Abstract:
:A case of gliosarcoma composed of glioblastoma and liposarcoma is presented. A 70-year-old Japanese man was admitted to hospital because of dysarthria and aphasia. Magnetic resonance imaging indicated a brain tumor located in the temporal-parietal area of the left hemisphere. He rejected any therapy and died of respiratory failure. At autopsy the tumor was well-demarcated with firm consistency and myxoid appearance, accompanied by necrosis and hemorrhage. Microscopically the tumor consisted of both glial and sarcomatous components, compatible with a gliosarcoma. Lipoblast-like tumor cells were identified in the sarcomatous area. Glial component was observed in the periphery and was diffusely positive for CD56 and S100 protein and focally for glial fibrillary acidic protein. Only a small number of tumor cells in the sarcomatous area expressed neurogenic markers. Lipoblast-like tumor cells were positive for S100 protein but negative for any other neurogenic markers. A significant number of tumor cells were positive for retinoblastoma protein (pRB) in the glial area, whereas only a few of them were positive in the sarcomatous area, indicating alteration of pRB in sarcomatous component. The present tumor is a rare gliosarcoma with liposarcomatous differentiation; alteration of pRB may play a role in sarcomatous transformation of glial component.
journal_name
Pathol Intjournal_title
Pathology internationalauthors
Fukuda T,Yasumichi K,Suzuki Tdoi
10.1111/j.1440-1827.2008.02242.xsubject
Has Abstractpub_date
2008-06-01 00:00:00pages
396-401issue
6eissn
1320-5463issn
1440-1827pii
PIN2242journal_volume
58pub_type
杂志文章abstract::Autosomal recessive polycystic kidney disease (ARPKD) is caused by genetic mutations of the gene encoding fibrocystin, and is characterized by the collecting duct cysts and congenital hepatic fibrosis. We report an autopsy-proven case of ARPKD in a 77-year-old male who presented with rapidly progressive renal and live...
journal_title:Pathology international
pub_type: 杂志文章
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journal_title:Pathology international
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journal_title:Pathology international
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journal_title:Pathology international
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journal_title:Pathology international
pub_type: 杂志文章
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journal_title:Pathology international
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journal_title:Pathology international
pub_type: 杂志文章
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journal_title:Pathology international
pub_type: 杂志文章
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journal_title:Pathology international
pub_type: 杂志文章
doi:10.1111/pin.12624
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journal_title:Pathology international
pub_type: 杂志文章
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journal_title:Pathology international
pub_type: 杂志文章,评审
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更新日期:2003-02-01 00:00:00
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journal_title:Pathology international
pub_type: 杂志文章
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更新日期:2004-08-01 00:00:00
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journal_title:Pathology international
pub_type: 杂志文章,多中心研究,评审
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journal_title:Pathology international
pub_type: 杂志文章
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更新日期:2010-02-01 00:00:00
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journal_title:Pathology international
pub_type: 杂志文章
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更新日期:1997-06-01 00:00:00
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journal_title:Pathology international
pub_type: 杂志文章,评审
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更新日期:1999-11-01 00:00:00
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journal_title:Pathology international
pub_type: 杂志文章
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journal_title:Pathology international
pub_type: 杂志文章
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journal_title:Pathology international
pub_type: 杂志文章
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journal_title:Pathology international
pub_type: 杂志文章
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journal_title:Pathology international
pub_type:
doi:10.1111/pin.12945
更新日期:2020-08-01 00:00:00
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journal_title:Pathology international
pub_type: 杂志文章
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更新日期:1997-06-01 00:00:00
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journal_title:Pathology international
pub_type:
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更新日期:2019-06-01 00:00:00
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journal_title:Pathology international
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doi:10.1111/pin.12445
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journal_title:Pathology international
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journal_title:Pathology international
pub_type: 杂志文章
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journal_title:Pathology international
pub_type: 杂志文章
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journal_title:Pathology international
pub_type: 杂志文章
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更新日期:1999-12-01 00:00:00
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journal_title:Pathology international
pub_type: 杂志文章,评审
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