A Case of Primary Malignant Fibrous Histiocytoma of the Lung |
Joong Sik Kim1, Bang Sun Kim2, Hwa Sik Moon2, Wan Kook Lee2, Jae Cheol Ro2, Seung Hak Park2, Hae Won Pyun2, Eun Joo Seo3 |
1Department of Internal Medicine, Dong Boo City Hospital, Seoul, Korea 2Department of Internal Medicine, Catholic Medcial College, Seoul, Korea 3Department of Clinicopatholoy, , Catholic Medcial College, Seoul, Korea |
폐에 발생한 원발성 악성 섬유성 조직구종 1예 |
김중식1, 김방선2, 문화식2, 이완국2, 노재철2, 박성학2, 변해원2, 서은주3 |
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Abstract |
Malignant fibrous histiocytoma was originally considered as a rare variant of common benign fibrous histiocytoma, but recently reclassified as a distinct form of sarcoma. A storiform pattern with admixture of fibroblasts and histiocytes, as well as xanthomatous and giant cells, is characteristic histological findings. This tumor is a deep seated soft tissue sarcoma of the extremities and trunk.
Although the lung is a frequent site for distant metastasis of this tumor, primary malignant fibrous histicoytoma of the lung is quite rare. We present a case of primary malignant fibrous histiocytoma of the lung with a discussion of its clinical and pathological manifestations |
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