Table 1.
No. | LGL leukemia type | Mutations | Sex | Age at diagnosis, y | WBC count at diagnosis, 109/L | Lymph count at diagnosis, 109/L | Lymphocyte count, 109/L* | CD8+ Vβ † | Concomitant disorders | Therapy‡ |
---|---|---|---|---|---|---|---|---|---|---|
1 | CD3+CD8+CD56+ T cell | STAT5b Y665F | F | 71 | 11.8 | 7.0 | 8.5 | Vb22, 91% | Collagenosis | No |
2 | CD3+CD8+CD56+ T cell | STAT5b Y665F | F | 49 | 16.1 | 12.9 | 13.7 | Vb17, 94% | None | No |
3 | CD3+CD8+CD56+ T cell | STAT5b N642H | M | 74 | 90.0 | 85.5 | 85.5 | Vb21, 87%§ | Pancytopenia, neutropenia, splenomegaly | Yes |
4 | CD3negCD56+ NK cell | STAT5b N642H | M | 75 | 164.7 | 131.8 | 131.8 | Vb7, 27%§Vb3, 16%§ | Hemolytic anemia, neutropenia, splenomegaly, MGUS | Yes |
F, female; M, male; MGUS, monoclonal gammapathy of unknown significance; WBC, white blood cell.
Lymphocyte count at the time point when the sample was taken.
Proportion of Vβ clone of CD8+ cells.
Pharmacological treatment at any time point.
Proportion from total T-cell fraction.