子宫平滑肌分化的恶性周围神经鞘瘤(MPNST)--病例报告,强调诊断陷阱和 DNA 甲基化分析的价值。

IF 3.1 2区 医学 Q2 GENETICS & HEREDITY Genes, Chromosomes & Cancer Pub Date : 2024-11-07 DOI:10.1002/gcc.70006
Horace M. H. Cheung, Anthony P. Y. Liu, Maximus C. F. Yeung
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引用次数: 0

摘要

恶性周围神经鞘瘤(MPNST)是一种罕见的原发性间叶肿瘤,发生于女性生殖道,文献报道的病例不超过二十几例。大多数病例发生在中年人身上,组织学分级高,临床结果不佳,且无 1 型神经纤维瘤病史。该病例在该部位极为罕见,这无疑给常规临床实践带来了诊断上的挑战。在下文中,我们将报告另一例发生在一名 49 岁中国女性身上的子宫 MPNST 病例,该病例最初被误诊为子宫肌瘤。原发肿瘤显示出两种独特的成分--一种是高分化差的成分,其中有明显的多形性纺锤形细胞,呈包膜样排列;另一种是类子宫肌瘤(LMS)成分,其中的肿瘤细胞显示出明显的肌样分化。不到两年后,患者再次复发,复发肿瘤显示出与原发肿瘤高级别成分相似的特征。尽管患者接受了靶向治疗和化疗,但46个月后再次复发,最终不治身亡。在回顾性分子分析中,RNA 测序没有检测到与临床相关的融合转录本。有趣的是,DNA甲基化分析表明,该肿瘤属于德国癌症研究中心(DKFZ)肉瘤分类中的 "MPNST "组。该肿瘤还被发现存在EED基因同源缺失、多个拷贝数改变以及高级别和LMS样成分中H3K27me3表达缺失。结合组织学和所有辅助检查结果,诊断结果最符合 MPNST。我们的病例凸显了女性生殖道多发性骨髓瘤的诊断误区,以及DNA甲基化分析的潜在临床用途。
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Malignant Peripheral Nerve Sheath Tumor (MPNST) With Smooth Muscle Differentiation of the Uterus—A Case Report With Emphasis on Diagnostic Pitfalls and Value of DNA Methylation Analysis

With no more than two dozen cases reported in the literature, malignant peripheral nerve sheath tumor (MPNST) is a rare primary mesenchymal neoplasm arising in the female genital tract. Most cases occurred in middle-aged adults with high grade histology, unfavorable clinical outcome, and no history of neurofibromatosis type 1. Its extreme rarity in this site no doubt poses a diagnostic challenge during routine clinical practice. In the following, we report an additional case of uterine MPNST occurring in a 49-year-old Chinese woman, which was initially misdiagnosed as a leiomyosarcoma. The primary tumor showed two distinctive components—a high-grade poorly differentiated component with markedly pleomorphic spindle cells arranged in a peritheliomatous pattern; and a leiomyosarcoma-like (LMS-like) component with tumor cells displaying obvious myoid differentiation. The patient suffered a recurrence less than 2 years later with the recurrent tumor demonstrating similar features to the high-grade component of the primary tumor. The patient eventually succumbed 46 months later after developing another recurrence despite receiving targeted therapy and chemotherapy. On retrospective molecular analysis, no clinically relevant fusion transcript was detected on RNA sequencing. Interestingly instead, DNA methylation analysis showed the tumor clustered with the “MPNST” group in the German Cancer Research Center (DKFZ) sarcoma classifier. The tumor was also found to have EED gene homozygous deletion, multiple copy number alterations and loss of H3K27me3 expression in both high-grade and LMS-like components. Combining histology with all the ancillary tests results, the diagnosis was most consistent with MPNST. Our case highlights the diagnostic pitfalls for MPNST arising in the female genital tract and the potential clinical utility of DNA methylation analysis.

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来源期刊
Genes, Chromosomes & Cancer
Genes, Chromosomes & Cancer 医学-遗传学
CiteScore
7.00
自引率
8.10%
发文量
94
审稿时长
4-8 weeks
期刊介绍: Genes, Chromosomes & Cancer will offer rapid publication of original full-length research articles, perspectives, reviews and letters to the editors on genetic analysis as related to the study of neoplasia. The main scope of the journal is to communicate new insights into the etiology and/or pathogenesis of neoplasia, as well as molecular and cellular findings of relevance for the management of cancer patients. While preference will be given to research utilizing analytical and functional approaches, descriptive studies and case reports will also be welcomed when they offer insights regarding basic biological mechanisms or the clinical management of neoplastic disorders.
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