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1
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2
Perivascular epithelioid cell tumor ('PEComa') of the uterus: a subset of HMB-45-positive epithelioid mesenchymal neoplasms with an uncertain relationship to pure smooth muscle tumors.子宫血管周上皮样细胞瘤(“PEComa”):一组HMB-45阳性上皮样间叶肿瘤,与纯平滑肌肿瘤的关系尚不明确。
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Extremely late-onset pulmonary metastasis from uterine PEComa.极为晚期的肺转移:源自子宫的 PEComa。
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Malignant perivascular epithelioid cell tumor (PEComa) of the uterus.子宫恶性血管周上皮样细胞肿瘤(PEComa)。
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引用本文的文献

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Malignant perivascular epithelioid cell tumor (PEComa) of the uterus.子宫恶性血管周上皮样细胞肿瘤(PEComa)。
BMC Womens Health. 2022 Dec 16;22(1):523. doi: 10.1186/s12905-022-02119-9.
2
Primary retroperitoneal PEComa: an incidental finding.原发性腹膜后上皮样血管平滑肌脂肪瘤:偶然发现。
BMJ Case Rep. 2022 Nov 11;15(11):e250466. doi: 10.1136/bcr-2022-250466.
3
Extremely late-onset pulmonary metastasis from uterine PEComa.极为晚期的肺转移:源自子宫的 PEComa。
Pathologica. 2022 Aug;114(4):312-315. doi: 10.32074/1591-951X-762. Epub 2022 Sep 8.
4
A successful case of complete surgical resection via left upper and right lower lobectomy for bilateral lung metastases of a perivascular epithelioid cell tumor in the colon: a case report.经左上叶和右下叶切除实现结肠血管周上皮样细胞瘤双侧肺转移完全手术切除的成功病例:病例报告
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Natural History and Treatment Strategies of Advanced PEComas: A Systematic Review.晚期血管周上皮样细胞瘤的自然史与治疗策略:一项系统评价
Cancers (Basel). 2021 Oct 18;13(20):5227. doi: 10.3390/cancers13205227.
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A Retrospective Case Study of 13 Uterine Perivascular Epithelioid Cell Neoplasm (PEComa) Patients.13例子宫血管周上皮样细胞瘤(PEComa)患者的回顾性病例研究
Onco Targets Ther. 2021 Mar 9;14:1783-1790. doi: 10.2147/OTT.S300523. eCollection 2021.
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Perivascular Epithelioid Cell Tumour of the Uterus: a Case Report.子宫血管周上皮样细胞瘤:一例报告
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Computerized Tomography and Magnetic Resonance Imaging Findings in Malignant Perivascular Epithelioid Cell Tumors of the Ovaries with Pulmonary Metastasis.卵巢恶性血管周上皮样细胞瘤伴肺转移的计算机断层扫描和磁共振成像表现
Iran J Radiol. 2016 Aug 1;13(4):e34712. doi: 10.5812/iranjradiol.34712. eCollection 2016 Oct.
9
Angiomyolipoma and Malignant PEComa: Discussion of Two Rare Adrenal Tumors.血管平滑肌脂肪瘤与恶性PEComa:两种罕见肾上腺肿瘤的探讨
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10
Expression of CD44 and CD29 by PEComa cells suggests their possible origin of mesenchymal stem cells.PEComa细胞中CD44和CD29的表达表明它们可能起源于间充质干细胞。
Int J Clin Exp Pathol. 2015 Oct 1;8(10):13023-33. eCollection 2015.

本文引用的文献

1
Perivascular epithelioid cell tumor ('PEComa') of the uterus: a subset of HMB-45-positive epithelioid mesenchymal neoplasms with an uncertain relationship to pure smooth muscle tumors.子宫血管周上皮样细胞瘤(“PEComa”):一组HMB-45阳性上皮样间叶肿瘤,与纯平滑肌肿瘤的关系尚不明确。
Am J Surg Pathol. 2002 Jan;26(1):1-13. doi: 10.1097/00000478-200201000-00001.
2
Abdominopelvic sarcoma of perivascular epithelioid cells. Report of four cases in young women, one with tuberous sclerosis.血管周上皮样细胞腹部盆腔肉瘤。4例年轻女性病例报告,其中1例患有结节性硬化症。
Mod Pathol. 2001 Jun;14(6):563-8. doi: 10.1038/modpathol.3880351.
3
[A uterine pecoma: a case report].
G Chir. 1999 Apr;20(4):163-4.
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Epithelioid lymphangioleiomyomatosis-like tumour of the uterus in a patient without tuberous sclerosis: a lesion mimicking epithelioid leiomyosarcoma.
Histopathology. 1998 Jul;33(1):91-3. doi: 10.1046/j.1365-2559.1998.0415g.x.

子宫血管周上皮样细胞瘤的晚期肺转移

Late pulmonary metastasis in uterine PEComa.

作者信息

Dimmler A, Seitz G, Hohenberger W, Kirchner T, Faller G

机构信息

Institute of Pathology, University of Erlangen-Nuremberg, Krankenhausstrasse 8-10, 91054 Erlangen, Germany.

出版信息

J Clin Pathol. 2003 Aug;56(8):627-8. doi: 10.1136/jcp.56.8.627.

DOI:10.1136/jcp.56.8.627
PMID:12890819
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1770029/
Abstract

Perivascular epithelioid cell tumours (PEComas) other than angiomyolipoma, clear cell "sugar" tumour of the lung, and lymphangioleiomyomatosis are very rare mesenchymal tumours. The uterus seems to be the most prevalent site of involvement, but only 13 cases of uterine PEComa have been described. Three of these cases exhibited local aggressive behaviour and only one showed metastasis. Because of the extremely small number of cases, PEComas are considered tumours of uncertain malignant potential. This report describes a 68 year old woman, who presented with multiple pulmonary lesions seven years after the initial diagnosis of well differentiated endometrial stromal sarcoma. Histological and immunohistochemical analysis of the pulmonary lesions, in addition to re-evaluation of the primary uterine tumour, led to the final diagnosis of metastatic uterine PEComa. The findings indicate that any PEComa might have malignant potential. Spreading of this tumour to other organs might become evident even several years after primary manifestation.

摘要

除血管平滑肌脂肪瘤、肺透明细胞“糖”瘤和淋巴管平滑肌瘤病外,血管周上皮样细胞瘤(PEComas)是非常罕见的间叶组织肿瘤。子宫似乎是最常受累的部位,但仅有13例子宫PEComa的病例报道。其中3例表现出局部侵袭性,仅有1例发生转移。由于病例数量极少,PEComas被认为是恶性潜能不确定的肿瘤。本报告描述了一名68岁女性,在最初诊断为高分化子宫内膜间质肉瘤7年后出现多发肺部病变。对肺部病变进行组织学和免疫组化分析,并对原发性子宫肿瘤进行重新评估后,最终诊断为转移性子宫PEComa。这些发现表明,任何PEComa都可能具有恶性潜能。即使在原发表现出现数年之后,这种肿瘤向其他器官的扩散也可能变得明显。