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2023, Number 1

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Arch Inv Mat Inf 2023; 14 (1)

Congenital telangiectatic cutis marmorata. About a case

Pérez-Elizondo AD, Urrutia-Torres FJ
Full text How to cite this article 10.35366/113547

DOI

DOI: 10.35366/113547
URL: https://dx.doi.org/10.35366/113547

Language: Spanish
References: 6
Page: 31-34
PDF size: 190.01 Kb.


Key words:

congenital telangiectatic cutis marmorata, vascular malformation, dermatology.

ABSTRACT

Congenital telangiectatic cutis marmorata (CTCM) is a rare low-flow vascular malformation involving capillaries and venous vessels, characterized by the presence of a localized or generalized asymmetric pattern of erythematous-violaceous reticulated macules present from or shortly after birth. The diagnosis is clinical and the prognosis good, although it depends on the presence of associated congenital anomalies. A 13-year-old female patient is presented with erythematous-violaceous lesions in a reticulated pattern with peripheral telangiectasias, located on the face, trunk and extremities, compatible with a diagnosis of congenital phlebectasia with systemic congenital anomalies.


REFERENCES

  1. Frieden I, Enjorlas O, Esterly N. Vascular birthmarks and other abnormalities of blood vessels and lymphatics. In: Schacner LA, Hansen RC (editors). Pediatric dermatology. 3rd ed. London: Mosby; 2003. pp. 833-862.

  2. van Lohuizen CHJ. Uber eine seltene angerborene hautanomalie (cutis marmorata telangiectatica congenita). Acta Derm Venereol. 1922; 3: 201-211.

  3. del Boz-González J, Serrano-Martín MM, Vera-Casaño A. Cutis marmorata telangiectásica congénita. Revisión de 33 casos. An Pediatr (Barc). 2008; 69 (6): 557-564.

  4. Kramer HD, Alfaro CP, Muñoz MP. Cutis marmorata telangiectático congénito: a propósito de cuatro casos. Rev Chil Pediatr. 2010; 81 (3): 241-245.

  5. Nagore A, Tórrello A, Zambrano A. Cutis marmorata telangiectásica congénita. Revisión de 28 casos. Actas Dermosifiliogr. 1999; 90: 433-438.

  6. Kienast AK, Hoeger PH. Cutis marmorata telangiectatica congenita: a prospective study of 27 cases and review of the literature with proposal of diagnostic criteria. Clin Exp Dermatol. 2009; 34 (3): 319-323.




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Arch Inv Mat Inf. 2023;14