Desmoid type fibromatosis: A case report with an unusual etiology

doi:10.4251/wjgo.v9.i9.385

Advanced Search

BPG is committed to discovery and dissemination of knowledge

Home / Archive / Volume 9, Issue 9

This Article

Academic Content and Language Evaluation of This Article

CrossCheck and Google Search of This Article

Academic Rules and Norms of This Article

Citation of this article

Corresponding Author of This Article

Research Domain of This Article

Article-Type of This Article

Open-Access Policy of This Article

Times Cited Counts in Google of This Article

Number of Hits and Downloads for This Article

Total Article Views (6989)

All Articles published online

The chart showing PDF series, WORD series, HTML series, Figures (1-5) series.

Item

Count

PDF

415

WORD

310

HTML

3376

Figures (1-5)

295

Sum=4396

Publishing Process of This Article

The chart showing Browse series, Download series.

Item

Count

Browse

1102

Download

1399

Sum=2501

Sep 15, 2017 (publication date) through Dec 22, 2024

Times Cited of This Article

Times Cited (7)

Journal Information of This Article

Publication Name

World Journal of Gastrointestinal Oncology

ISSN

1948-5204

Publisher of This Article

Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

Case Report

World J Gastrointest Oncol. Sep 15, 2017; 9(9): 385-389
Published online Sep 15, 2017. doi: 10.4251/wjgo.v9.i9.385

Full Size Figure Download Figure

Figure 5 Beta-catenin immunohistochemistry: Positive, diffuse, plump myofibroblast nuclear staining, faint cytoplasmic staining characteristic of desmoid type fibromatosis.

Citation: Jafri SF, Obaisi O, Vergara GG, Cates J, Singh J, Feeback J, Yandrapu H. Desmoid type fibromatosis: A case report with an unusual etiology. World J Gastrointest Oncol 2017; 9(9): 385-389
URL: https://www.wjgnet.com/1948-5204/full/v9/i9/385.htm
DOI: https://dx.doi.org/10.4251/wjgo.v9.i9.385