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dc.contributor.authorYeo, Zann
dc.contributor.authorDor, Riaz
dc.date.accessioned2025-08-01T09:38:50Z
dc.date.available2025-08-01T09:38:50Z
dc.identifier.citationCureus. 2025 Apr 18;17(4):e82512. doi: 10.7759/cureus.82512.en_US
dc.identifier.urihttp://hdl.handle.net/20.500.12904/19676
dc.description.abstractHepatic portal venous gas (HPVG) is a rare but significant radiological finding traditionally associated with severe abdominal pathology, particularly bowel ischaemia. However, advances in imaging have led to the recognition of benign and self-limiting causes. We report the case of a 34-year-old female with longstanding type 1 diabetes mellitus, autonomic dysfunction, and stage 4 chronic kidney disease (CKD), who presented with severe vomiting, abdominal pain, and malaise. CT revealed HPVG without any evidence of bowel compromise or ischaemia. The patient was successfully managed with conservative treatment, including intravenous fluids, antiemetics, and insulin therapy, resulting in rapid clinical improvement and resolution of the HPVG on follow-up imaging. This report underscores the importance of recognising vomiting-induced HPVG as a benign phenomenon and highlights the essential role of careful clinical assessment in avoiding unnecessary surgical interventions.
dc.subjectGastroenterologyen_US
dc.titleBenign Vomiting-Induced Hepatic Portal Venous Gas: A Case Report.en_US
dc.typeArticleen_US
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US
rioxxterms.versionNAen_US
rioxxterms.versionofrecord10.7759/cureus.82512.en_US
rioxxterms.typeJournal Article/Reviewen_US
refterms.dateFOA2025-08-01T09:38:51Z
refterms.panelUnspecifieden_US
refterms.dateFirstOnline2025-04
html.description.abstractHepatic portal venous gas (HPVG) is a rare but significant radiological finding traditionally associated with severe abdominal pathology, particularly bowel ischaemia. However, advances in imaging have led to the recognition of benign and self-limiting causes. We report the case of a 34-year-old female with longstanding type 1 diabetes mellitus, autonomic dysfunction, and stage 4 chronic kidney disease (CKD), who presented with severe vomiting, abdominal pain, and malaise. CT revealed HPVG without any evidence of bowel compromise or ischaemia. The patient was successfully managed with conservative treatment, including intravenous fluids, antiemetics, and insulin therapy, resulting in rapid clinical improvement and resolution of the HPVG on follow-up imaging. This report underscores the importance of recognising vomiting-induced HPVG as a benign phenomenon and highlights the essential role of careful clinical assessment in avoiding unnecessary surgical interventions.en_US
rioxxterms.funder.project94a427429a5bcfef7dd04c33360d80cden_US


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