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J Thorac Cardiovasc Surg 2003;126:1204-1207
© 2003 The American Association for Thoracic Surgery
Brief communication |
a Department of Thoracic and Cardiovascular Surgery, Rouen University Hospital-Charles Nicolle, Rouen, France
b Department of Radiology, Rouen University Hospital-Charles Nicolle, Rouen, France
c Department of Anesthesiology, Rouen University Hospital-Charles Nicolle, Rouen, France
Received for publication March 13, 2003; accepted for publication April 24, 2003.
* Address for reprints: Pierre-Yves Litzler, MD, Department of Thoracic and Cardiovascular Surgery, Charles Nicolle University Hospital, 1, rue de Germont, 76000 Rouen, France
pierre-yves.litzler@chu-rouen.fr
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A 35-year-old woman with a medical history of hereditary and recurrent epistaxis and lip telangiectasia was admitted with sudden left thoracic pain and dyspnea. There was no recent history of fever or thoracic trauma. Biologic data were as follows: hemoglobin level, 8.8 g/L; hematocrit level, 28%; oxygen saturation, 97%; and fraction of inspired oxygen, 10 L/min. Chest radiography and computed tomographic (CT) scanning revealed a left hemothorax with a suspicion of a vascular malformation in the left lower lobe (Figure 1). There were no aortic or pericardial abnormalities.
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