Canalis R F, Gussen R
Arch Otolaryngol. 1980 May;106(5):290-3. doi: 10.1001/archotol.1980.00790290042014.
Temporal bone rhabdomyosarcomas are rare tumors that occur almost exclusively in children. They arise most commonly in the middle ear, from which they extend through the mastoid and petrous portions of the temporal bone, eventually invading the cranium. We report the histopathologic findings of a rhabdomyosarcoma with anterior and medial displacement, predominantly involving the petrous bone. Recognition and separate study of this type of tumor is clinically important. Predominantly petrosal rhabdomyosarcomas are less prevalent than similar lesions with lateral expansion and tend to develop significant ear symptoms late in the course of the disease. When first diagnosed, these lesions usually exhibit signs of intracranial extension, and consequently are less amenable to treatment and are more rapidly fatal.
颞骨横纹肌肉瘤是罕见肿瘤,几乎仅发生于儿童。它们最常起源于中耳,由此延伸穿过颞骨的乳突部和岩部,最终侵犯颅骨。我们报告了1例横纹肌肉瘤的组织病理学表现,该肿瘤向前内侧移位,主要累及岩骨。识别并单独研究这类肿瘤具有重要临床意义。以岩骨为主的横纹肌肉瘤比具有外侧扩展的类似病变少见,且往往在疾病后期才出现明显耳部症状。初次诊断时,这些病变通常已表现出颅内扩展迹象,因此较难治疗,且死亡更快。