EOR Flashcards

1
Q

LICHEN PLANUS

A
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2
Q

Pityriasis rosea

A
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3
Q

Drug Eruptions

  1. Erythema Multiform
    1. Etiology
    2. Presentation
    3. Treatment/Prognosis
  2. SJS/TEN
    1. Differences
    2. Treatment
A

Erythema Multiform:

  1. Etiology: Herpes Simplex Virus
    1. Similarities in clinical and histopathologic findings have led to controversy over the distinction between EM and Stevens-Johnson syndrome (SJS), an often drug-induced disorder that may present with cutaneous, targetoid lesions and mucosal erosions. However, there is suggestive evidence that EM with mucous membrane involvement and SJS are different diseases with distinct causes [1]. The term erythema multiforme major should not be used to refer to SJS

SJS/TEN

  1. According to a widely accepted classification, SJS and TEN are considered a disease continuum and are distinguished chiefly by severity, based upon the percentage of body surface affected by blisters and erosions (table 1) [2,3]:

●SJS is the less severe condition, in which skin detachment is <10 percent of the body surface (picture 1A-C).

●TEN involves detachment of >30 percent of the body surface area (BSA) (picture 2A-D).

●SJS/TEN overlap describes patients with skin detachment of 10 to 30 percent of BSA.

We will use the term “SJS/TEN” to refer collectively to SJS, TEN, and SJS/TEN overlap syndrome.

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4
Q

MEASLES (Rubeola)

A
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5
Q

IMMUNOGLOBULIN A VASCULITIS

A
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6
Q

KAWASAKI DISEASE

A
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7
Q

Laryngeotracheitis

  1. Etiology: Pathogen?
  2. Dx:
  3. Tx
A
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8
Q

Necrotising Entericolitis

A
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9
Q
A

Candidal Rash

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10
Q

Staphylococcal scalded skin syndrome (SSSS)

A
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11
Q

Patellofemoral Pain syndrome

A
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12
Q

MARFAN SYNDROME

A
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13
Q

Legg-Calvé-Perthes disease

A
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14
Q

Intestinal Malrotation with MIDGUT VOLVULOUS

A
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15
Q

HAND, FOOT, MOUTH

What is the pathogen?

A
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16
Q

neurofibromatosis type 1

A

The boy has both café-au-lait macules and cognitive disability, raising concern for neurofibromatosis type 1, or von Recklinghausen’s disease. Neurofibromatosis is a neurocutaneous disorder caused by a mutation on NF1 on chromosome 17. Cutaneous findings of neurofibromatosis type 1 include café-au-lait macules, axillary and inguinal freckling, Lisch nodules, and neurofibromas. Neurofibromas are peripheral nerve sheath tumors that may be focal and cutaneous or plexiform. Cutaneous neurofibromas are small, sessile or pedunculated lesions that move with the skin. They are non-tender and occur primarily on the trunk. Cutaneous neurofibromas most commonly develop during adolescence, although subtle lesions may be noted earlier in angled light. The number of neurofibromas on an affected individual may range from a few to thousands. Plexiform neurofibromas are present in half of patients with neurofibromatosis and cause a very different clinical picture. They may be superficial, deep, or both. The entangled nerves can become large, complex, and often disfiguring due to associated overgrowth of surrounding tissues. Deep plexiform neurofibromas may compress internal structures, including the airway and spinal cord. Individuals with neurofibromatosis are also at increased risk of bony abnormalities, including bony dysplasia, pseudoarthroses, scoliosis, osteoporosis, and short stature. Additionally, affected individuals are predisposed to a variety of tumors, including optic nerve gliomas and soft tissue sarcomas such as rhabdomyosarcoma, malignant peripheral nerve sheath tumors, and glomus tumors.

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17
Q

Most common pathogens causing Osteomyelitis?

  1. MC
  2. Neonates
  3. Sickle Cell
A
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18
Q

Meckel Diverticulum

A
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19
Q

Neonatal cephalic pustulosis

A
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20
Q

Pertussis- Whooping Cough

  1. Pathogen
  2. Presentation
  3. Treatmnet
A
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21
Q

Diaphragmatic Hernia

A
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22
Q

Gastroschisis vs omphalocele

A

Dx: Clinical

Tx: Silo

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23
Q

Extrophy of the Bladder

A
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24
Q

Biliary Atresia

A

Dx:

  1. US = No Ducts
  2. Hitascan after 7 days of phenobarbitol
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25
Q

Acute Rheumatic Fever

  1. Etiology: Pathogen
  2. Presentation:
  3. Dx: Think in the Criteria Pneumonic
  4. Criteria
  5. Tx:
A
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26
Q

Hypertrophic Cardiomyopathy

  1. Genetics: Dominant or resessive
  2. Presentation:
    1. Murmur type?
    2. What increases the Murmur
    3. What decreases the murmur
  3. EKG findings
  4. Treatment: What is the combination of medications
A
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27
Q

Syncope

  1. Causes
    1. Systems/Etiology
  2. Tests
    1. Labs
    2. Imaging
    3. Special Tests
A
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28
Q

Inguinal Hernias

  1. Indirect vs. Direct
    1. MC
    2. Hesselbaack Triangle
  2. Patient:
    1. Age Ranges
  3. Tx: What determines a emergent vs non-emergent Tx.
  4. Which type has a higher risk of Strangulation
A
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29
Q

Niacin Deficiency

  1. What is the Vitamin?
  2. What are the 3 Ds?
  3. What diet results in niacin Deficiency?
A
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30
Q

Vitamin A Deficiency

  1. Presentation?
  2. What organ is affected the most.
A
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31
Q

Vitamin C Deficiency?

  1. Name of the Vitamin?
  2. Name of the disease it causes?
  3. Presentation?
  4. 4H’s
  5. Treatment:
    1. What foods?
A
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32
Q

Vitamin D Deficiency

  1. Metabolism
  2. Pathology in
    1. Childhood
    2. Adults
  3. Treatment:
    1. ?????
A
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33
Q

Lactose Intolerance

  1. Presentation
  2. Dx
  3. Tx:
A
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34
Q

GERD: Infants

A
  1. Avoid Smoke Exposure
  2. Breastfeeding is better than Formula
  3. Avoid Overeating

Pharmacology:

  1. Mild Cases (“Happy Spitter”) < 1 yo -Pharmacotherapy is not indicated
  2. PPI is better than H2Blocker
  3. PPI- -prazole (omeprazole) PPI- Have been studied in children.
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35
Q

Pediculosis Capitis-

  1. Management
A
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36
Q

Scabies:

  1. Presentation
  2. Treatment
    1. Infant Safe
    2. Outbreak oral treatment
A
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37
Q

Bacterial Conjunctivitis

  1. MC Pathogens (3)
  2. Presentation
  3. Treatment
    1. Contact Wearer
    2. Non Contact wearer
A
  1. Treatment:
    1. Trimethprim-Polymyxin B
      1. Cheaper and just as effective
    2. Erythromycin
  2. Contact Wearer
    1. Moxifoxacin
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38
Q

Allergic Conjunctivitis

  1. Presentation
    1. Think dusty roads
  2. Tx:
A
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39
Q

Viral Conjunctivitis

  1. MC pathogen
  2. Presentation
  3. Treatmnent
A
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40
Q

Chlamydial Conjunctivitis/Neonatal Conjunctivitis

  1. Presentation
    1. Timeframe
A
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41
Q

Orbital Cellulitis

A
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42
Q

Strabismus

A
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43
Q

Ottitis Media

A
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44
Q

Otitis Externa

A
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45
Q

Mastoiditis

A
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46
Q

TM Perforation

  1. What do you need to remember when treating TM perforation.
A
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47
Q

Hearing Loss

Condutive Vs. Senroineural

A
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48
Q

Epiglottitis

A
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49
Q

Allergic Rhinitis

A
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50
Q

Epistaxis

A
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51
Q

Pharyngitis (Acute Pharyngotonsillitis)

A
52
Q

Peritonsillar Abscess

A
53
Q

Oral Candidiasis

A
54
Q

Gastroenteritis

A
55
Q

Dehydration-Pediatrics

  1. Presentation Chart for mild, moderate, severe
  2. Tx:
A
  1. Tx:
    1. Severe
      1. Isotonic Crystaloid Solution- IV infusion
    2. Moderate/Mild
      1. Oral Rehydration
      2. Only a 3% of pt had to revert back to IV infusion when started on oral Rehydration.
56
Q

Appendicitis

  1. Presentation?
    1. Signs=- 4 of them
  2. When to use antibiotics vs surgery
A
57
Q

Cryptorchidism

A
58
Q

Hydrocele

A
59
Q

Balanitis

A

Tx: No neomycin

Polysporin + Aquaphor

60
Q

Enuresis

A
  1. DDX
    1. Constipation
    2. Sleep Apnea
    3. ADHD
  2. Goals:
    1. ●Staying dry on particular occasions (eg, sleepover)

●Reducing the number of wet nights

●Reducing the impact of enuresis on the child and family

●Avoiding recurrence

61
Q

Ovarian Torsion

A
62
Q

Paraphimosis/Phimosis

A
63
Q

Tesitcular Torsion

A
64
Q

Hypospadiasas

A
65
Q

Vesicoureteral Reflux (VUR)

A
66
Q

Glomerulonephritis

A
67
Q

Cystitis

A
68
Q

Atypical Mycobacterial Disease

A
69
Q

Influenza

A
70
Q

Neonatal Herpes Simplex Virus

A
71
Q

Juvenile Rheumatoid Arthritis

A
72
Q

Drug Eruptions

A
73
Q

Acne Vulgaris

A
74
Q

Androgenetic Alopecia

A
75
Q

Exanthems

  1. Erythema Multiforme
  2. Erythema Marginatum
  3. Erythema Nodosum
  4. Erythema Migrans
  5. Erythema Infectiosum
A
76
Q

Verrucae Plantaris

A
77
Q

Burns

  1. Classification
    1. Thickness
    2. Degree
    3. Depth of burn
A
78
Q

Allergic Contact Dermatitis

A
79
Q

Atopic Dermatitis

A
80
Q

Nummular Eczema

A
81
Q

Acute Palmoplanta Eczema (Dyshidrotic Eczema)

A
82
Q

Tinea Pedis

A
83
Q

Tinea Cruris

A
84
Q

Tinea Capitis

A
85
Q

Tinea Corposis

A
86
Q

Impetigo

A
87
Q

Tinea Versicolor

A
88
Q

Volvulus

A
89
Q

Child Abuse

A
90
Q

ADHD

A
91
Q

Autism

A
92
Q

Bulimia Nervosa

A
93
Q

Anorexia Nervosa

A
94
Q

Major Depressive Disorder

A
95
Q

Persistent Depressive Disorder

A
96
Q

Conduct Disorder

A
97
Q

Generalized Anxiety Disorder

A
98
Q

Specific Phobias

A
99
Q

Suicide Behaviors

A
100
Q

Normal Sexual Development in Females

A
101
Q

Tanner Staging Males

A
102
Q

Contraceptives

A
103
Q

Absence Seizures (petit Mal)

A
104
Q

Status Epilepticus

A
105
Q
A
106
Q

Viral Meningitis

A
107
Q

Bacterial Meningitis

A
108
Q

Acute Lymphocytic Leukemia

A
109
Q

Chronic Lymphocytic Leukemia

A
110
Q

Acute Myeloid Leukemia (AML)

A
111
Q

Chronic Myelogenous Leukemia (CML)

A
112
Q

Hemophilia A

A
113
Q

Hemophilia B

  1. Name
A
114
Q

FACTOR XI

A
115
Q

DISORDERS OF COAGULATION (SUMMARY)

A
116
Q

IRON DEFICIENCY ANEMIA

A
117
Q

Megaloblastic Anemia

  1. Which one has Neurologic Symptoms
A
118
Q

Anemia of Chronic Disease

A
119
Q

Lead Poisoning/Lead Toxicity

A
120
Q

RSV

High Risk Patients

A
  1. High-risk Populations
    1. <29 w Gestation
    2. <32w with Premature lung development
    3. <24m requiring oxygen
    4. <24m Immunocompromised
121
Q

Bronchiolitis

A
122
Q

Bacterial Pneumonia

  1. Pathophysiology
  2. Managment
A
123
Q

Cystic Fibrosis

A

Respiratory Infections or Failure to Thrive ====== Cystic Fibrosis

124
Q

Failure to Thrive

A
  1. Beta Thalassemia
  2. Patent Ductus Arteriosis
125
Q
A