Human pathology

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intramuscular myxoma

Intramuscular myxoma is a benign soft-tissue tumor that presents as a deeply seated mass confined to skeletal muscle.

Synopsisi

- hypocellular, hypovascular regions
- cytologically bland stellate and bipolar fibroblasts separated by abundant extracellular myxoid matrix
- areas of increased cellularity and vascularity that can lead to a mistaken diagnosis of sarcoma

  • The hypercellular regions are not associated with cytologic atypia of the constituent cells, mitotic activity, or necrosis. (9777984)

Cytogenetics

- hyperdiploidy
- trisomy 18

Differential diagnosis

- myxofibrosarcoma
- low-grade fibromyxoid sarcoma
- myxoid liposarcoma

Prognosis

- Surgical excision is virtually always curative. - Recurrence, even after incomplete resection, is exceptional.

References

- Nielsen GP, O’Connell JX, Rosenberg AE. Intramuscular myxoma: a clinicopathologic study of 51 cases with emphasis on hypercellular and hypervascular variants. Am J Surg Pathol. 1998 Oct;22(10):1222-7. PMID: 9777984