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Asian Cardiovasc Thorac Ann 2002;10:189-190
© 2002 Asia Publishing EXchange Pte Ltd

CASE STUDY

Mediastinal Myelolipoma

Gao Bing, MD, Hiroshi Sugimura, MD, Shuichiro Sugimura, MD, Yoshinobu Hattori, MD, Tadashi Iriyama, MD, Hideki Kano, MD

Department of Thoracic Surgery Fujita Health University School of Medicine and Health University College Toyoake City, Aichi, Japan
Gao Bing, MD Tel: 81 75 751 3784 Fax: 81 75 751 4960 email: gaobing_cn{at}yahoo.com Department of Cardiovascular Surgery, Faculty of Medicine, Kyoto University, 54 Kawara-cho, Shogoin, Sakyo-ku, Kyoto 606-8507, Japan.
Myelolipoma is a rare tumor, and a mediastinal location is extremely unusual. The main pathologic feature is the coexistence of mature adipose tissue and bone marrow cells; the presence of megakaryocytes is essential for diagnosis. The successful removal of a mediastinal myelolipoma in a 59-year-old man is described.




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 Ann. Thorac. Surg.Home page
M. Vaziri, A. Sadeghipour, A. Pazooki, and L. Z. Shoolami
Primary mediastinal myelolipoma.
Ann. Thorac. Surg., May 1, 2008; 85(5): 1805 - 1806.
[Abstract] [Full Text] [PDF]


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