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

作者信息

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

机构信息

Clínica Materno-Fetal, Florianópolis, SC, Brazil.

出版信息

Ultrasound Obstet Gynecol. 2000 Jun;15(6):537-41. doi: 10.1046/j.1469-0705.2000.00040.x.

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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