Journals / Haydarpaşa Numune Eğitim ve Araştırma Hastanesi Tıp Dergisi / 2012 / Cilt: 52 - Sayı: 3

Cutis marmoratatelangiectatica congenita: case report

Konjenital kutis marmoratus telenjiektazi

Pages
159–161
Publication Date
2022-10-17
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Our purpose to report the case is to call attention to a rare benign disease which can alsobe multi-systemic involvement.

📌 3 Key Takeaways

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Objective & Hypothesis:Cutis marmorata telangiectatica congenital is rare sporadic congenital vascular anomaly characterized by telangiectasia, phlebectasia and persistent cutis marmorata, generally seen in newborn period, likely to be associated with multisystem congenital abnormalities, was describedby van Lohuizen in 1922.
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Key Findings & Data:In our case, we reportthe baby who had persistent cutis marmorata onthe anterior of the lower extremities and a little onthe abdomen region just after birth.
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Conclusion & Impact:Our purpose to report the case is to call attention to a rare benign disease which can alsobe multi-systemic involvement.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Cutis marmorata telangiectatica congenital is rare sporadic congenital vascular anomaly characterized by telangiectasia, phlebectasia and persistent cutis marmorata, generally seen in newborn period, likely to be associated with multisystem congenital abnormalities, was describedby van Lohuizen in 1922. In our case, we reportthe baby who had persistent cutis marmorata onthe anterior of the lower extremities and a little onthe abdomen region just after birth. There wasany finding revealing associated congenital anomaly either in the physical examination of the patient or laboratory evaluation or imaging modalities. Our purpose to report the case is to call attention to a rare benign disease which can alsobe multi-systemic involvement.

Özet

Konjenital kutis marmoratus telenjiektazi, kutanöz damar yapısının tutulumu ile seyreden, telenjiektaziler, flebektazilerle ve persiste eden kutis marmoratus ile karakterize, genellikle yeni doğan döneminde ortaya çıkan, multisistem konjenital anomalilerin efllik edebildiği, 1922 yılındavan Lohuizen tarafından tarif edilmifl nadir görülen sporadik bir hastalıktır. Sunduğumuz vakamızda doğumdan hemen sonra saptanan, karınbölgesinde ve bacakların ön yüzünde persisteeden kutis marmoratus bulunmaktaydı, hastanınyapılan fizik muayenesinde, laboratuar tetkiklerve görüntüleme yöntemlerinde herhangi bir efllikeden anomali saptanmadı. Bu vakayı sunmamızın amacı genellikle selim olan ancak multisistem tutulum da gösterebilen nadir görülen buhastalığa dikkat çekmektir.

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Cite This Article

ERDOĞAN, F., ÇİFTÇİ, M., DÜNDAR, M. (2022). Cutis marmoratatelangiectatica congenita: case report. Haydarpaşa Numune Eğitim ve Araştırma Hastanesi Tıp Dergisi, Cilt: 52 - Sayı: 3, 159–161. https://ajindex.com/articles/535418

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References (1)

  1. Chatterjee R, Dey S. Cutis marmorata telangiectatica congenita with skin ulcerations in a new born. Indian J Dermatol 2009;54:375-7. 2.South DA, Jacobs AH. Cutis marmorata telangiectatica congenita (congenital generalized phlebectasia). J Pediatr 1978;93:944-9. 3. Amita- i DB, Fichman S, Merlob P, Morad Y, Lapidoth M, Metzker A: Cutis marmorata telangiectatica congenita: clinical findings in 85 patients. Pediatr Dermatol 2000;17(2):100-4. 4.Devillers AC, de Waard-van der Spek FB, Oranje AP: Cutis marmorata telangiectatica congenita: clinical features in 35 cases. Arch Dermatol 1999;135(1):34-8. 5.Gerritsen MJ, Steijlen PM, Brunner HG, Rieu P: Cutis marmorata telangiectatica congenita: report of 18 cases. Br J Dermatol 2000;142(2):366-9. 6.Picascia DD, Esterly NB. Cutis marmorata telangiectatica congenita: Report of 22 cases. J Am Acad Dermatol 1989;20:1098-1104.