| Literature DB >> 27134953 |
Ali Ozgur Ersoy1, Efser Oztas1, Erdinc Saridogan1, Sibel Ozler1, Nuri Danisman1.
Abstract
Fetal lymphangioma is a hamartomatous congenital anomaly of the lymphatic system, which is embracing the fetal skin (sometimes mucous membranes) and the subcutaneous tissue. The general consensus is that it occurs as a result of failure in lymphatic drainage. A 36-year-old pregnant woman was referred to our perinatology clinic at 22 weeks' gestation, because of a fetal right-sided axillary mass revealed by ultrasonography. The mass measuring 5x7x7cm in three dimensions had a multilocular structure without colour Doppler flow and well-circumscribed borders. Amniocentesis revealed a normal constitutional karyotyping. Lymphangioma was considered as prediagnosis. A healthy female baby weighing 3470 grams was delivered at term. Neonatal examination and the postnatal MRI confirmed the diagnosis. The baby is still on follow-up with the medical treatment of Sirolimus an anti-proliferative drug, and the mass got smaller significantly in 8 months after delivery.Entities:
Keywords: Axillary mass; Chest wall mass; Karyotyping; Magnetic resonance imaging
Year: 2016 PMID: 27134953 PMCID: PMC4843338 DOI: 10.7860/JCDR/2016/18516.7513
Source DB: PubMed Journal: J Clin Diagn Res ISSN: 0973-709X