Successful resection of a re-occurred pulmonary myosarcoma in a patient with Turner syndrome mosaic

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Abstract

We describe a patient who underwent thoracic radiation therapy for biopsy-proven pulmonary spindle cell sarcoma in the left lower lobe, 15 months after birth. At the age of 37 she developed shoulder pain, fatigue, and progressive exertion dyspnoea. Chest X-ray revealed a pulmonary mass in the left lower lobe due to a cytology-proven malignant tumour. The patient underwent left pneumonectomy. Histology revealed a myosarcoma of the lung, similar to the previous sarcoma. Furthermore, the patient was diagnosed to have Turner syndrome mosaic and chromosomal analysis revealed a translocation t(1;13) in 3/50 metaphases. However a germline mutation of the p53 tumour suppressor gene was excluded. After 2 years of follow-up the patient is stable and there are no signs of recurrence of the tumour. We conclude a re-occurrence of this very rare malignant disorder of the lung after a 36-year interval in a patient with Turner syndrome mosaic. Following initial curative radiation therapy, with a remission over 36 years, lung resection was now successfully performed.

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Brauer, V. F. H., Reichenberger, F., Müller, A., Steinert, M., Froster, U. G., Wirtz, H. R. W., & Schauer, J. (2002). Successful resection of a re-occurred pulmonary myosarcoma in a patient with Turner syndrome mosaic. Sarcoma, 6(4), 141–143. https://doi.org/10.1080/1357714021000066395

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