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Vol. 53. Núm. 4.
Páginas 350-354 (octubre 2000)
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Vol. 53. Núm. 4.
Páginas 350-354 (octubre 2000)
Acceso a texto completo
Síndrome de Klippel-Trenaunay: a propósito de tres nuevas observaciones
Klippel-trenaunay syndrome: report of 3 new cases
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20842
P. Gimeno Pita, P. Pérez Martín, M. Marco Tello, V. Rebage Moisés*
Unidad Neonatal. Hospital Miguel Servet. Zaragoza
J. López-Pisóna, M. Romeo Uleciab, N. Galeano Ricañoc
a Servicios de Neuropediatría. Hospital Miguel Servet. Zaragoza
b Cirugía Infantil. Hospital Miguel Servet. Zaragoza
c Cirugía Plástica. Hospital Miguel Servet. Zaragoza
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Se comunican tres nuevas obervaciones de síndrome de Klippel-Trenaunay (SKT) de distinta evolución y extensión, que reúnen criterios diagnósticos, evaluados por examen físico, técnicas de imagen, estudios radiológicos y de laboratorio. La malformación vascular e hipertrofia de tejidos blandos era evidente en los tres casos, en dos de ellos existían lesiones internas y agrandamiento óseo, y en uno anomalías digitales. Se revisan, además, los principales aspectos de esta importante angiodisplasia.

Palabras clave:
Síndrome de Klippel-Trenaunay (SKT)
Malformación vascular

We report three new cases of Klippel-Trenaunay Syndrome (KTS), with differing evolution and involvement, in which the diagnostic criteria were confirmed by physical evaluation, imaging techniques, radiologic and laboratory studies. Vascular malformation and soft tissue hypertrophy were evident in all three patients: two showed internal lesions and bony hypertrophy and one patient showed digital deformities. We review the main features of this important angiodysplasia.

Key words:
Klippel-Trenaunay Syndrome (KTT)
Vascular malformation
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