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1
Dedifferentiated Solitary Fibrous Tumor: A Concise Review.去分化孤立性纤维性肿瘤:简要综述。
Arch Pathol Lab Med. 2018 Jun;142(6):761-766. doi: 10.5858/arpa.2016-0570-RS.
2
Solitary Fibrous Tumour A rare cause of acute abdomen.孤立性纤维瘤:急性腹痛的罕见病因。
Ann Ital Chir. 2017 Mar 29;6:S2239253X17026767.
3
A Review of the Surgical Management of Extrathoracic Solitary Fibrous Tumors.胸外孤立性纤维性肿瘤的外科治疗综述
Am J Clin Oncol. 2018 Jul;41(7):687-694. doi: 10.1097/COC.0000000000000348.
4
Solitary Fibrous Tumor of the Sigmoid Colon Masquerading as an Adnexal Neoplasm.伪装成附件肿瘤的乙状结肠孤立性纤维瘤。
Case Rep Pathol. 2016;2016:4182026. doi: 10.1155/2016/4182026. Epub 2016 Sep 8.
5
Successful laparoscopic treatment of a giant solitary fibrous tumor of the mesorectum: A case report and literature review.腹腔镜成功治疗巨大直肠系膜孤立性纤维瘤:病例报告及文献复习
Asian J Endosc Surg. 2017 Feb;10(1):51-54. doi: 10.1111/ases.12322. Epub 2016 Sep 5.
6
Solitary fibrous tumor of small bowel mesentery with postoperative bowel obstruction: a case report and review of literature.小肠系膜孤立性纤维瘤伴术后肠梗阻:1例报告并文献复习
Int J Clin Exp Pathol. 2015 Sep 1;8(9):11691-7. eCollection 2015.
7
Nuclear expression of STAT6 distinguishes solitary fibrous tumor from histologic mimics.STAT6 的核表达可将孤立性纤维性肿瘤与组织学模拟物区分开来。
Mod Pathol. 2014 Mar;27(3):390-5. doi: 10.1038/modpathol.2013.164. Epub 2013 Sep 13.
8
Solitary fibrous tumor of all sites: outcome of late recurrences in 14 patients.所有部位的孤立性纤维瘤:14例晚期复发患者的结局
Clin Sarcoma Res. 2013 Apr 3;3:4. doi: 10.1186/2045-3329-3-4. eCollection 2013.
9
Solitary fibrous tumors and so-called hemangiopericytoma.孤立性纤维性肿瘤及所谓的血管外皮细胞瘤。
Sarcoma. 2012;2012:690251. doi: 10.1155/2012/690251. Epub 2012 Apr 8.
10
HEMANGIOPERICYTOMA: A VASCULAR TUMOR FEATURING ZIMMERMANN'S PERICYTES.血管外皮细胞瘤:一种以齐默尔曼周细胞为特征的血管肿瘤。
Ann Surg. 1942 Jul;116(1):26-33. doi: 10.1097/00000658-194207000-00004.

盲肠壁孤立性纤维瘤:下消化道出血的罕见病因

Solitary fibrous tumour of caecum wall: an unlikely cause of low gastrointestinal haemorrhage.

作者信息

Santos Mariana Nogueira, Tavares Amelia Brandao, Viveiros Fernando Arruda, Baldaia Helena

机构信息

General Surgery, Centro Hospitalar de Vila Nova de Gaia Espinho EPE, Vila Nova de Gaia, Portugal.

Anatomical Pathology, LAP-Laboratório Anatomia Patológica-Unilabs, Porto, Portugal.

出版信息

BMJ Case Rep. 2018 Oct 25;2018:bcr-2018-227238. doi: 10.1136/bcr-2018-227238.

DOI:10.1136/bcr-2018-227238
PMID:30366899
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6203041/
Abstract

Solitary fibrous tumour (SFT), previously denominated as haemangiopericytoma, is a rare, spindle cell neoplasm that was first described in the thoracic pleura. It is now known that this tumour may develop from almost any anatomic location. We report a case of SFT, in a 65-year-old man, which was located in the muscularis propria layer of the caecum with involvement of the serosa and the ileocecal appendix, location never described in the literature, and with an uncommon clinical presentation of hematochezia. A radical right hemicolectomy was performed, and the patient was asymptomatic without evidence of metastasis or relapse after 6 months of follow-up.

摘要

孤立性纤维瘤(SFT),以前被称为血管外皮细胞瘤,是一种罕见的梭形细胞肿瘤,最初在胸膜中被描述。现在已知这种肿瘤几乎可以在任何解剖位置发生。我们报告一例65岁男性的SFT,肿瘤位于盲肠固有肌层,累及浆膜和回盲部阑尾,该部位在文献中从未有过描述,且临床表现为便血较为罕见。患者接受了根治性右半结肠切除术,随访6个月后无症状,无转移或复发迹象。