Reis SC, Ferreira HIF, Tranquillini G, Tadeu VR, Franco FL, Bedin V

Language: Portugués
References: 8
Page: 133-135
PDF size: 257.71 Kb.

ABSTRACT

Phacomatosis pigmentovascularis is defined as the association of a vascular malformation with an extensive pigmented nevus. Currently, it is classified into three groups: cesioflammea, spilorosea and cesiomarmorata. A case of an infant with 5 months of age who presented the association of vascular malformation and aberrant mongolian spots since birth, without systemic involvement, is presented. The interest in this case relates to the rarity and need to recognize the syndrome and its repercussions.

REFERENCES

1. Happle R. Phacomatosis pigmentovascularis revisited and reclassified. Arch Dermatol. 2005; 141: 385-388.

2. Fernández MG, Boixeda P, de las Heras E, Aboin S, Millán CG, Olasolo PJ. Phakomatosis pigmentovascularis: clinical findings in 15 patients and review of the literature. J Am Acad Dermatly. 2008; 58: 88-93.

3. Seckin D, Yucelten D, Aytug A, Demirkesen C. Phacomatosis pigmentovascularis tipe IIIb. Int J Dermatol. 2007; 26: 960-963.

4. Hall BD, Cadle RG, Morrill-Cornelius SM, Bayet CA. Phakomatosis pigmentovascularis: implications for severity with especial reference to Mongolian spots associated with Sturge-Weber and Klippel-Trenaunay syndromes. Am J Med Genetics. 2007;143A: 3047-3053.

5. Landro AD, Tadini GL, Marchesi L, Cainelli T. Phakomatosis pigmentovascularis: a new case with renal angiomas and some considerations about the classification. Pediatr Dermatol. 1999; 16: 25-30.

6. Hasegawa Y, Yasuhara M. Phakomatosis pigmentovascularis type IVa. Arch Dermatol. 1985; 121: 651-655.

7. Noriega-Sanchez A, Markland ON, Herndon JH. Oculocutaneous melanosis associated with the Sturge-Weber syndrome. Neurology. 1972; 22: 256-262.

8. HuangCY, Lee PY. Phakomatosis pigmentovascularis IIb with renal anomaly. Clin Exp Dermatol. 2000; 25: 51-54.