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伴有脂肪肉瘤成分、骨浸润及颅外生长的胶质肉瘤。

Gliosarcoma with liposarcomatous component, bone infiltration and extracranial growth.

作者信息

Borota O C, Scheie D, Bjerkhagen B, Jacobsen E A, Skullerud K

机构信息

Department of Pathology, The University Hospital Rikshospitalet-Radiumhospitalet, Sognsvannsveien 20, 0027 Oslo, Norway.

出版信息

Clin Neuropathol. 2006 Jul-Aug;25(4):200-3.

Abstract

Gliosarcoma is a highly malignant brain tumor consisting of both a glioblastoma and a mesenchymal component. The latter typically resembles fibrosarcoma, but differentiation patterns resembling osteosarcoma, chondrosarcoma, angiosarcoma and rhabdomyosarcoma have also been described. Molecular-genetic studies have shown that both glioblastoma and the mesenchymal component share identical cytogenetic abnormalities or mutations, suggesting a monoclonal origin from glial cells. We report an unusual case of gliosarcoma that presented as a large intracerebral tumor with infiltration of the temporal bone and the soft tissues in the infratemporal fossa. Microscopically, the tumor consisted of alternating areas of glioblastoma and fibrosarcoma. Focally, areas ofosteosarcomatous and liposarcomatous differentiation were found. Although gliosarcoma with transcranial penetration is very rare, it should be suspected in case of intracranial tumor with glioblastoma-imaging features, infiltration of bone and extracranial growth. Our case of liposarcomatous differentiation in gliosarcoma--together with another very recently reported similar case--expands the morphologic heterogeneity of this peculiar brain tumor.

摘要

胶质肉瘤是一种高度恶性的脑肿瘤,由胶质母细胞瘤和间充质成分组成。后者通常类似于纤维肉瘤,但也有报道其分化模式类似于骨肉瘤、软骨肉瘤、血管肉瘤和横纹肌肉瘤。分子遗传学研究表明,胶质母细胞瘤和间充质成分具有相同的细胞遗传学异常或突变,提示其起源于神经胶质细胞的单克隆性。我们报告了一例不寻常的胶质肉瘤病例,该病例表现为巨大的脑内肿瘤,侵犯颞骨和颞下窝软组织。显微镜下,肿瘤由胶质母细胞瘤和纤维肉瘤交替区域组成。局部可见骨肉瘤样和脂肪肉瘤样分化区域。尽管经颅穿透性胶质肉瘤非常罕见,但对于具有胶质母细胞瘤影像学特征、骨质侵犯和颅外生长的颅内肿瘤应怀疑有此病。我们报道的胶质肉瘤脂肪肉瘤样分化病例,连同最近报道的另一例相似病例,扩展了这种特殊脑肿瘤的形态学异质性。

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