| Literature DB >> 33944824 |
Alfredo Annicchiarico1, Mario Giuffrida2, Paolo Del Rio3, Elena Bonati4, Gennaro Perrone5, Fausto Catena6.
Abstract
Diaphragmatic hernia (DH) can be congenital or acquired. DH is a potentially life-threatening condition and the management in emergency setting remain unclear. Nonspecific symptoms can delay the diagnosis. We report a case of a 63-year-old man admitted for abdominal pain and nausea. He was successfully treated with damage control surgery.Entities:
Year: 2021 PMID: 33944824 PMCID: PMC8142769 DOI: 10.23750/abm.v92iS1.10096
Source DB: PubMed Journal: Acta Biomed ISSN: 0392-4203
Figure 1.Sagittal and coronal CT-Scan shows a large diaphragmatic defect on the left side which allows the passage of the stomach in the absence of signs of ischemia.
Figure 2.The forward displacement of the gastric bubble, the missing of the gastric folds and the absence of contrast enhancement in gastric’s walls suggest a failure of conservative management and impose surgical treatment.
Figure 3.Intraoperative findings. Surgical exploration shows a left posterolateral diaphragmatic defect.
Figure 4.Open Abdomen. Negative pressure wound therapy was chosen for temporary abdominal closure
Figure 5.Previous CT-Scan. The patient reports the absence of previous trauma and a CT-Scan performed 5 years earlier excludes a diaphragmatic defect related to CDH.