Hematology 1: Leukopoiesis, WBC Disorders, and Laboratory Diagnostics

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Vocabulary review flashcards covering leukopoiesis, benign and malignant leukocyte disorders, cytochemical staining methods, and microscopy essentials based on Hematology 1 examination material.

27 Terms

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Granulopoiesis Maturation Sequence

The morphologic developmental sequence of granulocytes: myeloblast, promyelocyte, myelocyte, metamyelocyte, band cell, and mature segmented granulocyte.

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Mast Cells

Tissue cells that share a similar morphologic appearance and functional profile to peripheral blood basophils.

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CD34

A surface glycoprotein marker expressed by hematopoietic stem cells utilized for their identification.

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Primary (Azurophilic) Granules

Early cytoplasmic granules containing myeloperoxidase (MPO\text{MPO}) that first appear during the promyelocyte stage of granulocytic maturation.

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Toluidine Blue

A special metachromatic stain used to identify basophils and mast cells in bone marrow or tissue specimens.

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Myelocyte

The granulocytic precursor stage distinguished by the initial formation of secondary (specific) granules and the last stage in the series capable of mitotic division.

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Leukocyte Alkaline Phosphatase (LAP) Stain

A cytochemical stain used to differentiate chronic myelogenous leukemia (CML\text{CML}, which displays a decreased score) from a leukemoid reaction (which displays an elevated score).

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Philadelphia Chromosome

A characteristic cytogenetic abnormality formed by a reciprocal translocation between chromosome 9 and chromosome 22, designated as t(9;22)t(9;22), seen in chronic myelogenous leukemia (CML\text{CML}).

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Chédiak-Higashi Syndrome

A hereditary anomaly characterized by abnormal granulocyte maturation with the presence of giant, abnormal lysosomal granules in leukocytes.

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Smudge Cells

Fragile, ruptured leukocyte remnants commonly observed in chronic lymphocytic leukemia (CLL\text{CLL}), which can be prevented on blood smears by the addition of albumin.

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t(15;17)

A specific cytogenetic translocation characteristic of acute promyelocytic leukemia (APL\text{APL} / FAB M3\text{FAB M3}), which is frequently complicated by disseminated intravascular coagulation (DIC\text{DIC}).

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CD41

A platelet glycoprotein surface marker expressed by megakaryocytic lineage blasts in acute megakaryoblastic leukemia (FAB M7\text{FAB M7}).

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Mott Cells

A morphologic variant of plasma cells characterized by abundant cytoplasmic inclusions of immunoglobulins (Russell bodies) that resemble grape clusters.

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Reed-Sternberg Cells

Large, distinctive multinucleated or bilobed giant cells that serve as the defining diagnostic finding in lymph node biopsies of Hodgkin lymphoma.

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Pelger-Huët Anomaly

A benign hereditary leukocyte disorder marked by failure of granulocytes to segment beyond the two-lobed ('dumbbell' or 'pince-nez') or band stage, displaying coarse, hyperclumped nuclear chromatin.

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Auer Rods

Rod-shaped cytoplasmic inclusions formed by fused primary/azurophilic lysosomal granules found in myeloblasts and promyelocytes in acute myeloid leukemia.

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Waldenström Macroglobulinemia

A malignant lymphoproliferative disorder involving lymphoplasmacytoid cells that secrete monoclonal immunoglobulin M (IgM\text{IgM}).

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Tartrate-Resistant Acid Phosphatase (TRAP)

A cytochemical staining reaction that remains persistently positive in the neoplastic B-lymphocytes of hairy cell leukemia following the addition of L-tartaric acid.

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Specific Esterase (Naphthol AS-D Chloroacetate Esterase)

A cytochemical stain that demonstrates strong positive enzyme activity primarily in cells of the granulocytic (neutrophilic) lineage.

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Non-Specific Esterase (Alpha-Naphthyl Acetate Esterase)

A cytochemical stain used to identify blast cells of monocytic lineage by demonstrating strongly positive enzymatic activity.

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Döhle Bodies

Light blue, oval or round leukocyte inclusions composed of ribosomal RNA (rough endoplasmic reticulum) seen in the cytoplasm of granulocytes on Wright-stained peripheral smears.

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Alder-Reilly Anomaly

A hereditary metabolic storage disorder in which leukocytes accumulate abnormal mucopolysaccharides, forming dense azurophilic granules that closely resemble toxic granulation.

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May-Hegglin Anomaly

An inherited disorder characterized by Döhle-like cytoplasmic inclusion bodies in neutrophils, thrombocytopenia, and giant, poorly granulated platelets.

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LE Cell

A segmented neutrophil that has ingested a denatured, homogeneous mass of nuclear protein (antinuclear antibody-coated chromatin).

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Tart Cell

A monocyte or histiocyte that has engulfed an intact, morphologically recognizable cell nucleus, distinct from an LE cell.

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Terminal Deoxynucleotidyl Transferase (TdT)

A specialized DNA polymerase and intracellular enzyme whose elevated activity is a sensitive marker for primitive lymphoid cells in acute lymphoblastic leukemia (ALL\text{ALL}).

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Microscope Condenser

The sub-stage lens system responsible for concentrating and directing light through the specimen slide to ensure uniform, even illumination.