Results 21 to 30 of about 8,758 (225)

Desmoid tumor: an unusual case of gross hematuria

open access: yesTherapeutic Advances in Urology, 2015
Desmoid tumors are rare soft-tissue masses originating from the proliferation of fibroblasts in the fibroconnective tissues. Intra-abdominal desmoid tumors pose special diagnostic challenge due to multiplicity of differential diagnoses, and difficulty to
Sudhir Isharwal   +4 more
doaj   +1 more source

Multicentric extra-abdominal desmoid tumors arising in bilateral lower limbs

open access: yesRare Tumors, 2010
Extra-abdominal desmoid tumors preferentially affect the shoulders, arms, backs, buttocks, and thighs of young adults. Multicentric occurrence is rather rare but seems to be another distinctive feature of extra-abdominal desmoid tumors.
Nobuhiro Fukushima   +5 more
doaj   +1 more source

Complete resection of a rectus abdominis muscle invaded by desmoid tumors and subsequent management with an abdominal binder: a case report

open access: yesJournal of Medical Case Reports, 2018
Background Desmoid-type fibromatosis is characterized by desmoid tumors, which are benign soft tissue tumors that can be locally aggressive but typically do not metastasize.
Tatsuhiko Ogawa
doaj   +1 more source

Desmoid-type fibromatosis of the splenic hilum: A rare tumor at an unusual location

open access: yesNigerian Journal of Surgery, 2020
Desmoid-type fibromatoses (DTFs), also known as desmoid tumors, are benign but infiltrative neoplasms that often appear next to previous surgical site. Intra-abdominal tumors usually involve the mesentery, but splenic hilum is an unusual localization. We
Ana Sanchez-Gollarte   +7 more
doaj   +1 more source

Idiopathic desmoid-type fibromatosis of the pancreatic head: case report and literature review [PDF]

open access: yes, 2014
Desmoid-type fibromatosis (DTF) is an uncommon nonmetastatic fibrous neoplasm. Sporadic intraperitoneal DTF is rarely described in current literature. We herein report a case of DTF of unknown cause involving the pancreatic head.
Baoling Tian   +5 more
core   +2 more sources

Abdominal desmoid tumors

open access: yesSurgical Oncology, 2007
Desmoid tumors are rare, benign, fibromatous lesions that are the result of abnormal proliferation of myofibroblasts. Desmoid tumors can be classified as extra-abdominal and abdominal. Abdominal desmoid tumors are either superficial or intraabdominal.
Sakorafas, George H.   +2 more
openaire   +3 more sources

Aggressive intraabdominal fibromatosis [PDF]

open access: yes, 2006
Background. Intraabdominal or mesenteric fibromatosis is a rare benign nonmetastatic neoplasm that appears as a sporadic lesion or in patients with familiar polyposis. Its evolution is unpredictable.
Grubor Nikica   +5 more
core   +1 more source

The paradox of cancer genes in non-malignant conditions: implications for precision medicine. [PDF]

open access: yes, 2020
Next-generation sequencing has enabled patient selection for targeted drugs, some of which have shown remarkable efficacy in cancers that have the cognate molecular signatures.
Adashek, Jacob J   +3 more
core  

Desmoid Tumours in Familial Adenomatous Polyposis: Review of 17 Patients from a Portuguese Tertiary Center [PDF]

open access: yes, 2016
INTRODUCTION: Desmoid Tumours (DT) are benign tumours with an estimated incidence of 2-4 per million per year. Between 7-16% of them are associated with Familial Adenomatous Polyposis (FAP) and are mostly parietal or intra-abdominal.
Martins, V.   +3 more
core   +1 more source

Resection and Abdominal Wall Reconstruction of a Desmoid Tumor with Endometrioma Features

open access: yesCase Reports in Surgery, 2016
Desmoid tumors are rare, musculoaponeurotic mesenchymal origin tumors arising from the proliferation of well-differentiated fibroblasts. Desmoid tumors may arise from any location with the abdominal cavity, abdominal wall and extremity locations being ...
Jaqueline Majors   +3 more
doaj   +1 more source

Home - About - Disclaimer - Privacy