Tarhan N C, Yologlu Z, Tutar N U, Coskun M, Agildere A M, Arikan U
Department of Radiology, Baskent University School of Medicine, Bahcelievler Ankara, Turkey.
Eur Radiol. 2000;10(10):1678-80. doi: 10.1007/s003300000323.
We present the case of a 44-year-old woman with chondromyxoid fibroma of temporal bone origin. Since this is the least common bone tumor of cartilaginous origin, it is highly unusual to find this tumor in the skull. In fact, the literature describes 18 cases of this form of neoplasia arising in the skull, only 4 of these having originated in the temporal bone. To date, the radiological features of these tumors, and especially features detected using the latest imaging modalities, have not been described in detail. This report is unique in that it is the first to present a case of chondromyxoid fibroma of the temporal bone accompanied by detailed CT and MRI findings.
我们报告一例起源于颞骨的软骨黏液样纤维瘤的44岁女性病例。由于这是起源于软骨的最罕见骨肿瘤，在颅骨中发现这种肿瘤非常罕见。事实上，文献中描述了18例起源于颅骨的这种肿瘤，其中只有4例起源于颞骨。迄今为止，这些肿瘤的放射学特征，尤其是使用最新成像方式检测到的特征，尚未得到详细描述。本报告的独特之处在于，它首次呈现了一例伴有详细CT和MRI表现的颞骨软骨黏液样纤维瘤病例。
