Final FINAL-Table 1 Flashcards

1
Q

What are 2 important diagnostic tests for anemia?

A

Reticulocyte count, Hgb

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2
Q

What does a high retic count with high bilirubin indicate?

A

Bone marrow is working!

Most likely d/t destruction or loss of RBCs (hemolytic)

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3
Q

(acute/chronic) anemias are well tolerated in children

A

Chronic

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4
Q

Anemic disorder characterized by bone marrow aplasia

A

Diamond Blackfan anemia

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5
Q

Diamond Blackfan anemia responds to ____treatment, and is cured by ____

A

Steroids

Bone Marrow Transplant (BMT)

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6
Q

3 yo pt with cc of lethargy x3 days. Pt is pale, jaundiced, w/ palpable spleen. CBC shows low Hb, High retic count, and increased LDH. What do you suspect?

A

Hemolytic anemia

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7
Q

In the case above, which findings were indicative of hemolysis?

A

Jaundice

Splenomegaly

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8
Q

___ hemolysis can be due to Hereditary spherocytosis, G6PD deficiency, and hemoglobinopaties

A

Intrinsic

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9
Q

____ hemolysis can be due to AIHA, DIC, or IV hemolysis

A

Extrinsic

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10
Q

What common virus can produce a low retic count and red cell aplasia?

A

Parvovirus B19

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11
Q

Your patient presents with anemia + Petechiae. You suspect:

A

Leukemia or HUS

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12
Q

Which lab would show you the presence of spherocytes?

A

Peripheral blood smear

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13
Q

When does Fe deficiency anemia first appear?

A

After the first 4-5 mo of life

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14
Q

What should you check if a pt presents with neutropenia or thrombocytopenia?

A

Bone marrow fxn

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15
Q

Name the iron studies for Fe Deficient anemia

A
Serum ferritin (low)
Serum iron (low)
Total Fe binding capacity (inc)
Transferrin saturation  (low)
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16
Q

Children who drink cow’s milk are at risk for developing__ deficiency

A

Iron

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17
Q

Kids who drink goat’s milk are at risk for developing__ deficiency

A

Folate

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18
Q

Age range for kids with Diamond Black-fan anemia

A

Birth-1 year

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19
Q

B-12 deficiency is a common finding in this GI disorder

A

Crohn’s

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20
Q

Smooth beefy red tongue may indicate

A

B-12 deficiency

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21
Q

Fanconi and Diamond-Blackfan anemias are ____ forms of normocytic anemia

A

Congenital

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22
Q

Age range for Fanconi anemia

A

2-10 years

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23
Q

What is TAR and what condition is it found in?

A

Thrombocytopenia with absent radius. Fanconi anemia

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24
Q

____anemias are characterized by Anemia, Jaundice, Splenomegaly

A

Hemolytic

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25
Q

Longstanding spherocytosis and sickle cell disease can cause _____

A

Gallstones

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26
Q

What is the most common inherited enzyme defect?

A
G6PD deficiency 
(2nd is Pyruvate Kinase Deficiency)
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27
Q

G6PD manifests as _____ cells on peripheral blood smear

A

Blister cells

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28
Q

G6PD commonly presents with this finding

A

Hyperbilirubinemia

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29
Q

B12/folate deficiency presents as _____ RBCs on peripheral blood smear

A

Macrocytic

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30
Q

This hemoglobinopathy is found in carriers only

A

Thalassemia trait

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31
Q

Hemophilias, vitamin K deficiency, and DIC are all disorders of _____

A

Coagulation

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32
Q

Intrinsic clotting pathway is measured by a

A

PTT

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33
Q

Extrinsic pathway measured with a

A

PT

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34
Q

A pt who is bleeding into their joints should be worked up for

A

Hemophilia

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35
Q

More common mechanism of thrombocytopenia

A

Increased consumption/ breakdown of RBCs

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36
Q

Kasabach-merritt syndrome is associated with sepsis and ____

A

Thrombocytopenia

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37
Q

DIC, Liver disease, and HSP are all _____ types of bleeding disorder

A

Acquired

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38
Q

____ is a type of thrombocytopenia associated with severe illness or shock

A

DIC

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39
Q

Most common bleeding disorder of CHILDhood

A

ITP (idiopathic thrombocytopenia purpura)

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40
Q

ITP usually shows up after____

A

A viral infection

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41
Q

Treatment for ITP includes

A
Steroids
IV Ig (in severe cases)
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42
Q

Factor ___- and Von Willebrand work together

A

VIII

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43
Q

Hemophilia B, aka _____, is x-linked and are assoc w/ factor IX deficiency

A

Christmas Disease

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44
Q

_____ is the most common INHERITED bleeding disorder among Caucasians (though it can be acquired…)

A

Von Willebrand disease

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45
Q

VW disease can be treated with _________, which releases vWF from endothelial stores

A

Desmopressin

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46
Q

FFP contains____

A

All coag factors

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47
Q

If you have abnormal PT/PTT, you would give

A

FFP

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48
Q

If you have normal PT/PTT values, you would give

A

Cryoprecipitate

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49
Q

In ___ syndrome, bilirubin is elevated in times of stress, causing jaundice

A

Gilbert’s Syndrome

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50
Q

Most common death by disease in children

A

Cancer

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51
Q

___ has inc. incidence of Trisomy 21, NF type 1, and fanconi’s anemia

A

ALL

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52
Q

First labs for a CA workup

A

CBC w/ diff

Peripheral blood smear

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53
Q

ALL occurs most commonly in kids aged _____-______

A

2-10 (peak at 4)

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54
Q

Most common CA treatment for kids

A

Chemo

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55
Q

Philadelphia chromosome is associated with ____

A

CML (Chronic Myelogenous Leukemia)

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56
Q

Pt presents with firm, non-tender lymph node and hx cough. What do you order?

A

CBC
CXR
Lymph biopsy

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57
Q

What are you looking for on x-ray for a kid with suspected ALL?

A

Mediastinal widening/ mass

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58
Q

This type of lymphoma peaks in adolescence and again after age 50

A

Hodgkins Disease

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59
Q

Biopsy for suspected hodgkin’s disease would show this type of cell:

A

Reed-Sternberg cells

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60
Q

Hodgkin’s is characterized by ______ adenopathy

A

Painless cervical

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61
Q

Mediastinal lymphadenopathy or mass can present with: __ or ___

A

Cough, dyspnea

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62
Q

Most common type of solid tumor in kids:

A

Brain tumor

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63
Q

Classic triad of brain tumors

A

Papilledema
Morning headache
Vomiting (w/o nausea)

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64
Q

Most common tumor of childhood

A

Astrocytoma

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65
Q

Young children most often get ______ brain tumors

A

Infratentorial

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66
Q

Older children more often get ____ brain tumors (which are WORSE)

A

Supratentorial

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67
Q

Abdominal mass that crosses midline

A

Neuroblastoma

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68
Q

Painless abdominal mass that does NOT cross the midline

A

Wilms Tumor (nephroblastoma)

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69
Q

Most common solid neoplasm OUTSIDE the CNS

A

Neuroblastoma

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70
Q

This type of tumor is common in Beckwith-Widemann syndrome

A

Wilms tumor

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71
Q

Most common sign of a retinoblastoma

A

White pupillary reflex

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72
Q

How do you diagnose retinoblastoma

A

MRI

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73
Q

Most common soft tissue sarcoma in childhood

A

Rhabdomyosarcoma

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74
Q

3 types of Rhabdomyosarcoma

A

Orbital, nasal, bladder

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75
Q

____ is a definitive test for osteosarcomas

A

Tissue biopsy

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76
Q

____ present with a painful, palpable mass and lytic lesions with calcifications on x-ray

A

Osteosarcoma

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77
Q

___ commonly presents with femur and pelvic pain, fever, and wt loss.

A

Ewing sarcoma

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78
Q

Most important diagnostic tools in ortho

A

PE and Radiographic imaging

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79
Q

Hip dysplasia (is/is not) a disease of dislocation

A

Is NOT

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80
Q

____ is the abnormal relationship between the prox femur & acetabulum

A

Hip Dysplasia

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81
Q

Hip dysplasia can be diagnosed using these techniques

A

Barlow’s and Ortolani’s

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82
Q

______ are indicative (not diagnostic) of hip dysplasia, occurring in up to 40% of cases

A

Asymmetric Skin folds

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83
Q

If diagnosed in the first 4-6 mo of life, hip dysplasia can be treated with __

A

Pavlik harness

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84
Q

You find a palpable mass in your patient’s neck, and note that their head is twisted to the side. X-ray reveals no cervical deformities. What is your ddx?

A

Torticollis

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85
Q

Children with this congenital connective tissue disorder can have subluxed ocular lenses, thoracic aortic aneurysms.

A

Marfan syndrome

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86
Q

This disorder is characterized by in-utero fractures and blue sclera

A

Osteogenesis imperfecta

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87
Q

_____ show promise for decreasing incidence of fractures in OI

A

Bisphosphonates

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88
Q

The most common form of short-limbed dwarfism:

A

Achondroplasia

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89
Q

Patients with achondroplasia have a greater risk for ___

A

Scoliosis

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90
Q

Your patient has a 20˚ scoliosis curvature. Your next step is:

A

No tx required

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91
Q

Name 4 types of congenital vertebrae abnormalities

A

Wedge vertebra
Hemivertibra
Congenital bar
Block vertebra

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92
Q

Most common cause of limping and hip pain for kids in the US:

A

Transient Synovitis

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93
Q

Most common organism implicated in septic arthritis of the hip

A

Staph aureus

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94
Q

Treatment course for septic arthritis

A

ABX then surgery if needed

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95
Q

Your 7 year old male patient presents with an atraumatic painless limp and decreased internal rotation. You suspect:

A

Legg-Calve-Perthes Dz

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96
Q

Treatment for Perths disease includes

A

Protecting the joint w/o limiting mobility

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97
Q

3 x-ray views for diagnosing Perths disease

A

AP, Lateral, Frog-leg

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98
Q

____ is an orthopedic emergency, characterized by pain in hip, medial knee, and anterior thigh.

A

SCFE

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99
Q

Radial head subluxation is also known as

A

Nursemaid’s Elbow

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100
Q

Typical posture associated with radial head subluxation

A

“my arm” posture

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101
Q

SCFE is most common in this age group

A

Adolescents 10-16

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102
Q

Genu ____ is normal between infancy and 2 years

A

Varum

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103
Q

Genu ____ is normal between 2-8 years

A

Valgum

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104
Q

___ is the abnormal growth of the medial aspect of the proximal tibial epiphysis, resulting in a progressive varus deformity

A

Blout’s

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105
Q

Most common cause of in-toeing in kids under the age of 2

A

Tibial torsion

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106
Q

The recommended treatment for W-sitters

A

Bicycle/skating

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107
Q

Patellofemoral Pain Syndrome presents with _______pain, worse with activity, stairs, prolonged sitting

A

Anterior knee pain

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108
Q

___ can cause microfractures to the tibial tuberosity bone overgrowth

A

Osgood-Schlatter Disease

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109
Q

_______ is a MSS problem of intrauterine positioning and will resolve spontaneously

A

Calcaneovalgus

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110
Q

What should you look for on physical exam if the patient also presents with metatarsus varus?

A

Check for hip dysplasia

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111
Q

Most ___ is caused by congenital hypoplastic tarsal bones (esp the Talus)

A

Talipes Equinovarus

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112
Q

Torus fractures are also known as

A

Buckle fracture

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113
Q

Torus fractures affect these bones

A

Radius/ulnar

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114
Q

___ is an oblique fracture of the distal tibia without a fibula fracture

A

Toddler’s Fracture

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115
Q

Salter Harris classification describes ______ fractures

A

Epiphyseal

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116
Q

A type _____ S-H fracture through a portion of the physis and epiphysis into the joint that may result in complication because of intra-articular component and because of disruption of the growing or hypertrophic zone of the physis.

A

Type III

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117
Q

A type ____ S-H fracture presents as a crush injury to the physis with a poor functional prognosis (aka the WORST)

A

Type V

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118
Q

This type of S-H fracture has joint involvement

A

Type III

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119
Q

Types _&__ are a closed reduction and are treated with a cast

A

Types I & II

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120
Q

Osteosarcomas most commonly occur in ______ bones

A

Long bones

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121
Q

Most common bone tumor in children (benign)

A

Osteochondroma

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122
Q

Most common malignant bone tumor in children

A

Osteosarcoma

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123
Q

____ can present like an osteomyelitis with fever and leukocytosis, but shows lytic lesions on x-ray

A

Ewing Sarcoma

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124
Q

Anterior thigh and knee pain may be presentations of a ___ problem

A

Hip

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125
Q

Joint pain can be an early presentation of ___-

A

Crohns Disease

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126
Q

____ is the inflammation at the insertion of a ligament to a bone

A

Enthesitis

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127
Q

Pleuritis, pericarditis, or peritonitis are all types of _____

A

Serositis

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128
Q

Most common chronic Rheumatic Disease of children is ___

A

JIA/JRA

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129
Q

Young girls with ____ JRA and a positive ANA are at highest risk of uveitis

A

Pauciarticualr

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130
Q

You order an ANA on your patient. It comes back positive. What should be on your differential?

A

Lupus

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131
Q

Most common site of pauciarticular arthritis

A

Knee

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132
Q

___ often presents with a cyclic fever, salmon pink macular rash, and HSM

A

Systemic Form of JRA

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133
Q

The 3 P’s of systemic JRA

A

Polyserositis
Pleuritis
Pericarditis

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134
Q

____ in kids usually affects males >10 yrs, and typically presents with a positive HLA-B27, elevated ESR, and CRP

A

Spondyloarthropathy

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135
Q

1st & 2nd line tx for JRA

A

1 – NSAIDs

2 – Methotrexate

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136
Q

First lab to order for suspected SLE

A

ANA

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137
Q

Mainstay treatment for SLE

A

Steroids

  • methylprednisolone/ prednisone
  • hydroxychloroquin
  • NSAIDs
138
Q

Leading cause of death from SLE

A

Renal disease (diffuse proliferative nephritis)

139
Q

Most common vasculitis in childhood

A

Henoch Schonelien Purpura

140
Q

___is a rare inflammatory disease of muscles and skin that presents w/ fatigue, malaise, progressive muscle weakness, w/ low grade fever & rash

A

Dermatomyositis

141
Q

Most likely cause of HA in kids

A

Migraine or tension HA

142
Q

Secondary gain is common in this type of headache

A

Chronic Tension Headache

143
Q

Migraines are usually (unilateral/bilateral)

A

Unilateral

144
Q

1st line treatment for migraines in kids

A

Ibuprofen/APAP

145
Q

Cluster headaches are best treated with ____

A

100% oxygen

146
Q

Define epilepsy:

A

2 or more unprovoked seizures

147
Q

___ epilepsy is a benign condition w/ unilateral focal seizures and speech abnormalities

A

Rolandic epilepsy

148
Q

Typical age range for febrile seizures

A

6mo – 6 yrs

149
Q

___ seizures are associated with GI or upper respiratory infections

A

Febrile seizures

150
Q

Most common type of seizure in childhood

A

Partial/focal (40-60%)

151
Q

Role of an EEG in diagnosing seizures

A

Adjunct test (hx is most important)

152
Q

The majority of febrile seizures are ______

A

Generalized

153
Q

Treatment for febrile seizures includes

A

Phenobarbital, Valproic Acid

Rectal Diazepam

154
Q

The majority of epileptic seizures are ______

A

Partial/focal

155
Q

Type of impairment of consciousness in simple focal seizures

A

NO impairment

156
Q

Type of impairment of consciousness in complex focal seizures

A

Impairment = staring

157
Q

Type of impaired consciousness in secondary generalized focal seizures

A

Generalized convusion

158
Q

____ = no impairment of consciousness

A

Simple

159
Q

____= impairment of consciousness (staring)

A

Complex

160
Q

____= simple or complex partial seizure that ends in a generalized convulsion

A

Secondary Generalized

161
Q

____ can be mistaken for colic, reflux, or startle

A

Infantile spasms

West Syndrome

162
Q

Infantile spasms are associated with _____, which presents with ash leaf spots on the skin

A

Tuberous Sclerosis

163
Q

Treatment for Status Epilepticus includes:

A

ABCs then IV benzos

Diazepam or lorazepam

164
Q

The AAP recommends ____ for obtaining LP

A

Low threshold

165
Q

The majority of febrile seizures are (simple/complex)

A

Simple

166
Q

Febrile seizures that are focal, prolonged, or multiple are:

A

Complex

167
Q

Treatment (if any) for febrile seizures

A

Rectal diazepam

168
Q

Sleep disorders, migraine variants, benign breath-holding spells, syncope, movement disorders, and pseudoseizures are all_______

A

Spells that mimic seizures

169
Q

An infant pt presents with lethargy and vomiting. Upon PE you find that his fontanelles are bulging. What is the cause?

A

Increased Intracranial Pressure

170
Q

Sign visible in the eyes of younger children that indicates ICP

A

“Setting sun sign”

171
Q

An obese teenage girl presents to your clinic with a complaint of HA, tinnitus, and loss of vision. You perform an MRI to exclude hydrocephalus and intracranial mass. What do you suspect?

A

Pseudotumor Cerebri

172
Q

Most common cause of stroke in children

A

Cyanotic heart disease

+sickle cell anemia, meningitis, hypercoagulable states

173
Q

Most common cause of concussion in kids

A

Falls

174
Q

Management for children with amnesia or who were unconscious

A

ER Evaluation

175
Q

HA, dizziness, forgetfulness, inability to concentrate, slowing of response time, mood swings, and irritability after a concussion is known as:

A

Post-concussive Syndrome

176
Q

Meningomyelocele are usually identified using this screening tool

A

Ultrasound (+ high AFP)

177
Q

Arnold Chiari types I and II are types of ______

A

NTDs

178
Q

Arnold Chiari III defect is also known as

A

Anencephaly

179
Q

Migrational disorder associated with severe delay and seizures, with a “smooth brain” on MRI

A

LIssencephaly

180
Q

The premature closure of sutures

A

Craniosynostosis

181
Q

You notice ash leaf spots on your patient. Which neurocutaneous disorder do you suspect?

A

Tuberous Sclerosis

182
Q

____ is an autosomal dominant disorder characterized by café au lait spots, axillary freckling, and learning disabilities

A

Neurofibromatosis

183
Q

Characterized by benign tumors in vital organs (brain, eyes, kidneys, heart, skin) and can often cause infantile spasms

A

Tuberous Sclerosis

184
Q

This neurocutaneous disease presents with a unilateral port wine stain over the upper face

A

Sturge-Weber syndrome

185
Q

Up to 90% of Sturge Weber patients have this vascular anomaly

A

Leptomeningeal Vascular Anomaly

186
Q

2 common causes of ataxia in children

A

Post-infectious

Drug intoxication

187
Q

A neuromuscular disorder of the Anterior Horn

progressive weakness, wasting of skeletal muscle resp failure

A

SMA (Spinal Muscular Atrophy)

188
Q

A neuromuscular disorder of the Peripheral Nerve

ascending symmetrical weakness, post-infectious

A

Guillian Barre

189
Q

A neuromuscular disorder of Neuromuscular Transmission

ptosis, loss of facial expression

A

Myasthenia Gravis

190
Q

A neuromuscular disorder of Muscle Tissue

X-linked, proximal muscle wasting, pseudohypertrophic calf

A

Muscular Dystrophy

191
Q

Pelvic weakness seen in Duchenne Muscular Dystrophy results in a positive _____ sign on physical exam

A

Gower Sign

192
Q

Most common type of cerebral palsy

A

Spastic

193
Q

5 types of cerebral palsy

A

Spastic, athetoid, rigidity, tremor, ataxic

194
Q

Most common nutritional disorder affecting children and adolescents in the developed world?

A

Obesity

195
Q

No other source of protein is needed in the 1st 6 mo of life except ___

A

Breastmilk

196
Q

Who needs more kcal/kg….a 2 year old or a 10 year old?

A

2 year old (102 vs 70)

197
Q

RDA for protein ranges for 2.2g/kg/day for 0-6 mo, to ____g/kg/day for adolescents

A

1 g

198
Q

Breast milk provides about ___% calories from fats

A

50%

199
Q

During the first year, weight increases ____% and brain size ____

A

200%, doubles

200
Q

The last measurement to change in a child with malnutrition is _____

A

Head circumference

201
Q

The American Academy of Pediatrics recommends human milk as the sole source of nutrition for______, with continued intake for the first year and as long as desired thereafter

A

the first 6 mo of life

202
Q

A new mom comes in and asks if she can breastfeed while on methadone treatment. What do you say?

A

YES!

203
Q

SIDS is more common in this type of household:

A

Smoking

204
Q

Is breastfeeding recommended in mothers infected with HIV?

A

No, unless water source for formula is unsafe

205
Q

How do you assess adequacy of milk intake in an infant?

A

rate of wt gain is most objective indicator of adequate intake

206
Q

Breast milk stools typically look ____

A

Seedy

207
Q

A well-hydrated infant voids ___-___ times per day

A

6-8

208
Q

Standard formulas contain ____cal/oz (same as breast milk)

A

20

209
Q

You should use special formulas (soy, lactose free) for infants with:

A

Malabsorption, gastroschesis,

210
Q

What kind of TERM infant might need extra calories

A

Heart disease

211
Q

What vitamin does breast milk lack?

A

Vitamin D (supplement 200IU/day)

212
Q

At what point do full term breast-fed babies need supplemental iron?

A

4-6 mo of age (1mg/kg/day)

213
Q

Formula fed infants should get Fe fortified formula for ______

A

1st year of life

214
Q

When can you start solid foods in infants?

A

6 mo

215
Q

What is the max amount of cow’s milk per day that is recommended?

A

Not >24 oz/day (over 1 yr old)

216
Q

At what point should bottle feeding be discontinued?

A

12-18 mo

217
Q

Most common form of malnutrition in children living in poverty?

A

Iron deficiency anemia

218
Q

Brain growth triples by age ___

A

6

219
Q

____ is a leading cause of death in children under 5 years of age

A

Protein-energy malnutrition

220
Q

Less than 5% of failure to thrive is due to ____ causes

A

Organic

221
Q

This type of adolescent may be especially vulnerable to IDA

A

Student athletes

222
Q

Best indicator that baby is getting enough calories

A

Growth rate in length, weight, and FOC

223
Q

11yo children who are overweight are more than ___x as likely to remain overweight at age 15 than 7yo children.

A

2 times

224
Q

SCFE, Pseudomotor Cerebri, DM Type II, HTN, and low self esteem are all consequences of ____

A

Childhood obesity

225
Q

Bacteria that causes cavities

A

Strep Mutans

226
Q
CRITICAL CARE
Bites/Stings
Hyperthermia/hypothermia
Burns
Shock
Respiratory Failure (status asthmaticus, ARDS)
A
NORMAL ABG VALUES
pH          7.35-7.45
CO2       35 – 45
O2          70 –100 
O2 sat    93-98 % 
HCO3     22 – 26
227
Q

3 important differences in the pediatric patient

A
  • Greater body surface area
  • Internal organs are more anterior, protected by less fat
  • Airway structural differences
228
Q

A child’s BP may be maintained with up to _____% acute blood loss

A

30%

229
Q

1st step in assessing the seriously ill child:

A

ABCDE’s

Rapid clinical assessment

230
Q

What does the term “exposure” refer to?

A

Hypo/hyperthermia and also

Exposing the patient to assess for injuries

231
Q

Dehydration d/t gastroenteritis is an example of something that can cause _______ shock in a child

A

Hypovolemic

232
Q

Epiglottitis is an (upper/lower) airway disorder leading to resp distress

A

Upper

233
Q

_____ presents as the main compensatory mechanism for blood loss

A

Tachycardia

234
Q

A goal of resuscitation is to identify and restore abnormalities of __ and __

A

Oxygenation, Perfusion

235
Q

Most children with shock have ______causes

A

Non-cardiac

236
Q

____ is most common cause of hypovolemic shock in kids

A

Dehydration

237
Q

Kid showing up in 1st week of life in shock…you suspect a ___ cause

A

Sepsis, Cardiac, Or metabolic

238
Q

Hypoxic injury to the ___may cause seizures, cerebral edema, infarction.

A

Brain

239
Q

Hypoxic injury to the ___may cause ATN, ARF

A

Kidney

240
Q

____ is the most common cause of unplanned hospitalization in kidd 3-12yr

A

Asthma

241
Q

____ is due to severe bronchospasm, excessive mucus secretions, or inflammation/edema of airways, causing airway obstruction that may progress to respiratory failure

A

Status Asthmaticus

242
Q

Labs to order for suspected status Asthmaticus

A

O2sat, ABG, CXR

243
Q

Therapy for Status Asthmaticus

A

Humidified O2
B2 agonist (nebulized or bolus)
IV corticosteroids

244
Q

___ is the most common precipitant of ARDS

A

Infection

245
Q

Appropriate labs to order for your peds patient with ARDS

A

ABGs, daily CXR, CBC (infection surveillance)

246
Q

Loss of acid occurs with ____/_____

A

Vomiting/ NG suctioning

247
Q

Bicarb loss occurs with ____

A

Diarrhea

248
Q

Treatment of DKA includes

A

NS
Insulin, then D5
Na given via NS
*NO bicarb given!

249
Q

Airway obstruction, pneumonia, ARDS, PE, trauma, and respiratory depression can all lead to_____

A

Respiratory Acidosis

250
Q

H+ loss and bicarb gain can lead to____

A

Metabolic acidosis

251
Q

Anxiety, pain, altitude, excessive ventilation, PE, asthma, edema, or salicylate overdose can lead to ____

A

Respiratory Alkalosis

252
Q

Lactic acidosis, ketoacidosis, and exogenous acid consumption are all types of metabolic acidosis with a ______ anion gap

A

Increased

253
Q

Septic, anaphylactic, and spinal shock are all ____ types of shock

A

Distributive

254
Q

Type of shock where organ perfusion is maintained

A

Compensated

255
Q

Most common cause of shock in children

A

Hypovolemic shock

256
Q

This syndrome occurs in response to distributive shock, with fever, tachycardia, tachypnea, and abnormal WBC counts

A

SIRS (systemic inflammatory response syndrome)

257
Q

Gram (+ /- ) organisms use endotoxins which cause release of cytokines which can lead to septic shock

A

Gram Negative

258
Q

Gram (+ /- ) organisms use pyrotoxic superantigens, which cause massive lymphocyte activation and release of T-cell cytokines, leading to cellular injury, organ failure, and shock

A

Gram Positive

259
Q

Which are more painful, 2nd or 3rd degree burns?

A

2nd degree

260
Q

Burns > ____cm need grafting

A

1 cm

261
Q

___ is a life threatening failure of thermoregulation, characterized by high fever, CNS dysfunction, and incoherence

A

Heat Stroke

262
Q

___ in children is defined as core body temp

A

Hypothermia

263
Q

Most common cause of burns in children

A

Scalding

264
Q

A 5 y/o presents with a deep, white and dry burn on his arm. The skin blanches when you touch it. What degree burn is this and how long should it take to heal?

A

Partial thickness 2nd Degree

Could take a month or more

265
Q

What types of findings on PE would make you suspect an inhalation injury?

A

Facial burns, singed hair, carbonaceous sputum

266
Q

Labs/vitals to order/monitor for a burn patient

A

Urine output, CBC, electrolytes, renal function, urinalysis, tetanus prophylaxis

267
Q

What is the time limit for using activated charcoal for poison tx?

A

w/in 1 hour

268
Q

Most common poisoning in kiddos

A

Acetaminophen

269
Q

Treatment for carbon monoxide poisoning w/ cerebral edema

A

100% O2

270
Q

Your 4 year old patient comes in with a bite on his hand after sticking it into a hole in the woods. You don’t know what bit him, but you should do this for all bites.

A

Irrigation

271
Q
  1. What congenital orthopedic/skeletal problem is characterized by blue sclera?
A

Osteogenesis imperfect

(also see broken bones pre and post natal – if you see it in US, it is almost pathopneumonic

272
Q
  1. What meds are used to treat OI?
A

bisphosphonate

273
Q
  1. Most common form of short-limb dwarfism?
A

Achondroplasia

274
Q
  1. A patient is diagnosed with achondroplasia. What long-term orthopedic problem are they at increased risk for?
A

Scoliosis

275
Q
  1. A mother brings her 6 y/o son in with complaints that he has been limping. He denies any trauma, and says it doesn’t hurt. On PE you note poor internal rotation and abduction. What is your suspicion?
A

Legg-Calf-Perthes disease

276
Q
  1. What exams would you order and what would you expect to find?
A

XRAY: Necrotic bone (avascular necrosis of hip)
LABS: CBC, ESR
TX: protect joint, limit movement.

277
Q
  1. Toxic synovitis is usually an autoimmune response following:
A

An infection, esp URI

278
Q
  1. Clinical features distinguishing L-C-P dz and septic arthritis of the hip include:
A
    • fever in septic arthritis

- + pain in septic arthritis (LCP = PAINLESS)

279
Q
  1. What is “nursemaid’s elbow” and how is it treated.
A

Subluxation of the radial head

TX: Flex the FA, supinate the elbow

280
Q
  1. This type of fx is described as “oblique fx of the distal tibia without fibular involvement” and usually manifests in children ages 1-3 without hx of significant trauma, and with only minimal pain/swelling.
A

Toddler’s Fx

281
Q
  1. A common fracture of the forearm, usually about 1/3 way up the radius, is a ____
A

Buckle fracture (aka Taurus Fx)

282
Q
  1. Describe the various Salter-Harris classifications.

Which is worst?

A

Class V = worst (crushed growth plate, likely to arrest growth)

(III and IV bad too, b/c go into joint space)

283
Q
  1. Describe distinguishing factors of a limp caused by SCFE
A

Slipped Capital Femoral Epiphysis

  • Adolescents 10-16
  • especially very active or obese males
  • Vague syptoms: + limp, +pain knee/med thigh/ hip
  • limited internal rotation
  • SURGICAL EMERGENCY
284
Q
  1. Congenital deformity of the foot, characterized by inward deviation with angulation at the base of the 5th metatarsal.
A

Metatarsus varus

285
Q
  1. ID Causes of #14. Differentiate from club foot
A

Intrauterine positioning

MV can be passively moved to midline, club foot is a rigid skeletal abnormality.

286
Q
  1. An infant born with metatarsus varus is at increased risk of what OTHER ortho finding?
A

Hip dysplasia (2-10%)

287
Q
  1. 14/F presents with lump on knee. She is an active soccer player and says it hurts every now and then, but usually doesn’t bother her. She appears very thin but well –nourished. The lump is visible and makes her nervous. You note a 3-4cm hard, palpable mass on the medial side of the knee. You suspect?
A

Ostechondroma (most common bone neoplasm)

TX: typically benign, you can leave it there, or surgically remove if problematic

288
Q
  1. What is the most common malignant bone tumor in kids? Where are they typically found?
A
  • Osteosarcomas

- Typical in long bones

289
Q
  1. What is the first treatment done for osteosarcoma?
A
- Chemotherapy
THEN Excision (excision = curative)
290
Q
  1. 6 y/o Female presents with pain in L arm, especially if you touch it. Pain worsens day by day. She also presents with fever. What are your differentials?
A
  • Ewing’s sarcoma vs. Osteomyelitis
  • Do Labs + XRay to ID. Fever + lytic lesion in bone = osteomyelitis
  • Fever, Inc WBC also osteomyelitis
291
Q
  1. An infant is diagnosed with hip dysplasia. You want to apply an orthopedic splint called ____
A
  • Pavlik Harness
292
Q
  1. A 4 year old presents in status epilepticus. What is your first-line treatment?
A
  • Diazepam (Valium)
293
Q
  1. EEG’s _____ (can/not) be used to diagnose epilepsy
A

They are NOT used

294
Q
  1. What is the most common type (manifestation) of childhood epilepsy?
A
  • partial seizures (usually due to genetics)
295
Q
  1. A form of epilepsy characterized by very brief spasms, severe EEG, and poor prognosis is called:
A
  • Infantile spasms
296
Q
  1. Describe facts associated with febrile seizures. When would you work them up?
A
  • Typically ages 6m – 6y
  • Usually do not progress to epilepsy
  • If resolves quickly and returns to normal, no workup need. If difficult to arouse or vomiting after seizure, work up neuro
297
Q
  1. Patient presents for 2m check up. Home birth with educated midwife. NB Screen and vaccines done by midwife. Mom’s concern – baby not eating in last week or so, separated sutures and bulging fontanelle. What do you think of?
A
  • Increased ICP – mass? Hydrocephalus?
298
Q
  1. What symptoms would you expect to see in a child with increased ICP?
A
  • HA (may be worse in AM, worsens with cough, vagal, or bending over)
  • Strabismus, diplopia, wandering eye
  • Vomiting WITHOUT nausea
299
Q
  1. 13/F overweight, presents with complaint of HA. Mother states she complains a lot, but recently also complains of tinnitus and vision being off. What is your concern?
A

*most commonly= idiopathic cause

300
Q
  1. Most common causes of childhood stroke?
A
  • cyanotic heart disease
  • sickle cell disease
  • meningitis
  • hypercoagulable state
  • Sxs: similar to adult: u/l flaccidity, facial droop
301
Q
  1. Neurofibromatosis, Tubosclerosis, and Sturge-Webber are all associated with what finding?
A

Seizures

302
Q
  1. 5 y/o presents with concerned grandparents due to him “not like other kids”, has to climb to stand. What do you suspect? What is this finding called?
A
  • Suspect Muscular dystrophe

- Gower sign

303
Q
  1. What pathopneumonic finding would further heighten suspicion of MD?
A
  • calves appear full (hypertrophic)
304
Q
  1. Match diseases to their pathologies:
    a) Muscular dystrophy
    b) Guillan-Barre
    c) Myesthenia gravis
    d) Spinal Muscular Atrophy (SMA)
A

a) Muscle fiber
b) nerve
c) Neuromuscular junction
d) Anterior horn

305
Q
  1. 15y/o mom brings him in in a panic because hisfeet felt numb, by lunch he felt weird standing up. He can talk but he feels like he’s getting weaker in his upper legs. Hx significant for URI this week. You suspect? How do you treat?
A
  • Suspect Guillan-Barre
  • Tx: supportive care, ADMIT
  • May need ventilator support
306
Q
  1. A 12 y/o presents with purpuric rash 1 week following a URI. She also has a blood-shot eye and red colored urine. You suspect?
A
  • Henloch Schenlein pupura (autoimmune against blood vessels)
307
Q
  1. Describe tx for meningomyeloceles.
A
  • Surgery

- * be sure to assess for paralysis at birth (active & symmetric movement? Incontinence? )

308
Q
  1. Compare and contrast Henoch-Shonlein vs Idiopathic Thrombocytic Purpura
A

BOTH: Autoimmune, Purpuric rashes, Hx URI (or infection).
HSP = autoimmune a/g blood vessels
ITP = autoimmune a/g platelets

309
Q
  1. 18m/f brought in for pallor. Family think something’s wrong because she’s getting pale and they’re dark Hispanic. Nml diet, no PMH. Normal vitals… You only note pallor. No hepatosplenomegaly, lymphadenopathy, no bruising. What do you consider?
A
  • consistent with anemia

- Order: CBC, Iron studies

310
Q
  1. What lab would you order in #40 to ID whether this is an acute or chronic anemia and how the body is compensating?
A
  • Order reticulocyte count. High reticulocyte count = enough time AND able to make new cells.
  • Low retic = acute onset OR aplastic/hypoplastic (use hx!)
311
Q
  1. 3 y/o female in ER presents with jaundice, fatigue x 3 days, Low hgb, high retic. She also has organomegaly. You want to consider what?
A
  • Hemolytic/destructive anemias (organs large from processing broken cells/ bilirubin excess):
  • sickle -G6PD
  • spherocytosis - thalassemias
312
Q

43.T/F heart murmurs are commonly associated with anemia.

A

TRUE

313
Q
  1. Diamond Black-fan is a _____ anemia that can be treated by ____ and cured by ___
A
  1. Congenital hypo/aplastic anemia
  2. tx by steroids
  3. cured by bone marrow transplant
314
Q
  1. Diamond black-fan has __ (more/less) association with other anomalies than it’s cousin Fanconi’s anemia
A

Less: 30% dbf, 50% Fanconi

315
Q
  1. How is Fanconi’s managed?
A
  • steroids or IVIG, BM trasfusion

- 20% self-limited auto-immune and often grow out of it.

316
Q
  1. Differentiate Fanconis vs DBF:
A

DBF: onset @ birth-1yr, short stature, autosomal recessive,

Fanconis” onset 2-10 yrs, higher rate congenital problems, autosomal recessive

317
Q
  1. 4 y/o male with pallor, fatigue x 2 months. You order a CBC and find low RBC, WBC, AND platelets. What do you think?
A
  • 2+ depressed cell lines think leukemia

- age 4, boy, most common leukemia in kids = ALL

318
Q
  1. What lab finding would be consistent with your differential in #48?
A
  • high lymphoblast numbers (overgrow the BM so the BM can’t work)
319
Q
  1. Most common cancer in teens?
A

Lymphomas (3rd most common cancer of all: #1- ALL, #2-brain tumors #3-lymphoma)

320
Q
  1. What are the two types of lymphoma? Which is worse?
A
  • Hodgkin vs non-Hodgkin lymphoma

- non-Hodge = worse (also less common)

321
Q
  1. What clinical findings would you find in a pt with Hodgekin lymphoma? What would you use to confirm?
A
  • Findings: PAINLESS lymphadenopathy without illness, splenomegaly, nml CBC
  • Do CXR to confirm: look for mediastinal widening/mass, enlarged thymus
322
Q
  1. What characteristic finding will differentiate between Hodgekin and non-Hodgekin lymphoma?
A
  • Reed Steinberg cells in Hodgekin lymphoma

- hodgekin = cervical lymph most common

323
Q
  1. A patient presents with a triad of symptoms including papilledema, HA worse in AM, and vomiting. You recognize this as alarming for ___
A

Increased ICP

324
Q
  1. What is the most common brain tumor in kids?
A

Astrocytoma

325
Q
  1. A brain tumor where allows for the best prognosis?
A

SUPRAtentorial

326
Q
  1. Definitive tx for a brain tumor includes:
A

Surgical removal (successful in 50-60% of all CA)

327
Q
  1. A 3y/o presents with poor feeding, abd distention, and refuses to walk. When you pick him up, he cries loudly. He also appears pale and miserable. On exam you note a large, palpable abdominal mass and HTN. What do you consider?
A

-Diff dx: HTN=renal?, mass = neuro/nephroblastoma

328
Q
  1. Differentiate between neuroblastoma and nephroblastoma. Which is called Willm’s tumor?
A
  • Neuroblastoma can cross midline

- Nephrobllastoma (Willms) does not cross midline

329
Q
  1. The most common sign of retinoblastoma is:
A
  • absence of red reflex (white reflex)

- Strabismus

330
Q
  1. Tx for retinoblastoma includes:
A

radiation (mainstay)surgery if ineffective.

− monitor for metastisization (fatal if mets)

331
Q
  1. The soft tissue tumor aka most common sarcoma of childhood is called:
A

-Rhabdomyosarcoma

332
Q
  1. Differentiate presentation of rhabdomyosarcoma by age.
A
  • Young – head, neck, GU

- Older kids: extremities, trunk

333
Q
  1. A patient presents with jaundice. It is determined that they do not posess the enzyme that metabolizes and conjugates bilirubin. This diagnosis is called ___
A

Guilbert’s (specifically elevation in unconjugated bilirubin d/t deficiency of conjugating enzyme.

334
Q
  1. ID types of congjugating enzyme deficiencies.
A
  • No enzyme AT ALL = Kraigler Najar. (requires tx or fatal; tx = phenobarbiotol)…)
  • Diminished activity (Guilberr’s) (usually benign, but keep a close eye out. Often don’t require tx)
335
Q
  1. Protein C deficiency, antitrombin 3 deficiency, and protein S deficiency all result in what?
A
  • Hypercoagulation state (clotting problems)
336
Q
  1. A pt presents with septic shock. You also note hematuria, bleeding gums, etc. What labs should you order?
    What is the most likely diagnosis?
    What is the treatment?
A
  • CBC, PTT, PT, fibrinogen, INR
  • DIC highly associated with sepsis

Tx: FFP (contains a lot of clotting factors)

337
Q
  1. How can you treat severe thrombocytopenia?
A
  • transfusion of platelets
338
Q
  1. A 14 y/o presents with heavy periods and occasional nose bleeds. She denies any spontaneous bruising though. What problem might you check for?
A
  • VonWillebrands
339
Q
  1. Define whether each problem is due to a problem with production, consumption, or abnormal function:
    a) ITP
    b) Leukemia
    c) Sickle cell (in crisis)
A

a) Destruction (auto immune)
b) production
c) function

340
Q
  1. ID and differentiate between most common childhood leukemias.
A

ALL (acute lymphoblastic leukemia (most common = 75%
AML (15-20%)
CML (