Search results
Results from the WOW.Com Content Network
Aggressive fibromatosis or desmoid tumor is a rare condition.Desmoid tumors are a type of fibromatosis and related to sarcoma, that can spread to other soft tissues, such as muscles, tendons, cartilidge, organs, blood vessels and arteries.
The FDA approval was supported by data from a late-stage trial, which tested 142 adults with progressing desmoid tumors, where the treatment showed a 71% lower risk of disease progression or death ...
Desmoplastic small-round-cell tumor (DSRCT) is an aggressive and rare cancer that primarily occurs as masses in the abdomen. [4] Other areas affected may include the lymph nodes, the lining of the abdomen, diaphragm, spleen, liver, chest wall, skull, spinal cord, large intestine, small intestine, bladder, brain, lungs, testicles, ovaries, and the pelvis.
The white tumor infiltrates the adjacent skeletal muscle (red tissue – lower left) and fat (yellow tissue – upper left). This tendency for invasion of adjacent normal tissues and structures is the reason that desmoid-type fibromatosis has a relatively high rate of local recurrence, even after surgical removal. Specialty: Oncology
The Desmoid Tumor Research Foundation (DTRF) is an American non-profit organization which funds research on desmoid tumors (aggressive fibromatosis), a rare soft-tissue tumor affecting 5–6 people per million per year. [1] Its goal is to improve treatments and find a cure. [2] The organization was founded in 2005 by Marlene Portnoy and Jeanne ...
Fibroblastic and myofibroblastic tumors. Fibroblastic and myofibroblastic tumors (FMTs) are tumors which develop from the mesenchymal stem cells which differentiate into fibroblasts (the most common cell type in connective tissue) and/or the myocytes / myoblasts that differentiate into muscle cells. FMTs are a heterogeneous group of soft tissue ...
Familial adenomatous polyposis (FAP) is an autosomal dominant inherited condition in which numerous adenomatous polyps form mainly in the epithelium of the large intestine. While these polyps start out benign, malignant transformation into colon cancer occurs when they are left untreated. Three variants are known to exist, FAP and attenuated ...
Gardner syndrome is an autosomal dominant form of polyposis characterized by the presence of multiple polyps in the colon together with tumors outside the colon. [3] The extracolonic tumors may include osteomas of the skull, thyroid cancer, epidermoid cysts, fibromas, [4] as well as the occurrence of desmoid tumors in approximately 15% of ...