ArticleSurgical and radiologic anatomy : SRA2016
Situs inversus with levocardia, infrahepatic interruption of the inferior vena cava, and azygos continuation: a case report.
Article in Surgical and radiologic anatomy : SRA, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed, 14 citations in OpenAlex.
- CT Findings of Azygos Venous System: Congenital Variants and Acquired Structural Changes.Journal of the Korean Society of Radiology · 2024Review
- A Case Report of Dextrocardia with Situs Inversus: A Rare Condition and Its Clinical Importance.Case reports in medicine · 2024Article
- Surgical Treatment of Lung Cancer in Situs Inversus Totalis-A Case Report.Reports (MDPI) · 2023Article
- Situs Inversus Totalis: A Clinical Review.International journal of general medicine · 2022Review
- Oblique lateral interbody fusion to treat lumbar spinal stenosis in a patient with situs inversus totalis: a case report.The Journal of international medical research · 2021Article
- Azygos and hemiazygos continuation: An occasional finding in emergency department.Radiology case reports · 2019Article
- Letter to the editor regarding "Situs inversus with levocardia, infrahepatic interruption of the inferior vena cava, and azygos continuation: a case report".Surgical and radiologic anatomy : SRA · 2015Article
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4 authors at 3 institutions in 1 country.
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No grant is acknowledged in the PubMed record.
Abstract
Situs inversus incompletus is a rare congenital condition in which the major abdominal organs are reversed or mirrored from their normal positions. It is often associated with multiple congenital anomalies. We present the case of a 38-year-old woman with dyspnea and a clinical history of chronic kidney disease and kidney transplantation. Echocardiography showed a right atrial mass, and analysis of multidetector computed tomography angiography revealed the interruption of the inferior vena cava with an increase of the azygos vein and azygos continuation. These congenital malformations are often associated with deep vein thrombosis and/or pulmonary thromboembolism and explained the occurrence of dyspnea. Cardiac magnetic resonance with contrast medium confirmed the presence of the right atrial mass, the characteristics of which were attributed to interatrial thrombus, which was further confirmed by the success of thrombolytic therapy and the remission of symptoms. In conclusion, we described a case of situs inversus with levocardia in association with infrahepatic interruption of the inferior vena cava, and azygos continuation with cardiac thrombus and chronic renal failure.
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