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首页> 外文期刊>European journal of gynaecological oncology >Uterine perivascular epithelioid cell neoplasms (PEComas): Report of two cases and literature review
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Uterine perivascular epithelioid cell neoplasms (PEComas): Report of two cases and literature review

机译:子宫血管周围上皮样细胞瘤(PEComas):两例报告并文献复习

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摘要

Perivascular epithelioid cell tumors (PEComas) are rare tumors characterized by co-expression of melanocytic and smooth muscle markers. PEComas have been reported in a wide variety of anatomic sites. In the female genital tract, PEComas most frequently affect the uterus. PEComas which occur in non-classic anatomic distributions are known as perivascular epithelioid cell tumor-not otherwise specified (PEComa-NOS). PEComas have an unpredictable biologic behavior, with some tumors being unresectable or metastatic at the time of diagnosis. The risk of aggressive behavior of these tumors has been linked to a number of factors evaluable on histopathological review following initial surgical resection. The authors report two cases of PEComa-NOS of the uterus: one with disease confined to uterus and the other case with lung and liver metastasis.
机译:血管周上皮样细胞瘤(PEComas)是罕见的肿瘤,其特征在于黑素细胞和平滑肌标志物的共表达。 PEComas已经在各种各样的解剖部位被报道。在女性生殖道中,PEComas最常影响子宫。发生在非经典解剖分布中的PEComas被称为血管周上皮样细胞瘤(未另作说明)(PEComa-NOS)。 PEComas具有不可预测的生物学行为,某些肿瘤在诊断时无法切除或转移。这些肿瘤侵袭性行为的风险与许多因素有关,这些因素可在初次手术切除后进行组织病理学评估。作者报告了2例子宫PEComa-NOS:1例局限于子宫,另一例发生肺和肝转移。

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