• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

家族性腺瘤性息肉病中硬纤维瘤的CT表现:进一步观察

CT appearances of desmoid tumours in familial adenomatous polyposis: further observations.

作者信息

Brooks A P, Reznek R H, Nugent K, Farmer K C, Thomson J P, Phillips R K

机构信息

Department of Diagnostic Radiology, St Bartholomew's Hospital, London.

出版信息

Clin Radiol. 1994 Sep;49(9):601-7. doi: 10.1016/s0009-9260(05)81875-6.

DOI:10.1016/s0009-9260(05)81875-6
PMID:7955885
Abstract

Intra-abdominal desmoid tumours represent a major cause of morbidity and mortality in patients with familial adenomatous polyposis (FAP), and such patients are also liable to develop musculoskeletal desmoids. We have reviewed the CT appearances of 44 desmoid lesions (28 intra-abdominal and 16 musculoskeletal) in 20 patients with FAP. We found a considerable heterogeneity in the CT appearance of musculoskeletal and intraabdominal desmoids, with respect to their density, definition and change in size or density on follow-up, not only between different patients but also in patients with multiple lesions, who rarely showed identical appearances of all lesions. In some cases, mesenteric tumours may initially present as ill-defined soft tissue infiltration of mesenteric fat, becoming larger and more mass-like with time. On medical treatment, shrinkage was seen infrequently in musculoskeletal desmoids, and not at all with mesenteric lesions. CT evidence of bowel involvement by intra-abdominal lesions was frequent, most commonly appearing as 'tethering' or encasement of bowel loops. The presence of a large mesenteric mass (> 10 cm diam.), multiple mesenteric masses, extensive small bowel involvement and/or bilateral hydronephrosis were associated with ultimate death.

摘要

腹内硬纤维瘤是家族性腺瘤性息肉病(FAP)患者发病和死亡的主要原因,此类患者还容易发生肌肉骨骼系统的硬纤维瘤。我们回顾了20例FAP患者中44个硬纤维瘤病灶(28个腹内病灶和16个肌肉骨骼病灶)的CT表现。我们发现,肌肉骨骼和腹内硬纤维瘤的CT表现存在相当大的异质性,不仅在不同患者之间,而且在有多发病灶的患者中,其密度、边界以及随访时大小或密度的变化方面很少有所有病灶表现均相同的情况。在某些病例中,肠系膜肿瘤最初可能表现为肠系膜脂肪界限不清的软组织浸润,随着时间推移会变得更大且更像肿块。在药物治疗方面,肌肉骨骼硬纤维瘤很少出现缩小,肠系膜病灶则根本没有缩小。腹内病灶累及肠管的CT证据很常见,最常见的表现是肠袢“受牵拉”或被包绕。存在大的肠系膜肿块(直径>10 cm)、多个肠系膜肿块、广泛的小肠受累和/或双侧肾积水与最终死亡相关。

相似文献

1
CT appearances of desmoid tumours in familial adenomatous polyposis: further observations.家族性腺瘤性息肉病中硬纤维瘤的CT表现:进一步观察
Clin Radiol. 1994 Sep;49(9):601-7. doi: 10.1016/s0009-9260(05)81875-6.
2
Stepwise progression of familial adenomatous polyposis-associated desmoid precursor lesions demonstrated by a novel CT scoring system.一种新型CT评分系统显示家族性腺瘤性息肉病相关硬纤维瘤前体病变的逐步进展。
Dis Colon Rectum. 2003 Apr;46(4):481-5. doi: 10.1007/s10350-004-6586-1.
3
Desmoid disease in patients with familial adenomatous polyposis.家族性腺瘤性息肉病患者的硬纤维瘤病
Dis Colon Rectum. 2000 Mar;43(3):363-9. doi: 10.1007/BF02258303.
4
Desmoid tumours in patients with familial adenomatous polyposis and desmoid region adenomatous polyposis coli mutations.家族性腺瘤性息肉病患者及韧带样型纤维瘤病区域腺瘤性息肉病(APC)基因突变患者中的韧带样型纤维瘤病
Br J Surg. 2007 Aug;94(8):1009-13. doi: 10.1002/bjs.5633.
5
Identification and progression of a desmoid precursor lesion in patients with familial adenomatous polyposis.家族性腺瘤性息肉病患者韧带样瘤前体病变的识别与进展
Br J Surg. 1998 Jul;85(7):970-3. doi: 10.1046/j.1365-2168.1998.00773.x.
6
Prior pregnancy ameliorates the course of intra-abdominal desmoid tumors in patients with familial adenomatous polyposis.既往妊娠可改善家族性腺瘤性息肉病患者腹腔内硬纤维瘤的病程。
Dis Colon Rectum. 2000 Apr;43(4):445-50. doi: 10.1007/BF02237185.
7
Desmoid tumors in patients with familial adenomatous polyposis.家族性腺瘤性息肉病患者的硬纤维瘤
Cancer. 1994 Aug 15;74(4):1270-4. doi: 10.1002/1097-0142(19940815)74:4<1270::aid-cncr2820740415>3.0.co;2-7.
8
Carbon ion radiotherapy for desmoid tumor of the abdominal wall: a case report.腹壁硬纤维瘤的碳离子放射治疗:一例报告
World J Surg Oncol. 2016 Sep 13;14(1):245. doi: 10.1186/s12957-016-1000-8.
9
A 10-year review of surgery for desmoid disease associated with familial adenomatous polyposis.家族性腺瘤性息肉病相关韧带样瘤病手术治疗的10年回顾。
Br J Surg. 2006 Oct;93(10):1258-64. doi: 10.1002/bjs.5425.
10
MR appearances of desmoid tumors in familial adenomatous polyposis.家族性腺瘤性息肉病中硬纤维瘤的磁共振成像表现
AJR Am J Roentgenol. 1997 Aug;169(2):465-72. doi: 10.2214/ajr.169.2.9242755.

引用本文的文献

1
Unravelling Peritoneal Carcinomatosis Using Cross-Sectional Imaging Modalities.利用横断面成像方式解析腹膜癌病
Diagnostics (Basel). 2023 Jul 3;13(13):2253. doi: 10.3390/diagnostics13132253.
2
Multimodality imaging features of desmoid tumors: a head-to-toe spectrum.硬纤维瘤的多模态成像特征:从头到脚的图谱
Insights Imaging. 2020 Sep 25;11(1):103. doi: 10.1186/s13244-020-00908-0.
3
Duodenum-derived fibromatosis that invaded the muscular layer of intestinal wall: A rare case report.十二指肠来源的纤维瘤病侵犯肠壁肌层:一例罕见病例报告。
Medicine (Baltimore). 2017 Aug;96(31):e7684. doi: 10.1097/MD.0000000000007684.
4
An atypical presentation of small bowel obstruction and perforation secondary to sporadic synchronous intra-abdominal desmoid tumours.散发性同步腹腔内硬纤维瘤继发小肠梗阻和穿孔的非典型表现
Int J Surg Case Rep. 2016;20:147-50. doi: 10.1016/j.ijscr.2016.01.014. Epub 2016 Feb 1.
5
Sclerosing mesenteritis, a rare mesenteric disorder, in a patient with ulcerative colitis.一名溃疡性结肠炎患者患有硬化性肠系膜脂膜炎,这是一种罕见的肠系膜疾病。
Clin J Gastroenterol. 2009 Aug;2(4):257-261. doi: 10.1007/s12328-009-0086-8. Epub 2009 May 2.
6
Mesenteric desmoid-type fibromatosis causing secondary hypertension in a young woman.肠系膜硬纤维瘤病导致一名年轻女性继发性高血压。
Obstet Gynecol Sci. 2014 Sep;57(5):412-4. doi: 10.5468/ogs.2014.57.5.412. Epub 2014 Sep 17.
7
Intra-abdominal desmoid tumor mimicking gastric cancer recurrence: a case report.酷似胃癌复发的腹腔内硬纤维瘤:一例报告
World J Surg Oncol. 2014 May 10;12:146. doi: 10.1186/1477-7819-12-146.
8
Retroperitoneal fibromatosis presenting as a presacral mass.表现为骶前肿块的腹膜后纤维瘤病
Acta Radiol Short Rep. 2014 Feb 25;3(2):2047981614523760. doi: 10.1177/2047981614523760. eCollection 2014 Feb.
9
Mesenteric fibromatosis presenting as a diagnostic dilemma: a rare differential diagnosis of right iliac fossa mass in an eleven year old-a rare case report.肠系膜纤维瘤病表现为诊断难题:一名11岁儿童右下腹包块的罕见鉴别诊断——一例罕见病例报告
Case Rep Surg. 2013;2013:569578. doi: 10.1155/2013/569578. Epub 2013 Dec 2.
10
Giant mesenteric fibromatosis: Report of a case and review of the literature.巨大肠系膜纤维瘤病:病例报告及文献复习。
World J Gastrointest Surg. 2012 Mar 27;4(3):79-82. doi: 10.4240/wjgs.v4.i3.79.