Data di Pubblicazione:
2022
Abstract:
CBL syndrome is a Noonan-like RASopathy with heterogeneous clinical phenotype and predisposition to juvenile myelomonocytic leukemia (JMML). Here we describe two patients with identical germline CBL mutation and clinical and immune-hematological overlapping features with autoimmune lymphoproliferative syndrome (ALPS) and B-cell expansion with NF-κB and T-cell anergy (BENTA) syndrome. Increased immature/transitional B cells can be depicted in CBL syndrome, ALPS, and BENTA. Nonetheless, our patients here described showed peculiar B-cell phenotype due to increased immature/transitional CD34+ B cells. This feature differentiates CBL syndrome from BENTA, pointing toward an abnormal proliferation of B-cell early precursors.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
ALPS; BENTA; CARD11; CBL; lymphocytosis; RALD; RASopathies; splenomegaly
Elenco autori:
Saettini, F.; Coliva, T. A.; Vendemini, F.; Galbiati, M.; Bugarin, C.; Masetti, R.; Moratto, D.; Chiarini, M.; Guerra, F.; Iascone, M.; Badolato, R.; Cazzaniga, G.; Niemeyer, C.; Flotho, C.; Biondi, A.
Link alla scheda completa:
Pubblicato in: