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Primary adenoid cystic carcinoma of the trachea: a report of two cases and literature review


Mohammed El Marjany
Adil Arsalane
Hassan Sifat
Khalid Andaloussi
Mohamed Oukabli
Khalid Hadadi
El Hassan Kabiri
Hamid Mansouri

Abstract

Adenoid cystic carcinoma (ACC) of the trachea is rare, it represents 1% of all respiratory tract cancers. It’s generally considered as a slowgrowing, with pronlonged clinical course. Most patients present with dyspnea, and the symptoms often mimic those of asthma or chronic bronchitis Surgical resection is the mainstay of treatment often combined to radiotherapy because of close surgical margins. When surgery isn’t possible, most tumors respond to radiotherapy alone wich often results in long periods of remission We report two  cases of primary ACC of trachea: a 49 year old male presented a distal unresectable tracheal ACC treated with chemo-radiotherapy who developed a recurrence and died 7 years after the diagnosis. And a 50 years old  female with a proximal tracheal tumor treated by surgical resection and end- to- end anastomosis followed by adjuvant radiotherapy. At 10 months follow-up, our patient shows no evidence of disease with negative  histological findings.

Key words: Adenoid cystic carcinoma, trachea, tracheal resection, radiotherapy


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eISSN: 1937-8688