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首页> 外文期刊>Case Reports in Pathology >Malignant Trigeminal Nerve Sheath Tumor and Anaplastic Astrocytoma Collision Tumor with High Proliferative Activity and Tumor SuppressorP53 Expression
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Malignant Trigeminal Nerve Sheath Tumor and Anaplastic Astrocytoma Collision Tumor with High Proliferative Activity and Tumor SuppressorP53 Expression

机译:具有高增殖活性和抑癌基因P53表达的恶性三叉神经鞘膜肿瘤和间变性星形细胞瘤碰撞肿瘤

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摘要

Background. The synchronous development of two primary brain tumors of distinct cell of origin in close proximity or in contact with each other is extremely rare. We present the first case of collision tumor with two histological distinct tumors.Case Presentation. A 54-year-old woman presented with progressive atypical left facial pain and numbness for 8 months. MRI of the brain showed left middle cranial fossa heterogeneous mass extending into the infratemporal fossa. At surgery, a distinct but intermingled intra- and extradural tumor was demonstrated which was completely removed through left orbitozygomatic-temporal craniotomy. Histopathological examination showed that the tumor had two distinct components: malignant nerve sheath tumor of the trigeminal nerve and temporal lobe anaplastic astrocytoma. Proliferative activity and expressed tumor protein 53 (TP53) gene mutations were demonstrated in both tumors.Conclusions. We describe the first case of malignant trigeminal nerve sheath tumor (MTNST) and anaplastic astrocytoma in collision and discuss the possible hypothesis of this rare occurrence. We propose that MTNST, with TP53 mutation, have participated in the formation of anaplastic astrocytoma, or vice versa.
机译:背景。两种极为接近或彼此接触的起源细胞不同的原发性脑肿瘤的同步发展极为罕见。我们介绍了第一例碰撞肿瘤,其中有两种组织学不同的肿瘤。一名54岁的妇女表现为进行性非典型性左面部疼痛和麻木,持续8个月。脑部MRI显示左中颅窝异质性肿块延伸至颞下窝。在手术中,发现了一个独特但混合的硬膜内和硬膜外肿瘤,该肿瘤通过左眶oz颞颞开颅手术完全切除。组织病理学检查显示该肿瘤具有两个不同的成分:三叉神经的恶性神经鞘瘤和颞叶间变性星形细胞瘤。在这两种肿瘤中均证实了其增殖活性和表达的肿瘤蛋白53(TP53)基因突变。我们描述了首例恶性三叉神经鞘膜瘤(MTNST)与间变性星形细胞瘤发生碰撞,并讨论了这种罕见情况的可能假说。我们建议具有TP53突变的MTNST参与了间变性星形细胞瘤的形成,反之亦然。

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