Fibromatosis: Difference between revisions

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{{SK}} Fibromyxoma; myxofibroma; musculoaponeurotic fibromatosis
==Overview==
==Overview==
The term '''fibromatosis''' refers to a group of [[benign]] [[soft tissue]] [[tumor]]s which have certain characteristics in common, including absence of cytologic and clinical [[malignant]] features, a [[histology]] consistent with proliferation of well-differentiated [[fibroblasts]], an infiltrative growth pattern, and aggressive clinical behavior with frequent local recurrence. Other names include "musculoaponeurotic fibromatosis," referring to the tendency of these tumors to be adjacent to and infiltrating deep [[skeletal muscle]], and "desmoid tumor," an obsolete term which more specifically refers to the occurrence of these tumors in the [[abdominal wall]] of a pregnant woman. Treatment includes prompt radical excision with a wide margin and/or [[Radiation therapy|radiation]]. Despite the local infiltrative and aggressive behavior of these tumors, mortality secondary to these tumors is minimal to nonexistent.
The term '''fibromatosis''' refers to a group of [[benign]] [[soft tissue]] [[tumor]]s which have certain characteristics in common, including absence of cytologic and clinical [[malignant]] features, a [[histology]] consistent with proliferation of well-differentiated [[fibroblasts]], an infiltrative growth pattern, and aggressive clinical behavior with frequent local recurrence. Other names include "musculoaponeurotic fibromatosis," referring to the tendency of these tumors to be adjacent to and infiltrating deep [[skeletal muscle]], and "desmoid tumor," an obsolete term which more specifically refers to the occurrence of these tumors in the [[abdominal wall]] of a pregnant woman. Treatment includes prompt radical excision with a wide margin and/or [[Radiation therapy|radiation]]. Despite the local infiltrative and aggressive behavior of these tumors, mortality secondary to these tumors is minimal to nonexistent.
 
==Classification==
Subtypes of fibromatosis include juvenile fibromatosis, fibromatosis colli, infantile digital fibromatosis, infantile myofibromatosis, lipofibromatosis, fibromatosis hyalinica multiplex, penile fibromatosis (Peyronie's disease), and palmar fibromatosis (Dupuytren's contracture). Multiple fibromatoses are seen in [[Gardner's syndrome]], a syndrome which also includes multiple [[colon polyp]]s and osteomas. Fibromatosis is a different entity from [[neurofibromatosis]].
Subtypes of fibromatosis include juvenile fibromatosis, fibromatosis colli, infantile digital fibromatosis, infantile myofibromatosis, lipofibromatosis, fibromatosis hyalinica multiplex, penile fibromatosis (Peyronie's disease), and palmar fibromatosis (Dupuytren's contracture). Multiple fibromatoses are seen in [[Gardner's syndrome]], a syndrome which also includes multiple [[colon polyp]]s and osteomas. Fibromatosis is a different entity from [[neurofibromatosis]].


==References==
==References==
* {{eMedicine|derm|778}}
{{reflist|2}}
* [http://www.maxillofacialcenter.com/BondBook/softtissue/fibromatosis.html maxillofacialcenter]
{{Diseases of the musculoskeletal system and connective tissue}}
* Rosai, J. ''Rosai and Ackerman's Surgical Pathology''. Mosby Inc., 2004. pg 2249-2252.


{{Diseases of the musculoskeletal system and connective tissue}}
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Latest revision as of 02:45, 31 October 2012

Fibromatosis
ICD-10 M72.9
MeSH D005350

WikiDoc Resources for Fibromatosis

Articles

Most recent articles on Fibromatosis

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Review articles on Fibromatosis

Articles on Fibromatosis in N Eng J Med, Lancet, BMJ

Media

Powerpoint slides on Fibromatosis

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Evidence Based Medicine

Cochrane Collaboration on Fibromatosis

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TRIP on Fibromatosis

Clinical Trials

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Guidelines / Policies / Govt

US National Guidelines Clearinghouse on Fibromatosis

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Books

Books on Fibromatosis

News

Fibromatosis in the news

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Commentary

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Definitions

Definitions of Fibromatosis

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Patient resources on Fibromatosis

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Patient Handouts on Fibromatosis

Directions to Hospitals Treating Fibromatosis

Risk calculators and risk factors for Fibromatosis

Healthcare Provider Resources

Symptoms of Fibromatosis

Causes & Risk Factors for Fibromatosis

Diagnostic studies for Fibromatosis

Treatment of Fibromatosis

Continuing Medical Education (CME)

CME Programs on Fibromatosis

International

Fibromatosis en Espanol

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Business

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Patents on Fibromatosis

Experimental / Informatics

List of terms related to Fibromatosis

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Synonyms and keywords: Fibromyxoma; myxofibroma; musculoaponeurotic fibromatosis

Overview

The term fibromatosis refers to a group of benign soft tissue tumors which have certain characteristics in common, including absence of cytologic and clinical malignant features, a histology consistent with proliferation of well-differentiated fibroblasts, an infiltrative growth pattern, and aggressive clinical behavior with frequent local recurrence. Other names include "musculoaponeurotic fibromatosis," referring to the tendency of these tumors to be adjacent to and infiltrating deep skeletal muscle, and "desmoid tumor," an obsolete term which more specifically refers to the occurrence of these tumors in the abdominal wall of a pregnant woman. Treatment includes prompt radical excision with a wide margin and/or radiation. Despite the local infiltrative and aggressive behavior of these tumors, mortality secondary to these tumors is minimal to nonexistent.

Classification

Subtypes of fibromatosis include juvenile fibromatosis, fibromatosis colli, infantile digital fibromatosis, infantile myofibromatosis, lipofibromatosis, fibromatosis hyalinica multiplex, penile fibromatosis (Peyronie's disease), and palmar fibromatosis (Dupuytren's contracture). Multiple fibromatoses are seen in Gardner's syndrome, a syndrome which also includes multiple colon polyps and osteomas. Fibromatosis is a different entity from neurofibromatosis.

References

Template:Diseases of the musculoskeletal system and connective tissue


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