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Persistence of the embryonic lateral marginal vein: report of two cases
Rojas Martinez, Raúl; Puech-Leäo, Pedro; Paulo Motta, Guimaräes; Baptista, Muraco Netto.
  • Rojas Martinez, Raúl; University of Säo Paulo. Faculty of Medicine. Hospital das Clínicas. Department of Vascular Surgery. Säo Paulo. BR
  • Puech-Leäo, Pedro; University of Säo Paulo. Faculty of Medicine. Hospital das Clínicas. Department of Vascular Surgery. Säo Paulo. BR
  • Paulo Motta, Guimaräes; University of Säo Paulo. Faculty of Medicine. Hospital das Clínicas. Department of Vascular Surgery. Säo Paulo. BR
  • Baptista, Muraco Netto; University of Säo Paulo. Faculty of Medicine. Hospital das Clínicas. Department of Vascular Surgery. Säo Paulo. BR
Rev. Hosp. Clin. Fac. Med. Univ. Säo Paulo ; 56(5): 159-162, Sept.-Oct. 2001. ilus
Artigo em Inglês | LILACS | ID: lil-305078
RESUMO

PURPOSE:

Congenital venous malformations of the lower limbs represent a particular challenge for the vascular surgeon. Persistence of fetal veins is a rare malformation, and the most common is the persistence of the lateral marginal vein usually observed in patients with Klippel-Trenaunnay Syndrome. The persistence of this embryonic vein as an isolated venous malformation without the other characteristics of the Klippel-Trenaunnay Syndrome has not yet been reported. This paper describes two cases.

METHODS:

Two patients, a 17-year-old male patient and a 16-year-old female, have had since their birth a large venous trunk in the lateral aspect of the right leg and thigh. The limbs underwent duplex scanning and phlebography. The surgical removal of the lateral marginal vein was performed.

RESULTS:

Surgical treatment resulted in very good functional and aesthetic results. Follow-up at 26 months showed no evidence of varicose vein recurrence.

CONCLUSIONS:

To achieve good results, surgical intervention may be indicated in cases of orthopedic deformity, hemorrhage, symptomatic, and unaesthetic lesions
Assuntos
Texto completo: DisponíveL Índice: LILACS (Américas) Assunto principal: Veias / Síndrome de Klippel-Trenaunay-Weber / Perna (Membro) Tipo de estudo: Estudo observacional / Estudo prognóstico Limite: Adolescente / Feminino / Humanos / Masculino Idioma: Inglês Revista: Rev. Hosp. Clin. Fac. Med. Univ. Säo Paulo Assunto da revista: Medicina Ano de publicação: 2001 Tipo de documento: Artigo País de afiliação: Brasil Instituição/País de afiliação: University of Säo Paulo/BR

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Texto completo: DisponíveL Índice: LILACS (Américas) Assunto principal: Veias / Síndrome de Klippel-Trenaunay-Weber / Perna (Membro) Tipo de estudo: Estudo observacional / Estudo prognóstico Limite: Adolescente / Feminino / Humanos / Masculino Idioma: Inglês Revista: Rev. Hosp. Clin. Fac. Med. Univ. Säo Paulo Assunto da revista: Medicina Ano de publicação: 2001 Tipo de documento: Artigo País de afiliação: Brasil Instituição/País de afiliação: University of Säo Paulo/BR