播散性腹膜平滑肌瘤病基因组图谱分析:3例

Viviani, Cavillon, É. Boudier, Averous, S. Croce, N. Sananès, J. Baldauf, B. Langer, C. Akladios
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引用次数: 0

摘要

摘要弥散性腹膜平滑肌瘤病(DPL)是一种罕见的疾病,属于生长不确定的平滑肌肿瘤。它的特点是腹膜腔内多个平滑肌结节增生,类似恶性过程,如腹膜癌,但组织学研究证明是良性的。它的起源仍然未知。DPL病例的基因组分析对了解其发病机制和后续病程很有意义,但目前的研究很少。在这篇文章中,我们列出了基因组图谱,通过基于阵列的比较基因组杂交(array-CGH)分析了两例子宫肌瘤分块后检测到的DPL的腹膜和子宫病变,以及一例“散发性”DPL病例。阵列- cgh结果显示,这三个病例的基因组图谱都是扁平的。由于没有不平衡的重排,不可能仅根据基因组谱在两个病变之间建立遗传谱系。CGH在这类疾病中并不是决定性的。对外显子组的分析可以为我们提供新的信息,尤其是关于这些肿瘤癌变的驱动事件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Analysis of the Genomic Profile in Disseminated Peritoneal Leiomyomatosis: Three cases
Disseminated peritoneal leiomyomatosis (DPL) is a rare disease entity belonging to the category of smooth muscle tumours of uncertain growth. It is characterized by proliferation of multiple smooth muscle nodules in the peritoneal cavity mimicking a malignant process such as peritoneal carcinomatosis but which when studied histologically proves to be of benign nature. Its origin is still unknown. Genomic analysis of DPL cases is of interest in order to understand its pathogenesis and subsequent course, but there are few extant studies. In this article we set out the genomic profiles, analysed by array-based comparative genomic hybridization (array-CGH), of peritoneal and uterine lesions in two cases of DPL detected after previous uterine morcellation for fibroids, as well as a "sporadic" case of DPL. Array-CGH findings revealed in all three cases a flat genomic profile. It is not possible to establish a genetic lineage between two lesions on the basis of the genomic profiles alone, owing to the absence of an unbalanced rearrangement. CGH is not conclusive enough in this type of disorder. Analysis of the exome could provide us with fresh information, not least about driving events in the cancerogenesis of these tumours.
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