[HTML][HTML] Prenatal diagnosis of fetal gallbladder duplication associated with uncommon chromosomal anomaly (46, XX, t (X; 10)(p11. 2; q24. 3)[20])

EH Comert, H Sal, C Kart, ESG Guven… - … Obstetrics & Gynecology, 2019 - imrpress.com
EH Comert, H Sal, C Kart, ESG Guven, S Guven
Clinical and Experimental Obstetrics & Gynecology, 2019imrpress.com
Fetal gallbladder duplication is a rare congenital malformation. In the literature only a few
cases of fetal gallbladder duplication in utero is reported. A 22-year-old woman was referred
to this hospital at 26 weeks of gestation for a routine ultrasound examination. A fetal
duplication of gallbladder accompanied was diagnosed with ultrasonography (axial section
of fetal abdomen on sonography showed two hypoechoic cyst-like structures). The diagnosis
of duplication of gallbladder, was also confirmed with MRI. The result of cordocentesis was …
Fetal gallbladder duplication is a rare congenital malformation. In the literature only a few cases of fetal gallbladder duplication in utero is reported. A 22-year-old woman was referred to this hospital at 26 weeks of gestation for a routine ultrasound examination. A fetal duplication of gallbladder accompanied was diagnosed with ultrasonography (axial section of fetal abdomen on sonography showed two hypoechoic cyst-like structures). The diagnosis of duplication of gallbladder, was also confirmed with MRI. The result of cordocentesis was reported as 46, XY, t(X;10) (p11.2;q24.3) [20]. Antenatal/natal/postnatal care was unremarkable. A novel chromosomal mutation (46, XX, t(X;10) (p11.2;q24.3) [20]) with duplicated fetal gallbladder which has not been reported previously was described.
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