Ultrasound is well established for the evaluation of fetal abnormalities. Studies of the normal adrenal glands of the fetus' and neonate2 have been previously described. However, no descriptions of fetal adrenal tumors diagnosed ultrasonographically have been found. In this case report, a case of co
Prenatal sonographic diagnosis of adrenal neuroblastoma
✍ Scribed by Alvaro Grandó; Vicente Monteggía; Carlos Gandara; Rodrigo Ruano; Victor Bunduki; Marcelo Zugaib
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 351 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0091-2751
- DOI
- 10.1002/jcu.1029
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Neuroblastoma is the most frequent extracranial solid tumor in childhood, but it is seldom diagnosed prenatally. We report a case of adrenal neuroblastoma identified at 39 weeks' menstrual age and successfully treated by postnatal surgery and chemotherapy. Sonography revealed a hyperechoic mass in the right upper quadrant of the fetal abdomen associated with hydramnios and hydronephrosis. Two days after delivery, the tumor was resected. No metastasis was identified. The infant received 6 cycles of chemotherapy, and at 2 years of age she was well, with no signs of recurrence. © 2001 John Wiley & Sons, Inc. J Clin Ultrasound 29:250–253, 2001.
📜 SIMILAR VOLUMES
Neuroblastoma is well recognized in the newborn, and has also been detected in the fetus. We report a case of metastases in the liver diagnosed in utero and later confirmed to be from a neuroblastoma of the left adrenal gland.
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
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