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Primary Pulmonary Myxoid Liposarcoma with Translocation t(12;16)(q13;p11) in a Young Female Patient: A Brief Case Report

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¼ÕÃáÈñ, ÃÖÇÊÁ¶, ³ë¹Ì¼÷,
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¼ÕÃáÈñ ( Son Choon-Hee ) 
Dong-A University College of Medicine Department of Internal Medicine

ÃÖÇÊÁ¶ ( Choi Phil-Jo ) 
Dong-A University College of Medicine Department of Thoracic and Cardiovascular Surgery
³ë¹Ì¼÷ ( Roh Mee-Sook ) 
Dong-A University College of Medicine Department of Pathology

Abstract


Primary liposarcoma of the lung is an extremely rare disease. To date, only 14 cases have been reported in the literature. We experienced a case of myxoid liposarcoma of the lung treated by surgery. The tumor was well-defined, solid, lobulated mass measuring 3.5¡¿2 cm, involving the bronchus of the left lower lobe. Microscopically, myxoid liposarcoma was identified. The fluorescence in situ hybridization confirmed the presence of a reciprocal translocation involving DNA damage-inducible transcript 3 (DDIT3) and fused in sarcoma (FUS) genes. The patient is still alive with no recurrence or metastasis at the time of writing this report (on 20 months postoperatively). To our knowledge, this is the first cytogenetic case report of pulmonary myxoid liposarcoma.

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Lung; Liposarcoma; In situ hybridization; fluorescence

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