Case Report
Copyright ©The Author(s) 2022.
World J Clin Cases. Feb 16, 2022; 10(5): 1572-1579
Published online Feb 16, 2022. doi: 10.12998/wjcc.v10.i5.1572
Table 2 Primary differential diagnosis
Tumor type
Epidemiology
Clinical features
Size
Histopathology
Immunophenotype
Genetics
Nodular fasciitisYoung adults, no gender differenceGrows rapidly, painless, recurrence is rareMedian size, ≤ 2 cm (always < 5 cm)Spindle-shaped fibroblasts, growth in S- or C- shaped, interstitium is loose and myxoid, visible exosmosis of erythrocytesPositive: SMA, Calponin, CD10; negative: S100, CD34, nuclear β-cateninMYH9–USP6 gene fusion
Low-grade fibromyxoid sarcomaTypically affect young adults, no gender differenceSlow growth, no pain, easy recurrenceMedian size, 5 cm (1-20 cm)Original glue and myxoid region are mixed, spindle cell, small blood vessels, early formation of collagen rosettesEMA positive from focally to 80%, MUC4 positive has high sensitivity and specificityFUS-CREB3L2 or FUS-CREB3L1 gene fusion
Low-grade myofibroblastic sarcomaPredominantly in adults, 40-50 yr see more, slight predominance in malesEnlarging mass, painless, easy recurrenceMedian size, 4 cm (1.4-17 cm)Diffusely infiltrative growth, spindle cells arranged in a storiform pattern or fasciclesPositive: actin, desmin, calponin, CD34 (focal); negative: S100, nuclear β-cateninOnly one showed a circular chromosome
Low-grade myxofibrosarcomaElderly patients, over 60 yr, slight predominance in malesSlowly enlarging, painless, easy recurrenceLarger volume (range variable)Spindle cells, mild atypia, curvilinear thin-walled blood vessels, pseudolipoblastsPositive: SMA, negative: Desmin and histiocyte-specific markersNo specific aberration