Aplastic anemia presenting as hemophagocytic lymphohistiocytosis

Two unusual cases of hemophagocytic lymphohistiocytosis (HLH) complicating aplastic anemia (AA) are described. Each patient had a history of preexisting acute hepatitis of unknown cause at the time of HLH diagnosis and i...

Hierarchical Involvement of Myeloid-Derived Suppressor Cells and Monocytes Expressing Latency-Associated Peptide in Plasma Cell Dyscrasias

Objective: Plasma cell dyscrasias (PCDs) are disorders of plasma cells having in common the production of a monoclonal M-protein. They include a spectrum of conditions that may represent a natural progression of the same...

Genotype-Phenotype Correlations of β-Thalassemia Mutations in an Azerbaijani Population

β-Thalassemia is the most common inherited disorder in Azerbaijan. The aim of our study was to reveal genotype-to-phenotype correlations of the most common β-thalassemia mutations in an Azerbaijani population. Patients w...

About Chediak-Higashi, Hemoglobin Lansing, and Hemoglobin Jabalpur

Uylukta Şişliğin Nadir Rastlanan Bir Sebebi: Ekstramedullar Myeloid Tümör