Familial myxovascular fibromas

Familial myxovascular fibromas are a rare type of fibroma that primarily affect the skin and subcutaneous tissues. They are characterized by the presence of myxoid and vascular components, and are often associated with a family history of similar lesions.

Etiology[edit | edit source]

The exact cause of familial myxovascular fibromas is unknown. However, they are believed to be the result of a genetic mutation that leads to abnormal growth of fibrous tissue. Some researchers suggest that they may be associated with certain genetic disorders, although this has not been definitively proven.

Clinical Presentation[edit | edit source]

Familial myxovascular fibromas typically present as small, painless nodules under the skin. They can occur anywhere on the body, but are most commonly found on the extremities. The lesions are usually slow-growing and do not cause any symptoms unless they compress nearby structures.

Diagnosis[edit | edit source]

The diagnosis of familial myxovascular fibromas is typically made based on the clinical presentation and a biopsy of the lesion. The biopsy will show characteristic features of myxoid and vascular tissue, which helps to distinguish it from other types of fibromas.

Treatment[edit | edit source]

The primary treatment for familial myxovascular fibromas is surgical removal of the lesion. This is usually curative, although recurrence is possible. In some cases, radiation therapy or chemotherapy may be used to treat large or recurrent lesions.

Prognosis[edit | edit source]

The prognosis for individuals with familial myxovascular fibromas is generally good. The lesions are benign and do not typically cause any symptoms unless they compress nearby structures. However, recurrence is possible, particularly if the entire lesion is not removed during surgery.