Desmoid tumor: Difference between revisions
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{{CMG}} {{AE}}{{S.M.}}{{Faizan}} | {{CMG}} {{AE}}{{S.M.}}{{Faizan}} | ||
{{SK}} Aggressive fibromatosis, Deep musculoaponeurotic fibromatosis, Deep | {{SK}} Aggressive fibromatosis, Deep musculoaponeurotic fibromatosis, Deep fibromatosis, Familial infiltrative fibromatosis, Hereditary Desmoid tumor, Musculoaponeurotic fibromatosis, Nonmetastasizing fibrosarcoma, Fibromatosis of soft tissue, Grade I fibromatosis, Well-differentiated non-metastasizing fibromatosis | ||
==[[Desmoid tumor overview|Overview]]== | ==[[Desmoid tumor overview|Overview]]== | ||
Revision as of 19:06, 31 August 2019
For patient information click here
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Desmoid tumor Microchapters |
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Diagnosis |
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Treatment |
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Case Studies |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Sara Mohsin, M.D.[2]Faizan Sheraz, M.D. [3]
Synonyms and keywords: Aggressive fibromatosis, Deep musculoaponeurotic fibromatosis, Deep fibromatosis, Familial infiltrative fibromatosis, Hereditary Desmoid tumor, Musculoaponeurotic fibromatosis, Nonmetastasizing fibrosarcoma, Fibromatosis of soft tissue, Grade I fibromatosis, Well-differentiated non-metastasizing fibromatosis
Overview
Historical Perspective
Classification
Pathophysiology
Causes
Differentiating desmoid tumor from other Diseases
Epidemiology and Demographics
Risk Factors
Natural History, Complications and Prognosis
Diagnosis
Diagnostic study of choice | History and Symptoms | Physical Examination |Laboratory Findings | CT | MRI | Other Imaging Findings | Other Diagnostic Studies
Treatment
Medical Therapy | Surgery | Cost-Effectiveness of Therapy | Future or Investigational Therapies