| Literature DB >> 22187338 |
Yohsuke Yagi1, Akira Machida, Shuta Toru, Takayoshi Kobayashi, Tomonari Amano, Katsuiku Hirokawa, Masanobu Kitagawa.
Abstract
A 58-year-old man developed muscle weakness and had more than 1,000 CTG repeats in the myotonin protein kinase gene. He was diagnosed as having myotonic dystrophy. At the time of diagnosis, a large tumor was detected in his abdominal cavity on CT scan examination. He died from pneumonia 6 years later. At autopsy, the abdominal tumor was diagnosed as a lipoma. Several types of tumor have been reported to be associated with myotonic dystrophy type 1; however, this is the first detailed clinical case demonstrating the possible relationship between myotonic dystrophy and lipoma.Entities:
Mesh:
Year: 2011 PMID: 22187338 DOI: 10.1007/s10072-011-0896-6
Source DB: PubMed Journal: Neurol Sci ISSN: 1590-1874 Impact factor: 3.307