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- W2327260836 abstract "A 52-year-old man was admitted because of cough and a tumor-like shadow on his chest roentgenogram. Thoracotomy was performed without a definitive diagnosis. Frozen sections of the tumor examinated during operation revealed mesenchymal malignant cells, so left lower lobectomy with dissection of lymph nodes was performed. Histologically, the tumor cells showed a typical storiform-pleomorphic arrangement and immunohistochemical stains demonstrated positive reactions for vimentin, α 1-antitrypsin and α 1-antichymotrypsin, leading to a diagnosis of MFH. Ultrastructurally, the tumor cells were of three types : fibroblastic cells, histiocytic cells and primitive mesenchymal cells. No adjuvant therapy was administered. A brain metastasis was diagnosed six months later, and he died 12 months after operation.Primary MFH of internal organs is rare, and MFH of the lung is especially rare. A review of the literatures indicates that the prognosis of this disease is poor since there is a high incidence of metastases via hematogenous routes." @default.
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- W2327260836 date "1990-01-01" @default.
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- W2327260836 title "Malignant fibrous histiocytoma (MFH) of the lung-a case report-" @default.
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- W2327260836 doi "https://doi.org/10.2995/jacsurg1987.4.354" @default.
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