Table 3 Literature review of peripheral T cell lymphoma
Name | year | Numberof Cases | Age/sex | Primary site of tongue | Cytologic Features | IHC characters and gene rearrangment | Clinical feature | Stage | IPI | Treatment | Survival (months) |
|---|---|---|---|---|---|---|---|---|---|---|---|
Uherova P,et al. [12] | 2002 | 1 | 56/M | – | small to intermediate, with round nuclei and abundant pale to clear cytoplasm, like marginal zone B-Cell lymphoma | CD3+,CD43+,CD45+; TCR+ | – | – | – | – | – |
May SA, et al. [13] | 2007 | 1 | 40/F | right ventrolate | atypical small- to medium-sized lymphoid infiltrate with involvement of the overlying squamous epithelium. Having irregular nuclear contours and scant cytoplasm | CD2,3,4,5+ CD43+; TCR+ Ki-67 25% | nodule | IA | Low | CVD and CM | 32 months free of disease until research published |
Lee JH, et al. [14] | 2014 | 1 | 59/M | right side of the tongue base | – | CD3+, TIA+, granzyme B+ CD56-Ki-67 80% | fungating mass | IIA | low | CHOP plus RT and VMAT | Died 17 months later |
Narla S, et al. [15] | 2016 | 1 | 50/F | left half of anterior portion | small lymphoid cells with scanty cytoplasm, irregular hyperchromatic nucleusand inconspicuous nucleoli | CD3,4,8+;TCR+Ki67 30–40% | nodule | I | low | No adjunctive therapy | 1 year later lost followed up |