WBC, LYMPH NODES, SPLEEN, AND THYMUS I Flashcards

1
Q

normal hematopoiesis

definitive _____________ arise several weeks later in the mesoderm of the intraembryonic aorta/gonad/mesonephros region

A

definitive hematopoietic stem cells

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2
Q

normal hematopoiesis

formed elements of blood - ____,_____,____,_____, and _____ - have a common origin from HSCs, pluripotent cells that sit at the apex of a hierarchy of bone marrow progenitors

r,g,m,p,p

A

red cells
granulocytes
monocytes
platelets
progenitors

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3
Q

normal hematopoiesis

HSC’s have two essential properties that are required for the maintenance of hematopoiesis:

________ and ________

A

pluripotency
capacity of cell renewal

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4
Q

normal hematopoiesis

the marrow response to short term physiologic needs is regulated by hematopoietic growth factors through their effects on the committed progenitors

these growth factors are called ____________ because they were discovered by their ability to support the growth of colonies of blood cells in vitro

A

colony stimulating factors

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5
Q

normal hematopoiesis

_________ of hematopoietic origin are often associated with mutations that block progenitor cell maturation or abrogate their growth factor dependence

A

tumors

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6
Q

disorders of white blood cells can be classified into two broad categories: ______ in which there is expansion of leukocytes and ______ which are defined as a deficiency of leukocytes

A

proliferative disorders
leukopenias

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7
Q

neutropenia agranulocytosis

______ occurs in aplastic anemia, and a variety of infiltrative marrow disorders; in these conditions granulocytopenia is accompanied by anemia and thrombocytopenia

diseased states associated with ineffective hematopoiesis such as _______- and myelodysplastic syndrome in which defective precursors die in the marrow

A

suppression of HCS
megaloblastic anemia

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8
Q

neutropenia, granulocytosis

alterations in the ________- vary with cause. with excessive destruction of neutrophils in the periphery, the marrow is usually hypercellular due to a compensatory increase in granulocytic precursors

____- are a common consequence of agranulocytosis.

A

bone marrow
infections

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9
Q

_________ refers to an increase in the number of white cells in the blood
it is a common reaction to a variety of inflammatory states

A

leukocytosis

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10
Q

leukocytosis

_________ which are coarser and darker than normal neutrophilic granules represent abnormal azurophilic primary granules

_______ are patches of dilated endoplasmic reticulum that appear as sky-blue cytoplasmic “puddles”

A

toxic granules
dohle bodies

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11
Q

leukocytosis

at other times particularly in severe infections many immature granulocytes appear in the blood, mimicking a myeloid leukemia (_____ reaction)

A

leukemoid reaction

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12
Q

lymphadenities

_______ in the cervical region is most often due to drainage of microbes or microbial products from infections of the teeth or tonsils, while in the axillary or inguinal regions is most often caused by infections in the extremities

A

acute nonspecific lymphadenitis

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13
Q

chronic nonspecific lymphadenitis morphology

____________ is caused by stimuli that activate humoral immune responses

defined by the presence of large oblong germinal centers ( secondary follicles), which are surrounded by a collar of small resting naive B cells (the mantle zone)

A

follicular hyperplasia

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14
Q

chronic nonspecific lymphadenitis morphology

_________ is caused by stimuli that trigger T cell mediated immune responses such as acute viral infections (e.g., infectious mononucleosis)

__________ (also called reticular hyperplasia) is marked by an increase in the number and size of the endothelial cells that line lympathic sinusoids and increased numbers of intrasinusoidal macrophages

A

paracortical hyperplasia
sinus histiocytosis

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15
Q

_____________ is a reactive condition marked by cytopenias and signs and symptoms of systemic inflammation refered to macrophage activation

for this reason, it is also sometimes referred to as macrophage activating syndrome

A

hemophagocytic lymphohistiocytosis

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16
Q

hemophagocytic lymphohistiocytosis

common features of all forms of HLH systemic activation of macrophages and _____ cytotoxic T cells

A

CD8 cytotoxic t cells