Desmoplastic fibroma

Desmoplastic fibroma is a rare, benign, locally aggressive fibrous neoplasm that typically arises in the metaphysis of long bones or in the mandible. It is a type of fibroma that is characterized by the presence of abundant collagen and a relatively small number of fibroblasts.

Clinical Presentation[edit | edit source]

Patients with desmoplastic fibroma often present with pain and swelling in the affected area. The tumor may also cause pathological fractures. The age of onset is usually in the first two decades of life, but it can occur at any age.

Diagnosis[edit | edit source]

The diagnosis of desmoplastic fibroma is based on the clinical presentation, radiographic findings, and histopathological examination. Radiographically, the tumor appears as a lytic, well-defined, non-calcified mass. Histologically, it is composed of spindle-shaped fibroblasts embedded in a dense collagenous stroma.

Treatment[edit | edit source]

The treatment of choice for desmoplastic fibroma is wide surgical excision. However, due to the aggressive nature of the tumor and its tendency to recur, complete removal may not always be possible. In such cases, adjuvant therapies such as radiation therapy or chemotherapy may be considered.

Prognosis[edit | edit source]

The prognosis for patients with desmoplastic fibroma is generally good, as the tumor is benign and does not metastasize. However, the local aggressiveness of the tumor and the potential for recurrence can lead to significant morbidity.

References[edit | edit source]

Fletcher, CDM, Bridge JA, Hogendoorn P, Mertens F. WHO Classification of Tumours of Soft Tissue and Bone. IARC Press: Lyon 2013.

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