Tuberc Respir Dis > Volume 38(3); 1991 > Article
Tuberculosis and Respiratory Diseases 1991;38(3):309-316.
DOI: https://doi.org/10.4046/trd.1991.38.3.309    Published online September 1, 1991.
A case of primary malignant fibrous histiocytoma of the lung.
In Cheol Shin1, Sun Woo Lee1, Moon Jun No1, In Won Park1, Byoung Whui Choi1, Sung Ho Hue1, Mi Kyoung Kim2, Kye Yong Song2, Dong Suep Sohn3, Ki Min Yang3
1Department of I nterna/ Medicine, College of Medicine, Chung.Ang University, Seoul, Korea
2Department of Anatomical Pathology, College of Medicine, Chung.Ang University, Seoul, Korea
3Department of Chest Surgery, College of Medicine, Chung.Ang University, Seoul, Korea
Abstract
Malignant fibrous histiocytoma (MFH ) is the most common soft tissue sarcoma of late adult life This tumor occurs principally as a mass on an extremity or in the abdominal cavity or retroperitoneum of adult but primary pulmonary MFH is rare. MFH may be subclassified into storiform. pleomorphic, myxoid. giant cell, inflammatory, and angiomatoid type and the prognosis is no different among the histologic subtypes We experienced one patient who was consistent with primary MFH of the lung. The patient complained dyspnea and intermittent hemoptysis and showed bilateral suprahilar mass on simple chest film and chest CT. Histological findings by open lung biopsy was storiform-pleomorphic type and individual cells showed histiocyte. like and fibroblast .like appearance


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