Kaya Ö, Yoldaş T, Karademir S, Örün UA, Sarı E. A pediatric case of Ortner`s syndrome caused by heritable pulmonary arterial hypertension and review of the literature. Turk J Pediatr 2019; 61: 963-966. An 11-year-old male, who complained of hoarseness and fatigue on effort presented to our institution for evaluation. Left vocal cord paralysis and severe pulmonary hypertension was diagnosed. The patient had an enlarged pulmonary artery due to pulmonary hypertension which was responsible for compression to left vocal cord paralysis causing hoarseness. Ortner`s syndrome or cardiovocal syndrome is known as hoarseness due to left vocal cord paralysis secondary to cardiac pathologies. Although hoarseness of voice is frequently encountered in the otorhinolaryngology clinics, pulmonary hypertension related hoarseness is an unusual presentation in childhood.
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http://dx.doi.org/10.24953/turkjped.2019.06.022 | DOI Listing |
Ortner's syndrome, also known as cardiovocal syndrome, is a rare cause of hoarseness due to compression of the left recurrent laryngeal nerve caused by pathology of cardiovascular structures in the mediastinum. It was first described by Norbert Ortner in 1897, who associated the syndrome with mitral stenosis. It typically presents as paresis of the left recurrent laryngeal nerve, which is mechanically compressed in the area of the aortic arch.
View Article and Find Full Text PDFRadiol Case Rep
December 2024
Department of Radiology, Mohammed VI University Hospital of Tangier, Tangier, Morocco.
Ortner's syndrome or cardiovocal syndrome is a rare condition referring to laryngeal recurrent nerve paralysis due to cardiovascular conditions. We report the case of a 66-year-old man, with a medical history of active smoking, who complained of hoarseness of voice secondary to vocal cord palsy. A neck and thoracic CT scan revealed severe enlargement of pulmonary main artery, which caused compression of the left recurrent laryngeal nerve in the aortopulmonary window The prolonged course of the left laryngeal nerve makes it susceptible to injury from cardiovascular structures in the mediastinum.
View Article and Find Full Text PDFBMJ Case Rep
August 2024
Department of Radiology, Imperial College Healthcare NHS Trust, London, UK
Am J Case Rep
August 2024
Department of Cardiology, Cardiovascular Institute, Hospital Clínico San Carlos, Madrid, Spain.
Cureus
June 2024
Radiodiagnosis, All India Institute of Medical Sciences, Bathinda, Bathinda, IND.
Polycystic kidney disease (PKD) is a genetic disease characterized by the formation of multiple cysts in bilateral kidneys. While renal complications are predominant, cardiovascular manifestations such as aortic aneurysms can also occur. Although there are a few case reports of giant aortic arch aneurysms, to the best of our knowledge, this has been rarely reported in patients with PKD.
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