Literature DB >> 18401685

Tracheal chondrosarcoma.

Hideo Umezu1, Motohiko Tamura, Satoru Kobayashi, Noriyoshi Sawabata, Koichi Honma, Shinichiro Miyoshi.   

Abstract

Tracheal chondrosarcomas are rare, with only 14 cases previously documented. We report a case of chondrosarcoma of the trachea and review other published cases. Our patient was a 34-year-old man who began to feel shortness of breath 8 months after initial hemoptysis. Transverse and coronal computed tomography demonstrated a tumor that was obstructing nearly 80% of the tracheal lumen at the thoracic inlet. A bronchoscopic biopsy specimen led to an initial diagnosis of chondroma. Five tracheal rings from the third to the seventh including the tumor were completely resected, and an end-to-end anastomosis was performed. The histological diagnosis of the surgical specimen showed it to be a chondrosarcoma. The patient was alive without recurrence at 6 years 4 months after surgery. Because recurrence after incomplete resection and malignant transformation can occur with chondromas, radical resection of the trachea is recommended for all cartilaginous tumors of the trachea.

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Year:  2008        PMID: 18401685     DOI: 10.1007/s11748-007-0218-3

Source DB:  PubMed          Journal:  Gen Thorac Cardiovasc Surg        ISSN: 1863-6705


  8 in total

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  8 in total
  7 in total

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Journal:  Cancer Rep (Hoboken)       Date:  2021-09-02
  7 in total

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