胃组织细胞肉瘤中的NF1突变和TUBB3扩增:病例报告和文献综述。

IF 1.2 4区 医学 Q3 PATHOLOGY Medical Molecular Morphology Pub Date : 2024-09-01 Epub Date: 2024-06-24 DOI:10.1007/s00795-024-00393-0
Yi Yang, Wei Fan, Xiaoping Liu, Qiongrong Chen
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引用次数: 0

摘要

组织细胞肉瘤是一种罕见的成熟组织细胞肿瘤,临床病程凶险,对治疗反应差。原发性胃组织细胞肉瘤较为罕见,仅有零星报道。组织细胞肉瘤是一种罕见的成熟组织细胞肿瘤,临床病程凶险,对治疗反应差。原发性胃组织细胞肉瘤较为罕见,仅有零星报道。患者为一名 71 岁女性,因上腹疼痛加重一年入院。CT 扫描显示胃体小弯处有一个隆起的肿块,随后患者接受了内镜下粘膜下剥离术。显微镜下,非粘连性肿瘤细胞弥漫浸润固有膜和粘膜下层,弥漫表达 LCA、CD4、CD163、CD68 (KP1)、细胞周期蛋白 D1、溶菌酶和波形蛋白。PD-L1(22CS)表达评估为 CPS 60。最终病理诊断为胃组织细胞肉瘤。随后,新一代测序确定了NF1基因第21外显子的无义突变[c.2446C > T (p.R816*)]和TUBB3基因扩增(拷贝数:4.55)。患者拒绝进一步治疗,半年后死于肿瘤。该病例拓宽了胃癌的鉴别诊断范围,强调了免疫组化和分子检测在组织细胞肉瘤准确诊断中的价值。此外,我们还对11例胃组织细胞肉瘤进行了文献综述,以加强对其临床病理特征、治疗和预后的了解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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NF1 mutation and TUBB3 amplification in gastric histiocytic sarcoma: a case report and literature review.

Histiocytic sarcoma is a rare neoplasm of mature histiocytes with an aggressive clinical course and poor response to treatment. Primary gastric histiocytic sarcoma is rarer and just reported sporadically.Histiocytic sarcoma is a rare neoplasm of mature histiocytes with an aggressive clinical course and poor response to treatment. Primary gastric histiocytic sarcoma is rarer and just reported sporadically. A case of a 71-year-old female admitted with a one-year history of upper abdominal pain exacerbated after meals. After CT scans revealed a bulged mass at the lesser curvature of the gastric body, the patient underwent endoscopic submucosal dissection. Microscopically, non-cohesive neoplastic cells diffusely infiltrated lamina propria and submucosa, and diffusely expressed LCA, CD4, CD163, CD68 (KP1), Cyclin D1, Lysozyme, and Vimentin. PD-L1 (22CS) expression evaluated as CPS 60. The final pathological diagnosis was gastric histiocytic sarcoma. Subsequently, next-generation sequencing identified a nonsense mutation in exon 21 of NF1 gene [c.2446C > T (p.R816*)] and the TUBB3 gene amplification (copy number: 4.55). The patient refused further treatment and died of the tumor half a year later. This case broadens the spectrum of differential diagnosis of gastric cancer and emphasizes the value of immunohistochemical and molecular tests in the accurate diagnosis of histiocytic sarcoma. Furthermore, we performed literature review of 11 cases of gastric histiocytic sarcoma so as to strengthen the understanding of the clinicopathologic features, treatment, and prognosis.

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来源期刊
Medical Molecular Morphology
Medical Molecular Morphology 医学-病理学
CiteScore
2.90
自引率
5.60%
发文量
30
审稿时长
>12 weeks
期刊介绍: Medical Molecular Morphology is an international forum for researchers in both basic and clinical medicine to present and discuss new research on the structural mechanisms and the processes of health and disease at the molecular level. The structures of molecules, organelles, cells, tissues, and organs determine their normal function. Disease is thus best understood in terms of structural changes in these different levels of biological organization, especially in molecules and molecular interactions as well as the cellular localization of chemical components. Medical Molecular Morphology welcomes articles on basic or clinical research in the fields of cell biology, molecular biology, and medical, veterinary, and dental sciences using techniques for structural research such as electron microscopy, confocal laser scanning microscopy, enzyme histochemistry, immunohistochemistry, radioautography, X-ray microanalysis, and in situ hybridization. Manuscripts submitted for publication must contain a statement to the effect that all human studies have been reviewed by the appropriate ethics committee and have therefore been performed in accordance with the ethical standards laid down in an appropriate version of the 1964 Declaration of Helsinki. It should also be stated clearly in the text that all persons gave their informed consent prior to their inclusion in the study. Details that might disclose the identity of the subjects under study should be omitted.
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