Pathology Trigger Words Flashcards

1
Q

[Neoplasm] Cells seen in patients with lymphoblastoma or metastatic carcinoma

A

Tart Cell

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2
Q

[Rheuma] Autoantibody which confer early disease onset of Sjogren Syndrome

A

Anti-Ro

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3
Q

[Rheuma] Autoantibody which confers diffuse scleroderma

A

Anti-Scl 70 (Anti-DNA topoisomerase I)

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4
Q

[Rheuma] Autoantibody which confers limited scleroderma

A

Anti-centromere

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5
Q

[Genetics] ___ is the 2nd most common cause of mental retardation

A

Fragile X Syndrome

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6
Q

[Genetics] Fragile X Syndrome confers what repeating expansion in what gene?

A

CGG, FMR1 Gene

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7
Q

[Genetics] Huntington disease confers what expansion in what gene?

A

CAG, HTT Gene

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8
Q

[Genetics] What enzyme is deficient in Chronic Granulomatous Disease?

A

NADPH oxidase

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9
Q

[Genetics] Syndrome which typically presents as albinism and bleeding diasthesis secondary to impaired phagolysosome function.

A

Chediak-Higashi Syndrome

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10
Q

[Genetics] Syndrome typically presenting with cardiac anomalies, abnormal facies, thyroid disorder and a deletion in chromosome 22.

A

DiGeorge Syndrome

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11
Q

[Genetics] Triad of 1) thrombocytopenia, 2) repeated infections, and 3) eczema

A

Wiskott-Aldrich Syndrome

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12
Q

[IDS] HIV virulent factor which allows the virus to integrate into the host cell.

A

gp41 (fusion protein)

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13
Q

[IDS] HIV virulent factor which allows the virus to attache to CXCR4 (lymphocytic) and CCR5 (macrophagocytic)

A

gp120

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14
Q

[IDS] CD4 threshold for each of the following infections in AIDS patients:

1) Toxoplasma
2) CMV chorioretinitis
3) Pneumocystis jirovecii
4) TB
5) Cryptosporidium
6) MAC

A

1) <100/uL
2) <50/uL
3) <200/uL
4) <500/uL
5) <200/uL
6) <50/uL

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15
Q

[Neoplasm] Hallmark of malignancy

A

Anaplasia

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16
Q

[Cell Mechanisms] Hallmark of tissue repaie

A

Granulation (not granuloma!)

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17
Q

[Neoplasm] Most commonly mutated protooncogene

A

RAS

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18
Q

[Neoplasm] Governor of the cell cycle, a tumor suppressor gene

A

Rb

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19
Q

[Neoplasm] Guardian of the genome, a tumor suppressor gene

A

p53

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20
Q

[Neoplasm] HPV is an oncogenic virus which causes inactivation of p53 by this protein

A

E6

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21
Q

[Neoplasm] Tumor suppressor gene mutated in breast and endometrial cancers

A

PTEN

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22
Q

[Neoplasm] Tumor suppressor gene mutated in FAP and colon cancer

A

APC

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23
Q

[Neoplasm] One of the most studied etiologic agent/ risk factor for Bladder SCCA

A

Schistosoma haematobium infection

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24
Q

[Neoplasm] Carcinogen associated with liver angiosarcomas

A

Vinyl chloride

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25
[Neoplasm] Carcinogen associated with AML
Benzene
26
[Neoplasm] Electrolyte imbalances in Tumor Lysis Syndrome
HyperK+, HyperPhos, HyperUricemia, Hypocalcemia
27
[IDS] Characteristic cells in lymph nodes, lung, and sputum of measles patients
Warthin Finkelday cells
28
[IDS] Pink to purple intranuclear inclusion bodies in HSV infection
Cowdry bodies (Type A)
29
[IDS] Test to differentiate infectious mononucleosis etiology
Monospot test/ heterophile test (+: EBV; -: CMV)
30
[IDS] Characteristic appearance of basophilic inclusion bodies of CMV infection
Owl's eye
31
[Neoplasm] Characteristic cells seen in malignancies with microcalcifications causing necrosis
Psamomma bodies
32
[Neoplasm] In which type of thyroid malignancy can orphan annie nuclei be seen?
Follicular thyroid Ca
33
[IDS] Characteristic cells seen in klebsiella granulomatis infection which show gram neg coccobacilli in macrophages
Donovan bodies
34
[IDS] In PRIMARY TB, this refers to consolidation at the subpleural space.
Ghon focus
35
[IDS] In PRIMARY TB, this refers to a consolidation with pulmonary hilar node involvement
Ranke complex
36
[IDS] In SECONDARY TB, this refers to consolidation usually at the apical area
Simmon focus
37
[IDS] Central coagulation necrosis surrounded by palisading macrophages and fibroblasts, plasma cell- rich infiltrate, few treponemes seen in tertiary syphillis infection
Gumma
38
[IDS] Triad of interstitial keratitis, hutchinson teeth (screwdriver or peg-shaped), and eight nerve deafness
Late Congenital Syphillis
39
[IDS] Psoriasiform hyperplasia or test tubes in a rack appearance is seen in this STD
Condyloma lata
40
[IDS] Phenomenon wherein too many antibodies prevent antibody-antigen complex formation leading to a false negative result in assays
Prozone phenomenon
41
[IDS] Structures of perivacular ring hemorrhages around vessels plugged with infected RBCs in cerebral malaria
Durck granulomas
42
[IDS] Protozoan which has a maltese cross pattern morphology
Babesia
43
[IDS] Classic appearance of loss of striations in trichinosis of striated muscle cells with rich blood supply
Nurse cells
44
[IDS] Meyers -Kouwenaar bodies are dead worms surrounded by hyaline, esosinophilic precipitates embedded in small epitheloid granulomas seen in ___.
Filariasis (Lung)
45
[IDS] Accentuation of sclerosing keratitis seen in onchocerca infection as a result of anti-filarial treatment.
Mazzotti reaction
46
[Cardio] Post-MI Pericarditis
Dressler Syndrome
47
[Cardio] Diastolic murmurs
1) Aortic Regurgitation 2) Pulmonic Regurgitation 3) Mitral stenosis 4) Tricuspid stenosis
48
[Cardio] Most common valvular defect secondary to rheumatic heart disease
Mitral stenosis
49
[Cardio] Most common KNOWN cause of MVP causing mitral insufficiency
Marfan Syndrome (fibrillin 1 defect)
50
[Cardio] Low-pitched diastolic rumbling murmur best heard at the apex concomitant with aortic regurgitation
Austin-Flint murmur
51
[Cardio] "Caterpillar cells" which are plump macrophages with condensed chromatin pattern in a slender wavy ribbon seen in RF
Anitschkow cells
52
[Cardio] Nodules found in the hearts of individuals with rheumatic fever
Aschoff bodies
53
[Cardio] Subendocardial thickenings secondary to regurgitant jets seen in patients with RHD
MacCallum plaques
54
[Cardio] Type of endocarditis associated with malignancy and endocardial trauma
Marantic endocarditis
55
[Cardio] Type of endocarditis associated with SLE
Libman - Sacks endocarditis
56
[Cardio] Concept which states that pressure decreases and velocity increases as fluid passes through a narrow opening
Venturi effect
57
[Cardio] Most common helminthic etiology for myocarditis
Trichenella spiralis
58
[Cardio] Most common parasitic etiology for myocarditis
T. cruzi (Chagas disease)
59
[Cardio] Most common primary cardiac tumor in children
Rhabdomyoma
60
[Cardio] Most common primary cardiac tumor in adults
Myxoma
61
[Cardio] Defect associated with paradoxical emboli
ASD
62
[Hema] Subtype of AML with the best prognosis
Acute Promyelocytic Leukemia FABM3, t (15,17)
63
[Hema] Cells seen in the PBS of CLL patients, the most common leukemia of adults of the Western World
Smudge cells
64
[Hema] Malignant transformation of CLL to Diffuse Large B Cell Lymphoma
Richter Syndrome
65
[Hema] Cells which appear as large multiple nuclei or single with multiple lobes; each with a nucleolus seen in Hodgkin Lymphoma
Reed- Sternberg cells
66
[Hema] HL subtype with RS predominance and a (+) CD20 immunohistochemistry
Lymphocyte predominant Hodgkin Lymphoma
67
[Hema] Most common HL subtype
Nodular sclerosing
68
[Hema] Proteinuria of multiple myeloma characterized by Ig light chains
Bence- Jones proteinuria
69
[Hema] Infiltration of epidermis and upper dermis T-cells with cerebriform nuclei and generalized exfoliative erythroderma seen in mycosis fungoides
Sezary Syndrome
70
[Hema] Gene mutation in CML
BCR-ABL
71
[Hema] Gene mutation in PV
JAK2
72
[Hema] Characteristic lytic bone lesions is seen in what hematologic disorder
Multiple Myeloma
73
[Hema] Polycythemia Vera may proceed to this hematologic disorder once in the spent phase
Primary Myelofibrosis
74
[Hema] Pathognomonic cells seen in Langerhans histiocytosis
Birbeck granules
75
[Hema] Dacrocytes or tear-shaped RBCs are seen in this hematologic disorder
Primary Myelofibrosis
76
[Hema] Gold standard diagnostic test for Hereditary Spherocytosis
Osmotic Fragility Test
77
[Hema] Inclusions within red blood cells composed of denatured hemoglobin seen in asplenic G6PD deficiency
Heinz bodies
78
[Hema] Common morphologic feature of RBCS in G6PD patients with a functional spleen
Degmacytes or Bite cells
79
[Hema] What mutation causes sickling of RBCs
Glutamate -> Valine
80
[Hema] Nuclear remnants seen in asplenic patients with Sickle cell anemia
Howell-Jolly bodies
81
[Hema] Extramedullary hematopoiesis to compensate for B Thalassemia are seen as this on radiographs
Crew-cut appearance
82
[Hema] Most common inherited bleeding disorder
von Willebrand disease
83
[Hema] Toxin responsible for symptoms of HUS
Shiga-like toxin
84
[Hema] Bilateral adrenal hemorrhage secondary to fibrin thrombi
Waterhouse-Friedrichsen Syndrome
85
[Hema] Syndrome wherein a hemangioma is accompanied by bleeding diasthesis
Kasabach-Merritt Syndrome
86
[Respi] Whorls of shed epithelium seen in Asthma
Curschmasnn spirals
87
[Respi] Eosinophilic crystals seen in the airway of asthmatic patients
Charcot- Leyden crystals
88
[Respi] The late stage of this airway disorder is characterized by Honeycomb fibrosis
Idiopathic Pulmonary Fibrosis
89
[Respi] Concretions of calcium and proteins seen in Sarcoidosis
Schaumann bodies
90
[Respi] Stellate inclusions in giant cells seen in sarcoidosis
Asteroid bodies
91
[Respi] The cough center
Nucleus tractus solitarius
92
[Respi] A histomorphologic phenomenon of incrustation of blood vessel wall with basophilic nuclear material seen in small cell carcinoma
Azzopardi effect
93
[Respi] Immunostains for squamous cell carcinoma
p63, p40
94
[GI] Hypoproteinemia secondary to protein-losing enteropathy
Menetrier disease
95
[GI] Mutations in HNPCC or Lynch Syndrome
MSH2, MLH1
96
[GI] Procedure performed to treat extrahepatic biliary atresia
Kasai procedure
97
[GI] Most common benign tumor of the GI tract
Cavernous Hemangioma
98
[GI] Thrombosis at the portal circulation causing a sharply demarcated area of red-blue discoloration, hepatocyte atrophy, and congestion
Infarct of Zahn
99
[GI] Syndrome of >= 2 thrombotic obstruction at the hepatic artery, ascites, hepatomegaly, and hypercoagulable state
Budd-Chiari Syndrome
100
[GI] Perihilar cholangiocarcinoma
Klatskin tumor