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首页> 外文期刊>Pathology International >Intramuscular dendritic fibromyxolipoma: Myxoid variant of spindle cell lipoma?
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Intramuscular dendritic fibromyxolipoma: Myxoid variant of spindle cell lipoma?

机译:肌内树突状纤维肌脂瘤:梭形细胞脂肪瘤的黏液样变体?

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摘要

Dendritic fibromyxolipoma (DFML) is an uncommon, recently described, benign soft tissue lesion that shares many clinical and pathological features with myxoid variants of spindle cell lipoma (SCL). As described, DFML is distinguished from SCL by the presence of dendritic cytoplasmic processes, abundant keloidal collagen and a prominent, often plexiform vascular pattern. We describe the first known reported case of an intramuscular DFML that occurred in the right shoulder region of a 73-year-old man. The tumor displayed the typical histopathological features of DFML but also included foci of chondroid metaplasia, a previously unreported finding. This report also discusses the differential diagnosis, particularly distinguishing DFML from SCL and myxoid liposarcoma. In view of the similarities in many clinical and pathological features between SCL and DFML, we speculate that DFML probably represents an unusual variant of myxoid SCL.
机译:树突状纤维粘液瘤(DFML)是一种罕见的,最近描述的良性软组织病变,与纺锤状细胞脂肪瘤(SCL)的粘液样变具有许多临床和病理学特征。如上所述,DFML与SCL的区别在于存在树突状细胞质过程,丰富的瘢痕loid胶原蛋白和突出的,通常为丛状的血管型。我们描述了第一例已知的肌内DFML病例,该病例发生在一名73岁男子的右肩区域。该肿瘤表现出DFML的典型组织病理学特征,但也包括软骨上皮化生灶,这是以前未报道的发现。该报告还讨论了鉴别诊断,特别是将DFML与SCL和粘液样脂肪肉瘤区分开来。鉴于SCL和DFML在许多临床和病理学特征上的相似性,我们推测DFML可能代表了粘液样SCL的不寻常变体。

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