New agents in development for paroxysmal nocturnal hemoglobinuria are showing promising results, both by reducing residual symptoms of the disease as well as by lessening the burden associated with the treatment itself.
Researchers in the U.K. took a critical look at systemic hematological manifestations and stent thrombosis, including an interesting case presentation of ST in a man with previously undiagnosed paroxysmal nocturnal hemoglobinuria.
There’s concern that patients with paroxysmal nocturnal hemoglobinuria or aplastic anemia may have an increased risk of more-severe SARS-CoV-2 infections. How did these populations do after being vaccinated?
Young patients who survive cancer or an inherited disorder that requires hematopoietic stem cell transplantation face challenges unlike those of other pediatric cancer survivors. This calls for a new approach to rehabilitation, say the authors of a recent study.
A large retrospective analysis of malignant evolution in patients with aplastic anemia and paroxysmal nocturnal hemoglobinuria has identified morphological, cytogenetic, and molecular high-risk features for secondary myeloid neoplasms.
Most patients with paroxysmal nocturnal hemoglobinuria who have been treated with at least 1 year of C5 inhibitor therapy still have hemoglobin levels below 12.0 g/dL. Continued fatigue and other symptoms related to this anemia were reported in this study.
The authors developed a new flow cytometry assay to determine the characteristics of paroxysmal nocturnal hemoglobinuria clones in white blood cells. Patients had different PNH abnormalities in different cell types.