MedTech Recall Notes
MedTech Recall Notes
2. Flotation waterbath: 45 to 50 C
3. To remove formalin pigments: Picric acid
4. To remove mercurial deposits: Iodine
5. Explosive when dry: Picric acid
6. Function of alum in hematoxylin: Mordant
7. Primary importance of Frozen Sections: RAPID DIAGNOSIS
8. Enzyme histochemistry: Frozen section
9. Second best choice for routine cytologic examination after Papanicolau: Phase contrast microscopy
10. NOT SUITABLE for kidney structures: Bouin's
11. Cell death due to ischemia (loss of blood supply) is known as infarction, and is manifested by
caharacteristic histologic appearance: COAGULATION NECROSIS
12. Pseudomembranous colitis and diarrhea: Clostridium difficile
13. Corynebacterium amycolatum: Most frequently recovered Corynebacterium species from human
clinical material. It is part of the normal skin microbiota.
14. Primary fungal pathogen in HIV patients: Candida albicans.
15. Doublewalled, wrinkled cyst form: Acanthamoeba castellanii
16. Intracellular form of blood and tissue flagellates: leishmanial form
17. Normal stool pH: pH 7 to 8
18. Stool pH associated with CHO disorders: pH 5.5 or less
19. Microhematocrit: 10,000 g for 5 minutes
20. Standing plasma test: creamy layer (chylomicrons); turbid (VLDL)
21. Microanatomical fixatives should never contain osmic acid/osmium tetroxide because it inhibits
hematoxylin.
22. Nuclear fixatives should contain glacial acetic acid due to its affinity for nuclear chromatin.
23. Cytoplasmic fixatives (Flemming's without HAc, Regaud's, Orth's, Helly's and formalin with post-
chroming). They should never contain Glacial Acetic Acid because it destroys the mitochondria and
Golgi bodies.
24. Manual paraffin wax infiltration and embedding: At least four (4) changes of wax are required at
15 minutes interval to ensure complete removal of the clearing agent from tissue. The specimen is
then immersed in another fresh solution of melted paraffin for approximately 3 hours to ensure
complete embedding or casting of tissue.
25. Cambridge/Rocking microtome: invented by Paldwell Treffall.
26. Bond between Best carmine and glycogen: Coulombic attraction/electrostatic bonds, hydrogen
bonds
27. Routine H and E: Regressive staining, it involves a differentiation step
28. Stains for the glomerular basement membrane: PAS, Azocarmine stain
29. Postmortem clotting: immediately after death, rubbery consistency
30. Antemortem thrombi: friable, characterized by fibrin precipitation
31. Leadership: DIRECTING
32. COMPONENTS OF FIBRIN GLUE: cryoprecipitate (fibrinogen) and topical thrombin
33. Donor deferral, measles (rubeola) vaccination: 2 weeks
34. Donor deferral, German measles (Rubella) vaccination: 4 weeks
35. When stained with Sternheimer-Malbin stain, GLITTER CELLS stain LIGHT BLUE as opposed to
the VIOLET COLOR usually seen with NEUTROPHILS.
35. After episodes of hemoglobinuria, yellow-brown granules may be seen in renal tubular epithelial
cells and casts or free-floating in the urine sediment. To confirm that these granules are hemosiderin,
the Prussian blue stain for iron is used and stains the hemosiderin granules a blue color. (RTE cells
with HEMOSIDERIN).
36. Second most prevalent protein in CSF: Prealbumin (transthyretin)
37. MECONIUM, which is usually defined as a newborn’s first bowel movement, is formed in the
intestine from fetal intestinal secretions and swallowed amniotic fluid. It is a dark green, mucus-like
material. It may be present in the amniotic fluid as a result of fetal distress.
38. Blood should NEVER be drawn from a vein in an arm with a cannula (temporary dialysis access
device) or fistula (a permanent surgical fusion of a vein and an artery).
39. Adverse reaction of Aminoglycosides: Nephrotoxicity and ototoxicity
40. TETANY: neuromotor irritability accompanied by muscular twitching and eventual convulsions;
generally due to low calcium levels (hypocalcemia)
61. BASAL STATE: early morning before the patient has eaten or become physically active. This is a
good time to draw blood specimens because the body is at rest and food has not been ingested
during the night.
62. ACID: substance than can yield a hydrogen ion or hydronium ion when dissolved in water
63. BASE: substance than can yield hydroxyl ions (OH-)
64. COLLIGATIVE PROPERTIES: properties of osmotic pressure, freezing point, boiling point and
vapor pressure
65. t-test: compare accuracy, mean (TAM)
66. f-test: compare precision, SD (SPF)
67. Random error: 1:2SD, 1:3SD, R:4S (ODD NUMBERS)
68. Systematic error: 2:2SD, 4:1SD, 10:x (EVEN NUMBERS)
69. ZERO-ORDER KINETICS: reaction rate is dependent on enzyme concentration only
70. FIRST-ORDER KINETICS: reaction rate is directly proportional to substrate concentration
71. Arteriosclerosis: thickening or hardening of the walls of arteries
72. Atherosclerosis: accumulation of lipid in the veins and arteries
73. Azotemia: elevated urea in blood
74. Addison’s disease: deficiency of adrenocortical hormones
75. Conn’s syndrome: aldosterone-secreting adrenal adenoma
76. Cushing’s syndrome: excessive production of glucocorticoids (cortisol) by adrenal cortex
77. Phaeochromocytoma: tumors of the adrenal medulla or symphatetic ganglia that produce and
release large quantities of catecholamines
78. Amenorrhea: cessation of menstruation
79. Cirrhosis: Greek work YELLOW; irreversible scarring process by which normal liver architecture is
transformed into abnormal nodular architecture
80. Gilbert’s syndrome: hereditary disorder in which there is DECREASED BILIRUBIN TRANSPORT
into the hepatocytes.
81. Crigler-Najjar syndrome: hereditary DEFICIENCY of the UDPG-TRANSFERASE ENZYME
82. Dubin-Johnson syndrome is associated with increased plasma conjugated bilirubin, inborn error of
metabolism
83. Rotor syndrome, possibly of viral origin, where there is also a block in the excretion of conjugated
bilirubin but without liver pigmentation
84. Wilson’s disease is a defect of copper transport from the liver resulting in overload of copper in
liver and brain
85. Menkes disease is an X-linked recessive disorder in which defective transport of copper from
mucosal cells results in copper deficiency.
86. Hashimoto’s thyroiditis: chronic autoimmune thyroiditis; it is the most common cause of primary
hypothyroidism
87. Graves’ disease: diffuse toxic goiter
88. Kwashiorkor: acute protein calories malnutrition
89. Marasmus: caused by caloric insufficiency without protein insufficiency so that the serum albumin
level remains normal; there is considerable loss of body weight
90. Leydig cells: cells of the testicles that produce testosterone