Cutis marmorata telangiectatica congenita

Cutis marmorata telangiectatica congenita (CMTC) is a congenital localized or generalized vascular anomaly characterized by a persistent cutis marmorata pattern with a marbled bluish to deep purple appearance, spider nevus-like telangiectasia, phlebectasia and, occasionally, ulceration and atrophy of the affected skin.

Cutis marmorata

A reticular discoloration of the skin with cyanotic (reddish-blue appearing) areas surrounding pale central areas due to dilation of capillary blood vessels and stagnation of blood within the vessels. Cutis marmorata, also called livedo reticularis, generally occurs on the legs, arms and trunk and is often more severe in cold weather.


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PMID (PMCID)
29020473
 FEMALE Young Adult
Cutis mormorata telangiectatica congenital successfully treated with intense pulsed light therapy: A case report.
Deshpande AJ.
J Cosmet Laser Ther. 2018;20(3):145-147.
Cutis marmorata telangiectatica congenita is a rare disorder characterized by cutis marmorata, telangiectasia with or without recurrent ulcerations.
18035989
 MALE Infant, Newborn
Adams-Oliver syndrome with widespread CMTC and fatal pulmonary vascular disease.
Dadzie OE, Tyszczuk L, Holder SE, Teixeira F, Charakida A, Scarisbrick J, Chu A.
Pediatr Dermatol. 2007;24(6):651-3.
We provide an overview of cutis marmorata telangiectatica congenita, distinguishing it from cutis marmorata, a common and benign physiologic cutaneous disorder seen in neonates.
17260324
 FEMALE Infant
[Bilateral congenital glaucoma in a child with cutis marmorata telangiectatica congenita: a case report].
Spitzer MS, Szurman P, Rohrbach JM, Aisenbrey S.
Klin Monbl Augenheilkd. 2007;224(1):66-9.
Cutis marmorata telangiectatica congenita is a rare, cutaneous and vascular anomaly characterised by congenital cutis marmorata, telangiectasis, and phlebectasia.
17766224
 OTHER Infant, Newborn
[Cutis marmorata telangiectatica congenita--case report].
Flach E, Kellermayer R, Ertl T, Vida G, Sarkany I, Funke S, Gyarmati J.
Orv Hetil. 2007;148(36):1717-20.
Cutis marmorata telangiectatica congenita is a rare, usually congenital, localized or generalized cutaneous vascular abnormality characterized by a persistent cutis marmorata pattern, spider naevus-like telangiectasia and ulceration or atrophy of the involved skin, which frequently improves with age.
17766224
 OTHER Infant, Newborn
[Cutis marmorata telangiectatica congenita--case report].
Flach E, Kellermayer R, Ertl T, Vida G, Sarkany I, Funke S, Gyarmati J.
Orv Hetil. 2007;148(36):1717-20.
The authors present a case of cutis marmorata telangiectatica congenita with typical clinical findings: phlebectasia of the scalp with ulceration, almost generalized persistent cutis marmorata, telangiectasia.
15337471
 MALE Infant, Newborn
A case of macrocephaly-cutis marmorata telangiectatica congenita and review of neuroradiologic features.
Akcar N, Adapinar B, Dinleyici C, Durak B, Ozkan IR.
Ann Genet. 2004;47(3):261-5.
Macrocephaly-cutis marmorata telangiectatica congenita (M-CMTC) is characterized by macrocephaly, cutis marmorata, capillary malformations, toe syndactily, joint laxity and pre-natal overgrowth.
12789192
 MALE Infant, Newborn
Cutis marmorata telangiectatica congenita with hemangiomatous histopathologic features.
Fujita M, Darmstadt GL, Dinulos JG.
J Am Acad Dermatol. 2003;48(6):950-4.
Cutis marmorata telangiectatica congenita (CMTC) is a congenital cutaneous vascular malformation that is diagnosed on the typical clinical findings of persistent cutis marmorata, telangiectasia, phlebectasia, occasional ulceration and atrophy, and tendency for clinical improvement.
11477607
 MIXED_SAMPLE Infant
Association of arrhythmia and sudden death in macrocephaly-cutis marmorata telangiectatica congenita syndrome.
Yano S, Watanabe Y.
Am J Med Genet. 2001;102(2):149-52.
Macrocephaly-cutis marmorata telangiectatica congenita (M-CMTC) constitutes a distinct entity characterized by prenatal overgrowth, macrosomia, hemihypertrophy, macrocephaly, nonobstructive hydrocephaly, frontal bossing, hypotonia, developmental delay, generalized or facial capillary malformation with upper philtral nevus flammeus and cutis marmorata, joint hypermobility, loose skin, toe syndactyly, and postaxial polydactyly.
10710221
 MIXED_SAMPLE
Macrocephaly-Cutis marmorata telangiectatica congenita without cutis marmorata?
Franceschini P, Licata D, Di Cara G, Guala A, Franceschini D, Genitori L.
Am J Med Genet. 2000;90(4):265-9.
Macrocephaly-Cutis marmorata telangiectatica congenita without cutis marmorata?
9511980
 MALE Infant
MRI findings in macrocephaly-cutis marmorata telangiectatica congenita.
Carcao M, Blaser SI, Grant RM, Weksberg R, Siegel-Bartelt J.
Am J Med Genet. 1998;76(2):165-7.
We describe a child with macrocephaly-cutis marmorata telangiectatica congenita (M-CMTC), cherry red macules, megalencephaly with hemifacial and segmental overgrowth, macrosomia, and cutis marmorata telangiectasia congenita of the trunk, and visceral and subcutaneous cavernous hemangiomas.
9588532
 FEMALE Infant
Strokes, cutis marmorata telangiectatica congenita, and factor V Leiden.
Gruppo RA, DeGrauw TJ, Palasis S, Kalinyak KA, Bofinger MK.
Pediatr Neurol. 1998;18(4):342-5.
Cutis marmorata telangiectatica congenita is an uncommon, congenital cutaneous condition typified by persistent cutis marmorata and other associated abnormalities.
9279946
 FEMALE
Ocular findings in cutis marmorata telangiectatica congenita. Bilateral exudative vitreoretinopathy.
Pendergast SD, Trese MT, Shastry BS.
Retina. 1997;17(4):306-9.
Cutis marmorata telangiectatica congenita is a rare, cutaneous, reticulated, vascular anomaly characterized by congenital persistent cutis marmorata, telangiectasis, and phlebectasis.