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Rare mediastinal leiomyoma in a child

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Abstract

Leiomyoma of the mediastinum is rare. They are thought to arise from the smooth muscle cells of the media of mediastinal vascular structures and structure containing smooth muscle. Most mediastinal leiomyomas are seen in association with oesophagus in the posterior mediastinum. We present a case of huge leiomyoma in a 1.5 years old male child arising in the lower anterior mediastinum with compression of heart, liver and deformity of rib cage. Median sternotomy and a separate concomitant right mini-thoracotomy was done and tumor excised. Histopathology proved it to be a leiomyoma.

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Acknowledgments

We acknowledge the support of the patient’s relatives in letting us report this case.

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Correspondence to Zubair Ashraf Hakeem.

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Hakeem, Z.A., Rathore, S.S. & Wahid, A. Rare mediastinal leiomyoma in a child. Gen Thorac Cardiovasc Surg 65, 415–417 (2017). https://doi.org/10.1007/s11748-016-0705-5

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  • DOI: https://doi.org/10.1007/s11748-016-0705-5

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