Path Heme/Onc/Pain/Suffering Flashcards

1
Q

Dacrocytes morph and seen in

A

daCRYcyte

Teardrop cells

Seen in bone marrow shit (myelofibrosis) bc squeezed

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2
Q

Schittocyctes seen in and morph

A

Helmet cells (shizo guy and his helmet)

Seen in hemolytic anemias

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3
Q

Degmacytes morph and seen in

A

dejame una mordida

G6Pd defficiency

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4
Q

Acanthocytes seen in and morph

A

Spur cells

Liver disease

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5
Q

Spherocytes morph and seen in

A

donut

heriditary spherocytosis

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6
Q

Target cells seen in

A

HALT

HbC dx
Asplenia
Liver dx
Thalassemia

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7
Q

howell jolly bodies: what are they?
where they seen

A

Nuclear remnant not removed by spleen

seen in splenic dx

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8
Q

Heinz bodies what is and seen in

A

Precipitated hemoglobin on side of RBC

Removed by taking a bite

PUT HEINZ b4 BITE

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9
Q

Microcytic anemia cutoff

A

MCV less than 80

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10
Q

Microcytic anemia caused by

A

Hemoglobin issues

Deffective in thalassemia

Deficiencies

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11
Q

Megaloblastic anemia caused by

A

Defective DNA

Either folate/b12 deficiency or fanconi anemia

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12
Q

Macrocytic non megaloblastic seen in

A

Liver dx and alcholism

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13
Q

Reticulocyte count tells you

A

How well body is replacing the RBCs

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14
Q

Iron defficiency labs

A

Down: Iron, ferritin

Up: TIBC

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15
Q

Anemia of chronic dx labs

A

Down: iron, TIBC

Up: ferittin, hepcidin

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16
Q

Transferrin interchangable w

A

TIBC

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17
Q

α-Thalassemia presentation

A

Microcitic anemia

severity depends on how many genes affected

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18
Q

Cis/trans in α-Thalassemia by race

A

Cis: asians
Trans: africans

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19
Q

β-Thalassemia increases risk of _____ (pathogen). leads to:

A

Parvovirus

leads to aplastic anemia

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20
Q

β-Thalassemia population

A

mediterrenans

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21
Q

β-Thalassemia presentation

A

Severe microcytic anemia

Crew cut xray due to marrow expansion

Skeletal deformity (chipmunk face)

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22
Q

Lead inhibits

A

Ferrochelatase and ALA dehydratase

causes anemia and neuro shit

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23
Q

Sideroblasic anemia caused by

A

Genetic: x-linked ALA

Myeloplastic anemia

Alcohol

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24
Q

Sideroblastic anemia treatment

A

Pyridoxine

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25
Sideroblastic anemia labs
Increased: iron, ferritin Decreased: TIBC
26
Megaloblastic anemia features
Multilobed neutrophils RBC enlargment
27
Folate vs B12 defficiency (labs and presentation)
Folate: ** Normal** methylmalonic acid, **no** neuro shit B12: **increased** methylmalonic acid, **neuro** problems (meth fucks your brain)
28
Megaloblastic anemia common presentation
GLOSSITIS large RBCs clog and sweel tongue
29
Fanconi anemia caused by
DNA repair defect, bone marrow failure
30
Aplastic anemia sx
Fatigue, malaise, pallor, **mucosal bleeding and petechiae**
31
G6PD cause and genes
Xlinked RBCs get oxidative stress Causes hemolysis **FAVA BEANS**
32
Aplastic anemia marrow biopsy
hypocellular bone marrow w/ fatty infiltration
33
hemolytic anemia in newborn usually due to
Pyruvate kinase deffiency
34
Paroxysmal nocturnal hemoglobinuria presentation
negative coombs pancytopenia venous thrombi caused by complement activation
35
Pyruvate kinase deffiency RBC morph
Burr cells BURR PKD
36
Nocturnal hemoglobinuria mutation in
PIGA fucks up GPI anchor which destabilizes membrane
37
Sickle cell genetics
Point mutation in B-globin gene. HbS instead of HbA Glutamic to valine
38
Sickle cell crisis due to
Oxidative stress, acidosis , low O2 deoxy hemoglobin S polymerizes
39
Sickle cell anemia aplastic crisis due to
Parvovirus
40
Sickle cell increased risk of (infection)
Salmonella osteomyelitis
41
Warm vs Cold autoimmune anemia (and similarities)
Warm: IgG (seen in lupus, CLL) Cold: IgM (seen in mycoplasma, EBV, CLL) Both: +Coombs, normocytic anemia
42
**Micro**angiopathic hemolytic anemia presentation and seen in
Seen in things that cause little clots mechanical RBC destruction
43
**Macro**angiopathic hemolytic anemia due to
Heart valves (stenotic or prosthetic) causing RBC destruction
44
Lead poisoning what accumulates
ALA and protoporphyrin
45
Intermittent porphyria due to
Porphobilogen acummulation
46
Porphyria cutanea sx
Blistering cutaneous photosensitivity Hyperpigment
47
Thrombitic thrombocytopenic purpura pathophys
Inhibittion of ADAMST13 leads to decreased vWF accumulation Platelets aggregate and make microthrombi
48
TTP vs HUS
TTP has feever HUS has bloody diarrhea
49
TTP and HUS presentation
Thrombocytopenia Hemolytic anemia (**micro**angiopathic) AKI
50
vWF is defect in ____pathway. (pt/ptt)
Intrinsic PTT
51
DIC labs
Increased bleeding, PT, PTT. Schistocytes, Increased D-dimer
52
Antithrombin defficiency labs
PT and PTT normal
53
Young woman w/ recurrent pregnancy loss think
Factor V leiden
54
Factor V leiden pathophys
Mutant factor V resistance to degradation by protein C
55
Protein C vs S
C: cancel S: stop
56
Lymphomas initial presentation
Constitutional sx (low fever, night sweats, weight loss)
57
Reed-steinberg cells seen in (and morph)
Seen in Hogdkin Owl eyes hoot hoot
58
reed steinberg cell origin
CD 15 and CD 30
59
Fibrous bands seen in
Hodgkin lymphoma
60
Burkit lymphoma presentation and gene defect
Young african w/ jaw tumor 8,14 translocation EBV
61
Diffuse large b cell lymphoma mutation
BCL2 BCL2 limits apoptosis normally
62
Mantle cell lymphoma seen in
MAN
63
Painless follicles in adults think
Follicular lymphoma
64
Mantle cell lymphoma progression
Very agressive disease AGGRESSIVE MAN
65
Marginal Cell lymphoma genes and seen in
gastritis MALT gene is 11,18’ **MUCOSAL**
66
Adult T-cell lymphoma seen in
Japs, caribbean, africa. **HTLV1 virus**
67
Multiple myeloma feautures
CRAB hyper**C**alcemia **R**enal shit **A**nemia **B**ack pain from **B**one lytic lesions
68
Multiple myeloma findings (microscope)
Rouleaux formation (high *rouller* stacks chips)
69
Waldenstrom macroglobulinemia causes _____
Hyperviscosity of blood
70
Myelodisplastic syndromes patho and risk
Ineffective hematopoesis Can become AML
71
ALL associations
Mostly kids (real bad in adults tho) Down syndrome
72
ALL better prognosis if (gene defect)
(12,21) mejor en niños
73
ALL main finding
Highly increased lympho**blasts**
74
Chronic Lymphocitic leukemia findings (3)
**Smudge cells** Slow progress in elderly Autoimmune hemolytic anemia
75
Hairy cell leukemia seen in (population)
Adult males
76
Hairy cell leukemia findings (4)
Filamentous projection on cells (look fuzzy) Marrow fibrosis (dry tap) **Splenomegaly** **Pancytopenia**
77
Hairy cell leukemia mutation
BRAF
78
Acute myelogenous leukemia findings
Auer rods Myeloperoxidase + Increased myeloblasts on smear
79
Leukemia after radiation/chemo think
Acute myelogenous leukemia
80
Acute myelogenous leukemia in down syndrome mutation (also AKA)
15,17 Acute Promyelocytic Leukemia
81
Acute promyelocytic leukemia responds to
Retonic acid aka vitamin A
82
DIC in down syndrome think
Acute promyelocytic leukemia
83
Chronic Myelogenous leukemia genetics
9,22 philadelphia chromosome BCR-ABL
84
Chronic myelogenous leukemia findings ()
Low leukocyte alk phos (LAP) Splenomegally
85
Polycethemia vera mutation
JAK2
86
Polycythemia vera presentation
Severe pain red-blue coloration Shower itch
87
Polycethemia vera lab finding
EPO low
88
Essencital thrombocytopenia findings
increased Large, malformed platelets
89
Myelofibrosis due to
Increased fibroblast activity
90
Myelofibrosis findings
Decreased RBCs, **teardrop RBCs**
91
Whjat is seen in leukomoid reaction
dohle bodies
92
Lagerhans histiocytosis presentation
Lytic bone lesion in a child Otitis media
93
Lagerhans histiocytosis findings
Birbeck granules (tennis rackets)
94
Hemophilia is defect of ____(pathway)
Intrinsic
95
Hemophilia A deffiency of ___ and inheritance
VIII A=8
96
Hemophilia B deffiency of ___ and gene
IX X-linked
97
Hemophilia C deficiency. of ___ and gene
XI Autosomal recessive
98
Hemophilia lab finding
PTT increased PT no chage
99
Vitamin K deficiency labs
Both Pt and PTT increased with **normal bleeding time**
100
Platelet disorder labs
Increased bleeding time, PT/PTT normal
101
Bernard soulier syndrome labs
Increased bleeding time Large platelets RISTOCETIN Chef soulier makes risoto
102
Glansmann Thrombasthenia defect
GpIIb/IIIa, decreased platelet to platelet agregation
103
Bernard soulier defect
GpIB
104
immune thrombocytopenia labs
Increased megakaryocytes Decreased platelets
105
Immune thrombocytopenia antibodies to
GpIIb/IIIa
106
Things that cause immue thrombocytopenia
Autoimmune, viruses, malignancy, drug reactions
107
vWF disease findings
Decreased platelet aggregation **with increased PTT**
108
Giant cell arteritis population
Elderly female
109
Giant cell arteritis presentation
Unilateral headache, jaw claudication Affects carotid branches
110
Takayasu arteritis due to
Granomalutous thickening and narrowing of aortic arch