Radiotherapy for Desmoplastic Fibroma of Bone: A Case Report

Nag, Hira Lal; Kumar, Rakesh; Bhan, S; Awasthy, Bhawana S.; Julka, P.K.; Ray, Ruma

doi:10.1177/230949900301100117

Cited by 23 publications

(17 citation statements)

References 5 publications

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“…and Nag et al . [18, 19] radiotherapy has also been shown to be a therapeutic option. Sanfiliippo et al .…”

Section: Discussionmentioning

confidence: 99%

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Desmoplastic Fibroma: A Case Report with Three Years of Clinical and Radiographic Observation and Review of the Literature

Nedopil¹,

Raab²,

Rudert³

2013

TOORTHJ

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Background:Desmoplastic fibroma (DF) is an extremely rare locally aggressive bone tumor with an incidence of 0.11% of all primary bone tumors. The typical clinical presentation is pain and swelling above the affected area. The most common sites of involvement are the mandible and the metaphysis of long bones. Histologically and biologically, desmoplastic fibroma mimics extra-abdominal desmoid tumor of soft tissue.Case Presentation and Literature Review:A case of a 27-year old man with DF in the ilium, including the clinical, radiological and histological findings over a 4-year period is presented here. CT scans performed in 3-year intervals prior to surgical intervention were compared with respect to tumor extension and cortical breakthrough. The patient was treated with curettage and grafting based on anatomical considerations. Follow-up CT scans over 18-months are also documented here. Additionally, a review and analysis of 271 cases including the presented case with particular emphasis on imaging patterns in MRI and CT as well as treatment modalities and outcomes are presented.Conclusion:In patients with desmoplastic fibroma, CT is the preferred imaging technique for both the diagnosis of intraosseus tumor extension and assessment of cortical involvement, whereas MRI is favored for the assessment of extraosseus tumor growth and preoperative planning. While tumor resection remains the preferred treatment for DF, curettage and grafting prove to be an acceptable alternative treatment modality with close follow-up when resection is not possible. Curettage and grafting have been shown to provide good clinical results and are associated with long recurrence free intervals.

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“…and Nag et al . [18, 19] radiotherapy has also been shown to be a therapeutic option. Sanfiliippo et al .…”

Section: Discussionmentioning

confidence: 99%

“…Similarily, Nag et al . [18] treated one patient with DF in the distal end of the femur with radiotherapy of 45 Gy in 25 fractions. Both authors reported deceleration of disease progression over a time period of 30 and 36 months, respectively.…”

Section: Discussionmentioning

confidence: 99%

Desmoplastic Fibroma: A Case Report with Three Years of Clinical and Radiographic Observation and Review of the Literature

Nedopil¹,

Raab²,

Rudert³

2013

TOORTHJ

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“…It is extremely rare, and less than 200 cases have been reported so far 12. The most common site of affection is the jaw, followed by pelvis and long bones 34.…”

Section: Introductionmentioning

confidence: 99%

Desmoplastic fibroma of ulna: Excision and reconstruction of olecranon with a fibular graft

Goyal

Rastogi

Trıpathy

2013

IJOO

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Desmoplastic fibroma is a rare, well differentiated, locally aggressive fibrous tumor usually arising from soft tissues, and rarely from bones. Involvement of forearm bones is extremely unusual. We present a large desmoplastic fibroma of right ulna in a 15-year-old male. The tumor was excised with a wide margin, and the bony defect was reconstructed with nonvascular autologous fibular graft. Reconstruction of the olecranon process was attempted using the fibular head and the remaining olecranon. At 2-years followup, there was no recurrence, flexion extension arc of the elbow joint was 40°–130° and there was no restriction of activities of daily living.

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“…Также применяется лучевая и химиотерапия, которая не обладает такой эффективностью, как предыдущие методы лечения, и считается опасной для доброкачественных опухолей. Применяется при невозможности проведения последних, или при отказе пациента хирургического вмешательства [5,6]. введение десмопластическая фиброма костной тканиредкая, локально агрессивная, доброкачественная опухоль, локализующаяся в костной ткани.…”

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Clinical and Х-Ray Patternsof Desmoplastic Fibromaof Mandibular Bone

Музыкин

Иорданишвили

Рыбакова

et al. 2017

HERALD of North-Western State Medical University named after I.

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This article presents the results of the clinical examination of the patient at the age of 41, who has been hospitalized according to the principle of OMC to the department of oral surgery and multi- specialized hospital of stomatology with a rare bone disease which affects the lower jaw -desmoplastic fibroma. The surveillance has been conducted for three years. Clinical characteristics and Хray patterns of the disease were revealed and the results of instrumental and histological studies were shown.

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Radiotherapy for Desmoplastic Fibroma of Bone: A Case Report

Cited by 23 publications

References 5 publications

Desmoplastic Fibroma: A Case Report with Three Years of Clinical and Radiographic Observation and Review of the Literature

Desmoplastic Fibroma: A Case Report with Three Years of Clinical and Radiographic Observation and Review of the Literature

Desmoplastic fibroma of ulna: Excision and reconstruction of olecranon with a fibular graft

Clinical and Х-Ray Patternsof Desmoplastic Fibromaof Mandibular Bone

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