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作 者:Emmanouil Pikoulis Constantine Bramis Othon Michail George Liapis Evangelos Felekouras Vassiliki Kyriakou John Griniatsos
机构地区:[1]First Department of Surgery Laikon Hospital,University of Athens Medical School,Athens 115-27,Greece [2]Department of Pathology Laikon Hospital,University of Athens Medical School,Athens 115-27,Greece
出 处:《Chinese Medical Journal》2007年第14期1284-1286,共3页中华医学杂志(英文版)
摘 要:Angiomyolipoma (AML) is a tumour of uncertain .histogenesis originally believed to be a hamartomatous lesion, but recently recognized as a usually benign clonal mesenchymal neoplasm. Along with lymphagiomyomatosis (LAM), clear cell "sugar" turnout (CCST) and clear cell myelomelanocytic tumour (CCMMT), AML was classified in the so called perivascular epithelioid cell (PEComa) neoplasm family.Angiomyolipoma (AML) is a tumour of uncertain .histogenesis originally believed to be a hamartomatous lesion, but recently recognized as a usually benign clonal mesenchymal neoplasm. Along with lymphagiomyomatosis (LAM), clear cell "sugar" turnout (CCST) and clear cell myelomelanocytic tumour (CCMMT), AML was classified in the so called perivascular epithelioid cell (PEComa) neoplasm family.
关 键 词:ANGIOMYOLIPOMA BUTTOCKS
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