Diagnosis of a rare case of neonatal intestinal duplication cyst isolated from the gastrointestinal tract - Case report

Duplication cysts are congenital anomalies that typically have some connection to the gastrointestinal (GI) tract, but in rare cases the cysts can be completed isolated from the GI tract. We present the case of an appropriate for gestational age male infant born at 40 weeks gestational age with neon...

Full description

Saved in:

Bibliographic Details
Published in:	Revista medicală Română Vol. 70; no. 2; pp. 89 - 94
Main Authors:	Racean, Maria-Andreea, Suciu, Laura Mihaela, Prisca, Radu Alexandru, Marginean, Cristina Oana
Format:	Journal Article
Language:	English
Published:	Amaltea Medical Publishing House 30-06-2023
Subjects:	cyst gastrointestinal tract infant intestinal duplication
Online Access:	Get full text
Tags:	Add Tag No Tags, Be the first to tag this record!

Description
Summary:	Duplication cysts are congenital anomalies that typically have some connection to the gastrointestinal (GI) tract, but in rare cases the cysts can be completed isolated from the GI tract. We present the case of an appropriate for gestational age male infant born at 40 weeks gestational age with neonatal intestinal duplication cyst isolated from the GI tract. Postnatal diagnostic methods included ultrasound (US) and magnetic resonance imaging (MRI) based on abnormal antenatal findings. The positive diagnosis was based on the imaging results. Duplication cysts may remain asymptomatic and that is the reason why antenatal and postnatal US screening plays an important key role in the diagnosis. Series of imaging may confirm the diagnosis, prevent future complication and help the clinician to determine the optimal operative moment.
ISSN:	1220-5478 2069-606X
DOI:	10.37897/RMJ.2023.2.4