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*[[Matrix]] [[mineralization]] is not present
*[[Matrix]] [[mineralization]] is not present
*In approximately 90% of cases widening of the host [[bone]] from gradual apposition of [[Periosteal reaction|periosteal]] new [[bone]] formation is seen
*In approximately 90% of cases widening of the host [[bone]] from gradual apposition of [[Periosteal reaction|periosteal]] new [[bone]] formation is seen
[[File:Desmoplastic fibroma.jpg|400px|thumb|none|X-ray revealed uneven density in the distal left femur, in which lamellate high-density opacity and bone destruction were observed.,Xu Y, Wang Y, Yan J, Bai X, Xing G. Desmoplastic fibroma of the femur with atypical image findings: A case report. Medicine (Baltimore). 2018;97(52):e13787. Published 2018 Dec 28. doi:10.1097/MD.0000000000013787,https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6314775/]]


===Pleural Fibroma===
===Pleural Fibroma===

Revision as of 16:00, 9 July 2019

Fibroma Microchapters

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Maneesha Nandimandalam, M.B.B.S.[2], Simrat Sarai, M.D. [3]

Overview

X-ray may be helpful in the diagnosis of fibroma. Findings on x-ray suggestive of a particular fibroma depends on the type of the fibroma. Findings on x-ray suggestive of non-ossifying fibromas include sharply demarcated, asymmetrical, and cortically based lucencies with a thin sclerotic rim. Findings on x-ray suggestive of ossifying fibroma include well-circumscribed lesion, intracortical osteolysis with a characteristic sclerotic band, cortical expansion, and a lytic thinning of the diaphyseal cortical bone with interspersed sclerosis. Findings on x-ray suggestive of chondromyxoid fibroma include a lobulated, eccentric radiolucent lesion. Findings on x-ray suggestive of desmoplastic fibroma include a lytic bone lesions with a geographic pattern of bone destruction and a narrow zone of transition and non-sclerotic margins.[1][1]

Ossifying Fibroma

The following radiographic features are noted on x-ray of ossifying fibroma:

Chondromyxoid Fibroma

The following features are seen on plain radiograph of chondromyxoid fibromas:

  • Chondromyxoid fibroma is seen as a lobulated, eccentric radiolucent lesion
  • Long axis is parallel to long axis of long bone
  • No periosteal reaction (unless a complicating fracture present)
  • In approximately 100% of cases geographic bone destruction is present
  • In approximately 85% of cases well defined sclerotic margin is present
  • In approximately 60% of cases there can be presence of septations (pseudo trabeculation)
  • In approximately 12.5% there can be presence of matrix calcification

Desmoplastic Fibroma

The following features are seen on plain radiograph of desmoplastic fibromas:

X-ray revealed uneven density in the distal left femur, in which lamellate high-density opacity and bone destruction were observed.,Xu Y, Wang Y, Yan J, Bai X, Xing G. Desmoplastic fibroma of the femur with atypical image findings: A case report. Medicine (Baltimore). 2018;97(52):e13787. Published 2018 Dec 28. doi:10.1097/MD.0000000000013787,https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6314775/

Pleural Fibroma

The following features are seen on plain radiograph of pleural fibromas:

Cemento-ossifying fibroma

The following features are seen on plain radiograph of cemento-ossifying fibromas:

Uterine Fibromas

References

  1. 1.0 1.1 1.2 Copley L, Dormans JP (1996). "Benign pediatric bone tumors. Evaluation and treatment". Pediatr Clin North Am. 43 (4): 949–66. PMID 8692589.

    X-Ray

    Non-ossifying Fibroma

    • On X-Ray, non-ossifying fibromas are characterized by sharply demarcated, asymmetrical, cortically based lucencies with a thin sclerotic rim.
    • They often appear multiloculated. They are located in the metaphysis, adjacent to the physis. As the patient ages, they seem to migrate away from the growth plate.
    • They have no associated periosteal reaction, cortical breach or associated soft tissue mass.
    • Nonossifying fibroma appear as well defined, small, eccentric, lytic, expansile lesions located in the metaphysis with scalloped sclerotic borders. Multiple lesions may be present.<ref name="pmid12544273">Yildiz C, Erler K, Atesalp AS, Basbozkurt M (2003). "Benign bone tumors in children". Curr Opin Pediatr. 15 (1): 58–67. PMID 12544273.


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