Endoscopy 1990; 22(6): 276-278
DOI: 10.1055/s-2007-1012870
© Georg Thieme Verlag KG Stuttgart · New York

Chondroma of the Diaphragm - Report of a Case

M. Itakura, K. Shiraishi, T. Kadosaka, S. Matsuzaki
  • Department of Internal Medicine, Tokai University School of Medicine, Tokyo Hospital, Tokyo, Japan
Further Information

Publication History

Publication Date:
17 March 2008 (online)

Summary

A rare case of chondroma of the diaphragm is reported. The patient was a 23-year-old female who had had recurrent upper abdominal pain for 4 years. Her symptoms and physical findings on admission suggested an intra-abdominal tumor. Roentgenological study disclosed a mass with a thick calcified wall in the upper abdomen. Laparoscopy revealed a multinodular while mass protruding from the left hemidiaphragm. The mass was surgically enucleated from the diaphragm. The resected tumor had a thick, calcified wall and a narrow lumen containing colorless fluid. Microscopic examination disclosed a hyaline chondroid matrix with mature chondrocytes, as well as extensive ossification.

Primary tumor of the diaphragm is an uncommon disease. Only one case of chondroma of the diaphragm has been reported in the literature. Laparoscopy was useful in confirming the tumor's location and in speculating on its nature.

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