Bone marrow biopsy showing numerous plasma cells

Plasma Cell Dyscrasias

Overview Plasma cell disorders involve the abnormal proliferation of plasma cells. These B-cell clones synthesize and secrete a single monoclonal immunoglobulin or its fragments e.g. free light chains, and free heavy chains. These monoclonal immunoglobulins are termed M proteins and…

Diffuse Large B-cell lymphoma

Lymphomas

Overview Lymphomas are tumors arising from lymphoid cells. They have a much less dramatic presentation than leukemias. They are classified into 2 major groups – Hodgkin’s and Non-Hodgkin’s – based on morphology and immunophenotype. 2/3 of lymphoma present with Lymphadenopathy.…

Howel-jolly bodies

Myelodysplastic Syndromes

Myelodysplastic syndromes are characterized by dysplastic and ineffective hematopoiesis – bone marrow failure**.** It is sometimes described as “pre-leukemic” since there is a risk of transformation into acute leukemia (30%). In MDS, there is varied anemia, thrombocytopenia, and leukopenia. Hence…

Blood film showing numerous granulocytic forms, including band cells and immature myeloid cells

Myeloproliferative Neoplasms

Overview Myeloproliferative neoplasms are abnormal proliferations of one or more terminal myeloid cell lines in the peripheral blood (RBCs, WBCs, platelets). Myeloproliferative neoplasms are poorly characterized and poorly undersood. They all cause a predilection to extramedullary hematopoiesis, myelofibrosis, and transformation…

Smudge cells

Chronic Lymphocytic Leukemia

CLL is characterized by a progressive accumulation of monoclonal, mature, non-functional B lymphocytes. CLL is usually discovered on routine blood tests as an isolated lymphocytosis. It is defined by a > 5000/uL B-lymphocytes in the peripheral blood that are marked…

Blast cell

Acute Leukemia

Overview Acute Leukemia is an abnormal proliferation of blasts in either the peripheral myeloid or lymphoid cell lines. Acute Leukemias are of rapid onset. The blasts dramatically affect the bone marrow and consume nutrients and other resources leading to a…

Sickle Cell Disease

Overview Sickle cell disease is a hereditary, autosomal recessive disease caused by a point mutation of the beta-globin gene resulting in the absence of HbA and the production of HbS. Hbs has a preponderance to “sickling” (esp. during hypoxia, dehydration,…

Schistocytes and helmet cells

Haemolytic Anaemia

Overview Hemolytic anemia is simply anemia due to the destruction of red blood cells. The destruction of red blood cells happens at an accelerated pace, beyond the capacity of the bone marrow to compensate. Usually, a normocytic anemia is present…

Macro-ovalocytes

Macrocytic Anaemia

Overview Macrocytic anemia is characterized by Low Hb and High MCV (> 100). B12 and folate are required for the maturation of RBCs. Immature RBCs are larger, hence the increase in MCV in B12/Folate deficiency. A false normal MCV can…