Results 1 to 10 of about 6,521 (135)
Obstructive Pyelonephritis Secondary to Ureteral Compression by an Intra-Abdominal Desmoid Tumor in Familial Adenomatous Polyposis: A Case Report. [PDF]
ABSTRACT In patients with familial adenomatous polyposis, intra‐abdominal desmoid tumors should be recognized as a rare but important cause of ureteral obstruction and obstructive pyelonephritis. Prompt cross‐sectional imaging, early recognition, and multidisciplinary management are essential for preserving renal function, treating infection, and ...
Mehrban A +5 more
europepmc +2 more sources
Locally Aggressive Desmoid Tumor With L4-L5 Vertebral Invasion and Progressive Neurological Deficit: A Case Report. [PDF]
ABSTRACT Desmoid‐type fibromatosis is a rare, non‐metastatic fibroblastic neoplasm that may cause major morbidity through locally infiltrative growth. Spinal involvement with vertebral destruction and neurological deficit is particularly uncommon and may mimic malignant spindle‐cell or primary osseous tumors.
AlAnsari GA +4 more
europepmc +2 more sources
Abdominal Wall Desmoid Tumor Misdiagnosed as Schwannoma: A Case Report. [PDF]
ABSTRACT We present the case of a 35‐year‐old woman with an abdominal wall mass initially diagnosed radiologically as a schwannoma. Histopathology revealed desmoid fibromatosis through β‐catenin positivity, despite no trauma or surgical history. Complete excision with negative margins was curative, highlighting immunohistochemistry's diagnostic value ...
Limaiem F, Hajri M.
europepmc +2 more sources
A case report of extra‐abdominal desmoid tumor after kidney transplantation [PDF]
Introduction Desmoid tumors are rare, locally invasive, non‐metastasizing intermediate grade neoplasms. According to the organ procurement and transplantation network report, approximately one million solid organ transplants have been performed globally,
Tsuyoshi Matsuda +7 more
doaj +2 more sources
Desmoid tumors are clonal fibroblastic neoplasms that arise in soft tissues. Patients with familial adenomatous polyposis (FAP) can develop intra-abdominal desmoid tumors. However, metachronous appearance of intra-abdominal desmoid tumor is rare, and its
Kenji Tsuchihashi +14 more
doaj +1 more source
Desmoid tumor is a rare disease, which is histologically characterized by local invasion, monoclonality, and fibroblast proliferation; and clinically characterized by a variable and often unpredictable course.
Jianzheng Wang +10 more
doaj +1 more source
Surgical management of recurrent desmoid tumor in a young male
Desmoid tumors are rare, aggressive fibroblastic soft tissue tumors. We report a case of a 20-year-old male with recurrence of desmoid tumor of the left shoulder after initial complete resection 3 years prior. Pathology revealed fibromatosis desmoid type.
Omar A. Santiago Báez +4 more
doaj +1 more source
A collision tumor is a neoplastic lesion comprised of two or more distinct cell populations with distinct borders. Desmoid fibromatosis (DF) is a rare musculoaponeurotic tissue tumor that grows deep in the connective tissue and shows locally aggressive ...
Lorenzo Gitto +3 more
doaj +1 more source
Desmoid Tumor and Implant-Based Breast Reconstruction
Desmoid tumors are rare locally aggressive myelodysplastic tumors that are usually abdominally based. They account for 0.2% of breast tumors. Certain factors like prior surgery, familial adenomatous polyposis, pregnancy, and high estrogen states are ...
Catherine Kilmartin +4 more
doaj +1 more source
Does A Vertebra Fracture Cause A Tumor? A Dorsolumbar Paraspinal Desmoid Tumor: Case Report
Extraabdominal desmoid tumors are uncommon soft-tissue tumors. The etiology of the tumor is still unclear. Injury is one of the etiological factors of soft-tissue tumors.
Zeki Serdar Ataizi +3 more
doaj +1 more source

