Fetal echocardiographic findings in the Klippel-Trenaunay-Weber syndrome.

Drose, Julia A.; Thickman, David; Wiggins, James W.; Haverkamp, Alexander

doi:10.7863/jum.1991.10.9.525

Cited by 21 publications

(23 citation statements)

References 4 publications

(4 reference statements)

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“…This phenomenon was not a feature of the fetus until the third trimester, the cutaneous haemangiomata being the dominant abnormality in the second trimester. Uncommonly, other associated features may be present antenatally, such as non-immune hydrops (Mor et al, 1988), cardiomegaly (Drose et al, 1991) and bony abnormalities (Meizner et al, 1994). A wide range of differential diagnoses were considered antenatally.…”

Section: Discussionmentioning

confidence: 99%

Prenatal sonographic appearances of Klippel-Trenaunay-Weber syndrome

et al. 1999

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Section: Discussionmentioning

confidence: 99%

Prenatal sonographic appearances of Klippel-Trenaunay-Weber syndrome

et al. 1999

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“…Nonimmune hydrops fetalis, polyhydramnios, cardiac failure, macrocrania, ventriculomegaly, and hepatomegaly are other prenatal features [7, 11, 12]. High-output cardiac failure and coagulopathy could be caused by hemangioma-associated diffused intravascular coagulation and intravascular hemolysis [7].…”

Section: Discussionmentioning

confidence: 99%

Sonographic Identification of Klippel-Trenaunay-Weber Syndrome

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et al. 2013

Case Reports in Obstetrics and Gynecology

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Klippel-Trenaunay-Weber syndrome is a rare cutaneous vascular disorder characterized by the presence of multiple hemangiomata, arteriovenous fistulas, and limb hypertrophy. We report the prenatal sonographic findings in a case of Klippel-Trenaunay-Weber (KTW) syndrome including fetal limb hypertrophy and large subcutaneous cystic lesions. Prenatal diagnosis is possible by ultrasound examination and recognition important for prevention of complications and future management.

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“…Cardiomegaly was reported in a prenatal diagnosis of KTW. 10 Each case of KTW has its own combination and varying degree of symptomatology. There is a male:female ratio of 1:1 associated with KTW.…”

Section: Bone or Soft-tissue Hypertrophymentioning

confidence: 99%

Sonographic Appearance of Klippel-Trénaunay-Weber Syndrome Diagnosed at 18 Weeks Gestation

Hubacz¹

2001

Journal of Diagnostic Medical Sonography

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Presented is a case of Klippel-Trénaunay-Weber (KTW) syndrome. This rare syndrome is associated with a triad of anomalies including varicose veins, cutaneous hemangiomas, and bony or soft tissue hypertrophy. The prominent sonographic finding is multiple cystic areas or localized edema most often located on the lower torso of the fetus. Findings suggestive of KTW syndrome were noted following an 18-week gestation fetal survey and were later confirmed at autopsy.

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Fetal echocardiographic findings in the Klippel-Trenaunay-Weber syndrome.

Cited by 21 publications

References 4 publications

Prenatal sonographic appearances of Klippel-Trenaunay-Weber syndrome

Prenatal sonographic appearances of Klippel-Trenaunay-Weber syndrome

Sonographic Identification of Klippel-Trenaunay-Weber Syndrome

Sonographic Appearance of Klippel-Trénaunay-Weber Syndrome Diagnosed at 18 Weeks Gestation

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