Why the study?
Diaphragmatic liver herniation is a known complication of trauma or congenital defects, but no cases had been described following pericardial windowing.
This case highlights a rare but severe complication of diaphragmatic herniation following a pericardial window, requiring emergency surgical repair.
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Clinicians should consider diaphragmatic hernia in post-pericardial window patients with hypoxia; leaves open true incidence and prevention strategies.
A 37-year-old woman presented to her local district general hospital with a cough, pleuritic chest pain and intermittent cyanosis. Eight months prior, she underwent a successful pericardial window for recurrent, symptomatic pericardial effusions. On presentation she was hypoxic but haemodynamically stable. Her chest radiograph raised the suspicion of a diaphragmatic hernia, confirmed by CT imaging. This identified herniation through the diaphragm of the transverse colon and left lobe of the liver resulting in cardiac compression and right ventricular dysfunction. She continued to deteriorate and required emergency intubation to allow safe transfer to a tertiary upper gastrointestinal unit. She underwent a laparotomy and repair of the diaphragmatic hernia with an uneventful inpatient recovery. In the literature, diaphragmatic liver herniation is a recognised complication secondary to trauma or congenital defects, however, to our knowledge, there are currently no cases described following pericardial windowing.
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Harsten et al. (2020) studied this question.
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