Exam 4- lecture 1 Flashcards

(175 cards)

1
Q

how are RBC with iron deficiency anemia?

A

microcytic (smaller than normal)

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2
Q

lack of development

A

aplasia

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3
Q

this is an insufficient amount of iron supposed to the bone for RBC development

A

iron deficiency anemia

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4
Q

what are some problems with infections when a patient has diabetes?

A

decreased resistance of infection such as skin infections, furybcles, UTI and TB..

poor wound healing

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5
Q

why is PTT used?

A

by MD to monitor heparin therapy (hemodialysis with renal failure)

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6
Q

what is prothrombin time most often used by?

A

MD to monitor anticoagulation therapy

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7
Q

this type is not sex linked and affects women and men

A

type c hemophelia

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8
Q

how does hyperparathyroidism appear radiographically?

A

well defined uni or multilocular RL

Central Giant cell granuloma

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9
Q

this is characterized by the presence of very immature cells (blast cells) and by a rapidly fatal course if not treated

A

acute leukemia

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10
Q

what is the cause of secondary aplastic anemia?

A

bone marrow failure is a result of a drug or chemical agent

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11
Q

result of long standing iron deficiency

A

plummer vinson syndrome

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12
Q

chemical substance produced in the body that has a specific regulatory effect on certain cells or organs

A

horomone

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13
Q

what is a major problem for patients with type 1 diabetes?

A

controlling blood glucose levels… glucose is controlled by multiple injections of insulin

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14
Q

this type of hemophelia is less severe bleeding with defect in factor IX… risk of post op bleeding, bleeding and PT are normal.. PTT is prolonged

A

Hemophelia

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15
Q

what is the most common cause of hyperparathyroidism?

A

parathyroid adenoma which is a benign tumor of parathyroid gland

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16
Q

this is protrusion of the eyeballs

A

exopthalmus

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17
Q

this is the production of ketone acid from the breakdown of fatty tissues and is life threatening

A

diabetes mellitus

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18
Q

autoimmunity of type 1 diabetes leads to the destruction of insulin producing beta cells which leads to

A

insulin deficiency

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19
Q

what disease is associated with as a result of decreased production of adrenal steroids, the pituitary gland increases its production of adrenocorticotopic hormone (ACTH)

A

addison’s disease

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20
Q

decreased number of neutrophils in blood

A

neutropenia

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21
Q

this is thickening of the blood vessel wall from fibrofatty plaques and is associated with diabetes

A

atherosclerosis

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22
Q

what is type 1 diabetes?

A

insulin dependent

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23
Q

what are the causes of hyperthyroidism?

A

hyperplasia of the gland

benign and malignant tumor of thyroid

pituitary gland disease

metastic tumor

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24
Q

marked reduction in circulating neutrophils

A

agranulocytosis

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25
what are the causes of relative polycythemia?
diuretic use, vomiting, diarrhea or excessive sweating
26
what bones does polyostatic fibrous dysplasia involve?
bones of the face, skull, clavicles and long bones
27
these types of hemophelia are linked diseases and are transmitted through an unaffected daughter or grandson
types A and B- inherited X
28
this type of hemophelia is most common and is caused by a deficiency of plasma thromboplastinogen (factor VIII)
type A characterized by severe hemorrhage
29
what are the types of polycythemia?
polycythemia vera (primary) secondary polycythemia relative polycythemia
30
malignant neoplasms of the hematopoitic stem cells (blood forming cells) or disorder in bone marrow/ excessive number of abnormal WBC in circulating blood
leukemia
31
what is folic acid essential for?
DNA synthesis
32
what is the cause of primary aplastic anemia?
unknown cause
33
insoluble protein that is essential to the clotting of blood
fibrin
34
this is also known as primary adrenal cortical insufficiency
addison's disease
35
what's necessary for fibrinogen to be converted to fibrin?
11 clotting factors
36
what are the clinical manifestations of chronic lymphocytic leukemia?
gingival bleeding and periodontal disease WBC count can increase 50,000 cells treat with chemo and bone marrow transplants
37
abnormal rarefaction of bone
osteoporosis
38
difficulty swallowing.. atrophy of the upper alimentary tract and predisposition to development of oral cancer
dysphagia
39
what are the clinical signs of iron deficiency anemia?
angular chellits, pallor of oral tissues or erythematous, smooth, painful tongue
40
who is hyperthyroidism more common in?
women
41
accumulation of acid in the body resulting from the accumulation of ketone bodies
ketacidosis
42
release of hemoglobin from RBC by destruction of the cells
hemolysis
43
excessive apatite.. associated with type 1 diabetes
polyphagia
44
how is paget's disease diagnosed and treated?
lab tests of elevated serum alkaline phosphates level no treatment. still experimenting
45
what does acute leukemia do orally?
causes bleeding gums, petchiae and ecchymoses present treat with bone marrow transplant
46
this is when hypothyroidism is present during infancy and childhood
cretinism
47
this is an excessive production of thyroid hormone
hyperthyroidism
48
reduction of the number of red blood cells, quantities of hemoglobin, or volume of packed RBC
anemia
49
what is it called when patients have a thickened tongue?
macroglossia
50
abnormally large blood cells
megaloblastic anemia
51
this is an inherited disorder of platelet function
von willebrands disease
52
how is pernicious anemia diagnosed and treated?
lab test of low serum vitamin b12 levels, gastric achlorydia and megalobalastic anemia treat with injection of b 12
53
what percent of patients are type II and when is the onset?
90% of patients usually in their 40's
54
this type of leukemia is a slow onset affecting adults?
chronic leukemia
55
this causes menses, pubic hair and breast development by the age of 2
precocious puberty
56
what is an increase in growth horomone production associated with hyperpituitarism?
gigantism
57
what is associated with the development of aplastic anemia?
chenotherapgy, radioactive isotopes, radium, or radiant energy
58
excess of glucose in blood
hyperglycemia
59
what is the normal platelet count?
150,000-400,000 mm cube
60
this is a chronic metronomic disease characterized by resorption, osteoblastic repair, demineralization of the involved bone... occurs in older men and in the maxilla
paget's disease
61
these are skin lesions associated with polyoststic fibrous dysplasia
cafe au lait spots
62
this is an increase in blood cells caused by a physiologic response to decreased oxygen
secondary polycythemia
63
this provided assessment of the adequacy of platelet function not platelet number and tests measures how long it takes to standardized skin incision to stop bleeding by the formation of temporary hemostasis clot
bleeding time
64
what are the factors causing a decrease in oxygen with secondary polycythemia?
pulmonary disease, heart disease, living in high altitudes and increase in carbon monoxide
65
what is thrombocytopenia?
a count of platelets less than 100,000
66
this is a complex process when blood vessels are damaged/ vasoconstriction occurs in an attempt to stop blood flow then platelets (thrombocytes) adhere to the damaged surface to form a temporary clot to stop bleeding permantley- fibrin must be produced
hemostasis
67
who does polycythemia vera occur in and what are the symptoms?
usually men 40-60 years of age. symptoms: headache, dizziness, pruritis increase in rbc/impaired blood flow, vascular stasis and poor circulation(thrombi can lead to death)
68
who does acute myoblastic leukemia?
adolescents with poor prognosis
69
blood disorder characterized by purplish or brownish red discolorations caused by bleeding into the skin or tissues
purpura
70
what is another term that hyperthyroidism is referred to as?
thyrotoxicosis
71
enlargement of the liver
hepatomegaly
72
what are immature granulocytes called?
acute myoblastic leukkemia
73
what are the systemic and oral signs of celiac sprue?
diarrhea, nervousness, and parasthesja of the extremities glossitis painful burning of tongue and atrophy of papillae and ulceration of oral mucosa
74
what is most severely affected with diabetes?
the vascular system
75
what is common with non insulin dependent patients?
obesity
76
what may be responsible for destruction of adrenal gland?
malignant tumor or TB
77
this is characterized by insufficient production of adrenal steroids
addison's disease
78
what does acute leukemia do?
enlargement of spleen (splenomegaly) and liver (hepatomegaly)
79
this type of leukemia is associated with a chromosomal abnormality aka the philadelphia chromosome
chronic myeloid leukemia
80
how do you diagnose and treat iron deficiency anemia?
lab test- low hemoglobin content of RBC and reduced hematocrit value treat with increasing iron intake
81
formation of a clot
coagulation
82
what is a type II diabetic?
non insulin dependent they have an increased insulin resistance
83
how do you treat hyperthyroidism?
surgery medication to suppress thyroid activity use of radioactive iodine (I 131)
84
what is hypersecretion of growth horomone associated with hyperpituitarism?
acromegaly
85
who is monostatic fibrous dysplasia common in and how does it appear clinically?
young children and young adults.. painless swelling or bulging of the jaws involving the buccal plate
86
what disease stimulated melanocytes which results in bronzing of the skin and melanotic macules of the oral mucosa?
addisons disease
87
this is due to decreased plasma volume and not an increase in RBC
relative polycythemia
88
hypercalcemia
excess of calcium in the blood
89
what drugs effect hemostasis?
coumadin aspirin NSAIDS warfarin
90
what are the causes of iron deficiency?
deficiency of iron intake blood loss (menstrual or GI), poor iron absorption and increased requirement for iron (pregnancy)
91
deficiency of phosphates in the blood
hypophosphatemia
92
small flat hemorrhagic patch on skin or mucous membrane (bruise)
ecchymosis
93
stoppage or cessation of bleeding
hemostasis
94
this is an excess horomone production in the anterior pituitary gland that is caused most often by a benign tumor that produces growth horomone (pituitary adenoma)
Hyperpituitarism
95
this involves the beta cells of the pancreas and is a chronic disorder of glucose metabolism that is characterized by abnormally high blood glucose levels
diabetes mellitus
96
how does hyperthyroidism appear clinically?
rosy complexion erythema of the palms excessive sweating (heat intolerance) fine hair exopthalmus
97
this type of polycythemia is a neoplastic proliferation of bone marrow stem cells that results in abnormally high number of circulating red blood cells(uncontrolled production of RBC)
polycythemia vera
98
how do you treat relative polycythemia?
most includes removal of causative agent, chemotherapy and phlebotomy (blood letting)
99
this is clinically an enlargement of the bone of alveolar ridges and is painful... it looks patchy RL and RO that has been referred to as cotton or wool
paget's disease
100
this type of fibrous dysplasia involves more than one bone and is more common in female children
polyoststic fibrous dysplasia
101
what are the symptoms of sickle cell anemia?
weakness, shortness of breath, fatigue and joint pain and nausea... radiograph changes in the skull have been described as hair on end patten treat with oxygen and IV fluids
102
how does fibrous dysplasia appear radiographically and what are the treatments
diffuse RO which has been described as looking like a ground glass surgically excise
103
what are the most common types of anemia?
iron, folic acid, and vitamin B12
104
this produces quantities or numeric evaluation of platelets
platelet count
105
who does osteomalacia occur in and what is it caused by?
young children and caused by a nutritional deficiency of vitamin D or rickets treat with Nutritional supplements of vitamin D and dietary calcium pathological fractures may occur with this
106
the volume percentage of RBC's in whole blood
hematocrit
107
what is the number one medicine used for hypothyroidism?
synthroid
108
disorder of blood coagulation that results in severely prolonged clotting time, known as free bleeders
hemophilia
109
what does parathyroid hormone maintain?
normal blood levels of calcium by its effects on the kidney, GItract and bone
110
excessive thirst and intake fluid... associated with type 1 diabetic
poydipsia
111
minute red spot on the skin or mucosa caused by the escape of s small amount of blood
petechia
112
this is excessive secretion of parathyroid hormone (PTH) and plays an important role in calcium and phosphorous metabolism
hyperparathyroidsm
113
this type of hemophelia is known as christmas disease and less common. defect in factor IV
type B
114
what is the normal WBC count and what does it fall to in agranulocytosis?
4,000-11,000 falls to less than 1000 cells
115
what is pernicious anemia caused by?
deficiency of intrinsic factor... extrinsic is necesssry for absorption of vitamin b12 (needed for DNA synthesis)
116
this measures ability to form a clot... measure time it takes for a clot to form when calcium and a tissue are added to the patients plasma
prothrombin time (PT)
117
disease of bone caused by a deficiency of calcium over a period of long time
osteomalacia
118
a group of inherited disorders of hemoglobin synthesis, associated with hemolytic anemia (damage to RBC membranes and destruction of RBC).. treat with blood transfusions/splenectomy
thalaseemia
119
what does hyperthyroidism cause orally?
premature exfoliation in children osteoporosis and affects alveolar bone decay and perio disease progress more rapidly burning tongue
120
what is the most severe form of polyoststic dysplasia?
albrights syndrome which is endocrine abnormalities and causes precocious puberty
121
this binds the platelets to form a clot
fibrin
122
the cessation of bleeding
heomstasis
123
parathyroid hormone
parathormone
124
low levels of blood phosphorus
hypophosphatemia
125
who does acute lymphoblastic leukemia occur in?
primarily children
126
marked decrease in number of granulocytes, particularly neutrophils
agranulocytosis
127
inherited disorder of the blood found predominately in black individuals, females before age 30... result in abnormal hemoglobin in RBC
sickle cell anemia
128
what is the normal prothrombin time?
11-16 seconds
129
what is the most common form of fibrous displays is and what does it involve?
monostatic fibrous dysplasia and it involves only bone.. the maxilla is affected more than mandible and sometimes ribs, femur and tibia
130
lack of HC acid
gastric achlorhydia
131
a surface of activating factor
kaolin
132
excessive urination... involved with type 1 diabetes
polyuria
133
what type of aplastic anemia is fatal?
primary
134
engagement of the spleen
Splenomegaly
135
what are the clinical manifestations of pernicious anemia?
angular chelitis, painful erythematous tongue (burning)
136
what are oral complications of diabetes?
candidiasis xerostomia accentuated response to plaque gingiva can be hyperplastic and erythematous periodontal disease, mobility and early tooth loss ABC medication, calculus and plaque removal and effective oral hygiene care
137
a substitute platter factor to the patients plasma
cephalon
138
what is present with aplastic anemia?
leukemia and thrombocytopenia(decrease in platelets)
139
elevated blood levels of calcium
hypercalcemia
140
what are immature lymphocytes called?
acute lymphoblastic leukemia
141
dramatic decrease in all circulating blood cells because of a severe depression of bone marrow activity
aplastic anemia
142
what are some effects of artherosclerosis?
leads to impaired circulation of blood which results in impaired transport of oxygen and nutrients to the tissues increased risk of ulceration and gangrene of the feet, high BP, kidney failure and stroke blood vessel changed in the eye can lead to hemorrhage as blindness(diabetic retinopathy)
143
what are the types of hemophelia?
ABC
144
this type of leukemia is most common form and accounts for about 1/4 of all cases of leukemia
chronic lymphocytic leukemia
145
what is the normal time for partial thromboplastin time?
25-40 seconds
146
what results from lack of insulin?
hyperglycemia
147
disc shaped structure found in blood and for blood coagulation
platelet
148
increase in the total RBC mass in the blood
Polycythemia
149
what is the normal bleedingtime?
1-6 minutes
150
RBC that is smaller than normal
Microcyte
151
platelet
thrombocytes
152
horomone produced in the pancreas that regulates glucose metabolism and is major fuel regulating horomone
insulin
153
what percent of patients with type II diabetes require insulin injections?
25-30%
154
what can trigger sickle cell anemia?
excessive, exertion, administration of general anesthetic, pregnancy or even sleep
155
chronic disorder associated with a sensitivity to dietary gluten... protein found in wheat and wheat products
celiac sprue
156
this measures the time it takes a clot to form after the addition of kaolin
partial thromboplastin time (PTT)
157
what is the onset and how many people are type 1 diabetes?
the inset is usually around 20 years of age and 5-10% of all diabetes patients
158
what is hyperparathyroidism characterized by?
elevated blood levels of calcium low levels of blood phosphorus abnormal bone metabolism
159
how are blood glucose levels controlled with non insulin dependent patients?
diet and weight reeducation or oral medications
160
muscle pain
myalgia
161
this is a chronic form of polycythemia in middle aged white men under physiologic stress, mildly over weight, hypertensive and heavy smokers (increase in cardiovascular accidents)
stress polycythemia
162
what are bleeding disorders caused by?
abnormalities in platelets or clotting factors
163
characterized by abnormal increase in number of circulating. RBC.. oral mucosa may appear deep red to purple and the gingiva red.. excessive bleeding after oral surgery
polycythemia
164
this is when hypothyroidism is present in older children and adults
myxedema
165
this is decrease output of thyroid hormone
hypothyroidism
166
this is a disease characterized by the replacement of bone with abnormal fibrous connective tissue containing calcifications
fibrous dysplasia
167
what is an important diagnosis of. blood disorder?
complete blood count and a series of tests that examines RBC, WBC and platelets
168
what is the current home management for type 1 diabetics?
multiple insulin injections proper diet exercise home monitoring of blood glucose levels
169
how long does a type 1 diabetic remind insulin dependent?
their whole life
170
dietary deficiency of folic acid and b 12 results in anemia and can occur in association with malnutrition and increased metabolic requirements (alcoholism)
folic acid / b12 anemia
171
what is pagets disease also referred to?
osteitis deformans
172
this causes the blood PH to be lowered
ketoacidosis
173
this is a reduction in the oxygen and carrying capacity of the blood
anemia
174
decrease in number of platelets circulating in blood
thrombocytopenia
175
how do you diagnose and treat hyperpituitarism?
diagnose by blood work of a measurement of growth horomone treat with pituitary gland surgery