Das desmoplastische Fibrom der Fibula - Die schwierige klinische, radiologische und histologische Diagnose -

Perlick, L.; Zander, Dani S.; Wallny, T.; Zhou, Hongyue

doi:10.1055/s-2000-10065

Cited by 8 publications

(7 citation statements)

References 14 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…Sex predilection remains unclear while some authors report higher rates of DF in female patients [6] and others report no detectable sex predilection [7]. DF can theoretically affect any bone, but the majority of cases occur in the mandible (22%) and the metaphysis of long bones (56%) [8]. The pelvis accounts for 12% of cases.…”

Section: Introductionmentioning

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

View full text Add to dashboard Cite

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.

show abstract

Section: Introductionmentioning

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

View full text Add to dashboard Cite

show abstract

“…The rates of recurrence are 55-72% without resection and 17% with resection (1,22,(24)(25)(26). Metastases have not been reported.…”

Section: Discussionmentioning

confidence: 96%

Desmoplastic fibroma in the proximal femur: A case report with long-term follow-up

Yang

et al. 2015

Oncology Letters

View full text Add to dashboard Cite

Abstract. Desmoplastic fibroma of the bone is an extremely rare primary benign tumor. The present study reports a case of desmoplastic fibroma of the bone with the longest published follow-up. A 21-year-old female presented to The First Hospital of Jilin University (Changchun, Jilin, China) with thigh pain. Radiography demonstrated a lytic expansile lesion in the proximal femur. Curettage was performed, followed by use of an allogeneic graft. One month later, the patient suffered a pathological fracture and was treated with an open reduction and internal fixation. There was no recurrence of the tumor over a 28-year follow-up period. In conclusion, desmoplastic fibroma in the proximal femur is rare and an intralesional resection is strongly recommended to prevent recurrence. The disease may be misdiagnosed as a bone cyst, so the diagnosis should be confirmed with a histological examination.

show abstract

“…3,4,18,19 Histologically characterized as a myofibroblastic sarcoma 10 8,14 and desmin-negative myofibroblastic tumor of the femur. 3 In this case report, we describe the history, diagnostic pathway and the therapeutic algorithm of a locally aggressive myofibroblastic tumor affecting the proximal phalanx of the second toe.…”

Section: Introductionmentioning

confidence: 99%

Myofibroblastic Bone Tumor of the Toe: Case Report

Wagner¹,

Anders²,

Katenkamp³

et al. 2009

Foot Ankle Int.

View full text Add to dashboard Cite

show abstract

Das desmoplastische Fibrom der Fibula - Die schwierige klinische, radiologische und histologische Diagnose -

Cited by 8 publications

References 14 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 in the proximal femur: A case report with long-term follow-up

Myofibroblastic Bone Tumor of the Toe: Case Report

Contact Info

Product

Resources

About