Shuangshoti S, Phonprasert C
J Neurol Neurosurg Psychiatry. 1976 Jun;39(6):531-5. doi: 10.1136/jnnp.39.6.531.
A case is reported of a primary rhabdomyosarcoma occurring in the right subfrontal region of a 16 year old girl. The patient suffered from dull frontal headache and proptosis for three months before hospitalization. The circumscribed and demarcated neoplasm involved the dura mater, and invaded the frontal sinus and roof of the orbit on the same side. The pathogenesis of the tumour is thought to be related to aberrant differentiation of unstable mesenchyme. A suggestion is made that the "medullomyoblastoma" should be classified as a type of neoplasm of mixed mesenchymal and neuroepithelial origin.
报告了一例发生在一名16岁女孩右额下区域的原发性横纹肌肉瘤病例。患者在住院前三个月出现前额钝痛和眼球突出。该肿瘤边界清晰,累及硬脑膜,并侵犯同侧额窦和眶顶。肿瘤的发病机制被认为与不稳定间充质的异常分化有关。有人提出“髓母细胞瘤”应归类为一种间充质和神经上皮混合起源的肿瘤。