Basbug Mustafa, Akgun Hulya, Ozgun Mahmut Tuncay, Turkyilmaz Cagdas, Batukan Cem, Ozcelik Bulent
Department of Obstetrics and Gynecology, Erciyes University, Faculty of Medicine, Kayseri, Turkey.
J Clin Ultrasound. 2009 Jun;37(5):298-301. doi: 10.1002/jcu.20557.
Splenogonadal fusion limb defect syndrome (SGFLD) is a very rare abnormality. We report on a case with prenatal sonographic findings of a fetus with postnatally diagnosed SGFLD syndrome. This is also the second case of prenatal ultrasonographic diagnosis of gastrointestinal malrotation associated with SGFLD. A 26-year-old primigravid woman was referred to our clinic because of nonvisualization of both fetal femoral bones at 20 weeks of gestation. A detailed sonographic examination showed complete bilateral absence of lower limbs, micrognathia, single umbilical artery and a right-sided stomach. Autopsy confirmed prenatal sonographic findings and additionally showed that the spleen was abnormally connected to the left gonad by a fibrous band. In conclusion, although all limbs and both sides were equally affected in most of the reported cases, SGFLD syndrome should be considered in cases with terminal limb defects of lower limbs.
脾性腺融合肢体缺陷综合征(SGFLD)是一种非常罕见的异常情况。我们报告了一例胎儿产前超声检查结果,该胎儿出生后被诊断为SGFLD综合征。这也是第二例产前超声诊断出与SGFLD相关的胃肠道旋转不良的病例。一名26岁的初产妇因妊娠20周时未观察到胎儿双侧股骨而转诊至我们的诊所。详细的超声检查显示双下肢完全缺如、小颌畸形、单脐动脉和右侧胃。尸检证实了产前超声检查结果,此外还显示脾脏通过一条纤维带与左侧性腺异常相连。总之,尽管在大多数报道的病例中所有肢体和双侧均受到同等影响,但对于下肢末端肢体缺陷的病例应考虑SGFLD综合征。