• Users Online: 1251
  • Print this page
  • Email this page
CASE REPORT
Year : 2016  |  Volume : 7  |  Issue : 1  |  Page : 32-35

Dowling–Degos disease with reticulate acropigmentation of Kitamura: Extended spectrum of a single entity


Department of Dermatology, Chirayu Medical College and Hospital, Bhopal, Madhya Pradesh, India

Correspondence Address:
Dr. Shyam Govind Rathoriya
Department of Dermatology, Chirayu Medical College and Hospital, Bhopal - 462 030, Madhya Pradesh
India
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/2229-5178.174307

Rights and Permissions

Dowling–Degos disease (DDD) and reticulate acropigmentation of Kitamura (RAK) are rare genodermatoses inherited as an autosomal dominant trait with variable penetrance. They are considered to be part of a spectrum of reticulate pigmentary dermatoses, characterized by the presence of hyperpigmented macules coalescing in a reticular fashion. The authors describe a 28-year-old male patient having hyperpigmented macules on the axillae, neck and face, reticulate acropigmentation of dorsum of the hands, forearms and feet, palmar pitting, and comedo-like lesions over back. The patient showed the unique clinical as well as histopathological overlap of both the rare diseases (DDD and RAK), substantiating the hypothesis that they represent two different features of a single entity with variable phenotypic expression.


[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
    Viewed2173    
    Printed16    
    Emailed0    
    PDF Downloaded286    
    Comments [Add]    
    Cited by others 2    

Recommend this journal