ArticleCase reports in radiology2016
Bilateral Morgagni Hernia: A Unique Presentation of a Rare Pathology.
Article in Case reports in radiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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Who cites it
3 citing papers in PubMed, 5 citations in OpenAlex.
- Ultrasound diagnosis of congenital Morgagni hernias: Ten years of experience at two Chinese centers.World journal of clinical cases · 2024Article
- Giant Morgagni hernia with transthoracic herniation of the left liver lobe and transverse colon: a case report.Journal of medical case reports · 2023Article
- Intrathoracic migration of ventriculo-peritoneal shunt via Morgagni hernia.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2021Article
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Authors and funding
2 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Morgagni hernia is an unusual congenital herniation of abdominal content through the triangular parasternal gaps of the anterior diaphragm. They are commonly asymptomatic and right-sided. We present a case of a bilateral Morgagni hernia resulting in delayed growth in a 10-month-old boy. The presentation was unique due to its bilateral nature and its symptomatic compression of the mediastinum. Diagnosis was made by 3D reconstructed CT angiogram. The patient underwent medical optimization until he was safely able to tolerate laparoscopic surgical repair of his hernia. Upon laparoscopy, the CT findings were confirmed and the hernia was repaired.
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