Leukocyte Disorders 2 Flashcards

(42 cards)

1
Q

generalized neoplastic proliferation or
accumulation of leukopoietic cells with or without
involvement of the peripheral blood

A

leukemia

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2
Q

group of malignant disorders affecting blood and
blood forming tissue of the bone marrow, lymph system and spleen

A

leukemia

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3
Q

the most common form of leukemia in children
characterized by a rapid increase in the numbers of immature blood cells

A

acute leukemia

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4
Q

characterized by the excessive
build-up of relatively mature, but
still abnormal, white blood cells

A

chronic leukemia

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5
Q

the predominant cells are all cells coming from
common myeloid progenitors

A

Granulocytic or Myelocytic Leukemia

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6
Q

common lymphoid progenitors

A

Lymphocytic/Lymphoid Leukemia

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7
Q

presence of immature or abnormal cells with WBC count greater than 15 x 10⁹/L

A

leukemic leukemia

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8
Q

with immature or abnormal cells in peripheral
blood and with WBC count less than 15 x 10⁹/L

A

SUBLEUKEMIC LEUKEMIA

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9
Q

with no immature cells in the peripheral blood and with WBC count less than 15 x 10⁹/L

A

ALEUKEMIC LEUKEMIA

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10
Q

a type of myeloblastic leukemia
malignant green colored tumor of myeloid cases

formation of tumors originating from periosteum, especially of skull, orbits, nasal sinuses, ribs and vertebrae

A

chloroma

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11
Q

a focal malignant tumor
composed of myeloblast or
early myeloid precursors
occurring outside of the
bone marrow

A

MYELOBLASTOMA

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12
Q

cancer of plasma cells

A

myeloma

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13
Q

proliferation of one of
the cell types of the
lymphopoietic reticular
tissue

A

lymphoma

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14
Q

is a reactive but excessive leukocytosis
characterized by the presence of immature cells in the peripheral blood

increase in the total of leukocyte count in which
mimics leukemia

A

leukamoid reaction

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15
Q

is a neoplastic clonal MPD that commonly manifests with panmyelosis in the bone marrow and increases in RBC, granulocytes, and platelets in the peripheral blood

A

polycythemia vera

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16
Q

presence of JAK 2 (janus kinase 2)
 JAK 2 is associated with bone
marrow disorder caused by the
production of too many blood
cells

A

polycythemia vera

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17
Q

treatment for polycythemia vera that prevents thrombosis

18
Q

given to a px with high risk for polycythemia

19
Q

classified as a MPD in which the proliferation of an abnormal type of BM stem cell results in fibrosis, or the replacement of the marrow with collagenous connective tissue fibers

A

Myelofibrosis

20
Q

treatment for myelofibrosis

A

Androgen theraphy
› Prednisone
› Danazol
› Splenomegaly – hydroxyurea

21
Q

Characterized by autonomous proliferation of the
megakaryocytic cell lines.
 Thrombocytosis is present without a reactive
cause.

A

thrombocythemia

22
Q

treatment for thrombocytopenia

A

Busulfan in older patients
› Low dose aspirin to prevent thrombosis
› - Hydroxyurea theraphy

23
Q

a MPD arising as a clonal process from a
pluripotential stem cell
 begins with a chronic clinical phase that
progresses to an accelerated phase in 3 to 4 years and often terminates as an acute leukemia

A

chronic myelogenous leukemia

24
Q

a characteristic feature present in proliferating
hematopoietic cells is the Philadelphia chromosome
 has overproduction of myeloid cellulite that
results in preponderance of immature cells in the
neutrophilic line

A

chronic myelogenous leukemia

25
Can mimic neutrophilic glucamoid reaction
chronic myelogenous leukemia
26
treatment for chronic myelogenous leukemia
Busulfan › Bone marrow stem cell transplantation
27
group of clonal disorder of neoplastic pluripotential stem cells characterized by a decrease in one or more types of peripheral blood cells due to abnormal maturation in the bone marrow
Myelodysplastic syndrome
28
represent a group of neoplastic conditions originating from cells of the lymphoreticular system
LYMPHOPROLIFERATIVE DISORDERS
29
composed of small B-lymphocytes with abundant cytoplasm and fine (hairy) cytoplasmic projections
HAIRY CELL LEUKEMIA
30
also known as Alibert-Bazin syndrome  the most common form of cutaneous T-cell lymphoma  is a lymphoreticular neoplasm primarily involving the skin
MYCOSIS FUNGOIDES
31
a malignant disorder characterized by painless, progressive enlargement of lymphoid tissue  Hallmark is a large binucleated or multinucleated cell with each nucleus bearing a very large nucleolus (Reed Sternberg Cell)
HODGKIN’S DISEASE
32
Owl’s eye appearance or popcorn cells
Reed-strenberg cell
33
Nodular lymphocyte-predominant Hodgkin lymphoma  is a B cell neoplasm composed of relatively rare neoplastic cells scattered within the nodules of reactive lymphocytes  no reed-sternberg cells
NONHODGKIN’S DISEASE
34
other names: Plasmatocytoma, Kohler’s Disease  is a neoplasmic proliferation of morphologically abnormal plasma cells primarily occurring in the BM either in nodules or diffusely.
MULTIPLE MYELOMA
35
is an uncommon condition which behaves as a slowly progressive lymphoma  is proliferation of cells which produce a monoclonal IgM paraprotein
WALDENSTROM’S MACROGLOBULINEMIA
36
Other name: Glandular Fever, Pfeiffer’s Disease, Kissing Disease (commonly called)
INFECTIOUS MONONUCLEOSIS
37
T cells reacting against B lymphocytes infected with Epstein-Barr (EB) virus
INFECTIOUS MONONUCLEOSIS
38
represent a group of diseases with abnormal proliferation of mesenchymal cells that are closely related to phagocytic histiocytes and to fat cells  due to inborn errors in metabolism genetically transmitted
HISTIOCYTOSES/ STORAGE DISEASE
39
is a collagen disease which affects women most commonly  characterized by skin rash, arthralgia, fever, renal, cardiac and vascular lesions, anemia, leukopenia, and thrombocytopenia
SYSTEMIC LUPUS ERYTHEMATOSUS
40
3 TYPES OF ANTIBODY of SLE
Anti-DNP Anti-DNA Anti-Nuclear
41
ACQUIRED IMMUNODEFICIENCY SYNDROME
a disorder secondary to an infection with the human immunodefficiency virus (HIV)
42
a RNA retrovirus that is cytotropic for CD4 positive T cells and macrophages
HIV