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Prenatal sonographic diagnosis of Klippel-Trenaunay-Weber syndrome: a case report.

Authors
Yang, JI; Kim, HS; Ryu, HS
Citation
The Journal of reproductive medicine, 50(4):291-294, 2005
Journal Title
The Journal of reproductive medicine
ISSN
0024-7758
Abstract
BACKGROUND: Klippel-Trenaunay-Weber syndrome is a rare congenital soft tissue anomaly with sporadic occurrence characterized by the triad of multiple hemangiomas, arteriovenous fistulas and unilateral limb hypertrophy.



CASE: A 27-year-old, pregnant woman was referred at 31 2/7 gestational weeks. On prenatal sonography, multiloculated cystic areas involving the left side of the thorax and hypertrophy of the upper portion of the left arm were diagnosed without diagnostic findings on color flow Doppler studies of the cutaneous hemangioma. There was no progression within the remainder of the gestational period, and the neonatal outcome was good.



CONCLUSION: Klippel-Trenaunay-Weber syndrome should be considered in the differential diagnosis of a fetal thoracic mass even if color flow Doppler studies of the mass are negative.
MeSH terms
AdultArm/pathologyArm/ultrasonographyCysts/ultrasonographyFalse Negative ReactionsFemaleHumansKlippel-Trenaunay-Weber Syndrome/ultrasonography*PregnancyThorax/pathologyThorax/ultrasonographyUltrasonography, Doppler, ColorUltrasonography, Prenatal*
PMID
15916215
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Obstetrics & Gynecology
AJOU Authors
양, 정인김, 행수유, 희석
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