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最初被诊断为血管外皮细胞瘤的复发性颅内孤立性纤维瘤。

Recurrent intracranial solitary fibrous tumor initially diagnosed as hemangiopericytoma.

作者信息

Hori Emiko, Kurimoto Masanori, Fukuda Osamu, Takahashi Chiaki, Nagai Shoichi, Oya Takeshi, Endo Shunro

机构信息

Department of Neurosurgery, Saito Memorial Hospital, Niigata, Japan.

出版信息

Brain Tumor Pathol. 2007;24(1):31-4. doi: 10.1007/s10014-006-0212-y. Epub 2007 May 25.

Abstract

We describe a case of an intracranial solitary fibrous tumor that recurred three times consecutively in an 11-year period. A 72-year-old man presented with a headache and gait disturbance. Magnetic resonance imaging (MRI) revealed a dumbbell tumor at the left tentorium. The tumor was removed but recurred. The first diagnosis was hemangiopericytoma, but all specimens showed a "patternless pattern" and few reticulin fibers, which features were not compatible with hemangiopericytoma. All tumors showed immunoreactivity for CD34 and bcl-2. These results point to a solitary fibrous tumor (SFT) and not to hemangiopericytoma. We present here a hypercellular spindle-cell tumor that was very similar to hemangiopericytoma but is better diagnosed as SFT.

摘要

我们描述了一例颅内孤立性纤维瘤,该肿瘤在11年期间连续复发三次。一名72岁男性出现头痛和步态障碍。磁共振成像(MRI)显示左侧小脑幕有一个哑铃形肿瘤。肿瘤被切除但复发。最初诊断为血管外皮细胞瘤,但所有标本均显示“无模式模式”且网状纤维较少,这些特征与血管外皮细胞瘤不符。所有肿瘤对CD34和bcl-2均呈免疫反应性。这些结果表明是孤立性纤维瘤(SFT)而非血管外皮细胞瘤。我们在此呈现的是一种细胞增多的梭形细胞瘤,它与血管外皮细胞瘤非常相似,但更好地诊断为SFT。

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