Adeleye Amos Olufemi, Fellig Yakov, Umansky Felix, Shoshan Yigal
Department of Neurosurgery, Hadassah - Hebrew University Medical Center, POB 12000, 91120, Jerusalem, Israel.
J Neurooncol. 2009 Apr;92(2):233-8. doi: 10.1007/s11060-008-9756-5. Epub 2008 Dec 10.
We present a case of de novo fibrosarcoma in a 43-year-old male, with MRI documented evolution from a 5 mm hyperintense area to 5 cm tumor mass in a 12-month period. The diagnosis of low-grade fibrosarcoma was established by three experienced neuropathologists. The patient underwent gross total resection with adjuvant fractionated conformal radiotherapy. Following first recurrence 3 months later, the patient was reoperated and stereotactic radiosurgery of a residual tumor was performed thereafter. The pathological diagnosis was similar, but with additional extensive radiation effects. Six months later the patient underwent aggressive surgical resection for second recurrence. The pathological diagnosis was WHO grade IV glioblastoma. The etiology of this highly unusual progression from primary mesenchymal neoplasm to high-grade glioma is discussed.
我们报告一例43岁男性的新发纤维肉瘤病例,MRI记录显示在12个月内从一个5毫米的高信号区域发展为一个5厘米的肿瘤肿块。由三位经验丰富的神经病理学家确诊为低级别纤维肉瘤。患者接受了全切除手术并辅以分次适形放疗。3个月后首次复发,患者再次接受手术,随后对残留肿瘤进行了立体定向放射外科治疗。病理诊断相似,但伴有额外的广泛放射效应。6个月后,患者因第二次复发接受了积极的手术切除。病理诊断为世界卫生组织IV级胶质母细胞瘤。本文讨论了这种从原发性间叶性肿瘤高度不寻常地进展为高级别胶质瘤的病因。