نتایج جستجو برای: desmoid tumor
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INTRODUCTION Primary chest wall sarcomas are rare mesenchymal tumors and their mainstay of therapy is wide surgical resection. We report our single-institution, multidisciplinary experience with full-thickness resection for primary chest wall sarcomas. METHODS A retrospective review of our prospectively maintained databases revealed that 51 patients were referred for primary chest wall sarcom...
Desmoid tumor is a rare monoclonal fibroblast proliferation that is regarded as benign. The clinical management of desmoid tumors is very complex and requires a multidisciplinary approach because of the unpredictable disease course. For those cases localized in the anterior abdominal wall, symptomatic and unresponsive to medical treatment, radical resection and reconstruction with a prosthetic ...
Desmoid tumors, also called deep or aggressive fibromatosis, are uncommon mesenchymal tumors characterized by proliferation of fibroblasts in an abundant collagen extracellular matrix. They rarely involve the pancreas, and the diagnosis is difficult to make if they do. Only eleven cases have previously been reported involving the pancreas in a review of the literature. In these reported cases, ...
Desmoid tumors are rare potentially aggressive benign tumors. Various etiologies and recurrent factors have been presented and discussed. A case of an abdominal desmoid tumor with vascular mesenteric invasion in a 32-year-old female, over 2 years after pregnancy is presented. Pre-operative biopsy was not contributive, diagnosis was made after surgery. Resection required two vascular bypasses. D...
Abstract Desmoid-type fibromatosis (DF) is a borderline tumor of soft tissues that has low malignant potential but described as infiltrative, locally aggressive and rapidly growing. In the pediatric population, it occurs in head neck. Presentation varies based on size location. Despite high recurrence rate, surgical excision remains modality choice with. Here, we report case 5-month-old boy, wi...
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