterized clinically by a distinctive ridge-like border and histologically by cornoid lamellae. Gardner's syndrome, a variant of familial adenomatous polyposis (FAP), is an autosomal dominant disease characterized by colorectal polyps, osteomas, epidermoid cysts and soft tissue tumors. Here we report a case of 18 yr old female who presented with porokeratosis of Mibelli with osteoma, multiple epidermoid cytsts, and solitary rectal polyp.

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