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Umbilical teratoma in a newborn

Authors :
Taylor Shaw
Hannah Cockrell
Ross Straughan
Dan Parrish
David Sawaya
Source :
Journal of Pediatric Surgery Case Reports, Vol 70, Iss , Pp 101873- (2021)
Publication Year :
2021
Publisher :
Elsevier, 2021.

Abstract

Congenital tumors of the umbilical cord are rare, and teratomas of the umbilical cord are exceedingly rare. Umbilical cord masses are often detected on routine prenatal ultrasound; however, umbilical teratomas are difficult to diagnose by imaging studies alone, and often require histopathologic examination for definitive diagnosis. Given the polymorphic presentation of umbilical cord teratomas and associated congenital anomalies, amniocentesis for genetic screening and fetal karyotyping should be offered. Here we report a case of a prenatally suspected umbilical cord angiomyxoma in an otherwise normal fetus who was found to be a mature teratoma on surgical pathology.

Subjects

Subjects :
Pediatrics
RJ1-570
Surgery
RD1-811

Details

Language :
English
ISSN :
22135766
Volume :
70
Issue :
101873-
Database :
Directory of Open Access Journals
Journal :
Journal of Pediatric Surgery Case Reports
Publication Type :
Academic Journal
Accession number :
edsdoj.1e269faa7502484a9586e759d1c37490
Document Type :
article
Full Text :
https://doi.org/10.1016/j.epsc.2021.101873