Feedback Flashcards

1
Q

The laboratory of perpetual help is:

A

Tertiary laboratory

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Capability of primary lab except:

A

Routine Chemistry

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Microbiology culture and sensitivity for aerobe and anaerobe:

A

Hospital-based Tertiary Laboratory

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Which of the following is not a characteristic of a leader:

A

Does things right

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Consists of the detailed day to day operations needed to meet the immediate needs of the laboratory:

A

Tactical Planning

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Most error in lab occurs in:

A. Pre-analytic
B. Analytic
C. Post-analytic

A

A. Pre-analytic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

This includes specimen processing:

A

Analytic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Competition from other local laboratories are example of:

A

Threats

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Use of modern technology and equipment:

A

Strength

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

The laboratory of AFP medical center is an example of:

A

Government-owned tertiary lab

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

All scope of clinical lab except:

A

None of the above

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Service capability of primary lab:

A

Qualitative platelet count

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q
  1. Which of the following is true:

A. Micrbiology aerobic and anearobic C&S hospital based only
B. Micrbiology aerobic and anearobic C&S hospital based and nonhospital based
C. Both
D. Neither

A

A. Micrbiology aerobic and anearobic C&S hospital based only
B. Micrbiology aerobic and anearobic C&S hospital based and nonhospital based
C. Both

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Which is not a purpose of the laboratory:

A

Dictate patient management

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Secondary lab KOH is done in hospital base only:

A

False

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

After the results, electronic copy signature is acceptable in accordance in E commerce law:

True or False

A

True

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Pre analytic error during post collection except:

A

Inadequate patient preparation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Refers to all complex steps that must take place before a specimen can be analyzed:

A. Pre-analytic
B. Analytic
C. Post-analytic

A

Pre-analytic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Must take into consideration multiple factors and variables that may affect the succeeding steps:

A. Pre-analytic
B. Analytic
C. Post-analytic

A

Pre-analytic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

Screening process…:

A. Pre-analytic
B. Analytic
C. Post-analytic

A

Analytic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Manual or automated:

A. Pre-analytic
B. Analytic
C. Post-analytic

A

Analytical

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

Final phase of the laboratory process:

A. Pre-analytic
B. Analytic
C. Post-analytic

A

Post-analytical

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

Keeping of records:

A. Pre-analytic
B. Analytic
C. Post-analytic

A

Post-analytic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

30 y/o patient with headache, fatigue, pallor, tachycardia… decreased haemoglobin, hematocrit, iron:

A

Microcytic, hypochromic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
25. Haptoglobin in hemolytic anemia: Increase Decrease No Change
DECREASE
26
INDIRECT BILIRUBIN in hemolytic anemia: Increase Decrease No Change
INCREASE
27
Reticulocyte count in hemolytic anemia: Increase Decrease No Change
INCREASE
28
RDW in hemolytic anemia: Increase Decrease No Change
INCREASE
29
Erythroid precursors from bone marrow in hemolytic anmeia: Increase Decrease No Change
INCREASE
30
A patient present with DIC was recently diagnosed and tested positive for micro coagulation testing. What does the D-dimer measure?
Cleaved crosslink
31
A 45 y.o. man was diagnosed with primary hypoaldosteronism. Which of the lab result is most consistent with the diagnosis? ``` Increase or Decrease of Na K sereum HCO3 Urine Na Urine K ```
decrease Na increase K decrease serum HCO3 increase urine Na decrease urine K
32
Man undergoes elective sigmoid resection. ``` ph ↓ pCO2 ↓ Bicarbonate ↓ Potassium ↑ BUN ↑ Creatinine ↑ ``` Diagnosis? ``` A. Excessive sodium intake B. Fluid deficit C. Acute renal failure D. Surgical resection of both ureters E. Fistula between ureter and colon ```
C. Acute renal failure
33
``` 70 y.o. man undergoes electrolyte sigmoid resection for diverticulitis. On the 2nd post-operative day his average urine output is only around 35-45mL/hr. IVF rate increase to 100mL/hr days after his urinary output is 50-55mL/hr. Lab study reveals the following: ph 7.25 pCO2 30 HCO3 50 K 5.0 BUN 85mg/dL Creatinine 4.1 Which of the following is most likely diagnosis? ``` ``` A. Excessive sodium intake B. Fluid deficit C. Acute renal failure D. Surgical resection of both ureters E. Fistula between ureter and colon ```
C. Acute renal failure
34
``` 34. A 60 yr old man is admitted to the hospital with a 2 week history of progressive lethargy and obtundation. Lab results are: Na 105 K 4.0 Plasma osmolality 22 Urine osmolality 604 Urine sodium 78 ``` What is the most likely diagnosis?
SIADH
35
Low sodium in plasma and urine; high urine osmolality:
SIADH
36
Substance that is absorbed but not secreted is administered to the patient until steady state plasma level of 0.1 mg/dL. Second urine specimen is 60 ml and the administered substance is 10 ml. What is the GFR?
100 ml
37
Chart is given, which is primary hyperthyroidism:
Low TSH | High T4
38
38. Respiratory Failure secondary to poliomyelitis and the respirator was set on high:
Normal slightly increase (pO), Markedly decrease (pCO), Decrease (ph)
39
``` A 60-year-old diabetic man notes bone pain, especially in his hands, for the past 6 months. Laboratory shows the following results: Sodium: Normal Potassium: Normal CO2: Normal Glucose: Elevated Creatinine: Elevated Calcium: Elevated Phosphorus: Elevated Total Protein: Normal Albumin: Normal ``` Which of the following conditions is this patient most likely to have?
Parathyroid hyperplasia
40
40. Select the letter that best depicts primary hypothyroidism:
High TSH, Low T4
41
riggers for histamine release are the following except: A. IgE mediated mast cell B. Physical injury C. Anaphylotoxins D. Cell adhesion molecules
D. Cell adhesion molecules
42
The following are important component in acute inflammation, except: A. Vasodilation B. Emigration of leukocytes C. Release of chemical mediators D. NOTA
D. NOTA
43
Activated by antigen-antibody complex:
Classical Pathway
44
Central convergence point for all pathways: C3 C4 C5 C6
C3
45
To facilitate communication between cells, to assist in up-regulation or down-regulation of the immune response:
Cytokines
46
This complement activation pathway appears to be important in early defense against pathogenic microorganims: A. Classical Pathway B. Alternative Pathway C. MBL Pathway D. NOTA
B. Alternative Pathway
47
True of complement system, except: A. Promote inflammation and host defense B. Microorganism identification C. Unregulated tissue damage is a possible complication D. Not necessary to measures the serum complement level to track disease activity
D. Not necessary to measures the serum complement level to track disease activity
48
In Classical pathway, antigen-antibody complex sequentially binds and activate the following component except: C3 C4 C5 C6
C3
49
Complement decreased in SLE and low levels in active disease: C3 C4 Both
Both C3 and C4
50
``` Functions of complement system, except: A. To promote host defense B. To promote clearance of apoptotic debris C. To regulate immune response D. NOTA ```
D. NOTA
51
Complex glycoprotein that bind living tissues together, mediate cell migration during embryogenesis, wound healing and inflammatory response:
Adhesion molecules
52
Cell mediators that involves calcium:
Cadherins
53
Cancer serum tumor markers CA-19-9 and CA125 are epitopes that represent this type of CAM:
Mucin
54
The simplest functional assay in the classical pathway ch50 measures total hemolytic complement activity. True or False
TRUE
55
The protein C5 is the central convergence point of the three activated complement pathways: True or False
FALSE
56
16. A patient with gram negative septicemia and pyogenic infection often have deficient C3 or components of alternative pathway.
TRUE
57
Complement plays a key role in the glomerular damage in many cases of glomerulonephritis.
TRUE
58
The kinin generating system is another inflammatory response pathway present in plasma that controls the generation of peptides important in the inflammatory response.
TRUE
59
``` Spontaneous bleeding in skin and mucosa such as petechia, echymosis is usually secondary to: A. Thrombocytopenia B. Platelet defect C. Liver disease D. Both A and B ```
D. Both A and B
60
The final common pathway of coagulation involves:
Formation of Thrombin
61
A defect in the aggregation of platelets is/are secondary to: A. vWF deficiency B. GP1b deficiency C. GPIIb/IIIa deficiency D. A and B are correct
C. GPIIb/IIIa deficiency-glanzman
62
A defect in platelet adhesion maybe secondary to: A. vWF deficiency B. GP1b deficiency C. GPIIb/IIIa deficiency D. A and B are correct
D. A and B are correct
63
The screening test for the diagnosis for coagulation problem are: Bleeding time PT PTT AOTA
All of the above (Bleeding time, PT, PTT)
64
Undetectable K: A. Factor II B. Factor V C. Factor IX D. AOTA
1972-vit k factors B. Factor V
65
The most common inherited bleeding disorder in humans:
Von Willebrand
66
A deficiency or inhibition of one or more factors VII, X, V, II is suggested by: A. prolonged ThrombinTime B. prolonged PT C. prolonged aPTT D. decrease fibrinogen
B. prolonged PT -extrinsic
67
Deficiency or defect in factors II, V, VIII, IX, X, XI, XII and fibrinogen? A. prolonged ThrombinTime B. prolonged PT C. prolonged aPTT D. decrease fibrinogen
Prolongation of aPTT -intrinsic
68
``` The following clotting factors are produced by the liver except: A. Fibrinogen B. Prothombin C. vWF D. Christmas factor ```
C. vWF
69
Vacutainer for coagulation assay: color
Blue top tube
70
The vacutainer tube for CBC is: | color
Purple top tube
71
The following are Vitamin K dependent except: ``` Factor II Factor V Factor VII Factor IX Factor X ```
Factor V
72
Deficiency or mutation in coagulation proteins or factor that leads to thrombophilia, except:
Factor VII
73
Which of the following are true about DIC? A. DIC is a severe form of consumptive coagulopathy B. Systemic activation of hemostasis leads to widespread intravascular fibrin deposition with associated depletion of prohemostatic and anticoagulant factors C. With parallel secondary fibrinolysis, potentially leading to a wide range of adverse outcomes, including thrombotic occlusion of small/ mid-sized vessels, organ dysfunction/failure, and/or bleeding. D. AOTA
D. AOTA
74
Triggers disseminated intravascular coagulation (DIC): A. Septicemia B. Cancer C. Systemic inflammatory response syndrome D. All of the above
D. All of the above
75
True of severe Hemophilia A and B:
All of the above
76
The following statements about Aspirin is FALSE:
Aspirin acetylated inhibition bind to cyclooxygenase 2-tama to so hindi ito yun sagot
77
``` Which of the following does not contribute to clot formation? A. Calcium B. Phospholipid C. Heparin D. Thrombin ```
C. Heparin-anticougulant
78
Major antagonist of Vitamin K:
Warfarin
79
Defect in platelet-platelet interaction (disorders of aggregation): A. Von willebrand disease (defect or defeciency in vwf) B. Bernard-soulier syndrome (defect or defeciency in gp1b) C. Congenital afibrinogenemia (defeciency in plasma fibrinogen) D. Storage pool deficiency
glanzman -lahat ng choices adhesion problem maliban sa C C. Congenital afibrinogenemia (defeciency in plasma fibrinogen)
80
The following is true of prothrombin time: A. Prolonged PT is caused by deficiency of Factor VII, Factor X, Factor IX, II and I B. INR is calculated as INR=(PT measured)/(PT mean)ISI C. PT is more sensitive than aPTT D. All are correct
D. All are correct
81
Most effective test for DIC:
D-Dimer test
82
Parasitologic easy-to-do test:
Direct Wet Mount
83
Most involves ingestion except:
Strongyloides
84
Not a characteristic of nematodes:
Incomplete digestive tract
85
Cellulose tape exam:
Enterobius
86
Causes rectal prolapse:
T. trichiura
87
Tissue biopsy reveals encysted larvae:
Trichina worm
88
What parasite causes human cysticercosis?
T. solium
89
Maltese cross formation:
Babeiosis
90
Soon after returning from a trip to Costa Rica, a 41-year-old woman develops recurrent chills and high fever that recur every 48h. Examination of her peripheral blood reveals red granules (Schüffner's dots) in enlarged, young erythrocytes. Which of the following organisms is most likely to have produced her signs and symptoms?
P. ovale
91
Responsible for bladder cancer and has apical spine:
Schistosoma hematobium
92
This amoeba causes intestinal ulcers, liver and lung abscesses:
E. histolytica
93
A visitor from overseas was hospitalized due to suspected tuberculosis. The laboratory received a bloody sputum sample with orange brown flecks. What is the suspected organism?
Paragonimus westermani
94
Causes fatal meningoencephalitis:
Naegleria fowleri
95
Visceral larva migrans:
Toxoplasma canis
96
Bronchial AIDS silver methenamine: ``` A. Stercoralis B. Gondii C. Carinii D. Bancrofti E. Parvum ```
C. Carinii
97
Thru tick bites and blood transfusions except: A. Babesia B. Trypanosoma C. Leishmanosis D. AOTA
C. Leishmanosis -sand flies
98
Demonstrates the characteristic "falling leaf" motility of trophozoites: 18. 19. 20. 21.
Giardia lamblia
99
Quartan Fever: P. falciparum P. ovale P. malariae P. vivax
P. malariae
100
James dot pigmentation: P. falciparum P. ovale P. malariae P. vivax
P. Ovale
101
Malignant (Tertian) Malaria: P. falciparum P. ovale P. malariae P. vivax
P. falciparum
102
Infect duffy blood group: P. falciparum P. ovale P. malariae P. vivax
P. vivax
103
New reported case. 1st seen in primates:
P. knowlesi
104
Scavenging of free radicals: Vitamin B12 Vitamin C Vitamin E Vitamin K
Vitamin E
105
Hydroxylation of collagen: Vitamin B12 Vitamin C Vitamin E Vitamin K
Vitamin C
106
Myelinization of spinal tracts: Vitamin B12 Vitamin C Vitamin E Vitamin K
Vitamin B12
107
DNA metabolism / Uric acid production:
Molybdenum
108
Metallothionein: ``` Chromium Cobalt Folate Manganese Molybdenum Selenium Zinc ```
Zinc
109
Hyperglycemia/Hyperlipidemia: ``` Chromium Cobalt Folate Manganese Molybdenum Selenium Zinc ```
Chromium
110
Keshan Syndrome/cardiomyopathy: ``` Chromium Cobalt Folate Manganese Molybdenum Selenium Zinc ```
KS-Sel | Selenium
111
Pancreas: ``` Chromium Cobalt Folate Manganese Molybdenum Selenium Zinc ```
Pa Manga | Manganese
112
Neural tube defects: ``` Chromium Cobalt Folate Manganese Molybdenum Selenium Zinc ```
Neural-Fo | Folate
113
Prostate: ``` Chromium Cobalt Folate Manganese Molybdenum Selenium Zinc ```
ProZinc | Zinc
114
Spleen: ``` Chromium Cobalt Folate Manganese Molybdenum Selenium Zinc ```
SpC | Chromium
115
Fat: ``` Chromium Cobalt Folate Manganese Molybdenum Selenium Zinc ```
at-ALt | Cobalt
116
Adrenals: ``` Chromium Cobalt Folate Manganese Molybdenum Selenium Zinc ```
AdMoly | Molybdenum
117
Not true regarding folate?
All folate content of food is lost during cooking
118
True about thiamine except:
Thiamine is absorbed in small intestine and bound to prothrombin
119
Vitamins are organic molecule needed in trace amounts for health, reproduction and growth. They are as follows except: A. Except for vitamin D essential vitamin are derived from food B. Synthesis in the small intestines, not nutritionally significant because they are poorly absorbed C. Deficiency causes clinical significance D. Humans do not synthesize ascorbic acid, they need supplementation to prevent scurvy
B. Synthesis in the small intestines, not nutritionally significant because they are poorly absorbed
120
True about trace elements except:
Quantitation is done using quantitative procedure
121
Vitamin D promotes absorption of calcium and phosphate in the small intestine. Deficiency results to or from, EXCEPT: A. Deficiency is due to inadequate intake B. Insufficient sunlight reaching the skin C. Inadequate absorption, as in fat malabsorption diseases D. Failure of conversion to active metabolite in adult respiratory distress syndrome E. Rickets in children, osteomalacia in adults
D. Failure of conversion to active metabolite in adult respiratory distress syndrome
122
``` Zinc deficiency is common in patients with the following except: A. Diabetes insipidus B. Alcohol abuse C. Liver disease D. Kidney disease ```
A. Diabetes insipidus
123
Manifestation of severe zinc deficiencies, except: A. Hypogonadism, dwarfism, deformed bones B. Poor wound healing, abnormal hair and nails C. Loss of taste, GI disturbances, poor chylomicron function D. Teratogenic in pregnancy with congenital malformations, prematurity E. NOTA
E. NOTA
124
Dietary iodine is normally ingested as iodine and is the basic element in the synthesis of thyroid hormone. The following statements are true regarding the processes involving thyroid hormone except:
It is transported from the thyroid follicle
125
True of Panthotenic acid except: A. Part of CoA (for TCA) and ACP (for lipid) B. Panthothenic acid transported in erythrocytes C. Highest concentration in liver, adrenals, kidneys, brain, heart, and testes D. Panthothenic acid rarely present in food
D. Panthothenic acid rarely present in food
126
Capability of primary lab except:
Routine Chemistry
127
Microbiology culture and sensitivity for aerobe and anaerobe:
Hospital-based Tertiary Laboratory
128
65 year old man. Fatigued for 10 mos, PE unremarkable, decreased hemoglobin, decreased hematocrit, increased MCV, what do you request?
Assay for folate and B12
129
Blood test levels typically seen in hemolytic anemia. Increase or Decrease Haptoglobin
DECREASE
130
Blood test levels typically seen in hemolytic anemia. Increase or Decrease Indirect bilirubin
INCREASE
131
Blood test levels typically seen in hemolytic anemia. Increase or Decrease Reticulocyte
INCREASE
132
Blood test levels typically seen in hemolytic anemia. Increase or Decrease RDW
INCREASE
133
Blood test levels typically seen in hemolytic anemia. Increase or Decrease Erythrocyte precursor rate
INCREASE
134
10. A 22-y/o female went to your clinic complaining of "feeling down". Physical exam showed waxy pale skin and mucous membres. Extremities also showed purplish spots that do not blanch when pressed. Blood test revealed low RBC, WBC, and platelets. Bone marrow showed predominantly fat with decreased amount of cells. What is the diagnosis?
Aplastic anemia
135
True of Hereditary Angioedema:
Cause is heterozygous decrease in C1-inh
136
Bullous pemphigoid and epidermolysis bullosa acquisita: C3 C4 C5a C3 and C4
C5a
137
Complement for SLE:
C3 & C4
138
Cell mediator of inflammation:
Neutrophils
139
True of complement system EXCEPT: A. Host defense B. Apoptosis C. Immune Response D. NOTA 16. 17. Vitamin K dependent: factors X, IX, VII, II except: Factor V
D. NOTA
140
Complex glycoproteins that bind living cells together:
Adhesion molecules
141
Act as chemoattractants to neutrophils: C3 C4 C5a C3 and C4
C5a
142
Vitamin K dependent except ``` Factor II Factor V Factor VII Factor IX Factor X ```
Except Factor V
143
Deficiency or mutation in coagulation proteins or factor that leads to thrombophilia except:
Factor VII
144
Which of the following ere true about DIC: A. DIC is a severe form of consumptive coagulopathy B. Systemic activation of hemostasis leads to widespread intravascular fibrin deposition with associated depletion of prohemostatic and anticoagulant factors C. With parallel secondary fibrinolysis, potentially leading to a wide range of adverse outcomes, including thrombotic occlusion of small/midium sized vessels organ dysfunction or failure and or bleeding D. AOTA
D. AOTA
145
Single-stranded DNA A. 1base+1triphospahate+1sugar B. 1base+2triphospahate+1sugar C. 1base+3triphospahate+1sugar D. 1base+4triphospahate+1sugar
A. 1base+1triphospahate+1sugar
146
Process where mRNA goes splicing and capping: A. Post translation B. Post transcription C. Methylation D. PolyA tail
B. Post transcription
147
Recognizes specific short DNA sequence base pair and cleaves DNA molecule at recognition site:
Endonuclease
148
Correct complement sequence for DNA G/C G/T G/A
G/C GAAGGAG-CTTCCTC
149
Sections of DNA that specify amino acid sequence of proteins?
Codon
150
Faster and more specific test which will determine a specific gene and mutation or presence of chromosomal derangement?
FISH
151
Amplifying DNA:
PCR
152
Isothermal template amplification technique that can be used to detect trace amounts of DNA or RNA of a particular sequence:
Strand displacement amplification
153
Clinical situation/s involving immune complex reactions A. Rheumatoid Arthritis B. PSGN (Post-Streptococcal Glomerulonephritis) C. Chaga's disease D. A and B
D. A and B
154
Clinical situation/s involving cytotoxic reactions: A. Autoimmune Hemolytic Disease B. Autoimmune Thrombocytopenia C. Myasthenia gravis D. All of the above
D. All of the above
155
Test for humoral B-cell immunity
Quantitative Igs
156
Test for Inflammation
ESR and CPR
157
32. Positive / Negative cutoffs: A. If the mean plus 2 standard deviation is chosen as the cutoff, approx. 2.5% of the healthy population will test + B. If the mean plus 3 standard deviation is chosen as the cutoff, approx. 0.15% of the health population should test + C. Both
C. Both
158
In Grave's disease, following pharmacologic therapy, what is the relationship of the titer of TSI with likelihood of remission?
The titer of TSI are inversely correlated with the likelihood of remission
159
Gladiatorum is produce by:
HSV
160
Antigenic shift: Influenza A Influenza B
SA | Influenza A
161
Antigenic drift: Influenza A Influenza B
DB | Influenza B
162
80% of the CROUP is caused by this virus A. Para-Influenza B. Herpes Simplex Virus C. Adenovirus D. Meta-pneumoniae
A. Para-Influenza
163
PIV is considered the 2nd most common cause of lower respiratory tract infection. What is the most common type of PIV causing this? PIV2 PIV3 PIV4
PIV3
164
Method of virus detection in general:
RT PCR
165
Non Replicative form of Chlamydial infection: Elementary Bodies Intracytoplasmic inclusions Reticulate Bodies
Elementary Bodies
166
Non Infectious form of Chlamydia: Elementary Bodies Intracytoplasmic inclusions Reticulate Bodies
Reticulate Bodies
167
Histologically, diagnosis of chlamydial infections is best demonstrated by: Elementary Bodies Intracytoplasmic inclusions Reticulate Bodies
Intracytoplasmic inclusions
168
Condition that affects the lymphatic and circulation:
LGV
169
Slightly more sensitive than CA15-3:
CA27-29
170
Breast CA:
CA15-3
171
Monitoring of clinical course of patients with breast cancer:
CA 15-3
172
Non-seminous, molar pregnancy:
B-HCG
173
Important prognostic and predictive tumor marker for breast cancer?
Her2/neu
174
CA-125:
Ovarian Cancer
175
CEA:
Colon Cancer
176
A visitor is hospitalized due to suspected tuberculosis. The laboratory received a blood-tinged sputum with orange brown flecks. Preliminary tuberculin test is negative. What organism is the cause?
P. westermani
177
Which of the ff. causes fatal meningoencephalitis?
N. Fowleri
178
Which of the ff organisms cause visceral larva migrans: ``` A. Brazilensis B. A. lumbricoides C. S. stercoralis D. T. carinii E. T. gondii ```
C. S. stercoralis
179
Transmitted to humans through tick bites and blood transfusion:
Babesia
180
Falling leaf like motility:
G. Lamblia
181
Differential diagnosis if cyrptosporidium pravum to cyclospora cayetenensis
oocyte size: cryptosporidium bigger
182
Hydroxylation of collagen
Vitamin C
183
DNA metabolism/ uric acid production:
Molybdenum
184
Methallothionine
Zinc
185
Keshan/Cardiomyopathy:
SELENIUM
186
Menke's:
COPPER
187
Wernicke-Korsakoff:
VITAMIN B1
188
Neural tube defect:
FOLATE
189
Haptoglobin binds with myoglobin in cases of rhabdomyolysis. TRUE or FALSE
FALSE
190
Serum protein electrophoresis can be used to screen patients suspected of having AAT deficiency: TRUE or FALSE
TRUE
191
Which one of the following options are appropriate indications for requesting protein electrophoresis? a) Lytic bone lesions b) Recurrent infections c) Incidental finding of increased serum total protein d) Unexplained bone pain or fracture e) AOTA
e) AOTA
192
A 10-year old boy presents with lethargy, hip pain, and high grade fever. Past medical history reveals several hospital confinements due to pneumonia. His neonatal history is unremarkable. His CBC results are within reference ranges. The child is negative for HIV antibody. Blood cultures yield S. aureus. Serum electrophoresis will most likely show which one of the following patterns?
Puro picture yun choices but A yun sagot. Yun may mataas na A1b and nonexistent na gamma, as in walang gamma.
193
A 36-year-old woman on oral contraceptives undergoes heparin treatment for pulmonary embolis. Her blood is drawn in a red tap tube for serum protein electrophoresis. A distinct band is noted just anodal to the gamma fraction. What is the most likely cause of this unexpected band? a) Haptoglobulin b) IgG c) Fibrinogen d) Transferrin e) Alpha-2-macroglobulin
c) Fibrinogen
194
``` Refer to the previous question. Your answer in #5 migrates to which one of the following fractions? ``` a) Alpha-1 b) Alpha-2 c) Beta-1 d) Beta-2 e) Beta gamma
e) Beta gamma
195
20/M brought to the ED following a vehicular crash. Examination finds small _____ draining from his right nasal passage. The physician is not sure if this draining fluid is CSF. He sends the fluid specimen to the lab for identification. Electrophoresis demonstrates double band. This extra band is due to a variant of: a) Ferritin b) Transferrin c) Albumin d) Haptoglobulin e) Alpha-2-macroglobulin
b) Transferrin
196
Refer to previous question. Your answer in #7 migrates to which one of the following fractions? a) Alpha-1 b) Alpha-2 c) Beta-1 d) Beta-2 e) Beta gamma
d) Beta-2
197
A previously healthy 20 year-old man developed bilateral leg swelling two years ago that was managed with diuretics and steroids. He denies any history of kidney disease, malaria, TB, and syphilis. This patient has been hospitalized several times over the past two years for the same complaint. His BP is 110/70 mmHg. PE is remarkable for peripheral edema and rales in both lower lung fields. Pedal edema (+2) is noted. Lab tests show the ff results: Hb = 13.9 g/dL (N: 13.5-17.5) Hct = 40% (N: 40-54) Cholesterol = 441 mg/dL (N<200) Triglycerides = 225 mg/dL (N:<150) Serum creatinine = 2.1 mg/dL (N: 0.6-1.2) 24-hour urine protein = 12g (N<100mg) Urinalysis SG = 1.042, 4+ proteins, large numbers of granular and hyaline casts, 2-5 WBC/HPF, 10-20 RBC/HPF. Serum protein electrophoresis is done. Which one of the following conditions most likely account for the patient’s findings? a) Multiple myeloma b) Liver cirrhosis c) Nephrotic syndrome d) Waldenstrom’s macroglobulinemia e) Lymphoma
c) Nephrotic syndrome
198
A 10 year old Nigerian boy presents with generalized edema, ascites and proteinuria. Over the next 3 weeks, he develops conjugated hyperbilirubinemia, severe coagulopathy, and prominent extrapyramidal features comprising of tremors at rest and in action, shuffling gate, and slurred speech. Slit-lamp examination of the eyes reveals a brownish-yellow ring on the corneo-scleral junction. The following are true of the case, except: a) Urinary copper excretion is most likely increased in the patient. b) The most likely diagnosis for this case can be excluded by a normal ceruloplasmin result. c) The case cannot be diagnosed with protein electrophoresis. d) The most likely diagnosis of this case cannot be proved or excluded solely on liver copper content.
b) The most likely diagnosis for this case can be excluded by a normal
199
The minimum acceptable hemoglobin level for a homologous blood donor: a) 11.0 g/L b) 11.5 g/L c) 12.0 g/L d) 12.5 g/L e) 13.0 g/L
d) 12.5 g/L
200
The following are reasons for permanent deferral for blood donations, EXCEPT: a) Neonatal history of hepatitis infection b) Confirmed case of HIV but with high CD4 c) History of sexual contact with anyone in exchange for monetary gain d) History of Tegison (etretinate) use e) All of the reasons above entail permanent deferral.
c) History of sexual contact with anyone in exchange for monetary gain
201
A potential blood donor with a history of Accutan (isotretinoin) use comes to you for screening. What is your call? a) Permanent deferral for the donor. b) Defer the donor for at least one month from receipt of the last dose. c) Defer the donor for at least two months from receipt of the last dose. d) Defer the donor for at least one year from receipt of the last dose. e) Defer the donor for at least two years from receipt of the last dose.
b) Defer the donor for at least one month from receipt of the last dose.
202
Platelet components are stored up to ____ days at 20-24OC with continuous agitation. a) 2 b) 5 c) 6 d) 7
b) 5
203
16. Platelets prepared from a whole blood donation require which one of the following: a) A light spin, then a heavy spin b) Two light spins c) A light spin and two heavy spins d) A hard spin, then a light spin e) Two heavy spins
a) A light spin, then a heavy spin
204
A 40 y/o man sustains major trauma following a car accident. He is blood type O negative. Which of the following blood products would be unacceptable to transfuse? a) B positive FFP b) AB positive FFP c) A negative platelets d) O positive red cells e) AB positive red cells
e) AB positive red cells
205
The labels have come off some testing reagents in your blood bank. Your medtech is trying to find her anti-B, and she asks you what anti-B should be. Your answer: a) Green b) Orange c) Blue d) Yellow e) Grey
d) Yellow
206
Tests were done to determine a patient’s blood type. Results are as follows: Patient erythrocyte + anti-A serum: no agglutination Patient erythrocyte + anti-B serum: agglutination Patient erythrocyte + anti-Rh(D) serum: no agglutination Patient serum + Type A erythrocytes: agglutination Patient serum + Type B erythrocytes: no agglutination Patient serum + Type O erythrocytes: no agglutination What is the patients’ blood type? a) A positive b) A negative c) B positive d) B negative
d) B negative
207
A 25 year old pregnant woman is preparing for her C-section tomorrow. Her forward typing is consistent with blood group O while her reverse typing is group A. What is the most common reason for error in typing? a) Bombay phenotype b) She is a non-secretor (??) c) Clerical errors or a sample mix-up d) Use of an uncalibrated centrifuge e) She has undiagnosed acute myelogenous leukemia.
c) Clerical errors or a sample mix-up
208
Which of the following statements characterizes a major crossmatch for RBC transfusion? a) Prevents transmission of infectious diseases b) Prevents formation of antibodies against donor blood group antigens c) Prevents febrile transfusion reactions d) Negative patient antibody screen e) Guarantees survival of infused donor RBCs
d) Negative patient antibody screen
209
Bond formation coupled with ATP:
D. ligases
210
Oxidation-reduction:
A. Oxidoreductase
211
Elimination of double bond:
C. Lyase
212
Hydrolysis reaction:
B. Hyrdolase
213
Activity of erythrocyte ACP can be distinguished from prostatic acid phosphatase by: a) Prostatic ACP is susceptible to formaldehyde, resistant to tartrate b) Erythrocyte ACP is susceptible to formaldehyde c) They cannot be distinguished from each other
b) Erythrocyte ACP is susceptible to formaldehyde
214
Exists predominantly in biliary tract as a marker for biliary dysfunction. It is also found in bone, bile ducts, intestine, and placenta. a) ACP b) ALP c) ALT d) AST
b) ALP
215
How do you distinguish bone and liver enzyme of ALP?
Heating
216
What is increased in intracellular liver damage (hepatitis, cirrhosis) and after MI? a) AST b) ALT c) ALP d) ACP
a) AST
217
Which is more specific for liver damage? a) AST b) ALT c) ALP d) ACP
b) ALT
218
Which is used for monitoring hepatotoxic drugs? a) AST b) ALT c) ALP d) ACP
a) AST
219
Carcinoid syndrome:
Urine 5-HIAA
220
Pseudomembranous colitis:
E. Stool Clostridium dofficile toxin assay
221
Celiac disease:
D. Anti-tissue transglutaminase antibody
222
Protein losing enteropathy:
A. Stool a1 antitrypsin
223
Pancreatic insufficiency disease:
B. Fecal elastase
224
Ulcerative colitis:
E. p-ANCA
225
Crohn’s disease:
D. ASCA, anti-saccaromyces cerevisiae antibody
226
Colon carcinoma:
A. show deletion in one p53 allele
227
95% of pancreatic cancers:
B. mutated Kras
228
Mirizzi syndome:
C. CA19-9
229
Hep A:
C. RT PCR of feces
230
Hep B:
E. anamnestic response to the vaccine
231
Hep C:
B. Viral load, predictor of severity
232
Hep D:
A. Coinfection/Superinfection
233
Hep G:
D. Post-transfusion hepa
234
True of direct immunofluorescence:
b) A primary antibody with a fluorophore group bound to it and directly behind the epitope of the antigen it is specific for
235
True of indirect immunofluoescence:
a) A secondary antibody with a flurophore group bound to it and bound to fc portion of the primary antibody
236
Diagnosis of systemic rheumatic disease should depend on: a) Clinical characteristics b) Lab testing and biopsy c) Exclusion of other disease d) AOTA
d) AOTA
237
Positive ANA test with a dilution of <1:160. The next step that the physician should do: a) Order a panel of ANA specificities b) Examine if there are symptoms, signs, and lab findings of a rheumatic disease c) Consider other autoimmune disease d) Consider infections or _____ disorders as the cause.
a) Order a panel of ANA specificities
238
Positive ANA with a dilution of >1:160. The next step of the physician should be: a) Order a panel of ANA specificities b) Examine if there are symptoms, signs, and lab findings of a rheumatic disease c) Consider other autoimmune disease d) Consider infections or _____ disorders as the cause.
a) Order a panel of ANA specificities
239
True of diabetic ketoacidosis, EXCEPT: a) It is a serious and potentially fatal hypergylcemi condition requiring urgent treatment. b) The ration of B-hydryoxybutyric acid to acetoacetic acid is greatly decreased. c) It is frequently associated with nausea, vomiting, abdominal pain, electrolyte disturbances, and severe dehydration. d) Type 2 diabetes patients who are poorly controlled, particularly in the presence of extreme stress or severe acute illness, can also develop DKA
b) The ration of B-hydryoxybutyric acid to acetoacetic acid is greatly decreased.
240
Hypoglycemia from endogenous secretion can be due to the ff, EXCEPT: a) Insulin-secreting beta cell tumors b) Congenital hyperinsulinism c) Autoantibodies to insulin in patient who have never been treated with insulin d) NOTA
d) NOTA
241
True of lactic acidosis, EXCEPT: a) It is a product of pyruvic acid metabolism b) Nucleoside reverse transcriptase inhibitors used in the treatment of human immunodeficiency virus infection can also induce lactic acidosis c) Approximately 1400 mmol of lactic acid is produced daily in healthy individuals d) High levels of lactic acid produced during strenous exercise are rapidly cleared by renal mechanisms only
d) High levels of lactic acid produced during strenous exercise are rapidly cleared by renal mechanisms only
242
Lactic acidosis is diagnosed by the presence of the following, except: a) High blood lactose levels b) High anion gap c) Low blood ph d) NOTA
d) NOTA
243
This autosomal recessive deffect results in failure of heptic glucose generation from gluconeogenic precursors: a) Essential fructosuria b) Hereditary fructose insufficiency c) Fructose 1,6 biphosphatse deficiency d) NOTA
d) NOTA
244
McArdle disease is secondary to defect in: a) Muscle phosphorylase b) Phosphoglycerate kinase c) Pyruvate muscle isoenzyme d) Phosphofructo kinase
d) Phosphofructo kinase
245
The following are associated with von Gierke disease, EXCEPT: a) Glucose-6-phosphate b) Lab findings are hypoglycemia, lactic acidosis, hyperuricemia, and dyslipidemia c) Autosomal recessive d) Phosphorylase kinase
d) Phosphorylase kinase
246
It is a non-reducing sugar composed of glucose and fructose connected by a glycosidic band. a) Maltose = reducing (glucose+glucose) b) Sucrose c) Lactose = reducing (glucose+galactose) d) NOTA
b) Sucrose
247
The following are functions of insulin except: a) Promotes glycolysis b) Promotes lipolysis c) Stimulates synthesis of AA from pyruvate d) Increases glucose entry into the cell
b) Promotes lipolysis
248
The following are true of galactokinase deficiency except: a) Galactose cannot be converted into galactose-1-phosphate and this leads to cataract formation b) Pseudotumor cerebri is another rare complication observed in this disorder c) The diagnosis is made by demonstrating an elevated blood galactose level with normal urydyl transferase. d) A galactose-free diet cannot reverse cataract even if it is started early in infancy.
d) A galactose-free diet cannot reverse cataract even if it is started early in infancy.
249
This enzyme converts testosterone to estradiol in peripheral tissues such as adipocytes: a) 21-____ b) AOTA c) Aromatase d) DHEA-5
c) Aromatase
250
Activeform of testosterone: a) DHT b) DHEA c) Both d) None
a) DHT
251
Primary regulating hormone of reproductive function secreted and synthesized in the hypothalamus. a) GNRH b) FSH c) LH d) Prolactin
a) GNRH
252
Blighted ovum is indicated by which one of the following: a) Increased estradiol and progesterone b) Decreased estradiol and progesterone c) Increased estradiol d) Increased progesterone
a) Increased estradiol and progesterone
253
L/S ration that indicates fetal lung maturity: a) 2.0 b) 2.5 c) 1.5 d) 1.0
b) 2.5
254
True or False: The primary risk to the fetus in hemolytic disease of the newborn is the accumulation of unconjugated bilirubin in the CNS. a) True b) False Hypoglycemia from endogenous insulin secretion can be due to the ff, EXCEPT: a) Insulin-secreting beta cell tumors b) Congenital hyperinsulinism c) Autoantibodies to insulin in patients who have never been treated with insulin d) NOTA
b) False
255
``` The primary risk to the fetus in hemolytic disease of the newborn is one of the ff: a) Unconjugated bilirubin b) Anemia c) Both d) None ```
c) Both
256
True of Type I diabetes, EXCEPT: a) Frequency of 5%-10% b) C-peptide levels are very low or undetectable c) Autoantibodies may be present
d) Autoantibodies are absent
257
Hypoglycemia from endogenous insulin secretion can be due to the ff, EXCEPT: a) Insulin-secreting beta cell tumors b) Congenital hyperinsulinism c) Autoantibodies to insulin in patients who have never been treated with insulin d) NOTA
d) NOTA
258
The ff are included in the diagnostic criteria for an insulinoma, EXCEPT: a) Presence of signs and symptoms of hypoglycemia with plasma glucose level ≤55 mg/dL b) Insulin level ≥3 uU/mL (18 pmol/L) by immunochemiluminometric assay c) C-peptide concentration ≥0.6 ng/mL (0.2 nmol/L) d) NOTA
d) NOTA
259
True of lactic acidosis, EXCEPT: a) It is a product of pyruvic acid metabolism b) Nucleoside reverse transcriptase inhibitors used in the treatment of human immunodeficiency virus infection can also induce lactic acidosis c) Approximately 1400 mmol of lactic acid is produced daily in healthy individuals d) High levels of lactic acid produced during strenous exercise are rapidly cleared by renal mechanisms only
d) High levels of lactic acid produced during strenous exercise are rapidly cleared by renal mechanisms only
260
Lactic acidosis is diagnosed by the presence of the following, except: a) High blood lactose levels b) High anion gap c) Low blood ph d) NOTA
d) NOTA
261
This autosomal recessive defect results in failure of hepatic glucose generation by gluconeogenic precursors such as lactate, glycerol, and alanine. a) Essential fructosuria b) Hereditary fructose intolerance c) Fructose-1,6-bisphosphatase deficiency d) NOTA
d) NOTA
262
It is produced in the delta cells which make up 5%-10% of the islet cells. a) Glucagon b) Somatostatin c) Incretins d) NOTA
b) Somatostatin
263
The following are used currently as predictive markers for diabetes, EXCEPT: a) ICA b) Anti-TPO c) Anti-GAD d) IAA e) IAA-2 autoantibodies
b) Anti-TPO
264
Antibodies deposits are seen in BMZ (basement membrane zone) using immunofluoroscence. a) Bullous phemphigoid b) Pemphigus vulgaris c) Pemphigus foliaceous d) AOTA
a) Bullous phemphigoid
265
p-ANCA is best associated with a) Ulcerative colitis b) Crohn’s disease c) Both UC and CD d) Hepatic and hepatobiliary autoimmunity
a) Ulcerative colitis
266
ASCA is a marker for: a) Hepatic and hepatibiliary disease b) Inflammatory bowel disease c) Pernicious anemia d) Lymphocytic gastritis
b) Inflammatory bowel disease
267
VGCC (voltage-gated calcium channel) autoantibody screening is for the ff autoimmune diseases a) Myasthenia gravis b) Multiple sclerosis c) Eaton Lambert myasthenic syndrome d) AOTA
c) Eaton Lambert myasthenic syndrome
268
This type of cutaneous autoimmune disease involves specifically type III collagen: a) IgA pemphigus b) Dermatitis herpetiformis c) Bullous pemphigoid d) Epidermolysis bullous
c) Bullous pemphigoid
269
Linear/granular pattern of C3 deposits in IF is a consistent finding of: a) Pemphigus vulgaris b) Pemphigus follaceous c) IgA pemphigus d) Pemphigoid ____
a) Pemphigus vulgaris
270
The ff are examples of organ-specific disease, EXCEPT: a) Celiac disease b) Pemphigoid lesions c) Goodpasteur syndrome d) Autoimmune hepatitis
c) Goodpasteur syndrome
271
HLA-DQ2/HLA-DQ8: a) Celiac disease b) UC c) CD d) Pernicious anemia
a) Celiac disease
272
Intradermal acantholysis is the hallmark of: a) Epidermolysis bullous b) Dermatitis herpetiformis c) Pemphigus follaceus d) Pemphigus vulgaris
d) Pemphigus vulgaris
273
In the normal immune system, CD4 will differentiate into TH1 and TH2. The ff substances will be relased from TH2, EXCEPT: a) IL2 b) TNF-alpha c) Interferon gamma d) IL4
d) IL4
274
Single best screening test for thyroid dysfunction: a) TSH b) T3 c) Total T4 d) Free T4
a) TSH
275
Characterized by thyroid stimulating immunoglobulin and is the most common cause of ______ a) Toxic multinodular goiter b) Plummer syndrome c) Hashimoto thyroiditis d) Grave’s Disease
d) Grave’s Disease
276
Lab test results that point to euthyroid sick syndrome: a) TSH – low b) T3 – high c) T4 – high d) rT3 – high
d) rT3 – high
277
The best screening test for this condition is ratio of plasma aldosterone concentration to plasma renin ____ a) Conn syndrome b) Addison disease c) Cushing syndrome d) Primary adrenal insufficiency
a) Conn syndrome
278
In dexamethason suppression test, a dose of dexamethasone that suppresses both ACTH and cortisol ____ seen in: a) Cushing syndrome b) Addison disease c) Conn disease d) Normal individuals
d) Normal individuals
279
The anterior pituitary gland secretes the ff, EXCEPT: a) Growth hormone b) Prolactin c) Oxytocin d) TSH
c) Oxytocin
280
Prolactin levels of or greater than is almost always indicative of pituitary tumor: a) 1 ug/L b) 25 ng/mL c) 100 ng/mL d) 200 ng/mL
d) 200 ng/mL
281
Initial screening test for clinically suspected acromegaly OGTT TRH IGF-1 TnRH
IGF-1
282
The adrenal cortex secretes the ff, except a) Epinephrine and NE b) Glucocorticoids c) Estrogen and androgen d) Aldosterone
a) Epinephrine and NE