Cutis marmorata telangiectatica congenita: Clinical findings in 85 patients

Citation
D. Ben Amitai et al., Cutis marmorata telangiectatica congenita: Clinical findings in 85 patients, PEDIAT DERM, 17(2), 2000, pp. 100-104
Citations number
25
Categorie Soggetti
Pediatrics
Journal title
PEDIATRIC DERMATOLOGY
ISSN journal
07368046 → ACNP
Volume
17
Issue
2
Year of publication
2000
Pages
100 - 104
Database
ISI
SICI code
0736-8046(200003/04)17:2<100:CMTCCF>2.0.ZU;2-4
Abstract
Cutis marmorata telangiectatica congenita (CMTC) is an uncommon, sporadic, congenital cutaneous condition presenting with persistent cutis marmorata, telangiectasia, phlebectasia and possible ulceration of the involved skin, skin atrophy, and undergrowth of the involved extremity. To further the cur rent understanding of this disorder, we analyzed the clinical features of a large series of patients with CMTC. The files of 85 patients with CMTC who were examined in our center over the last 20 years were reviewed. The data recorded included patient sex, age at onset, nature and distribution of th e lesions, associated abnormalities, and course of disease. CMTC was charac terized by early recognition of the lesions (94% at birth) and equal sex di stribution. The lesion was unilateral in 65% of patients and most commonly involved the limbs (69%), Additional capillary lesions, noted in 20% of pat ients, may well have been an extension of the CMTC itself. Associated anoma lies were found in 18.8% of patients. Almost half of the patients showed a definite improvement in the reticular vascular pattern on follow-up. No fam ilial cases of CMTC were noted. CMTC is more prevalent than previously reco gnized, affects both sexes equally, and has a mostly localized distribution ; additional vascular lesions are associated with the disorder, but other a nomalies occur less often, Prognosis is generally good.