• Users Online: 578
  • Print this page
  • Email this page
CASE REPORT
Year : 2011  |  Volume : 2  |  Issue : 2  |  Page : 94-96

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


1 Department of Dermatology and STD, Shadan Institute of Medical Sciences, Peerancheru, Hyderabad, Andhra Pradesh, India
2 Department of Pathology, Shadan Institute of Medical Sciences, Peerancheru, Hyderabad, Andhra Pradesh, India
3 Department of Surgery, Shadan Institute of Medical Sciences, Peerancheru, Hyderabad, Andhra Pradesh, India

Correspondence Address:
Syed Yousuf Ali
H.No: 9-4-77/A/79, Al Hasnath Colony, Toli Chowki, Hyderabad-500 008, Andhra Pradesh
India
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/2229-5178.86001

Rights and Permissions

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.


[FULL TEXT] [PDF]*
Print this article     Email this article
 Next article
 Previous article
 Table of Contents

 Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
 Citation Manager
 Access Statistics
 Reader Comments
 Email Alert *
 Add to My List *
 * Requires registration (Free)
 

 Article Access Statistics
    Viewed2969    
    Printed99    
    Emailed0    
    PDF Downloaded255    
    Comments [Add]    

Recommend this journal