Table 1.
Clinical Phenotypes and Organ Complications in CVID Patients (n = 33) | |
---|---|
No disease-related complications | 9 (27%) |
Bronchiectasis | 4 (12%) |
Splenomegaly | 7 (21%) |
Autoimmunity | 20 (60%) |
Thrombocytopenia | 10 (33%) |
Hemolytic anemia | 6 (18%) |
Addison–Biermer disease | 2 (6%) |
Vitiligo | 1 (3%) |
Chronic seronegative polyarthritis | 2 (6%) |
Alopecia areata | 1 (3%) |
Nonspecific inflammatory bowel disease | 1 (3%) |
Psoriasis | 3 (6%) |
Polyclonal lymphocytic infiltration | |
Generalized lymphadenopathy | 19 (57%) |
Granulomatous lesions (histopathological confirmation) | 9 (27%) |
Immunoglobulin replacement therapy | 29 |
Immunoglobulin naïve | 3 |
Prednisolone | 2; dose 5 mg/day |
Methotrexate and etanercept | 1 |
Rituximab in anamnesis | 2 |
Clinical data of SLE patients (n = 17) | |
SLEDAI2K | 3.6 (min 0–max 9) |
Treatment | 16/17 |
Prednisolone | 10 (58%); dose: 9 mg/day (min 5–max 15 mg) |
Antimalarials | 16 (94%) |
Immunosuppressive medication | |
Methotrexate | 2 (11%) |
Rituximab in anamnesis | 1 (5%) |
CVID: Common variable immunodeficiency, SLE: systemic lupus erythematosus, SLEDAI2K: Systemic Lupus Erythematosus Disease Activity Index 2000.