Multiple chondromatous hamartomas of the lung

A. Bini, M. Grazia, F. Petrella, M. Chittolini

Research output: Contribution to journalArticlepeer-review

Abstract

Multiple chondromatous hamartomas (MCH) of the lung are very rare: only 16 cases have been reported to date. In young women, the tumours may be a manifestation of Carney triad (gastric leiomyoblastoma, pulmonary hamartoma and extra-adrenal paraganglioma) or Cowden syndrome (mucocutaneous lesions, multiple benign tumors of internal organs and increased risk for breast, thyroid, urogenital and digestive tract cancer). We report the 17th case of MCH of the lung, diagnosed accidentally in a 66 year-old male patient, with suspected concomitant hamartomas and malignant tumours.

Original languageEnglish
Pages (from-to)78-80
Number of pages3
JournalInteractive Cardiovascular and Thoracic Surgery
Volume1
Issue number2
DOIs
Publication statusPublished - Dec 2002

Keywords

  • Carney triad
  • Cowden syndrome
  • Multiple chondromatous hamartomas of the lung

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine
  • Pulmonary and Respiratory Medicine
  • Surgery

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