Results 11 to 20 of about 10,048 (219)

Huge intrathoracic desmoid tumor

Annals of Thoracic Medicine, 2009
Desmoid tumors are soft-tissue neoplasms arising from fascial or musculo-aponeurotic structures. Most reported thoracic desmoid tumors originate from the chest wall. However, intrathoracic desmoid tumors are rare.
Ibrahim Majdi, Sandogji Hasan, Allam Abdullah   +2 more
doaj   +1 more source

Desmoid tumor: an unusual case of gross hematuria

Therapeutic 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, Vikas Desai, Adam Horn, Subodh M. Lele, Chad A. Lagrange   +4 more
doaj   +2 more sources

An Unusual case of large Desmoid tumour: A case report

MRIMS Journal of Health Sciences, 2014
Desmoid are rare soft tissue tumours most commonly seen in females between 20-40 years of age.They are known for their infiltrative pattern of growth and local recurrence.
D Kishori, V Sudhir Kumar, V Indira
doaj   +2 more sources

Multicentric extra-abdominal desmoid tumors arising in bilateral lower limbs

Rare 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, Tetsuya Hamada, Koji Hiraoka, Takanori Shoda, Kensei Nagata, Tokiko Shimoyama   +5 more
doaj   +2 more sources

Obstructive Pyelonephritis Secondary to Ureteral Compression by an Intra-Abdominal Desmoid Tumor in Familial Adenomatous Polyposis: A Case Report. [PDF]

Clin Case Rep
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, Karimi M, Hamidian MT, Masoumi M, Tari Najarkolaei E, Babamahmoodi A.   +5 more
europepmc   +2 more sources

Breast Fibromatosis: Clinical and Pathological Insights From Two Case Reports. [PDF]

Clin Case Rep
ABSTRACT Breast fibromatosis is a benign, locally aggressive spindle‐cell tumor mimicking carcinoma. We report two cases in patients aged 15 and 61 years, highlighting its wide age range. Accurate histopathology prevents overtreatment. Modern management emphasizes individualized care, including active surveillance, complete surgical excision when ...
Soleimani V, Jahanbin B, Nozheh A.
europepmc   +2 more sources

Locally Aggressive Desmoid Tumor With L4-L5 Vertebral Invasion and Progressive Neurological Deficit: A Case Report. [PDF]

Clin Case Rep
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, Alanzi A, Alatefi D, AlKhalaf M, AlSalmi S.   +4 more
europepmc   +2 more sources

The management of desmoid tumours: A joint global consensus-based guideline approach for adult and paediatric patients.

, 2020
Desmoid tumor (DT; other synonymously used terms: Desmoid-type fibromatosis, aggressive fibromatosis) is a rare and locally aggressive monoclonal, fibroblastic proliferation characterised by a variable and often unpredictable clinical course.
Desmoid Tumor Working Group,
core   +3 more sources

Percutaneous Management of Desmoid Tumors. [PDF]

Curr Oncol Rep
Purpose of Review To provide a comprehensive review of percutaneous image-guided techniques in the management of desmoid tumors including evolving thermal and non-thermal ablation options, as well as trans-arterial catheter options ...
Landinez GP, Ramasamy SK, Wu X, Naser-Tavakolian K, Sajan A, Siddiqui A, Moody J, Garcia-Reyes K, Raja J, Krishnasamy VP.   +9 more
europepmc   +2 more sources

Abdominal Wall Desmoid Tumor Misdiagnosed as Schwannoma: A Case Report. [PDF]

Clin Case Rep
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