Literature DB >> 17500183

Hamartochondroma arising from a tracheal bronchus.

Domenico Iusco1, Antonio Bobbio, Enrico Donadei, Paolo Carbognani.   

Abstract

Tracheal bronchus is a congenital abnormality rarely described in the literature. It is mostly completely asymptomatic. This condition may rarely be associated with inflammatory diseases. Exceptional are those cases in which the condition is associated with malignancy. We describe a case of a 45-year-old man in whom a 3-month history of non-productive cough and chest pain led to a diagnosis of a solitary pulmonary nodule associated with a tracheal bronchus. The histopathological examination after VATS enucleation showed the presence of a hamartochondroma. To the best of our knowledge this is the first case in which a hamartochondroma has been found to be associated with a tracheal bronchus.

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Year:  2007        PMID: 17500183

Source DB:  PubMed          Journal:  Chir Ital        ISSN: 0009-4773


  1 in total

1.  A case of tracheal hamartoma resected with loop electrocautery.

Authors:  Marios Panagiotou; Alexandros Kalkanis; Napoleon Karagiannidis; Vlasis Polychronopoulos
Journal:  Case Rep Pulmonol       Date:  2013-01-14
  1 in total

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