2023, Number 04
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Ginecol Obstet Mex 2023; 91 (04)
Klippel-Trenaunay syndrome and pregnancy. Report of three cases
Ibargüengoitia-Ochoa F, Lira-Plascencia J, López-Torres MF
Language: Spanish
References: 17
Page: 274-279
PDF size: 376.78 Kb.
ABSTRACT
Background: Klippel Trenaunay syndrome is a rare congenital disease characterized
by capillary and venous malformations, limb overgrowth and in some cases lymphatic
malformations. Sufferers have an increased risk of hemorrhage and thromboembolism.
Clinical cases: Three primigravid patients diagnosed with Klippel Trenaunay syndrome
with pregnancy complications that were terminated by cesarean section with
the birth of their healthy, full-term children in all cases.
Conclusions: Women with Klippel-Trenaunay syndrome and pregnancy are at
significant risk for aggravation of their symptoms, hemorrhage during birth, and thromboembolic
events, even after birth. Individualized, multidisciplinary care will help
mitigate associated complications and achieve optimal outcomes.
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