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Soft-tissue tumors

Benign fibrous histiocytoma

Soft tissueBenignFibrohistiocytic tumours

Epidemiology

On the skin it is very common and is called a dermatofibroma. The variant that belongs to this family of soft-tissue tumors is the deep one (deep benign fibrous histiocytoma), considerably rarer and managed more carefully. When it is superficial and typical it is usually managed simply; deep or atypical growth requires ruling out more aggressive diagnoses.

Basic features

The cutaneous dermatofibroma presents as a firm, small, slow-growing nodule in the skin. The deep variant, by contrast, forms a mass in the subcutaneous tissue or within the muscle and, because it is rare and resembles other lesions, requires pathological confirmation before surgery is decided.

Usual treatment

Observation, or local excision if it hurts, bleeds, changes, or the diagnosis is unclear.

Outcomes and prognosis

The prognosis is excellent; deep variants require more care because of a greater chance of recurrence.

This information is general and does not replace a medical evaluation. A musculoskeletal tumor must be interpreted together with imaging, physical examination, biopsy when appropriate and each patient's context.

Specialist evaluation

If you have a mass, a bone lesion or a report suggesting a tumor, book an evaluation.

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