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Sarcomatoid carcinoma is an extremely rare biphasic tumor characterized by a combination of malignant epithelial and mesenchymal cells. Limited data on sarcomatoid carcinoma showed that most cases occurred with advanced local disease and metastasis, and paraneoplastic syndromes were rare. We pre­sent the case of a 63-year-old man with lung sarcomatoid carcinoma associated with jejunum metastasis and leukocytosis, and its clinical, macroscopic, and histopathological features. This case emphasizes the import­ance of recognizing paraneoplastic syndromes and metastasis of sarcomatoid carcinoma at diagnosis

Predominant sarcomatoid carcinoma of the lung concurrent with jejunal metastasis and leukocytosis