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胃肠道血管周上皮样细胞瘤:病例报告及文献复习

Perivascular epithelioid cell tumor of gastrointestinal tract: case report and review of the literature.

作者信息

Lu Biyan, Wang Chenliang, Zhang Junxiao, Kuiper Roland P, Song Minmin, Zhang Xiaoli, Song Shunxin, Kessel Ad Geurts van, Iwamoto Aikichi, Wang Jianping, Liu Huanliang

机构信息

From the Guangdong Institute of Gastroenterology and the Sixth Affiliated Hospital, (BL, CW, JZ, MS, XZ, SS, JW, HL); Guangdong Key Laboratory of Colorectal and Pelvic Floor Diseases, (BL, CW, JZ, MS, XZ, JW, HL); Institute of Human Virology, (BL, CW, JZ, MS, XZ, HL) Key Laboratory of Tropical Disease Control (Ministry of Education); Sun Yat-sen University, Guangzhou (BL, CW, JZ, MS, XZ, HL); Dongguan Health School, Dongguan, China (BL); Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands (JZ, RPK, AGK); and Advanced Clinical Research Center, Institute of Medical Science, University of Tokyo, Tokyo, Japan (AI).

出版信息

Medicine (Baltimore). 2015 Jan;94(3):e393. doi: 10.1097/MD.0000000000000393.

Abstract

Perivascular epithelioid cell tumors of gastrointestinal tract (GI PEComas) are exceedingly rare, with only a limited number of published reports worldwide. Given the scarcity of GI PEComas and their relatively short follow-up periods, our current knowledge of their biologic behavior, molecular genetic alterations, diagnostic criteria, and prognostic factors continues to be very limited.We present 2 cases of GI PEComas, one of which showed an aggressive histologic behavior that underwent multiple combined chemotherapies. We also review the available English-language medical literature on GI PEComas-not otherwise specified (PEComas-NOS) and discuss their clinicopathological and molecular genetic features.Pathologic analyses including histomorphologic, immunohistochemical, and ultrastructural studies were performed to evaluate the clinicopathological features of GI PEComas, their diagnosis, and differential diagnosis. Immunohistochemistry, semiquantitative reverse transcriptase polymerase chain reaction, and DNA sequencing assays were carried out to detect the potential molecular genetic alterations in our cases. Microscopically, the tumors showed distinctive histologic features of PEComas-NOS, including fascicular or nested architecture, epithelioid or spindled cell type, and clear to eosinophilic cytoplasm. The tumor cells were immunohistochemically positive for melanocytic markers. Molecular pathological assays confirmed a PSF-TFE3 gene fusion in one of our cases. Furthermore, in this case microphthalmia-associated transcription factor and its downstream genes were found to exhibit elevated transcript levels.Knowledge about the molecular genetic alterations in GI PEComas is still limited and warrants further study.

摘要

胃肠道血管周上皮样细胞瘤(GI PEComas)极为罕见,全球仅有有限数量的报道。鉴于GI PEComas病例稀缺且随访期相对较短,我们目前对其生物学行为、分子遗传学改变、诊断标准及预后因素的了解仍然非常有限。我们报告2例GI PEComas,其中1例表现出侵袭性组织学行为并接受了多种联合化疗。我们还回顾了关于未另行指定的GI PEComas(PEComas-NOS)的英文医学文献,并讨论了它们的临床病理和分子遗传学特征。进行了包括组织形态学、免疫组织化学和超微结构研究在内的病理分析,以评估GI PEComas的临床病理特征、诊断及鉴别诊断。进行了免疫组织化学、半定量逆转录聚合酶链反应和DNA测序分析,以检测我们病例中的潜在分子遗传学改变。显微镜下,肿瘤表现出PEComas-NOS独特的组织学特征,包括束状或巢状结构、上皮样或梭形细胞类型以及透明至嗜酸性的细胞质。肿瘤细胞免疫组织化学检测黑素细胞标记物呈阳性。分子病理学分析证实我们的1例病例存在PSF-TFE3基因融合。此外,在该病例中发现小眼相关转录因子及其下游基因的转录水平升高。关于GI PEComas分子遗传学改变的知识仍然有限,值得进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79f1/4602642/01c025f6d210/medi-94-e393-g001.jpg

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