Results 81 to 90 of about 6,761,428 (165)
SET domain containing 5 (SETD5), a chromatin regulator involved in adipocytic differentiation. However, its immunohistochemical expression and prognostic significance in liposarcoma remain unclear. In our study, SETD5 expression was markedly elevated in the dedifferentiated component of dedifferentiated liposarcoma compared to the well‐differentiated ...
Makoto Abe +10 more
wiley +1 more source
Desmoid Tumor of the Porta Hepatis: A Rare Location With Unusual Clinical Presentation
Background Desmoid tumor is a locally aggressive fibroblastic/myofibroblastic neoplasm frequently arising in deep soft tissues. Although it can be well circumscribed, a desmoid tumor generally infiltrates surrounding tissues and tends to recur locally without metastasizing.
Adila Adilli +10 more
wiley +1 more source
Aggressive desmoid fibromatosis : first case in a Rwandan child [PDF]
CITATION: Kanyamuhunga, A. et al. 2013. Aggressive desmoid fibromatosis : first case in a Rwandan child. South African Journal of Child Health, 7(3):117-118, doi:10.7196/SAJCH.593.The original publication is available at http://www.sajch.org.zaDesmoid ...
Stefan, Daniela Cristina +4 more
core +1 more source
Desmoid Fibromatosis of Breast Resembling Carcinoma: A Diagnostic Conundrum
Desmoid fibromatosis of the breast is an uncommon, benign, and locally invasive fibroblastic tumor that may show signs of malignancy but cannot spread.
Yaminy Pradeep Ingale +3 more
doaj +1 more source
Slow Growing Desmoid-Type Fibromatosis of the Breast: A Case Report
Fibromatosis or desmoid tumor of the breast is a rare benign entity that has no metastatic potential but has significant risk of local recurrence. Its association with previous surgical or accidental trauma and Gardner's syndrome has been reported ...
Ah Reum Park +9 more
doaj +1 more source
Desmoid fibromatosis of the cruris: A rare case report
Desmoid Fibromatosis (DF) is a locally aggressive connective tissue neoplasm that arises within the musculoaponeurotic structures. It is also referred to by various terms, including aggressive fibromatosis, deep fibromatosis, musculoaponeurotic ...
Nuciana Siti Andrianti, MD +3 more
core +1 more source
Desmoid-Type Fibromatosis of the Neck with Brachial Plexus Involvement: A Rare Case Report
Introduction: Desmoid-type fibromatosis (DTF) is a rare soft tissue tumor arising from musculoaponeurotic connective tissue, characterized by locally aggressive growth and a high rate of local recurrence despite the absence of metastatic potential. Case
Viet Anh Nguyen +2 more
core +1 more source
Desmoid-type Fibromatosis of the Mesentery: A Case Report
Summary Desmoid-type fibromatosis is a rare mesenchymal neoplasm with locally aggressive, infiltrating and destructive growth that is not characterized by a metastatic potential.
Tatyana M. Betova +11 more
core +1 more source
Desmoid tumors represent a rare entity of monoclonal origin characterized by locally aggressive behavior and inability to metastasize. Most cases present in a sporadic pattern and are characterized by a mutation in the CTNNB1 gene; while 5–15% show
Karla Susana Martín-Tellez +7 more
core +1 more source
Aggressive Fibromatosis (Desmoid Tumor) Is Derived from Mesenchymal Progenitor Cells
The cellular origins from which most tumors arise are poorly defined, especially in mesenchymal neoplasms. Aggressive fibromatosis, also known as desmoid tumor, is a locally invasive soft tissue tumor that has mesenchymal characteristics.
Saied Nik-Amini +4 more
core +1 more source

