斜坡脊索瘤,产生于已存在的良性脊索细胞瘤,1例报告

Maryam Almurshed, Lamia Alsarraf
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引用次数: 0

摘要

脊索起源病变是罕见的外科病例,具有广泛的分化,从残余到良性肿瘤-即“良性脊索细胞瘤BNCT”-恶性脊索瘤。这些病变发生在椎体中轴骨、斜坡和腰椎的末端。脊索瘤是一种恶性的破坏性病变,从骨骼延伸到周围的软组织。假设它是由其罕见的良性对应物BNCT引起的,因为在罕见的病例报告中,它们在腰椎区域共存,在斜坡区域更罕见。这些良性形式在外科病理标本中甚至很少看到,如果不被识别,则在形态学上与恶性脊索瘤有相似之处。在此,我们报告一例由良性脊索细胞瘤(BNCT)引起的脊索瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clival Chordoma, Arising in Pre-existing Benign Notochordal Cell Tumor, Case Report
: Lesions of notochordal origin are unusual surgical cases that have a broad spectrum of differentiation, from remnants to benign tumors -namely “benign notochordal cell tumor BNCT”-to malignant chordoma. These lesions arise within the vertebral bodies at the ends of axial skeleton, clivus and lumbar areas. Chordoma, is a malignant destructive lesion extending from bone to surrounding soft tissue. It is hypothesized to arise from its rare benign counterpart, BNCT as evidenced by their co-existence in rare case reports, in lumbar area, an even more rare in clival region. These benign forms are even scarce to see in surgical pathology specimen and carry a histological resemblance in morphology to malignant chordoma if not recognized. Here, we report a case of chordoma arising from a benign notochordal cell tumor (BNCT)
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