Author/Authors :
ELMAS, Ömer Faruk Atatürk Üniversitesi - Tıp Fakültesi - Dermatoloji Anabilim Dalı, Türkiye , KIZILYEL, Okan Atatürk Üniversitesi - Tıp Fakültesi - Dermatoloji Anabilim Dalı, Türkiye , METİN, Mahmut Sami Atatürk Üniversitesi - Tıp Fakültesi - Dermatoloji Anabilim Dalı, Türkiye , KARAKUZU, Ali Atatürk Üniversitesi - Tıp Fakültesi - Dermatoloji Anabilim Dalı, Türkiye , BİLİCİ, Şule Atatürk Üniversitesi - Tıp Fakültesi - Dermatoloji Anabilim Dalı, Türkiye
Abstract :
Cutis marmorata telangiectatica congenita is a rare congenital disorder in which there are telangiectasia, phlebectasia, atrophy and ulcers in skin. Although etiology is not well known it is thought to be multifactorial. Anomalies are associated with 50% of cases. Our case was 17 years old boy presented with phlebectasia on his right lower extremity and atrophy and cutis marmoratus lesions on his back. There weren’t neurologic system and eye involvement. Routine laboratory and radiologic investigations were unremarkable. Diagnosis was cutis marmorata telangiectatica congenita. There was no need for treatment because there weren’t associated anomalies and subjective complaints of the patient. We decided to report this case because cutis marmorata telangiectatica congenita is a rare disease and our patient was undiagnosed until age of 17.
NaturalLanguageKeyword :
Atrophy , Cutis , Marmorata , Phlebectasia.
