Table 4.
Differential diagnosis of BSNS.
| Diagnosis | Histology | Immunohistochemistry | Genetics |
|---|---|---|---|
| Schwannoma | Cellular (Antoni A) and microcystic or loosely packed (Antoni B) areas, vessels with perivascular hyalinization | S100 (+), SMA (−), beta-catenin (−), PAX3 (−) | - |
| Malignant Triton tumor | Nuclear pleomorphism and hyperchromasia, brisk mitotic activity, necrosis | H3K27me3 (−), S100 (+, focal), Myogenin (+), beta-catenin (−), PAX3 (−) | SUZ12 or EED mutation, NF1 mutation |
| Synovial sarcoma | Dense cellular sheets of uniform spindle-shaped dark blue cells | EMA (+), TLE-1 (+) | SS18-SSX1/2/4 |
| Glomangiopericytoma | Short fascicles and whorls, perivascular accentuation, grenz zone | SMA (+), beta-catenin (−), S100 (−), desmin (−) | CTNNB1 mutations |
| Solitary fibrous tumor | Patternless growth pattern, variably cellular, ropey collagen bundles | CD34 (+), STAT6 (+), SMA (−), S100 (−) | NAB2-STAT6 fusion |
| Leiomyosarcoma | Elongated spindle cells with blunt-ended nuclei, perinuclear halos | SMA (+), desmin (+), beta-catenin (−), S100 (−) | - |
| Fibrosarcoma | Herringbone pattern, usually dense keloid-like collagen | SMA (−/+, focal), desmin (−), S100 (−), beta-catenin (−) | - |