Cutis Marmorata Telangiectatica Congenita

Devillers, A. C. A.; Spek, Flora B. de Waard‐van der; Oranje, Arnold P.

doi:10.1001/archderm.135.1.34

Cited by 101 publications

(131 citation statements)

References 15 publications

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“…Frecuentemente, las lesiones cutáneas se resuelven dentro de los primeros dos años de vida. 2 Presentamos el caso de un paciente con CMTC y manifestaciones de sindactilia y lesiones cutáneas en todas las extremidades, el tronco y el rostro.…”

Section: Piel Marmórea Telangiectásica Congénita Y Sindactilia En Un unclassified

“…El glaucoma es la anomalía ocular concomitante más frecuente; suele detectarse en pacientes con lesiones perioculares vasculares. 2,3 En nuestro paciente, el examen oftalmológico para detectar glaucoma fue normal.…”

Section: Figura 2 Lesión Eritematosa Reticulada Sobre Las Extremidadunclassified

“…1 Este trastorno de etiología desconocida suele presentarse al nacimiento. 2 La mayoría de las veces, la CMTC se diagnostica sobre la base de las características clínicas. En general, se presentan anomalías asociadas, como asimetría corporal, malformaciones vasculares, úlceras y atrofia cutáneas, glaucoma,…”

Section: Introductionunclassified

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Piel marmórea telangiectásica congénita y sindactilia en un recién nacido prematuro. A propósito de un caso

İlhan¹,

Özer

Özdemir

et al. 2016

Arch Argent Pediat

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Arch Argent Pediatr 2016;114(2):e111-e113 / e111Presentación de casos clínicos RESUMEN La piel marmórea telangiectásica congénita (cutis marmorata telangiectatica congenita, CMTC) es una anomalía vascular congénita rara, a menudo benigna, localizada o generalizada, de etiología desconocida. Se caracteriza por piel marmórea persistente, telangiectasia y flebectasia. Podrían presentarse manifestaciones extracutáneas asociadas con la CMTC en el 18,8-70% de los casos. El diagnóstico de este trastorno se basa en los hallazgos clínicos. El pronóstico es bueno y suele mejorar dentro de los dos años de vida. En este artículo presentamos el caso de un varón recién nacido con CMTC en la piel de todas las extremidades, el tronco y el rostro, y una anomalía asociada, que incluía sindactilia. Presentamos este caso debido a su rareza. Palabras clave: piel marmórea telangiectásica congénita, recién nacido, sindactilia.

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Section: Piel Marmórea Telangiectásica Congénita Y Sindactilia En Un unclassified

Section: Figura 2 Lesión Eritematosa Reticulada Sobre Las Extremidadunclassified

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Piel marmórea telangiectásica congénita y sindactilia en un recién nacido prematuro. A propósito de un caso

İlhan¹,

Özer

Özdemir

et al. 2016

Arch Argent Pediat

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“…Case report commonly resolve within the first 2 years of life. 2 We report a case of CMTC with findings of syndactyly and skin lesions on all the limbs, trunk and face.…”

Section: Introductionmentioning

confidence: 96%

“…1 This disorder commonly presents at birth and its aetiology is unknown. 2 Diagnosis of CMTC is mostly made on the basis of clinical features. Associated anomalies such as asymmetry of the body, vascular malformations, skin ulceration or atrophy, glaucoma, psychomotor or mental retardation and limbs anomalies are generally defined.…”

Section: Introductionmentioning

confidence: 99%

Congenital cutis marmorata telangiectatica and syndactyly in a preterm. Case report

et al. 2016

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Cutis marmorata telangiectatica congenita (CMTC) is a rare, commonly benign, congenital, localized or generalized vascular anomaly of unknown aetiology. It is characterized by persistent cutis marmorata, telangiectasia and phlebectasia. Extracutaneous findings may be associated with CMTC in 18.8-70% of the cases. Diagnosis of the disorder is based on the clinical findings. The prognosis is good and improvement is observed within 2 years after birth. Herein, we report a case of a male neonate with CMTC presented on the skin of all his limbs, trunk and face, and an associated anomaly including syndactyly. We present this case because of its rarity.

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The Misnomer “Macrocephaly–Cutis Marmorata Telangiectatica Congenita Syndrome”

Wright¹,

Frieden²,

Orlow³

et al. 2009

Arch Dermatol

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Background: The condition known as macrocephalycutis marmorata telangiectatica congenita syndrome (M-CMTC) is a rare congenital syndrome of unknown etiology characterized by macrocephaly and vascular lesions that have been described as either cutis marmorata or cutis marmorata telangiectatica congenita (CMTC). Most patients also exhibit facial and limb asymmetry; somatic overgrowth; developmental delay; capillary malformations of the nose, philtrum, and/or upper lip; neurologic abnormalities; syndactyly or polydactyly; craniofacial abnormalities; and joint laxity or soft skin. Observations: We describe 12 patients with this condition from tertiary care medical centers (8 cases) and accrued via an M-CMTC support group Web site (4 cases). All patients showed reticulated or confluent port-wine stains (PWS), not CMTC. Seven of the 12 patients also had centrofacial capillary malformations. In our comprehensive review of 100 previously reported cases, only 34 were accompanied by photographs that were sufficiently clear to review for diagnostic purposes. None had true CMTC, with most having reticulated PWS or persistent cutis marmorata. Conclusions: Reticulated or confluent PWS and persistent capillary malformations of the central face, rather than CMTC, are the most characteristic cutaneous vascular anomalies seen in so-called M-CMTC syndrome. The name macrocephaly-capillary malformations (M-CM) more accurately reflects the features of this syndrome.

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Cutis Marmorata Telangiectatica Congenita

Cited by 101 publications

References 15 publications

Piel marmórea telangiectásica congénita y sindactilia en un recién nacido prematuro. A propósito de un caso

Piel marmórea telangiectásica congénita y sindactilia en un recién nacido prematuro. A propósito de un caso

Congenital cutis marmorata telangiectatica and syndactyly in a preterm. Case report

The Misnomer “Macrocephaly–Cutis Marmorata Telangiectatica Congenita Syndrome”

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