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本文引用的文献

1
Idiopathic desmoid-type fibromatosis of the pancreatic head: case report and literature review.胰头特发性韧带样型纤维瘤病:病例报告及文献复习
World J Surg Oncol. 2014 Apr 22;12:103. doi: 10.1186/1477-7819-12-103.
2
The role of APC and beta-catenin in the aetiology of aggressive fibromatosis (desmoid tumors).APC和β-连环蛋白在侵袭性纤维瘤病(韧带样瘤)病因学中的作用。
Eur J Surg Oncol. 2009 Jan;35(1):3-10. doi: 10.1016/j.ejso.2008.07.003. Epub 2008 Aug 21.
3
Desmoid tumors in a dutch cohort of patients with familial adenomatous polyposis.荷兰家族性腺瘤性息肉病患者队列中的硬纤维瘤
Clin Gastroenterol Hepatol. 2008 Feb;6(2):215-9. doi: 10.1016/j.cgh.2007.11.011.
4
Abdominal desmoid tumors.腹壁硬纤维瘤
Surg Oncol. 2007 Aug;16(2):131-42. doi: 10.1016/j.suronc.2007.07.009. Epub 2007 Aug 24.
5
Fibromatosis of the remnant pancreas after pylorus-preserving pancreaticoduodenectomy.保留幽门胰十二指肠切除术后残余胰腺纤维瘤病
J Gastrointest Surg. 2006 May;10(5):679-88. doi: 10.1016/j.gassur.2005.09.029.
6
Intraductal papillary-mucinous adenoma associated with unusual focal fibromatosis: a "postoperative" stromal nodule.导管内乳头状黏液腺瘤伴不寻常的局灶性纤维瘤病:一个“术后”基质结节。
Virchows Arch. 2002 Sep;441(3):308-11. doi: 10.1007/s00428-002-0686-x. Epub 2002 Jul 18.
7
Desmoid tumours complicating familial adenomatous polyposis.家族性腺瘤性息肉病并发硬纤维瘤
Br J Surg. 1999 Sep;86(9):1185-9. doi: 10.1046/j.1365-2168.1999.01222.x.
8
Desmoid tumors and mesenteric fibromatosis in Gardner's syndrome: report of kindred 109.
Arch Surg. 1979 Oct;114(10):1181-5. doi: 10.1001/archsurg.1979.01370340087015.

一例散发型硬纤维瘤:一种罕见的胰腺囊实性肿块。

A Sporadic Desmoid Tumor: an Exceptional Pancreatic Cystic-Solid Mass.

作者信息

Ardakani Jalal Vahedian, Mehrjardi Ali Zare, Wadji Massoud Baghai, Saraee Amir

机构信息

Firoozgar General Hospital, Iran University of Medical Sciences, Tehran, Iran.

出版信息

Indian J Surg. 2016 Aug;78(4):318-20. doi: 10.1007/s12262-015-1403-8. Epub 2015 Nov 13.

DOI:10.1007/s12262-015-1403-8
PMID:27574352
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4987560/
Abstract

Desmoid tumors are locally aggressive and non-metastatic neoplasms with a high rate of recurrence. Desmoid tumors of the pancreas are, however, very rare, and only a few cases have been reported in the literature. This paper reports an anecdotal case of a diffuse pancreatic desmoid tumor with the involvement of the pancreatic head, body, and-partially-tail. The patient underwent the Whipple procedure and subtotal pancreatectomy. Histopathological assessment showed that the tissues were partly positive for smooth muscle actin, but not for S100 or PanCK. The Ki67 index of the cells was only 1 %. Unfortunately, the patient died on the 10th postoperative day due to massive upper gastrointestinal bleeding.

摘要

硬纤维瘤是具有高复发率的局部侵袭性非转移性肿瘤。然而,胰腺硬纤维瘤非常罕见,文献中仅报道了少数病例。本文报告了一例累及胰头、胰体及部分胰尾的弥漫性胰腺硬纤维瘤的罕见病例。患者接受了惠普尔手术及胰腺次全切除术。组织病理学评估显示,组织平滑肌肌动蛋白部分呈阳性,但S100或细胞角蛋白全谱(PanCK)呈阴性。细胞的Ki67指数仅为1%。不幸的是,患者术后第10天因大量上消化道出血死亡。