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- W2257255283 abstract "Mucoepidermoid carcinoma of the tracheobronchial tree is an extremely rare variant of malignant neoplasm arising from the submucosal bronchial glands. We report the clinical manifestations, treatment, and prognosis of 7 patients with mucoepidermoid carcinoma of the tracheobronchial tree. Totally, 7 patients with histopathologically verified mucoepidermoid carcinoma, between January 1988 and February 2003, were enrolled into this study. There were 5 male and 2 female patients, with ages ranging from 19 to 47 years, and a mean of 35.4 years. The tumors were located at the left main (14%), right intermediate (14%), lobar (43%), and segmental (29%) bronchus; 5 cases (71%) in the left and 2 cases (29%) in the right. The main clinical symptoms were cough (86%), hemoptysis (43%), fever (43%), wheezing (29%), and chest pain (29%). Bronchoscopically, the tumors appeared as a polypoid-like endobronchial nodule or mass. Five patients received a transbronchial tumor biopsy, resulting in 2 cases with a correct diagnosis. The mean interval from symptom onset to diagnosis was 7.9 months, ranging from 2 to 24 months. All patients were treated by surgical resection; the postoperative follow-up period ranged from 10 months to 11 years, 8 months (mean, 5 years, 11 months), and there was no evidence of tumor recurrence or metastasis. In conclusion, mucoepidermoid carcinoma in the tracheobronchial tree is a rare airway tumor, and the correct diagnosis might be delayed because of nonspecific clinical manifestations and an inadequate bronchoscopic biopsy. However, mucoepidermoid carcinomas of the tracheobronchial tree in Taiwan are usually low grade; conservative pulmonary resection is preferred, and has a favorable prognosis." @default.
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- W2257255283 date "2005-10-01" @default.
- W2257255283 modified "2023-10-17" @default.
- W2257255283 title "A Clinicopathologic Analysis of Mucoepidermoid Carcinoma of the Tracheobronchial Tree" @default.
- W2257255283 doi "https://doi.org/10.29806/tm.200510.0002" @default.
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