Affiliation:
1. Department of Radiology, Mackay Memorial Hospital, Taipei, Taiwan
Abstract
Parachordoma is an extremely rare entity and there are only about 50 to 60 cases reported, in which there is only one definite pelvic parachordoma. We present a huge well-defined presacral tumor in a 48-year-old woman who has the symptoms of lower abdominal pain and difficulty in defecating. Radiological findings of the tumor on computed tomography and magnetic resonance imaging are described in detail. The reasons why we report the case are because the patient has rare clinical symptoms and because this is the second pelvic parachordoma. Then, we summarize the radiological features of parachordoma based on our study and the review of literature.
Reference11 articles.
1. LaskowskiJ Abstracts of papers, VIII international cancer congressMoscowMedgiz Publishing House1962262–262
2. Parachordoma of Soft Tissues of the Arm
3. Intraneural parachordoma of the arm with regional metastases
4. FletcherCDM UnniK MertensF World Health Organisation Classification of Tumours: Pathology and Genetics of Tumours of Soft Tissue and BoneIARC Press LyonWHO2002198–9
Cited by
6 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献