Sick Pre-Schooler Flashcards

(78 cards)

1
Q

hematological malignancy or cancer of the blood which develops in the bone marrow.

A

leukemia

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2
Q

most common childhood cancer

A

childhood leukemia

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3
Q

type of leukemia that develops and worsens quickly (over periods of days to weeks).

A

acute leukemia

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4
Q

type of leukemia that develops over a slower period of time (months), but it is more difficult to treat than acute leukemia, and is more common in adults than in children..

A

chronic leukemia

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5
Q

6 main types of leukemia that occur in children

A

• acute lymphoblastic leukemia
• acute myelogenous leukemia
• acute promyelocytic leukemia
• chronic myelogenous leukemia
• chronic lymphocytic leukemia
• juvenile myelomonocytic leukemia

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6
Q

the most common form of childhood leukemia, which makes up 75-80% of childhood leukemia diagnoses.

A

acute lymphoblastic leukemia

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7
Q

a form of leukemia that affects the lymphocytes, a type of White Blood Cells (WBC) which fights infection. when a patient has ALL, the bone marrow makes too many immature WBC and they do not mature correctly. these WBC also do not work correctly to fight infection. the WBC over-produce, crowding the other blood cells in the bone marrow.

A

acute lymphoblastic leukemia

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8
Q

accounts for most of the remaining cases of leukemia in children, comprising about 20% of childhood cancer.

A

acute myelogenous leukemia

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9
Q

a cancer of the blood in which too many myeloblasts (immature WBC) are produced in the bone marrow. the marrow continues to produce abnormal cells that crowd the other blood cells and do not work properly to fight infection.

A

acute myelogenous leukemia

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10
Q

what gets affected in ALL?

A

lymphocytes

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11
Q

what gets affected in AML?

A

myeloblasts

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12
Q

a specific type of AML.

A

acute promyelocytic leukemia

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13
Q

in this leukemia, promyelocytes are produced and build up in the bone marrow.

A

acute promyelocytic leukemia

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14
Q

what gets affected in APL?

A

promyelocytes

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15
Q

in acute promyelocytic leukemia, a specific chromosome translocation where genes on _ changes places with _. this genetic change prevents the promyelocytes from maturing properly.

A

in acute promyelocytic leukemia, a specific chromosome translocation where genes on chromosome 15 changes places with chromosome 17. this genetic change prevents the promyelocytes from maturing properly.

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16
Q

a chronic leukemia that develops slowly, over months to years.

A

chronic myelogenous leukemia

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17
Q

rare in children, but does occur.

A

chronic myelogenous leukemia

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18
Q

a chromosome translocation occurs in pt with chronic myelogenous leukemia where part of the _ breaks off and attaches itself to _, facilitating exchange of genetic material between these. the rearrangement of the chromosomes changes the positions and functions of certain genes, which causes uncontrolled cell growth.

A

a chromosome translocation occurs in pt with chronic myelogenous leukemia where part of the chromosome 9 breaks off and attaches itself to chromosome 22, facilitating exchange of genetic material between these. the rearrangement of the chromosomes changes the positions and functions of certain genes, which causes uncontrolled cell growth.

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19
Q

another form of chronic leukemia, but is extremely rare in children.

A

chronic lymphocytic leukemia

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20
Q

a form of leukemia in which myelomonocytic cells are overproduced.

A

juvenile myelomonocytic leukemia

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21
Q

what is affected in JMML?

A

myelomonocytic cells

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22
Q

it is sometimes considered a myeloproliferative neoplasm.

A

juvenile myelomonocytic leukemia

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23
Q

JMML is considered as _.

A

myeloproliferative neoplasm

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24
Q

JMML is rare and most commonly occurs in children _.

A

under the age of four

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25
in JMML, the myelomonocytic cells produced by the bone marrow and invade the _, _, and _.
• spleen • lungs • intestines
26
signs and symptoms of leukemia (11): CHILD CANCER
• continuous weight loss • headache, persistent nausea and vomiting with or without seizure • increased swelling or persistent pain in bones, joints, back or legs • lump or mass (swollen lymph nodes) — abdomen, neck, chest, armpits • development of rash, bleeding, bruises (including petechiae) • constant/recurrent infections • abdominal pain or fullness, which may cause shortness of breath or loss of appetite • noticeable paleness of skin • constant tiredness • eye or vision changes • recurrent or persistent fever
27
diagnosis for leukemia (5): BIBCS
• bone marrow aspiration and biopsy • immunophenotyping and cytogenic analysis • blood tests • complete blood count • spinal tap
28
treatment for leukemia (5): CSRTI
• chemotherapy • stem cell transplant • radiation therapy • targeted therapy • immunotherapy
29
treatment for leukemia: a treatment that uses chemicals to interfere with the cancer cells ability to grow and reproduce. it can be used alone or in combination with other therapies.it can be given either as a pill to swallow orally, an injection into the fat or muscle, and through an IV directly into the bloodstream or directly into the spinal column.
chemotherapy
30
treatment for leukemia: a process in which the blood-forming cells that are abnormal (like leukemia cells) or that were destroyed by chemotherapy are replaced with healthy new blood-forming cells.
stem cell transplant
31
treatment for leukemia that can help the human body produce more healthy WBC, RBC, or platelets.
stem cell transplant
32
treatment for leukemia that reduces the risk of life-threatening conditions such as anemia or hemorrhage.
stem cell transplant
33
stem cell transplants can be done by obtaining cells from the (2)
• bone marrow • blood or umbilical cord blood
34
stem cell transplants can use the cells from one’s cells, called _.
autologous stem cell transplant
35
stem cell transplant can use cells from another person, also known as _.
allogenic stem cell transplant
36
the type of stem cell transplants can used in childhood leukemia is typically _.
allogenic
37
two types of stem cell transplants.
• autologous • allogenic
38
treatment for leukemia that uses various types of radiation to kill cancer cells.
radiation therapy
39
treatment for leukemia that uses medication to specifically kill the cancer cells. the medication is able to leave healthy normal cells alone while it targets the cancer.
targeted therapy
40
treatment for leukemia that uses the child’s own immune system to fight the cancer. this therapy is currently in clinical trials.
immunotherapy
41
a cancerous tumor in the cells of the kidney. with the right treatment, it is highly treatable.
wilm’s tumor / nephroblastoma
42
signs and symptoms of wilm’s tumor (11): AAA FHNCLSH Funny Hippos Never Cook Leftover Spicy Hamburgers
• abdominal mass • abdominal swelling • abdominal pain • fever • hematuria (blood in the urine) • nausea and vomiting • constipation • loss of appetite • shortness of breath • high blood pressure
43
risk factors for wilm’s tumors (4): AFAH WDB
• african-american race • family history certain abnormalities: - aniridia - hemihypertrophy occurs as part of rare syndromes: - WAGR syndrome - denys-drash syndrome - beckwith-wiedemann syndrome
44
in the united states, _ children have a slightly higher risk of developing wilms' tumor than children of other races. _ children appear to have a lower risk than children of other races.
in the united states, **african-american** children have a slightly higher risk of developing wilms' tumor than children of other races. **asian-american** children appear to have a lower risk than children of other races.
45
wilm’s tumor occurs more frequently in children with certain abnormalities or syndromes present at birth including (2): AH
• aniridia • hemihypertrophy
46
risk factor of wilm’s tumor where the iris (the colored portion of the eye) forms only partially or not at all.
aniridia
47
risk factor of wilm’s tumor that means one side of the body or a part of the body is noticeable larger than the other.
hemihypertrophy
48
risk factor of wilm’s tumor that can occur as part of rare syndromes such as WAGR syndrome, which includes (4): WAGI
• wilm’s tumor • aniridia • genital and urinary system abnormalities • intellectual disabilities
49
risk factor of wilm’s tumor that can occur as part of rare syndromes such as denys-drash syndrome, which includes (3): WKM
• wilm’s tumor • kidney disease • male pseudohermaphroditism
50
a term describing a boy born with testicles but may exhibit female characteristics.
male pseudohermaphroditism
51
risk factor of wilm’s tumor that can occur as part of rare syndromes such as beckwith-wiedemann syndrome, which includes (5): MAMEE
• macrosomia • abdominal organs that jut out into the base of the umbilical cord • macroglossia • enlarged internal organs • ear abnormalities
52
risk factor of wilm’s tumor: children with this syndrome tend to be significantly larger than average (macrosomia). other signs may include abdominal organs that jut out into the base of the umbilical cord, a large tongue (macroglossia), enlarged internal organs and ear abnormalities.
beckwith-wiedemann syndrome
53
a chronic disease involving the airways in the lungs. these airways, or bronchial tubes, allow air to come in and out of the lungs.
asthma
54
the lungs and airways become easily inflamed when exposed to certain triggers, such as inhaling airborne pollen or catching a cold or another respiratory infection.
childhood asthma
55
in childhood asthma, the lungs and airways become easily inflamed when exposed to certain triggers, such as (3): RIC.
• respiratory infection • inhaling airborne pollen • catching cold
56
chronic runny or stuffy nose
rhinitis
57
inflamed sinuses
sinusitis
58
risk factors of asthma (9): EPAL OR HBB
• smoke exposure (exposure to tobacco smoke) • allergic history (skin reactions, food allergies, hay fever (allergic rhinitis) • lineage (family history of asthma, allergic rhinitis, hives, eczema) • town life (living in an urban area with increased exposure to air pollution) • obesity • respiratory conditions (rhinitis, sinusitis, pneumonia) • heartburn (gastroesophageal reflux disease GERD) • male • black
59
signs and symptoms of asthma (5): FASCC
• frequent, intermittent coughing • a whistling or wheezing sound when exhaling • SOB • chest congestion or tightness • chest pain other symptoms of childhood asthma includes: • trouble sleeping by SOB, coughing, wheezing • bouts of coughing or wheezing that get worse with a respiratory infection, such as cold or the flu • delayed recovery or bronchitis after a respiratory infection • trouble breathing may limit play or exercise • fatigue, which may be caused by poor sleep
60
diagnosis for asthma (5): PHATA
• presence of allergies or family history of asthma and allergies • history of recurrent or persistent wheeze • absence of physical findings that suggest an alternative diagnosis • tests that support the diagnosis (spirometry) • a consistent clinical response to an inhaled bronchodilator or preventer
61
it can be difficult to diagnose asthma in children aged 0-5 because (3):
• episodic respiratory symptoms such as wheezing and cough are very common in children, particularly in children aged under 3 years • objective lung function testing by spirometry is usually not feasible in this age group • a high proportion of child who respond to bronchodilator treatment do not go on to have asthma in later childhood (e.g. by primary school age)
62
types of asthma (2)
• allergic asthma • nocturnal asthma
63
allergic asthma may be caused by (6): DAF LMP
• dust mite • animal • food (food allergies rarely make asthma worse) • latex • mold • pollen
64
worsening of asthma at night is very common.
nocturnal asthma
65
causes of nocturnal asthma (6): DECGAD
• delayed allergic response, which may occur 3-8 hours after exposure • exposure to allergens in the bedroom, particularly dust mites • chronic sinus problems and/or post-nasal drip • gastroesophageal reflux • airway cooling from a drop in body temperature • decreased effect of medications during early morning hours • sleep apnea - brief, repetitive cessation of breathing during sleep caused by an upper airway obstruction
66
an infection in any part of the urinary system – kidneys, ureters, bladder and urethra. most infections involve the lower urinary tract – the bladder and the urethra.
urinary tract infection
67
organs part of the urinary system (4): KUBU
• kidneys • ureters • bladder • urethra
68
the lower urinary tract involves (2): BU
• bladder • urethra
69
_ are at greater risk of developing a UTI than _.
**women** are at greater risk of developing a UTI than **men**.
70
types of UTI (3): KUB
• kidney / acute pyelonephritis • urethra / urethritis • bladder / cystitis
71
general symptoms of UTI (3): PUS
• passing frequent, small amounts of urine • urine that appears cloudy • strong-smelling urine
72
signs and symptoms of acute pyelonephritis (4): HUNS
• high fever • upper back and flank pain • nausea and vomiting • shaking and chills
73
signs and symptoms of cystitis (4): PLFB
• pelvic pressure • lower abdomen discomfort • frequent painful urination • blood in urine
74
signs and symptoms of urethritis (1)
• burning sensation with urine discharge
75
risk factors of UTI (6): FUBS CR
• female - anatomy - sexual activity - birth control (diaphragm) - menopause • urinary tract abnormalities • blockages in the urinary tract - kidney stones/enlarged prostate • suppressed immune system - diabetes • catheter use • recent urinary procedure
76
diagnosis for UTI (6):
• voiding cystourethrogram (VCUG) • urinalysis • nuclear scan • computed tomography (CT-scan) • ultrasound • magnetic resonance imaging (MRI)
77
diagnosis for UTI that places fluid into the bladder through a tube to show any problems in the urethra or bladder when the child urinates.
voiding cystourethrogram
78
diagnosis for UTI that uses liquid that contains a small amount of radioactive material to see how well the kidneys work.
nuclear scan