Cleidocranial dysostosis is an autosomal dominant disorder characterized by absence or hypoplasia of the clavicles, skull abnormalities, and abnormal dentition. The prenatal diagnosis of this condition has been reported once previously in a known high-risk pregnancy. In this report we describe the p
Giant hemangioma of the thigh: Prenatal sonographic diagnosis
โ Scribed by Vincenzo Suma; Alberto Marini; Pier Giorgio Gamba; Claudia Luzzatto
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 383 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0091-2751
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โฆ Synopsis
Giant cutaneous hemangioma is a rare congenital anomaly that can cause dystocia due to its size.' We describe a case in which prenatal diagnosis of a giant hemangioma of the thigh, discovered by ultrasound examination during the 28th week, menstrual age (MA), was a useful indication that a cesarean section would be necessary.
sponding to menstrual age. Repeated, accurate, longitudinal, transverse, and oblique echographic scans showed no evidence of vascular lacunae or pulsatile structures. No anomalies of the brain, spinal cord, thorax, abdomen, upper limbs, or lower right limb were found.
The abdominal aorta and inferior vena cava had normal morphology and position. Sonographic examinations were repeated every week
CASE REPORT
A 34-year-old woman, primigravida, with a negative personal and family history, was referred to our Ultrasound Service after a routine sonogram. This examination, performed at 28 weeks, MA, showed a mass in the left thigh of the fetus.
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Agenesis of the vermis as detected during gestation by ultrasonography may indicate the existence of various malformation arrays or syndromes. We report on our observations of five cases of complete vermal agenesis that were detected at 22-31 weeks of gestation. All had a vertex presentation and tra
The aim of this study was to describe the prenatal detection of fetal nasal abnormalities by ultrasound. Transvaginal and transabdominal sonography was used for the detection of fetal malformations in 25 114 cases. The fetal nose was visualized in all the fetuses in an oblique section and in the lat
Purpose. We present a small series of prenatally diagnosed cases of ectopia cordis. Methods. Four fetuses with prenatally diagnosed ectopia cordis were sonographically evaluated and followed up. Results. The fetuses were diagnosed with ectopia cordis at 9, 13, 21, and 29 weeks' menstrual age. The