Module Seven: Pediatric Oncology, MSK, Neuromuscular, Endocrine, Mental Health, and Emergencies

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150 flashcards covering pediatric oncological, musculoskeletal, neuromuscular, endocrine, mental health, and emergency topics from Module 7.

Last updated 8:06 PM on 7/15/26
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152 Terms

1
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What is a fundamental principle regarding pediatric patients?

Pediatric patients are not little adults.

2
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What aspect should be incorporated into all aspects of pediatric care?

Play

3
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What are three types of pediatric organ neoplasms?

Wilms Tumor, Neuroblastoma, and Brain Organ Neoplasms.

4
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What are two types of pediatric blood neoplasms?

Acute Lymphoblastic Leukemia and Acute Myeloid Leukemia.

5
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What are three types of pediatric bone and soft tissue cancers?

Rhabdomyosarcoma, Osteosarcoma, and Ewing’s Sarcoma.

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What is the most common childhood cancer of the kidney?

Wilms Tumor

7
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What percentage of Wilms Tumor cases occur in children under the age of 55?

75%75\%

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What percentage of Wilms Tumor cases are considered familial?

5%5\%

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What is a key expected finding of a Wilms Tumor regarding its location?

A painless abdominal mass that does NOT cross the midline.

10
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What abdominal assessment action is strictly prohibited when a Wilms Tumor is suspected?

Palpating the abdomen, as it could cause the spread of tumor cells.

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What are the primary treatments for Wilms Tumor?

Surgery and Chemotherapy.

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What are common findings for Wilms Tumor besides an abdominal mass?

Weight loss, enlarged liver, spleen, and anemia.

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What is the most common cancer of infancy?

Neuroblastoma (affecting children <22mos<22\,mos).

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From which type of cells does a Neuroblastoma arise?

Fetal cells that form the adrenal medulla and the sympathetic nervous system (SNS).

15
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What is the primary site for a Neuroblastoma?

The abdomen

16
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What percentage of children with Neuroblastoma have metastasis prior to diagnosis?

70%70\%

17
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How does an abdominal mass in Neuroblastoma differ from a Wilms Tumor during physical assessment?

The firm, painless abdominal mass in Neuroblastoma CROSSES the midline.

18
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What urinary symptoms might a patient with Neuroblastoma exhibit?

Urinary frequency or retention due to bladder compression by the tumor.

19
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What are common signs and symptoms of Neuroblastoma metastasis?

Periorbital edema, supraorbital ecchymosis, exophthalmos, hepatomegaly, respiratory obstruction, fatigue, weight loss, and anorexia.

20
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What are the primary treatments for Neuroblastoma?

Surgery, radiation, and chemotherapy.

21
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What unusual phenomenon can sometimes occur with a Neuroblastoma tumor?

It may regress spontaneously.

22
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What accounts for 25%25\% of childhood cancers, making it the most common organ tumor in children?

Brain organ neoplasms

23
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In which parts of the brain do most pediatric brain tumors occur?

The brainstem or cerebellum.

24
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From which type of cells do pediatric brain tumors most commonly originate?

Glial cells (Glial tumors).

25
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What is the second most common cell origin for pediatric brain tumors?

Astrocytoma

26
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What is a classic expected finding for a child with a brain tumor upon awakening?

Headache

27
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What determines the expected findings for a brain tumor?

The location and size of the tumor.

28
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From which tissue does Rhabdomyosarcoma arise?

Muscle tissue

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What determines the clinical presentation of Rhabdomyosarcoma?

The location of the tumor and the resulting dysfunction or obstruction of the affected organ.

30
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What are the three treatment modalities for Rhabdomyosarcoma?

Surgery, Radiation, and Chemotherapy.

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What is the most common bone cancer in children?

Osteosarcoma

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In what age group is Osteosarcoma most frequently diagnosed?

Children over 1010 years old.

33
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Where do more than 50%50\% of Osteosarcoma cases occur?

The femur (specifically the metaphysis growth plate).

34
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What type of pain is characteristic of Osteosarcoma and how is it often relieved?

Localized pain often relieved with flexion.

35
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What are two surgical treatment options for Osteosarcoma?

Limb salvage or amputation.

36
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How does Ewing’s Sarcoma differ in location from Osteosarcoma?

Ewing’s Sarcoma presents in the diaphysis (shaft) of the bone, whereas Osteosarcoma is usually in the metaphysis.

37
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Which is rarer: Ewing’s Sarcoma or Osteosarcoma?

Ewing’s Sarcoma

38
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What is Hodgkin Disease (HD) Lymphoma?

A malignancy of the lymph system.

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In what age range is Hodgkin Disease most likely to occur?

Between 1515 and 1919 years of age.

40
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Where are painless enlarged nodes commonly found in Hodgkin Disease?

Subclavicular or cervical nodes.

41
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What are some constitutional symptoms of Lymphoma?

Nonproductive cough, abdominal pain, low-grade fever, anorexia, pruritus, night sweats, and weight loss.

42
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What is Acute Lymphoblastic Leukemia (ALL)?

A malignancy of the bone marrow characterized by an overproduction of immature white blood cells.

43
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What is the common age range for a child diagnosed with ALL?

22 to 66 years old.

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Which specific group is commonly associated with ALL?

White males with Down Syndrome.

45
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What are typical expected findings for ALL related to bone marrow failure?

Low-grade unresolving fever, pallor, bruising, petechiae, lethargy, joint pain, nausea/vomiting, weakness, and anorexia.

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What are the treatment options for ALL?

IV/Intrathecal Chemotherapy, Corticosteroids, Bone marrow transplant, and Hematopoietic stem cell transplant.

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Why is a port or central line placed for chemotherapy?

To deliver agent-specific chemotherapy safely into the bloodstream.

48
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How does chemotherapy affect cells throughout the body?

It affects rapidly growing cells.

49
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What are two major side effects of chemotherapy mentioned in the notes?

Immunosuppression and Pancytopenia.

50
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How is radiation therapy dosage typically delivered?

In divided treatments over several weeks.

51
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Why are tattoo marks used in radiation therapy?

To ensure the accurate delivery of the radiation beam.

52
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What are the localized side effects of radiation?

Lymphedema and scar tissue.

53
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What are four types of musculoskeletal disorders categorized as congenital?

Osteogenesis Imperfecta, Clubfoot, Hip Dysplasia, and Scoliosis.

54
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What are the risk factors for pediatric fractures?

Obesity, poor nutrition, and developmental characteristics.

55
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What are the clinical findings of a fracture?

Pain, crepitus, deformity, edema, ecchymosis, and decreased use of the affected area.

56
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Which type of fracture is also known as a 'compound' fracture?

Open fracture

57
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What is a greenstick fracture?

An incomplete fracture where one side of the bone is broken and the other is bent.

58
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What are the '5 Ps' included in neurovascular checks?

Pain, Pulse, Pallor, Paresthesia, and Paralysis (implied by the transcript's mention of sensation and pulses).

59
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What are the four types of traction listed?

Skin Traction, Skeletal Traction, Halo Traction, and Manual Traction.

60
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What are five potential complications of pediatric fractures?

Compartment Syndrome, Volkmann Contracture, Renal Calculi, Embolism, and Osteomyelitis.

61
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What is the clinical name for Clubfoot?

Talipes Equinovarus

62
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What is the physical presentation of Clubfoot?

The heel tilts down and the toes turn in.

63
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What is the progression of therapeutic interventions for Clubfoot?

Serial casting, followed by surgical correction of the tightened tendon, and then a brace for 22 to 44 years.

64
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What happens to the head of the femur in Legg-Calve Perthes Disease?

The blood supply is significantly reduced temporarily.

65
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What is a major potential complication of Legg-Calve Perthes Disease?

Avascular necrosis of the hip joint.

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How does Legg-Calve Perthes disease initially present?

An initial limp without pain.

67
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Which medication class is being tested for Legg-Calve Perthes Disease?

Bisphosphonates

68
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What birth presentation is commonly associated with Developmental Dysplasia of the Hip (DDH)?

Breech birth

69
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What physical signs indicate DDH?

Limited abduction, difference in leg length, asymmetric gluteal folds, and an audible click.

70
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What is the function of a Pavlik Harness?

It prevents hip flexion and adduction.

71
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How long is Pavlik Harness therapy typically used?

1212 weeks.

72
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What are the guidelines for Pavlik Harness wear time?

2323 hours per day.

73
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How often should the Pavlik Harness straps be readjusted by a provider?

Weekly

74
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What clothing should a child wear under a Pavlik Harness to protect the skin?

An undershirt and knee socks.

75
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What should be avoided on the skin of a child in a Pavlik Harness?

Lotions and powders.

76
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What is the goal of surgical reduction and Spica cast placement in DDH?

To place the femoral head into the acetabulum and maintain that position.

77
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What is a hallmark finding of Osteogenesis Imperfecta regarding the eyes?

Blue Sclera

78
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What are the findings associated with Osteogenesis Imperfecta?

Multiple bone fractures, blue sclera, early hearing loss, and small, discolored teeth.

79
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How is Osteogenesis Imperfecta diagnosed?

Bone biopsy

80
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What specific nursing action is required for blood pressure measurement in children with Osteogenesis Imperfecta?

Manual blood pressures (to prevent potential fractures from automatic cuffs).

81
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What is the definition of Scoliosis?

Abnormal lateral and rotational curvature of the spine.

82
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At what degree of curvature is a brace indicated for Scoliosis?

Between 2525 and 4545 degrees.

83
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At what degree of curvature is spinal fusion surgery indicated for Scoliosis?

Greater than 5050 degrees.

84
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What physical signs suggest Scoliosis during an exam?

Clothes hang unevenly, uneven shoulders, uneven shoulder blades (rib hump), and hips at different heights.

85
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What are the three categories of Cerebral Palsy (CP)?

Spastic, Dyskinetic, and Ataxic.

86
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What is the most common type of Cerebral Palsy?

Spastic CP

87
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How are muscles described in Spastic Cerebral Palsy?

Stiff and rigid.

88
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What is the difference between diplegia and quadriplegia in CP?

Diplegia affects two limbs; quadriplegia affects all four limbs.

89
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What characterizes Ataxic Cerebral Palsy?

It affects muscle movement and coordination.

90
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What are three prenatal risk factors for Cerebral Palsy?

Brain anomalies, maternal chorioamnionitis, and multiple births.

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What are three perinatal risk factors for Cerebral Palsy?

Low birth weight, premature birth, and asphyxia.

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What is a postnatal risk factor involving head trauma for CP?

Shaken baby syndrome

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What medications are used to manage Cerebral Palsy?

Baclofen, Diazepam, Botulinum Toxin A, and Valproic Acid/Carbamazepine.

94
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What causes Spina Bifida?

The neural tube fails to close.

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What nutritional deficiency is a major risk factor for Spina Bifida?

Folic Acid Deficiency

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What level of paralysis can occur with Spina Bifida?

Complete or incomplete paralysis below the level of the lesion.

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What are two common comorbidities of Spina Bifida?

Hydrocephalus and Chiari II malformation.

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What is a common allergy associated with children who have Spina Bifida?

Latex allergy

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What is Juvenile Idiopathic Arthritis?

An autoimmune disorder that targets the synovial joints.

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How does inactivity affect a child with Juvenile Idiopathic Arthritis?

Inactivity increases stiffness.