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本文引用的文献

1
Uterine epithelioid leiomyosarcomas with clear cells: reactivity with HMB-45 and the concept of PEComa.伴有透明细胞的子宫上皮样平滑肌肉瘤:与HMB-45的反应及血管周上皮样细胞瘤的概念
Am J Surg Pathol. 2004 Feb;28(2):244-9. doi: 10.1097/00000478-200402000-00013.
2
[Angiomyolipoma of the colon - case report and review of the literature].
Z Gastroenterol. 2003 Aug;41(8):715-8. doi: 10.1055/s-2003-41210.
3
Malignant transformation of renal angiomyolipoma.
Int J Urol. 2003 May;10(5):271-3. doi: 10.1046/j.1442-2042.2003.00620.x.
4
Angiomyolipoma of the colon: report of a case and review of the literature.
Dis Colon Rectum. 2003 Apr;46(4):547-9. doi: 10.1007/s10350-004-6598-x.
5
Clear cell 'sugar' tumor of the breast: another extrapulmonary site and review of the literature.乳腺透明细胞“糖”瘤:另一个肺外部位及文献综述
Am J Surg Pathol. 2002 May;26(5):670-5. doi: 10.1097/00000478-200205000-00014.
6
Pleomorphic Angiomyolipoma of Digestive Tract: A Heretofore Unrecognized Entity.消化道多形性血管平滑肌脂肪瘤:一种此前未被认识的实体瘤。
Int J Surg Pathol. 2000 Jan;8(1):67-72. doi: 10.1177/106689690000800112.
7
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.
8
Renal angiomyolipoma with epithelioid sarcomatous transformation and metastases: demonstration of the same genetic defects in the primary and metastatic lesions.肾血管平滑肌脂肪瘤伴上皮样肉瘤转化及转移:原发灶与转移灶中相同基因缺陷的证实
Am J Surg Pathol. 2000 Jun;24(6):889-94. doi: 10.1097/00000478-200006000-00017.
9
Angiomyolipoma of the large intestine: report of a case.
Mod Pathol. 1999 Dec;12(12):1132-6.
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Angiomyolipoma arising in the colon.
Am J Gastroenterol. 1996 Sep;91(9):1852-4.

具有单一型表达和主要上皮样成分的结肠血管平滑肌脂肪瘤。

Colonic angiomyolipoma with a monotypic expression and a predominant epithelioid component.

作者信息

Abdulkader M, Abercrombie J, McCulloch T A, Kaye P V

机构信息

Queens Medical Centre University Hospital, Nottingham NG7 2UH, UK.

出版信息

J Clin Pathol. 2005 Oct;58(10):1107-9. doi: 10.1136/jcp.2004.025130.

DOI:10.1136/jcp.2004.025130
PMID:16189161
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1770749/
Abstract

Angiomyolipomas are rare lesions, often arising in the kidney, and are part of a group of tumours with a diverse appearance and evidence of dual melanocytic and smooth muscle differentiation known as PEComas (tumours of perivascular epithelioid cell origin). This report describes an unusual case of a colonic PEComa in a 40 year old woman. Unlike most of the previous colonic angiomyolipomas/PEComas reported in the literature, this case formed a large, mainly extrinsic mass and was monotypic, and composed entirely of the myomatous component with no adipose tissue or typical vasculature.

摘要

血管平滑肌脂肪瘤是一种罕见的病变,通常发生于肾脏,是一组外观多样、具有黑素细胞和平滑肌双重分化证据的肿瘤(血管周上皮样细胞瘤)的一部分。本报告描述了一名40岁女性发生结肠血管周上皮样细胞瘤的罕见病例。与文献中报道的大多数既往结肠血管平滑肌脂肪瘤/血管周上皮样细胞瘤不同,该病例形成了一个主要为外生性的大肿块,且为单型,完全由肌瘤成分组成,无脂肪组织或典型脉管系统。