Volume 1, Issue 1 (3-2010)                   jdc 2010, 1(1): 44-46 | Back to browse issues page

XML Persian Abstract Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Ehsani A H, Nourmohammadpour P, Moradi A. Angiofibroma: A rare case. jdc 2010; 1 (1) :44-46
URL: http://jdc.tums.ac.ir/article-1-73-en.html
Abstract:   (9932 Views)

Tuberous sclerosis complex is a genetic disorder characterized by hamartoma formation in many organs. Its characteristic dermatologic manifestations include angiofibroma, shagreen patch, periungual fibroma and white macules. This disorder is usually accompanied by epilepsy and mental deficiency. Here, a 26-year-old man is presented who has been referred to a teaching hospital with a huge facial angiofibroma which had led to major psychological problems for him necessitating and appropriate treatment plan.

Full-Text [PDF 121 kb]   (1952 Downloads)    
Type of Study: Research | Subject: General
Received: 2009/09/30 | Accepted: 2009/10/28 | Published: 2013/07/16

Add your comments about this article : Your username or Email:
CAPTCHA

Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

© 2024 , Tehran University of Medical Sciences, CC BY-NC 4.0

Designed & Developed by : Yektaweb