| Literature DB >> 19541571 |
Yi-Chen Lai1, Hong-Jen Chiou, Hung-Ta Hondar Wu, Yi-Hong Chou, Hsin-Kai Wang, Paul Chih-Hsueh Chen.
Abstract
Alveolar soft part sarcoma (ASPS) is a rare soft-tissue sarcoma, commonly occurring in children and adolescents. The tumor mostly involves the lower extremities. The prognosis of the patient depends on whether there is metastasis. We present a 19-year-old female with ASPS in her right lower leg. Grayscale and color Doppler ultrasound showed a well-defined hypoechoic lesion with hypervascularity and very low resistive index (RI). Magnetic resonance imaging revealed iso signal intensity to muscle on T1-weighted images, high signal intensity to muscle on T2-weighted images with signal voids, and good enhancement after gadolinium administration. In a mass with hypervascularity and very low RI on sonography and hypervascularity with flow voids on magnetic resonance imaging, ASPS should be considered.Entities:
Mesh:
Year: 2009 PMID: 19541571 DOI: 10.1016/S1726-4901(09)70382-X
Source DB: PubMed Journal: J Chin Med Assoc ISSN: 1726-4901 Impact factor: 2.743