Clinical and Radiological Presentations of Pelvic Parachordoma

Author:

Huang Chun-Chao1,Cheng She-Meng1

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.

Publisher

SAGE Publications

Subject

Oncology,Histology

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

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