| Literature DB >> 33247814 |
Carmela Brillantino1, Eugenio Rossi1, Diana Baldari1, Rocco Minelli2, Elio Bignardi3, Giuseppe Paviglianiti4, Giulia Restivo5, Maria A Cangemi6, Raffaele Zeccolini7, Massimo Zeccolini8.
Abstract
In pediatric age, duodenal hematoma is rare and generally occurs following a closed abdominal trauma due to the crushing of the duodenum against the rigid plane of the spine; it rarely follows anticoagulant therapy, pancreatitis, bleeding disorders, vasculitis, tumors or upper digestive endoscopy. Duodenal hematoma is a rare cause of obstruction of the upper gastrointestinal tract and acute pancreatitis, and the diagnosis is sometimes difficult and late. On the other hand, the identification of the pathology in its initial stages allows the young patients to be subjected to a conservative treatment that resolves the issue most of the time, thus avoiding surgery. In this article we describe an unusual case of duodenal hematoma, following esophagus-gastro-duodenoscopy, in a 12-year-old boy with Di George syndrome.Entities:
Keywords: Abdominal mass; Duodenal hematoma; RM; TC; Ultrasound
Mesh:
Year: 2020 PMID: 33247814 PMCID: PMC9148366 DOI: 10.1007/s40477-020-00545-9
Source DB: PubMed Journal: J Ultrasound ISSN: 1876-7931