WBC Pathology I Flashcards
Histology morphology of the myeloblast:
Youngest
Scanty cytoplasm
Nucleolus
How is the promyelocyte differentiated from the myeloblast?
Primary granules are present
Immature WBC with specific granules:
Myelocyte
First immature WBC to appear in the peripheral smear; equivalent to a reticulocyte:
Intermediate cell
Most common cause of agranulocytosis:
Drug toxicity
Pathogenesis of leukopenias:
Inadequate or ineffective granulopoiesis
Increased destruction
Splenic sequestration
Kotsmann syndrome is:
Congenital inability to produce neutrophils
Peripheral WBC count is influenced by:
Size of precursor storage pools
Rate of cell release
Proportion of cells in the marginal pool
Rate of cell extravasation
Types of benign WBC proliferation in the bone marrow:
Leukocytosis
Leukemoid Reaction
Causes of neutrophilia:
Bacterial infection
Tissue necrosis
Pyogenic infection
Causes of lymphocytosis:
Chronic infection
Fungal, viral, immunologic reaction
Causes of eosinophilia:
Asthma
Allergy
Parasitic infection
Causes of monocytosis:
Chronic infection
Collagen disease
Basophilia is often indicative of:
Myeloproliferative disorder
PBS changes during a leukemoid reaction:
Toxic granules (Dohle bodies) No blasts, but stab cells present
B-cells are located in what area of the lymph node?
Follicular area
T-cells are located in what area of the lymph node?
Parafollicular area
Acute lymphadenitis in the cervical region indicates infection of:
Submandibular or neck area
Infection in the extremities manifests as acute lymphadenitis in which regions?
Axillary and inguinal regions
Three types of chronic lymphadenitis:
Follicular Hyperplasia
Parafollicular/Paracortical Hyperplasia
Sinus histiocytosis/reticular hyperplasia
In follicular hyperplasia, activated B-cells are located in the ___ while inactivated B cells are located in the ___ area:
germinal center; thin marginal
Two zones of germinal centers:
Centroblast (dark)
Centrocytes (light)
B-memory cells originate in the:
Centrocytes of the germinal center
Causes of follicular hyperplasia:
Rheumatoid arthritis
Toxoplasmosis
Early HIV
Features favoring a non-neoplastic hyperplasia:
Preservation of LN architecture
Variation in follicular shape and size
Mitotic figures and phagocytic macrophages
Characteristic cells in parafollicular hyperplasia:
Immunoblasts
Causes of parafollicular hyperplasia:
Drugs
IM
Vaccines
Hypertrophy of these cells are characteristic of sinus histiocytosis/reticular hyperplasia:
Lymphatic endothelial cells
Increase in macrophages
Structures indicative of follicular hyperplasia, located in the centrocytes:
Tingible bodies (phagocytosed B-cells)
Categories of Neoplastic proliferative states:
Lymphoid Neoplasm
Plasma cell dyscracias
Myeloid neoplasms
Histiocytoses
Originating cells of lymphoid neoplasm:
T-cells, B-cells, NK cells
3 categories of myeloid neoplasms:
Acute myeloid leukemia
Myelodysplastic syndrome
Chronic myeloproliferative disorders
Histiocytoses is a proliferation of these cells:
Macrophages and dendritic cells
Sinus histiocytosis is prominent in which cancers:
LN draining cancers (e.g. breast carcinoma)
Precursor B-cells cancers:
B Lymphoblastic Leukemia/Lymphoma (ALL)
Precursor T-cell cancers:
T lymphoblastic leukemia/lymphoma
Peripheral B-cell cancers:
Small Lymphocytic Leukemia Chronic Lymphocytic Leukemia Hairy cell leukemia Burkitt's Lymphoma Follicular Lymphoma
Peripheral T-cell cancers:
T-cell lymphoma
Anaplastic Large Cell Lymphoma
Mycosis Fungoides/Sezary Syndrome
Seen in all lymphocytic tumors, distinguishes from carcinoma:
CD 45 (Leukocyte Common Antigen)
Monocyte/macrophage antigens:
CD 14
CD 64