腹膜血管周围上皮样细胞瘤伴肺转移

Inês Margarida Neves Gomes, Ana Cristina Da Costa Ferreira De Vilhena, Inês Calvinho de de OLIVEIRA, Pedro Martinho SANTOS SEQUEIRA, Jorge Da Cunha Oliveira, C. Vinagre
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引用次数: 0

摘要

血管周围上皮样细胞瘤(PEComa)是一种罕见的间充质肿瘤。PEComas发生在多个部位,可发生转移、复发和侵袭性的临床过程。肺是PEComas最常见的转移部位。雌激素在PEComas中的作用尚不清楚。在人类中,雌激素可能通过MEK途径刺激PEComa肿瘤细胞,因为TSC2肿瘤抑制基因发生突变因此,阻断雌激素受体可能使MEK通路失活,并为治疗效果提供了理论依据关于子宫恶性PEComa合并肺转移的报道很少,使用激素治疗(包括他莫昔芬)的报道也较少。1-5我们报告一例恶性腹膜PEComa伴肺转移的病例,该病例已接受他莫昔芬治疗2年,到目前为止患者还活着,病情得到控制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Peritoneal Perivascular Epithelioid Cell Tumor with Pulmonary Metastasis
32 Perivascular epithelioid cell tumor (PEComa) is part of a rare family of mesenchymal tumors. PEComas occur at multiple sites and can undergo metastasis, recurrence, and aggressive clinical courses. The lung is a common metastatic site of PEComas. The role of estrogen in PEComas is unclear. In humans, estrogen might stimulate PEComa tumour cells because of a mutation in the TSC2 tumour suppressor gene, through MEK pathway.1 Blocking estrogen receptors might therefore inactivate the MEK pathway and provide a rationale for therapeutic efficacy.1 There are few reports about uterine malignant PEComa tumours with pulmonary metastases and fewer about the use of hormonal therapy, including tamoxifen.1-5 We report a case of a malignant peritoneal PEComa with pulmonary metastasis which has been treated for 2 years with tamoxifen and to the date the patient is alive and well, with a controlled disease.
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