Literature DB >> 11005126

Klippel-Trenaunay-Weber syndrome presenting as massive lymphangiohemangioma of the thigh: prenatal diagnosis.

L F Gonçalves1, M V Rojas, D Vitorello, E T Pereira, M Pereima, J A Saab Neto.   

Abstract

We report a case of Klippel-Trenaunay-Weber syndrome presenting prenatally as a massive congenital lymphangiohemangioma of the thigh. Routine ultrasonographic examination revealed multiple distorted cystic areas extending from the right flank through the right lower extremity of a 30-week fetus. A diagnosis of cystic lymphangioma of the thigh was suspected prenatally. Neonatal evaluation confirmed the prenatal findings. Neonatal color Doppler imaging revealed blood vessels within the tumor. The differential diagnosis is discussed together with available therapeutic procedures.

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Year:  2000        PMID: 11005126     DOI: 10.1046/j.1469-0705.2000.00040.x

Source DB:  PubMed          Journal:  Ultrasound Obstet Gynecol        ISSN: 0960-7692            Impact factor:   7.299


  3 in total

1.  Morphological changes observed via fetal ultrasound in prenatally diagnosed and isolated congenital lymphangiomas: three case reports.

Authors:  Yusuke Inde; Emi Yamagishi; Ikuno Kawabata; Atsuko Sekiguchi; Akihito Nakai; Toshiyuki Takeshita
Journal:  J Med Ultrason (2001)       Date:  2012-11-27       Impact factor: 1.314

Review 2.  Imaging evaluation of fetal vascular anomalies.

Authors:  Maria A Calvo-Garcia; Beth M Kline-Fath; Denise M Adams; Anita Gupta; Bernadette L Koch; Foong-Yen Lim; Tal Laor
Journal:  Pediatr Radiol       Date:  2014-12-10

3.  Prenatal diagnosis of Klippel-Trenaunay syndrome: Series of four cases and review of the literature.

Authors:  Olga Ivanitskaya; Elena Andreeva; Natalia Odegova
Journal:  Ultrasound       Date:  2019-10-17
  3 in total

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