WBC, LN, SPLEEN, THYMUS Flashcards

1
Q

Dohle bodies- sky blu cytoplasmic puddles

A

Sepsis

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2
Q

Neoplasms in bone marrow. Tumor cells found in peripheral blood

A

Leukemia

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3
Q

Immature leukemia

A

Acute leukemia

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4
Q

Mature leukemia

A

Chronic leukemia

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5
Q

MC cancer of children

A

Acute lymphoblastic leukemia

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6
Q

T(12,21)

A

ALL

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7
Q

Leukemia that is most responsive to tx

A

ALL

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8
Q

Primary chemitherapeutic drug for ALL? Wwhat is its catastrphic SE

A

Asparaginase - pancreatitis

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9
Q

Leukemia with very low alk phos

A

CML

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10
Q
A

Chronic phase

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11
Q

10-19% myeloblast

A

Accelerated phase

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12
Q

> 20% myeloblast

A

Blast crisis

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13
Q

Solid focus of leukemia outside the bone

A

Chloroma

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14
Q

Distinctive needle like azurophilic granules

A

Auer rods

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15
Q

Primary chemotherapeutic drug for CML. SE?

A

Imatinib - flyid retention, CHF

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16
Q

Most common leukemia in the elderly

A

Chronic lymphocytic leukemia (CLL)

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17
Q

Increase in WBC count with left shift and high alk phos.

Usually caused by infection

A

Leukemoid reaction

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18
Q

Leukemia in 15-39 y. O

A

AML

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19
Q

Leukemia in 25-60 yo

A

CML

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20
Q

Reed sternberg cells

A

Hodgkins lymphoma

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21
Q

MC hodgkins lymphoma

A

Nodular sclerosis

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22
Q

Most common hepatopoietic malignancy

A

Non hodgkins lymphoma

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23
Q

Most common form of indolent NOn hodgskins lymphoma

A

Follicular lymphoma

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24
Q

T(14:18

A

Follicular lymphoma

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25
MC NHL
Diffuse large cell lymphoma
26
Starry sky pattern. Comon in africans
Burkitts lymphoma
27
T(11;14)
Mantle lymphoma - poor prognosis
28
Neoplasm of CD4 + Tcell
Adult t cell lymphoma
29
T(15;17)
APML
30
t(9;22)
CML
31
t(8:14)
Burkitt lymphoma
32
Diffuse erythema and scaling of the entire body surhace
Sezary syndrome
33
MC and most deadly plasma cell neoplasm
Multiple myeloma
34
Defeerentiate waldenstroms macroglobulinemia from multiple myeloma
No lytic lesion in waldenstrom
35
Differentiate monoclonal gammopathy of endetermined significance MGUS FROM MULTIPLE MYELOMA
MGUS IS ASYMPTOMATIC
36
Teardrop cells or dacryocytes
Primary myelofibrosis
37
Tx for primary myelofibrosis
Bone marrow transplant
38
Birbeck granules ( tennis racket like appearance)
Langerhans cell histiocytes
39
Small yellow brown, brown or rust coloured foci in speel
Gandy gamna nodules
40
Swirling pattern of spindle shaped cells associated with myasthenia gravis
Thymoma
41
Differentiate extravascular hemolysis from intravascular hemolysis
Extravascular causes splenomegaly
42
Hemolytic anemia
Normocytic, normochromic
43
MCC of IDA
GI bleeding
44
Tx for hereditary spherocytosis
Splenectomy
45
Small dark nuclear remnants present in RBCs of asplenic patiens
Howell-jolky bodies
46
Episodic hemolysis in G6PD deficuency
Drugs: antimalarials, sulfonamides, nitofurantoins Food: fava beans
47
G6PD is the rate limiting step in which biochemical pathway
Pentose phosphate pathway Reduce NADP-NAPDH
48
Why are infants with sickle cell disease asumptomatic until 2-4 months of age?
Due to high amounts of fetal hemoglobin (Hbf)
49
Best initial diagnostic test for sickle cell anemia
Peipheral blood smear
50
Gold standard fir sickle cell anemia
Hemoglobin electrophoresis
51
DOC for sickle cell anemia
Hydroxyurea (increase Hbf)
52
Most severe form of a- thalassemia
Hydrops fetalis
53
Anemia in thalassemia
Microcytic,hypochromic
54
Decrease synthesis of adlut hemoglobin
Thalassemia
55
Primary tx for hemochromatosis
Phlebotomy
56
Hemochromatosis that does not respond to phlebotomy
Deferoxamine
57
Leading cause of death in paroxysmal nocturnal hemoglobinuria
Thrombosis
58
Caused by trauma to RBC IN INDIVIDUALS WITH cardiac valve prosthesis
Microangiopathic hemolytic anemia
59
Vit B 12 or folate deficiency
Megaloblastic anemia
60
Which oarasit infection can lead to megaloblastoc anemia?
Dyphyllibothrium latum
61
Schilling test
Pernicious anemia
62
Most common nutritional disorder in the world
Iron defiency anemia
63
Which parasite infection can lead to microcytic hypochromic anemia
Hookworms ( necator, ancylostoma) Albendazole
64
Iron deficiency anemia
Microcytic hypochromic anemia
65
Esophageal webs, microcytic hypochromatic anemia, atrophic glossitis
Plummer- vinson syndrome
66
IDA in elderly may be due to
Colorectal ca
67
Chronic primary hematopoietic failure and pancytopenia
Aplastic anemia
68
Chemical exposure which causes aplastic anemia
Benzene
69
Antiobiotic which causes aplastic anemia
Chloamphenicol
70
Aplastic anemia
Normocytic, normochromic
71
Deifferentiate aplastic anemia from myelodysplastic syndrome
In MDS , BM is hypercellular. In aplastic anemia, BM is hypocellular
72
Most feared complication ITP
Intracranial bleeding
73
That that cause neutropenia
Aminopyrine, PTU, chloramphenicol
74
Decreased gp1b leads to defective platelet adhesion. Decreased platelet count
Bernard soulier syndrome
75
Decreased gp IIb-IIIa leads to defective platelet aggregation. Normal platelet count
Glanzmann's thrmbathenia
76
MC inherent bleeding disorder
Von willebrand disease
77
Tx for vwd
Desmopressin | Factor VIII and vWF
78
MC hereditary disease associated with life threatening bleeding due to factor VIII deficinecy
Hemophilia A
79
Tx for hemophilia A
Factor VIII precipitate
80
Christmas disease
Hemophilia B. Factor IX concentrate
81
Sever meningococcemia
Waterhouse- friderichsen syndrome
82
Postpartum pituitary necrosis
Sheehan syndrone
83
Most specific test for DIC?
D-dimer
84
Dx test for pulmonary embolism
D- dimer
85
Dx test for herpes
Tzank smear
86
Cause of herpes labialis
HSV-1
87
95% of cancers if the head and neck
Squamous cell carcinoma