Department of Paediatrics, SSIMS & RC, Davangere, India
World Journal of Advanced Research and Reviews, 2022, 16(03), 236-238
Article DOI: 10.30574/wjarr.2022.16.3.0963
DOI url: https://doi.org/10.30574/wjarr.2022.16.3.0963
Received on 02 September 2022; revised on 16 November 2022; accepted on 19November 2022
It is uncommon for children to have celiac artery compression syndrome. We describe a case of celiac artery compression syndrome in a young child who initially reported to us with severe recurrent epigastric pain abdomen and nausea. Historical evidence of rapid weight loss over 15 days. When the child's symptoms persisted despite symptomatic treatment, comprehensive testing revealed that the child had celiac artery compression syndrome. In this report, we emphasize the significance of taking celiac artery compression syndrome into account as one of the differential diagnoses for acute severe epigastric pain that is unresponsive to standard gastritis treatment and when all investigations for pancreatitis, ureteric obstruction, and renal colic are normal.
MALS (Median Arcuate Ligament Syndrome); Celiac artery compression syndrome; Case; Children
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Shivanna N.K. , Kalappanavar Bhavya and Aanchal Khemani. A rare case of celiac artery compression syndrome. World Journal of Advanced Research and Reviews, 2022, 16(03), 236-238. Article DOI: https://doi.org/10.30574/wjarr.2022.16.3.0963
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