AI Article Synopsis

  • Portopulmonary hypertension (PoPH) is a serious complication linked to portal hypertension, especially in patients with liver cirrhosis, but is often underdiagnosed due to the variety of symptoms like dyspnea.
  • A comprehensive case study highlights the use of advanced imaging techniques, including dual energy CT and pulmonary perfusion imaging, to effectively diagnose PoPH.
  • This refined imaging protocol provides a noninvasive, efficient way to evaluate PoPH, complementing standard chest evaluations.

Article Abstract

Pulmonary arterial hypertension associated with portal hypertension, known as portopulmonary hypertension (PoPH) is one of the important and serious pulmonary complications in patients with portal hypertension. Although there are a large number of patients with portal hypertension due to mainly liver cirrhosis, the number of cases diagnosed with PoPH are far fewer because the causes of dyspnea in patients with cirrhosis are diverse and the disease entity of PoPH is poorly recognized by clinicians. We report here the case with PoPH suggested and assessed comprehensively by dual energy computed tomography (CT) including high-resolution pulmonary CT angiography, pulmonary perfusion imaging, myocardial late iodine enhancement imaging, and myocardial extracellular volume analysis. This refined CT imaging protocol can be used in conjunction with standard chest evaluation and offers a practical and useful approach for the noninvasive "one-stop shop" evaluation of PoPH.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10726335PMC
http://dx.doi.org/10.1016/j.radcr.2023.11.013DOI Listing

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