Ozdemir Mevci, Ozgural Onur, Bozkurt Melih, Torun Fuat Mehmet, Heper Aylin Okcu, Tuna Hakan
Pamukkale University, Faculty of Medicine, Department of Neurosurgery, Denizli, Turkey.
Turk Neurosurg. 2012;22(4):475-7. doi: 10.5137/1019-5149.JTN.3701-10.3.
We describe herein a patient with primary intracerebral malignant fibrous histiocytoma (MFH) to demonstrate this very rare central nervous system tumor. A 42-year-old male was admitted to our institute with the complaints of headache and speech impairment. Magnetic resonance imaging (MRI) revealed a tumor consistent with meningioma and we decided the surgery. The tumor was excised totally during the initial surgery. Histopathological examination revealed a mesenchymal tumor with an invasion of the adjacent brain and underlying dura mater. On the postoperative 4th month, the follow up MRI showed tumor recurrence at the same location and of similar size. Reoperation was performed and the tumor was again removed gross totally. However, the patient demonstrated a rapidly progressive course leading to death within the first year after the surgery. Two significant points of this case of primary central nervous system MFH are the rarity of its occurrence and its mimicking a meningioma.
我们在此描述一例原发性脑恶性纤维组织细胞瘤(MFH)患者,以展示这种极为罕见的中枢神经系统肿瘤。一名42岁男性因头痛和言语障碍入住我院。磁共振成像(MRI)显示一个与脑膜瘤相符的肿瘤,我们决定进行手术。在初次手术中肿瘤被完全切除。组织病理学检查显示为间叶性肿瘤,侵犯了相邻脑实质和硬脑膜。术后第4个月,随访MRI显示在同一部位出现大小相似的肿瘤复发。再次进行手术,肿瘤再次被大体完全切除。然而,患者病情迅速进展,在手术后第一年内死亡。原发性中枢神经系统MFH这一病例的两个重要特点是其发病率罕见以及它类似脑膜瘤。