Hematopoietic/Lymphoid Flashcards

0
Q

Most common cause of hereditary thrombophilia

A

Factor V leiden (resistance to protein C)

2nd most common cause: Prothrombin 20210A transition

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1
Q

Neutropenia + albinism + cranial and peripheral neuropathy + repeated infections

A

Chèdiak-Higashi Syndrome

Autosomal recessive

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2
Q

Iron deficiency + partially obstructing esophageal web is seen in which condition?

A

Plummer vinson syndrome

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3
Q

SE of Dilantin (Phenytoin)?

A

Folate deficiency

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4
Q

Most common cause of aplastic anemia?

A

Toxin

Others: Benzene, chloramphenicol, alkylating agents, parvovirus, Hep C

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5
Q

G6PD deficiency affects which pathway?

A

Failure of erythrohexose-monophosphate shunt

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6
Q

Defect in sickle cell

A

GAG (glu) > GTG (val)

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7
Q

Most common immune hemolytic anemia?

A

Warm body auto-immune hemolytic anemia

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8
Q

Cold agglutin disease is associated with which blood group antigen?

A

I blood group antigen

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9
Q

Hereditary spherocytosis is a defect in which structure?

A

Spectrin

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10
Q

Bite cells are also associated with which condition?

A

G6PD deficiency

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11
Q

Type of hemoglobin with increased resistance to M. falciparum

A

Hemoglobin S

G6PD deficiency and (-) duffy blood group

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12
Q

Osteomyelitis in patients with sickle cell is due to which organism?

A

Salmonella

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13
Q

Heinz bodies are also seen in which condition?

A

G6PD deficiency

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14
Q

Most common malignancy of children

A

ALL

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15
Q

Type of ALL most responsive to therapy

A

ALL Positive CD10

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16
Q

Autosplenectomy is also seen in which condition?

A

Sickle cell

17
Q

Auer rods is seen in which condtion?

18
Q

Smudge cells is associated with?

19
Q

Helmet cells are associated with which condition?

A

Thrombotic thrombocytopenic pupura

Traumatic injury; microangiopathic hemolytic anemia

20
Q

Heterophil-negative infectious mono is also known as?

21
Q

Teardrop-shaped erythrocytes is also seen in which condition?

A

Chronic idiopathic myelofibrosis

22
Q

Heterophil-positive infectious mono is also seen in which condition?

A

EBV

Presents with atypical lymphocytes

23
Q

Waldenstrom macroglobulinemia presents with?

A

M protein, Bence Jones proteins, Plasmacytoid lymphocytes

Important: abscence of bone lesion

24
Lytic bone lesions/punched-out lesions is seen in?
Multiple myeloma
25
Binucleated or multinucleated giant cells with eosinophilic inclusion-like nucleoli is also known as?
Reed-Sternberg cells
26
Reed-Sternberg cells is seen in which condition?
Hodgkin's lymphoma
27
Most frequently occuring form of Hodgkin lymphoma
Nodular sclerosis Hodgkin lymphoma
28
Most common form of non-Hodgkin lymphoma
Follicular lymphoma B-cell lymphoma; t(14;18)
29
Lymphoma that arises from sites of chronic inflammation/autoimmune disease is also known as?
MALToma
30
Starry sky appearance is seen in which lymphoma?
Burkitt Lymphoma Cell debris taken up by non-neoplastic macrophages
31
Pautrier microabscesses are seen in which type of infection?
Mycosis fungoides Small pockets of tumor cells w/in epidermis
32
M proteins are seen in?
Multiple myeloma Kappa or lambda light chain
33
Leukemic form of cutaneous T-cell lymphoma is known as?
Sezary syndrome
34
Hereditary hemorrhagic telangiectasia is also known as?
Osler-Weber-Rendu syndrome Localized malformations of venules and capillaries
35
Cytogenic change in Burkitt lymphoma?
t(8;14); Increased expression of c-myc
36
Bence Jones proteins are seen in which condition?
Multiple myeloma
37
Hereditary deficiency of platelet-surface IIb/IIIa
Glanzmann thrombasthenia
38
Hereditary lack of GP Ib/IX/V
Bernard-Soulier syndrome
39
Dutcher bodies are associated with which condition?
Waldenstrom's macroglobulinemia PAS (+) with IgM deposits around the nucleus