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British Journal of Radiology (2009) 82, e160-e163
© 2009 British Institute of Radiology
doi: 10.1259/bjr/32877860

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Liposarcoma of the sinonasal tract

S M THOMPSON, MD 1 C S DUQUE, MD 2 R N SHETH, MD 3 R R CASIANO, MD 4 J J MORCOS, MD, FRCS 3 and C R GOMEZ-FERNANDEZ, MD 1

1 Department of Pathology, University of Miami School of Medicine/Jackson Medical Center, 1611 NW 12 Avenue, Miami, FL 33136, USA, 2 Department of Oncology, Hospital Pablo Tobon Uribe, Medellin, Colombia, and Departments of, 3 Neurological Surgery and 4 Otolaryngology, University of Miami School of Medicine/Jackson Medical Center, 1611 NW 12 Avenue, Miami, FL 33136, USA

Correspondence: Sherry M Thompson, University of Miami School of Medicine/Jackson Medical Center, Department of Pathology, 1611 NW 12 Avenue, Miami, FL 33136, USA. E-mail: smthompson78{at}hotmail.com

Nasal and paranasal malignant tumours account for less than 5% of all head and neck malignancies. Epithelial malignancies overwhelmingly predominate, with squamous cell carcinomas representing the most frequent histological subtype in this location. Soft-tissue sarcomas of the nasal cavity and paranasal sinuses are exceedingly rare. Here, we report two cases of myxoid liposarcomas that occurred in the nasal and paranasal regions, both of which presented diagnostic challenges and could not be diagnosed definitively from intraoperative frozen sections. These cases reinforce the notion that, while they are uncommon, sarcomas in general and liposarcomas in particular should still be considered as part of the differential diagnosis in patients presenting with obstructive symptoms in the nasal and paranasal sinuses.







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