Table 1.
Patient cohort and different RTX regimes (n = 76).
Disease category | Patients | RTX interval | |
---|---|---|---|
1-4 weeks | >4 weeks | ||
Post-transplant lymphoproliferative disorder(5 after liver, 5 after kidney, 2 after bone marrow transplantation) | 12 | 11 | 1 |
Monomorphic (Burkitt lymphoma or diffuse large-cell B cell lymphoma) | 9 | ||
Polymorphic | 2 | ||
Unknown | 1 | ||
Organ transplant rejection(7 humoral, 1 cellular, 5 mixed cellular and humoral) | 13 | 0 | 13 |
Liver transplantation | 3 | ||
Kidney transplantation | 10 | ||
Autoimmune diseases | 24 | 5 | 19 |
Juvenile dermatomyositis | 2 | ||
Granulomatosis with polyangiitis | 3 | ||
Juvenile myasthenia gravis | 3 | ||
Systemic lupus erythematosus with Shrinking lung disease | 1 | ||
Atypical hemolytic uremic syndrome | 2 | ||
Thrombotic-thrombocytopenic purpura | 1 | ||
Anti-N-methyl-D-aspartate receptor (NMDAR)-encephalitis | 1 | ||
Membrano-proliferative glomerulonephritis type 1 | 1 | ||
Membrano-proliferative glomerulonephritis type 2 | 1 | ||
Microscopic polyangiitis | 1 | ||
Immunological disease associated with membrano-proliferativeglomerulonephritis type 1 | 1 | ||
Haemophilia with inhibitors to factor VIII | 1 | ||
Autoimmune hepatitis | 6 | ||
Oncological diseases | 6 | 5 | 1 |
Burkitt leukemia | 2 | ||
Acute lymphatic leukemia | 1 | ||
Mediastinal large B cell lymphoma | 1 | ||
Diffuse large centroblastic B cell lymphoma | 1 | ||
Unknown cervical lymphadenopathy | 1 | ||
Nephrotic syndrome | 13 | 0 | 13 |
Minimal-change glomerulonephritis (7 steroid-dependent, 2 steroid-sensitive) | 9 | ||
Focal-segmental glomerulosclerosis (1 steroid-resistant) | 1 | ||
Unknown | 3 | ||
Other diseases* | 8 | 2 | 6 |
Other diseases (n = 8) were.