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Cutis marmorata telangiectatica congenita in a preterm newborn – Case report and literature review

BACKGROUND: Cutis marmorata telangiectatica congenita (CMTC) is a sporadic congenital skin vascular abnormality. Significant number of patients has other congenital anomalies. CASE REPORT: We report a case of a preterm male newborn with cutis marmorata pattern presented on the skin of the face, righ...

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Autores principales: Matic, A, Pricic, S, Matic, Milan, Velisavljev Filipovic, G, Ristivojevic, A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kowsar 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3482331/
https://www.ncbi.nlm.nih.gov/pubmed/23115721
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author Matic, A
Pricic, S
Matic, Milan
Velisavljev Filipovic, G
Ristivojevic, A
author_facet Matic, A
Pricic, S
Matic, Milan
Velisavljev Filipovic, G
Ristivojevic, A
author_sort Matic, A
collection PubMed
description BACKGROUND: Cutis marmorata telangiectatica congenita (CMTC) is a sporadic congenital skin vascular abnormality. Significant number of patients has other congenital anomalies. CASE REPORT: We report a case of a preterm male newborn with cutis marmorata pattern presented on the skin of the face, right side of front of the trunk, whole back, glutei and both legs. Besides, microretrognatia and asymmetric, bad-formed, low-set ears were notable. Ophthalmologic findings showed visual impairment and pale optic nerve papilla. Monitoring of child showed mental underdevelopment and motor retardation. CONCLUSION: CMTC is a rare finding with good prognosis of skin malformations, with an obligation of dermatologist and paediatrician to investigate other associated congenital anomalies.
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spelling pubmed-34823312012-10-31 Cutis marmorata telangiectatica congenita in a preterm newborn – Case report and literature review Matic, A Pricic, S Matic, Milan Velisavljev Filipovic, G Ristivojevic, A Iran Red Crescent Med J Case Report BACKGROUND: Cutis marmorata telangiectatica congenita (CMTC) is a sporadic congenital skin vascular abnormality. Significant number of patients has other congenital anomalies. CASE REPORT: We report a case of a preterm male newborn with cutis marmorata pattern presented on the skin of the face, right side of front of the trunk, whole back, glutei and both legs. Besides, microretrognatia and asymmetric, bad-formed, low-set ears were notable. Ophthalmologic findings showed visual impairment and pale optic nerve papilla. Monitoring of child showed mental underdevelopment and motor retardation. CONCLUSION: CMTC is a rare finding with good prognosis of skin malformations, with an obligation of dermatologist and paediatrician to investigate other associated congenital anomalies. Kowsar 2012-09-30 2012-09 /pmc/articles/PMC3482331/ /pubmed/23115721 Text en Copyright © 2012, Iranian Red Crescent Medical Journal http://creativecommons.org/licenses/by/3/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Matic, A
Pricic, S
Matic, Milan
Velisavljev Filipovic, G
Ristivojevic, A
Cutis marmorata telangiectatica congenita in a preterm newborn – Case report and literature review
title Cutis marmorata telangiectatica congenita in a preterm newborn – Case report and literature review
title_full Cutis marmorata telangiectatica congenita in a preterm newborn – Case report and literature review
title_fullStr Cutis marmorata telangiectatica congenita in a preterm newborn – Case report and literature review
title_full_unstemmed Cutis marmorata telangiectatica congenita in a preterm newborn – Case report and literature review
title_short Cutis marmorata telangiectatica congenita in a preterm newborn – Case report and literature review
title_sort cutis marmorata telangiectatica congenita in a preterm newborn – case report and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3482331/
https://www.ncbi.nlm.nih.gov/pubmed/23115721
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