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肝脏血管周上皮样细胞肿瘤的临床病理观察
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作者 赵苏苏 余慧萍 +3 位作者 徐佳佳 周家华 章宜芬 余泽前 《临床肿瘤学杂志》 CAS 2023年第3期258-262,共5页
目的探讨肝脏血管周上皮样细胞肿瘤(PEComa)的临床病理学特征、诊断、治疗及预后。方法回顾性分析2016年10月至2021年3月10例肝脏PEComa的临床表现、影像学表现、组织病理学特征、治疗及预后。结果10例患者中,女性7例,男性3例;年龄30~74... 目的探讨肝脏血管周上皮样细胞肿瘤(PEComa)的临床病理学特征、诊断、治疗及预后。方法回顾性分析2016年10月至2021年3月10例肝脏PEComa的临床表现、影像学表现、组织病理学特征、治疗及预后。结果10例患者中,女性7例,男性3例;年龄30~74岁;除1例有背部疼痛、腹胀外,其余9例均无相关临床症状;肝左叶2例,肝右叶8例;肿瘤最大径为0.8 cm~6.5 cm,肿块与周围肝脏组织界限均较清楚;术前影像学检查仅2例诊断倾向PEComa;10例患者均接受手术切除;术后随访5~58个月,10例患者中除1例失访外均无复发和转移。显微镜下肿瘤细胞主要由上皮样细胞和脂肪细胞组成,以上皮样细胞占优势。免疫组化检查显示,肿瘤细胞均表达HMB-45、Malen-A、SMA和Vimentin,不表达CK、EMA、AFP和CD117,p53呈野生型,Ki-67均<5%。结论肝脏PEComa在影像学和病理形态学上都可以高度模拟肝细胞来源的肿瘤或者病变,其诊断和鉴别诊断应结合其特殊的影像学、病理形态学和免疫表型。肝脏PEComa患者预后良好。 展开更多
关键词 肝脏肿瘤 血管周上皮样细胞肿瘤 临床病理特征
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Perivascular epithelioid cell neoplasm of the colon 被引量:1
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作者 Hugh James Freeman Doug L Webber 《World Journal of Gastrointestinal Oncology》 SCIE CAS 2010年第4期205-208,共4页
A 17-year-old female presented with rectal bleeding from an ulcerated sigmoid mass in 1994.Initial pathological evaluation revealed a rare clear cell neoplasm of the colon,possibly originating from kidneys,adrenals,lu... A 17-year-old female presented with rectal bleeding from an ulcerated sigmoid mass in 1994.Initial pathological evaluation revealed a rare clear cell neoplasm of the colon,possibly originating from kidneys,adrenals,lung or a gynecologic source as a metastatic lesion.Extensive imaging studies were negative,and over the next 15 years,she remained well with no recurrence.The original resected neoplasm was reviewed and reclassified as a perivascular epithelioid cell neoplasm (PEComa).Although the long-term natural history of PEComas requires definition,increased clinical and pathological awareness should lead to increased recognition of an apparently rare type of colonic neoplasm that likely occurs more often than is currently appreciated. 展开更多
关键词 perivascular epithelioid cell neoplasm Carci noid TUMOR COLONIC adenocarcinoma Clear cell TUMOR
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Feasibility of laparoscopic isolated caudate lobe resection for rare hepatic mesenchymal neoplasms 被引量:1
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作者 Yang Li Kai-Ning Zeng +4 位作者 Dan-Yun Ruan Jia Yao Yang Yang Gui-Hua Chen Gen-Shu Wang 《World Journal of Clinical Cases》 SCIE 2019年第20期3194-3201,共8页
BACKGROUND Mesenchymal tumors such as perivascular epithelioid cell neoplasm(PEComa)and inflammatory pseudotumor-like follicular dendritic cell sarcoma(IPT-like FDC sarcoma)are relatively uncommon in the liver and are... BACKGROUND Mesenchymal tumors such as perivascular epithelioid cell neoplasm(PEComa)and inflammatory pseudotumor-like follicular dendritic cell sarcoma(IPT-like FDC sarcoma)are relatively uncommon in the liver and are particularly rare in the caudate lobe.The clinical manifestations and available imaging tests lack specificity for hepatic mesenchymal tumors.To the best of our knowledge,no caudate PEComa or IPT-like FDC sarcoma has been completely resected by laparoscopy.The standard laparoscopic technique,surgical approaches,and tumor margins for potentially malignant or malignant caudate mesenchymal tumors are still being explored.AIM To assess both the safety and feasibility of laparoscopic resection for rare caudate mesenchymal neoplasms.METHODS Eleven patients who underwent isolated caudate lobe resection from 2003 to 2017 were identified from a prospective database.Three consecutive patients with rare caudate mesenchymal tumors underwent laparoscopic resection.Patient demographic data,intraoperative parameters,and postoperative outcomes were assessed and compared with the open surgery group.RESULTS All procedures for the three resection patients with caudate mesenchymal tumors were completed using a total laparoscopic technique by two different approaches.The average operative time was 226 min,and the estimated blood loss was 133 mL.The average length of postoperative hospital stay was 6.3±0.3 d for the laparoscopy group and 15.5±2.3 d for the open surgery group(P<0.05).There were no perioperative complications or patient deaths in this series.CONCLUSION Laparoscopic isolated caudate lobe resection for rare mesenchymal neoplasms is a feasible and curative surgical option in selected patients. 展开更多
关键词 LAPAROSCOPIC liver RESECTION CAUDATE lobe perivascular epithelioid cell neoplasm Inflammatory pseudotumor-like follicular dendritic cell sarcoma
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伴TFE3基因易位的子宫颈PEComa 1例并文献复习 被引量:3
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作者 陈筱莉 蹇顺海 +2 位作者 杨慧敏 李丽 王小林 《重庆医学》 CAS 2020年第21期3569-3573,共5页
目的探讨伴转录因子E3(TFE-3)基因易位的子宫颈血管周上皮样细胞肿瘤(PEComa)的临床病理特征。方法结合相关文献,对1例TFE3基因易位的子宫颈PEComa临床资料、病理切片、免疫组织化学标记及荧光原位杂交(FISH)结果进行分析。结果肿瘤位... 目的探讨伴转录因子E3(TFE-3)基因易位的子宫颈血管周上皮样细胞肿瘤(PEComa)的临床病理特征。方法结合相关文献,对1例TFE3基因易位的子宫颈PEComa临床资料、病理切片、免疫组织化学标记及荧光原位杂交(FISH)结果进行分析。结果肿瘤位于子宫颈,大小4.0 cm×3.0 cm×2.5 cm,切面质地较嫩。组织学显示肿瘤细胞上皮样,细胞质丰富、透明,细胞核有中度异型,核仁可见,核分裂像约5个/50 HPF;瘤细胞间有大量纤细血管网。较多凝固性坏死,可见脉管侵犯。免疫组织化学染色显示肿瘤细胞弥漫表达TFE-3、人类黑素体单克隆抗体(HMB45)、黑素A(MelanA),不表达细胞角蛋白(CK)、结蛋白(Desmin)、平滑肌肌动蛋白(SMA);肿瘤高增殖活性区域Ki-67阳性细胞比例约30%。FISH检测出TFE3基因易位。结论伴TFE3基因易位的子宫颈PEComa诊断主要依据组织学、免疫组织化学及FISH检测TFE3基因状态;手术切除为主要治疗手段。 展开更多
关键词 血管周上皮样细胞肿瘤 转录因子E3 基因易位 鉴别诊断 文献复习
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