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Andrew Chatzis, Meletios Kanakis, Achilleas Lioulias, Fotios Mitropoulos, Unusual complication of neurofibromatosis, European Journal of Cardio-Thoracic Surgery, Volume 46, Issue 5, November 2014, Page 921, https://doi.org/10.1093/ejcts/ezu052
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A 14-year old boy with neurofibromatosis type I underwent surgery for severe kyphoscoliosis (Fig. 1A). Impaired ventilation led to the termination of the procedure. Investigation revealed tracheal compression by the innominate artery and a tumour (Fig. 1B–D). The latter was excised via right thoracotomy (Fig. 2). Histology revealed neurofibroma.

(A) Chest X-ray: severe kyphoscoliosis; (B–D): computed tomography scan: trachea compressed between the innominate artery and a tumour, identified after surgery as neurofibroma.

(A) Operative view. Tumour (arrowheads); (B) excised tumour; (C) skin neurofibromatosis lesions. I: innominate artery; T: trachea.