URx Flashcards

1
Q

Simple febrile seizures are managed with ___.

A

temperature control with antipyretics.

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2
Q

How can beta-blocker toxicity be differentiated from muscarinic toxicity (e.g. OP poisoning) clinically?

A

β-Blocker toxicity ≈ muscarinic toxicity common s/s: broncho-constriction -> wheezing, low SpO2

Other predominant s/s in β-blocker toxicity: low BP, low Bl. glucose, and seizures.

predominant s/s in muscarinic agent toxicity: lacrimation, nausea, vomiting, and diarrhea.

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3
Q

True/False?
In accordance with the shared decision-making approach, physicians should obtain information directly from minor patients and discuss treatment options with them, provided they are able to understand their medical history and articulate their wishes.

A

True

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4
Q

Shared medical decision-making typically begins with ___ and ______.

A

begins with the patient and physician.
*When the patient is a minor, a parent or guardian may also be involved.

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5
Q

A ______ presents at birth or within first few weeks of birth as a deeply hyperpigmented lesion that is minimally elevated (ie, a thin plaque) and has a texture that differs from that of the surrounding normal skin.

A

congenital melanocytic naevus (CMN);
aka giant hairy naevus/nevi (based on size and hair growth).

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6
Q

*CMNs develop in utero between ____ weeks GA d/t mostly sporadic localized genetic abnormalities esp. N-Ras mutation.

A

between 5-24 weeks GA

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7
Q

True/False?

When compared to acquired nevi, CMNs more commonly extend deeper into the dermis or subcutaneous fat layer.

A

True

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8
Q

Congenital melanocytic naevus (CMN) is usually seen in children of ____ age.

A

present at birth or develop within the first few weeks after birth (mostly);
may develop within 6 months of birth.

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9
Q

Approx. _____ % of newborns may present with or develop within first few weeks of birth, a congenital melanocytic naevus (CMN).

A

~1%

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10
Q

Small (<1.5 cm) and medium (1.5-20 cm) CMN have a lifetime risk of malignant melanoma of ____ %; the risk of malignant transformation in rarely occurring large (>20-40 cm) or “giant” (>40 cm) CMN, is about _____%.

A

risk of malignant transformation in

small/medium CMN is < 1%;
large/giant CMN is < 5%

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11
Q

True/False?

Coarse hair or texture on a CMN may increase the risk of transformation to a malignant melanoma.

A

False

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12
Q

A melanocytic nevus located in the epidermis is called a _____nevus; if in the dermis, it is called ____ nevus; and if present in both locations, it is called a _____ nevus.

A

epidermis: junctional nevus,

dermis: intradermal nevus, and

in both locations: compound nevus.

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13
Q

The differential diagnosis of a CMN include ______ conditions.

A

-café-au-lait macules (lack textural changes as seen in CMN),
-ephelides aka freckles (not congenital; lack textural changes as seen in CMN),
-junctional melanocytic nevi (not congenital; lack textural changes as seen in CMN), and
-lentigines (not congenital; lack textural change seen in CMN).

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14
Q

Ephelides aka ____ are non-congenital, very small (<3 mm), light brown macules located in sun-exposed areas, such as the face, upper chest, or back, which become darker with sun exposure and fade during cold weather months (when there is less sun exposure).

A

freckles;

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15
Q

A junctional melanocytic nevus can be clinically or histopathologically distinguished from a congenital melanocytic nevus based on ____ characteristics.

A

junctional melanocytic nevus:
-not congenital (unlike CMN)
-appear during childhood (unlike CMN).
-in the epidermis (CMNs are deep).
-usually light brown, and
-lack surface textural change.

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16
Q

The classic triad of c/p in infectious mononucleosis includes ___, ___, and _____ in addition to fever, myalgia, malaise, and fatigue.

A
  1. exudative pharyngitis
  2. lymphadenopathy (commonly cervical with mild tenderness),
  3. splenomegaly.

*Other s/s
-Hepatomegaly and/or jaundice in 5% to 10% of cases.
-Morbilliform skin rash in ~ 5% of patients (esp. if t/t with ampicillin for pharyngitis).

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17
Q

Blood smear showing _____ is a characteristic early lab finding of infectious mononucleosis in the presence of suggestive symptoms.

A

-lymphocytosis (>50% of total WBCs) with
-atypical lymphocytes (>10% of total lymphocytes).

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18
Q

The most feasible and widely used screening test for infectious mononucleosis (EBV infection) is the _____ test, which is positive in more than 90% of tested cases.

A

heterophile antibody (monospot) test.

*detects IgM to EBV by using horse, sheep, or bovine erythrocytes.

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19
Q

When are serologic tests (e.g. IgM antibodies to viral capsid antigen) indicated for the diagnosis of acute EBV infection?

A

-in heterophile antibody-negative cases, or
-in those with atypical presentations.

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20
Q

____ is the most common cause of osteomyelitis in patients with sickle cell disease in the US and Europe.

A

Salmonella

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21
Q

True/False?
A physician can provide confidential care to an adolescent for specific situations after discussing their reasons for not wanting to share the information with their parents, and then based on their response, encourage them to disclose the information to their family. However, it should be made clear that this is not necessary for him to receive care.

A

true.

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22
Q

Adolescents are considered minors and must rely on their parents for consent in almost all medical situations. Exceptions for which adolescents may receive confidential care include _____ situations.

A

STI testing and treatment, pregnancy testing, prenatal care, pregnancy termination and adoption, mental health services, and substance use treatment.

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23
Q

The differential diagnosis of hidradenitis suppurativa (HS) includes ____ conditions.

A

-Acne vulgaris (does not involve axillae),

-Extraintestinal Crohn’s disease (vulvar & perianal areas involved, +ve h/o intestinal Crohn’s disease),

-Folliculitis (superficial pustules), and

-Furuncles (usually transient, not recurrent or chronic).

*HS aka acne inversus, is chronic, inflammatory, and involves deep-seated nodules and abscesses, draining tracts, and fibrotic scars most commonly occur in intertriginous areas and areas rich in apocrine glands.

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24
Q

Intrapartum t/t for GBS is warranted for all patients with a positive GBS during pregnancy to avoid the risk of ______ d/t ____ reason.

A

to avoid the risk of GBS neonatal meningitis;

as antenatal t/t does not ensure eradication of GBS, and there is also a risk of recolonization after t/t.

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25
Q

____ is a common cutaneous fungal infection that causes itching, scaling, maceration, and fissuring of the interdigital spaces (e.g. toe webs).

A

Tinea pedis

*Less frequently, patients p/w
-scaling of the plantar and lateral surfaces of the foot (“moccasin” distribution), or
-vesicles or bullae on the instep of the foot (inflammatory tinea pedis).

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26
Q

Tinea pedis is common in ___ age group (s), and is often acquired from the decks surrounding swimming pools or from public showers.

A

preadolescents and teenagers;

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27
Q

The differential diagnosis of tinea pedis includes ____ conditions.

A
  1. Allergic contact dermatitis: erythema & scaling on the dorsum of the foot.
  2. Juvenile plantar dermatosis: 3-14 year old with fissures, redness & scaling of the plantar forefoot esp. great toe; a/w hyperhidrosis f/by quick drying (see attached image).
  3. Pitted keratolysis (aka ringed keratolysis): superficial bacterial infection p/with pitting & shallow erosions of the plantar foot (palms rare) with foot malodor (see attached image).

*none of the above involve interdigital spaces involved.
**Also, check 4th- 5th webspace for erythrasma in Tenia Pedis.

https://dermnetnz.org/topics/juvenile-plantar-dermatosis-images

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28
Q

Apnea of prematurity is defined as ____.

A

In an infant younger than 37 weeks of gestation, cessation of breathing for >20 seconds, or shorter if it involves bradycardia and/or desaturation.

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29
Q

Most episodes of apnea in preterm infants are ____, or _____.
(? central, obstructive, mixed).

A

central (physiologic immaturity of the respiratory drive),
or
mixed (both central and obstructive).

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30
Q

______ on clinical exam is suggestive of central apnea of prematurity.

A

absent inspiratory effort (d/t physiologically immature respiratory drive);

*whereas, in obstructive apnea, inspiratory efforts persist, but are ineffective in the presence of upper airway obstruction.

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31
Q

Apnea of prematurity occurs in approximately ___% of infants born between 33 and 34 6/7 weeks of gestation, and in virtually ____ % of infants <28 weeks GA.

A

~50% of infants born between 33 and 34 6/7 weeks GA, and
-in virtually all infants <28 weeks GA.

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32
Q

In comparison to apnea of prematurity, the incidence of apnea in term infants is very low, and is usually suggestive of an underlying ____ condition.

A

pathologic condition

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33
Q

A 2-day-old newborn p/with yellow skin, yellow sclera, elevated unconjugated bilirubin (UCB), a normal CBC, and normal liver enzymes. What is the most likely diagnosis?

A

Crigler-Najjar syndrome (liver cannot conjugate UCB d/t enzyme deficiency).

normal CBC rules out hemolysis, and normal liver enzymes rule out infective or inflammatory liver disease as cause of UCB hyperbilirubinemia.

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34
Q

Crigler-Najjar syndrome type I (more severe) can be distinguished from type II via _____ administration.

A

phenobarbital-> reduces sr. bilirubin in Crigler-Najjar syndrome type II;

-> no reduction in sr. bilirubin in Crigler-Najjar syndrome type I (more severe).

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35
Q

The differential diagnosis of unconjugated hyperbilirubinemia in the FIRST FEW DAYS of life includes ____ etiologies.

A

-breastfeeding jaundice (> common than Criggler-Najjar);
-hemolytic anemias (> common than Criggler-Najjar).
-hemolysis caused by maternal-fetal blood type incompatibility.
-Criggler-Najjar syndrome (liver cannot conjugate UCB).

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36
Q

A child presenting with a subdural hematoma and no h/o major trauma (eg, fall from a large height or motor vehicle accident) should be evaluated for ____.

A

non-accidental trauma.

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37
Q

Aside from accidental or non-accidental trauma, alternative diagnoses for life threatening intracranial bleeding in toddlers include _____ etiologies.

A

-AVM rupture (no subdural bleeding).

-hematologic: ITP, hemophilia, SCD (no subdural bleeding).

-malignancy (less chance of subdural hematoma).

*accidental or non-accidental trauma may present more commonly with a subdural hematoma.

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38
Q

____ is still a relevant and most common cause of epiglottitis in under- or unvaccinated children.

A

Hib

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39
Q

Acute epiglottitis, primarily caused by infection can lead to life-threatening airway obstruction; a lateral x-ray of the neck demonstrates the pathognomonic “______ sign.”

A

“thumb-print sign.”

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40
Q

Noninfectious causes of epiglottitis include ____ cause (s).

A

-thermal injury,
-direct trauma, or
-caustic ingestion.

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41
Q

The differential diagnosis of acute epiglottitis includes conditions such as ________.

A
  1. Croup: barking cough (unlike epiglottitis); distention of the hypopharynx on lateral X-ray neck (no thumb-print sign of epiglottitis).
  2. Peritonsillar or retropharyngeal infections: p/with drooling and neck extension.
  3. Foreign bodies: p/with drooling and respiratory distress.
  4. Diphtheria: s/s progress is typically more gradual with sore-throat, malaise, and low-grade fever with gray, sharply demarcated membranes.
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42
Q

A 5-year-old boy with no significant past medical history p/with fever, malaise, and a rash for 3 days that appeared on his hands and feet. On CE, vitals are all normal except for several shallow ulcers in the posterior pharynx, mild non-tender submandibular lymphadenopathy; and elliptical/oval vesicular rash on the palms, soles, and buttocks. What is the most likely diagnosis?

A

HFMD;
mc cause: Coxsackie virus A16;

*atypical HFMD is caused primarily by coxsackievirus A6.

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43
Q

How is the c/p of atypical HFMD different from typical HFMD?

A

Atypical HFMD p/with WIDESPREAD vesicles, bullae, and erosions often concentrated around the mouth and in the anogenital region.

Typical HFMD p/with oval or elliptical vesicles in hands, soles, and oral mucosa including the pharynx.

44
Q

Arthritic arthralgias in one or more joints for > 6 weeks with lack of systemic symptoms (e.g. fever, malaise) in a patient who is younger than 16 years, is characteristic of _____.

A

juvenile idiopathic arthritis (JIA);

*lack of systemic systems and fewer than five joints affected is consistent with the oligoarticular JIA subtype.

45
Q

____ screening is indicated in all JIA patients d/t increased risk of _____ in ANA +ve JIA patients.

A

eye screening ;

d/t increased likelihood of asymptomatic uveitis in ANA +ve JIA patients.

46
Q

ESR and CRP levels in JIA patients are ____ (? high, slightly high, normal).

A

-ESR ↑↑/slightly ↑/ normal, and
-CRP ↑↑/slightly ↑/ normal

47
Q

Multiple café-au-lait macules (CALM) are a feature of several syndromes such as _____ (list all).

A

-Neurofibromatosis (NF) type 1
-Legius,
-McCune-Albright,
-Silver,
-Bloom,
-Watson).

48
Q

The presence of six or more café-au-lait macules (CALMs) that measure >5 mm in prepubertal individuals, and >15 mm in postpubertal individuals is one of the diagnostic criteria for _____ disease, and is the earliest symptom to appear.

A

NF-1

49
Q

A 32-month-old boy with h/o premature birth via urgent C-section at 32 weeks GA, and PPV resuscitation in a NICU at birth is brought to the pediatrician for his routine 30-month well-child examination. Although his growth has been steady, he has a h/o global developmental delay for which he has been on early intervention services since infancy. He makes eye contact and lets the physician examine him with little reassurance. He walks with assistance on his tiptoes; muscle tone in his legs is high, patellar reflexes are brisk, and has ankle clonus bilaterally. There is no e/o muscle atrophy or hypertrophy. No h/o difficulty with social interactions or repetitive behaviors. Based on clinical observation and history provided by his mother, his emotional development seems to be appropriate. What is the most likely tentative diagnosis?

A

spastic cerebral palsy (CP) based on his increased tone, hyperreflexia, impaired fine motor function, delayed developmental milestones, and toe walking.

50
Q

_____ during the birthing process is a common reason children develop cerebral palsy (CP).

A

Loss of oxygen to the brain during birth (intra-natal period)

51
Q

Toxoplasmosis, a common congenital infection in newborns d/t mothers exposed to cat litter during pregnancy may p/with ___ s/s.

A
  1. Miscarriage, stillbirth, or neonatal death.

*Most affected newborns are symptom-free at birth. *

  1. Generalised disease (in ~ 20%): fever, anemia, jaundice, hepato-splenomegaly, or CNS s/s such as deafness, seizures, intellectual disability.
  2. Chorioretinitis with blindness in ~ 10% (chorioretinitis & CNS s/s may also develop later in life).
  3. Skin lesions (congenital): usually haemorrhagic or necrotic maculo-papular rash mainly on the trunk.

Skin lesions of acute acquired toxoplasmosis are variable and may resemble roseola, erythema multiforme, or papular urticaria; may be telangiectatic macules, papules, or vesicles, or p/with acute dermatomyositis-like syndrome.

52
Q

Contraindications to vaccines are limited, and include _____.

A

-h/o SEVERE ALLERGY to a vaccine component, or prior dose of vaccine.

-h/o encephalopathy within 7 days of prior pertussis vaccination.

-h/o allergy to eggs (Yellow fever vaccine contra-indicated; give influenza vaccine under supervision).

-*immunocompromised host (live vaccines contra-indicated).

-pregnant women (live vaccines contra-indicated).

*exception: patients with HIV may receive MMR and varicella vaccines if their CD4+ count is >200/cumm and both vaccines are given separately.

53
Q

Oral typhoid vaccine should not be administered to persons receiving ____ pharmaceutical agents.

A

sulfonamides

54
Q

True/False?
Antiviral drugs may affect the efficacy of live-virus vaccines.

A

true.

55
Q

True/False?
The CDC recommends regular vaccination of children even if they have low-grade fever, upper respiratory infection, colds, otitis media, and mild diarrhea.

A

True.

56
Q

Mediterranean ancestry and the presence of target cells (see attached image) in a patient with microcytic hypochromic anemia who is unresponsive to iron therapy should raise suspicion _____.

A

Thalassemia

57
Q

Thalassemia (major or minor) can often be mistaken for iron deficiency anemia because initial blood work reveals ____.

A

microcytic hypochromic anemia.

58
Q

Thalassemia is most common among people of ____ descent (s).

A

African, Middle Eastern, and Asian descent.

59
Q

_____ can also reveal “Target cells” on the peripheral smear (see attached image for target cells).

A

Liver disease.

60
Q

Thalassemia’s are caused by _____.

A

mutation in β-globin gene on chromosome 11.

61
Q

Thalassemia H is caused by a mutation in the ____ gene.

A

alpha-globin gene;
aka HbH disease.

62
Q

β-Thalassemia trait (heterozygous) is aka ____, and is characterized clinically by ____ s/s’s.

A

β-Thalassemia minor;
asymptomatic, or mild anemia.

63
Q

_____ is a highly transfusion-dependent thalassemia caused by homozygous mutation in the β-globin gene, and is characterized by ____ c/p.

A

β-Thalassemia major;

-severe anemia
-FTT
-jaundice
-Hepatosplenomegaly,
-bone abnormalities

*this is a highly transfusion-dependent condition, hence monitoring and m/m of iron overload/hemosiderosis is required.

64
Q

Since gastric fluid contains high concentrations of hydrochloric acid, repetitive vomiting can lead to ____ electrolyte disturbance.

A

depletion of chloride -> hypochloremia alkalosis (loss of both H+ and Cl- ions).

65
Q

Repeated vomiting can indirectly lead to hypokalemia d/t ____.

A

loss of H+ (HCl), creating an alkalotic state, which results in an intracellular shift of K+ in exchange for H+ exit from within the cell (to buffer the alkalosis);
in addition, K+ wasting occurs at the DCT in the renal system.

66
Q

Risk factors for hypertrophic pyloric stenosis include _____.

A

-male sex,
-first-born child,
-h/o prematurity, and
-exposure to macrolides in vitro.

67
Q

What are some major causes of vomiting in the newborn and early infancy period other than hypertrophic pyloric stenosis which also p/w vomiting?

A
  1. GI obstructions like
    -malrotation with volvulus (bilious emesis),
    -intestinal atresia (onset 1-4 wks. of birth).
    -Hirschsprung disease (onset 1-4 wks. of birth).
    -Intussusception (less common before 6 months of age).

*Also, children with all of the above conditions are usually irritable and do not want to feed after emesis.

68
Q

True/False?

Intussusception is less common before 6 months of life.

A

True

69
Q

Parental consent is required for ____ treatment in a minor who is not emancipated.

A

all nonemergent surgical intervention

70
Q

Variola virus causes _____, whereas poxvirus causes ____.

A

Variola virus causes smallpox;

poxvirus causes molluscum contagiosum.

71
Q

Simple febrile seizures last less than ____ minutes and are a/w a ____ -grade fever (rapid increase), whereas complex febrile seizures last more than ____ minutes, or occur more than once in a 24-hour period, and are a/w a ____- grade fever for several days.

A

Simple febrile seizures:
-last <15 minutes, and
-are a/w a high fever.

Complex febrile seizures:
-last > 15 minutes, or
-occur > once in a 24-hour period, and
-are a/w a low-grade fever for several days.

72
Q

True/False?

An isolated incidence of seizure in a febrile child indicates that the underlying cause of the seizure is fever and not an underlying seizure disorder.

A

True.

*in patients p/w a one-time simple febrile seizure, an EEG performed outside of the seizure event will most likely be normal.

73
Q

____ plus _____ is the feasible initial treatment for a patient with newly diagnosed type 1 DM.

A

Insulin glargine (long-acting)
+
insulin lispro (short-acting)

74
Q

A macular rash on the trunk, face, and extremities of a child (< 2 years of age) that appears within 12 - 24 hours of defervescence of fever (high) of 3-5 days duration is most likely ______ disease caused by ______.

A

Roseola infantum (aka exanthem subitum);
caused by HHV-6&raquo_space;> HHV-7

75
Q

Febrile seizures are commonly a/w infection with ____ virus, occurring in about ___ % of children infected with the same.

A

HHV-6 infection;
seen in ~ 10% to 15% of children infected with HHV-6.

76
Q

The characteristic _______ distinguishes Roseola from other infections that p/w fever and a generalized macular rash such as erythema infectiosum, measles, rubella, and infectious mononucleosis.

A

appearance of a maculo-papular rash following defervescence of fever (high).

77
Q

Initial management in newborns p/w signs and symptoms of duodenal atresia is ______ to prevent further vomiting and potential aspiration.

A

gastric decompression with a nasogastric tube

78
Q

____ is more appropriate for prenatal diagnosis of intestinal atresia, revealing findings such as ____ (list all).

A

Ultrasonography;
revealing
-polyhydramnios,
-dilated bowel, and
-increased bowel echogenicity.

79
Q

_____ is the most common cause of bronchiolitis during both epidemic and nonepidemic times of the year, followed by _____ agents.

A

-RSV is the mcc f/by

-parainfluenza viruses,
-rhinoviruses, and
-metapneumoviruses.

80
Q

High-risk bruising (ie, due to NAT or physical abuse) can be identified using the TEN-4, FACES P mnemonic. Explain.

A

TEN-4, FACES P mnemonic:
bruising involving the
-Torso, Ears, Neck, or
-located in any region in an infant < 4 months of age,
-involves the Frenulum, Angle of the jaw, Cheek, Eyelids, Subconjunctivae, or
-is Patterned.

81
Q

Describe the three forms in which Tinea pedis can present.

A
  1. Interdigital (most common): p/w erythema, scaling, and maceration of the interdigital spaces of the foot.
  2. Vesicular: p/w vesicles, bullae, and erosions on the instep of the foot.
  3. Moccasin: with erythema and scaling that involve much or all of the plantar surface and sides of the feet.
82
Q

Wood lamp exam is ____ in Tinea pedis.

A

negative.

83
Q

Conjugated hyperbilirubinemia is defined as direct bilirubin greater than ____ mg/dL.

A

direct bilirubin > 1 mg/dL (when total bilirubin is less than 5 mg/dL),
or
> 20% of the total bilirubin (when total bilirubin is greater than 5 mg/dL).

84
Q

___, ___, and ____ are suggestive symptoms of biliary obstruction.

A

jaundice, pale stools, and dark urine.

85
Q

____ jaundice is common, and causes a mild unconjugated hyper-bilirubinemia after the 3rd day of life.

A

Physiologic jaundice.

86
Q

Physiologic jaundice typically resolves without intervention by ___ -week in full-term neonates, and by ____-weeks in preterm neonates.

A

1 week in full-term neonates;

2 weeks in premature neonates.

87
Q

Parvovirus infection may cause ____ in children, ____in adults, ____ in patients with chronic hemolytic disorders, ____in the fetus, and _____ in immunocompromised patients.

A

-fifth disease aka erythema infectiosum in children;

-arthropathy mostly in adults;

-aplastic crisis in patients with chronic hemolytic disorders,

-hydrops fetalis in the fetus, and

-pure RBC aplasia in immuno-compromised patients.

88
Q

Definitive diagnosis of parvovirus B19 infection can only be made by ___ test (s).

A

-detection of specific IgM, or

-identification of the viral antigen or DNA in serum or tissue samples.

89
Q

____ is the typical presentation of Atopic Dermatitis (AD).

A

A child often with h/o asthma presents with a SYMMETRICAL, RECURRING erythematous, scaly, and PRURITIC rash on FLEXURAL surfaces such as the ante-cubital and popliteal fossae.

90
Q

The etiology of atopic dermatitis (AD) is unknown, but it is likely linked to _____.

A

immune dysregulation, barrier dysfunction, and the environment.

91
Q

The differential diagnosis of atopic dermatitis (AD) includes ____ conditions.

A
  1. Allergic contact dermatitis: rash on surfaces in contact with the allergen.
  2. Psoriasis: erythematous THICK SCALY (adherent) patches & plaques on EXTENSOR surfaces of the extremities.
  3. Seborrheic dermatitis: uncommon in children d/t low sebaceous gland activity.
    -erythematous scaly patches that are GREASY looking, and typically involve the scalp, eyebrows, alar folds, and intertriginous areas.
  4. Tinea corporis: round lesions that are erythematous with ELEVATED, SCALING borders and CENTRAL CLEARING.
    -not symmetrical
    -not typically recurring.
92
Q

Superficial infantile hemangioma (IH) formerly known as _____ typically appears around ___ age as a solitary, painless lesion on skin/mucus membrane, and has the potential to proliferate.

A

fka strawberry hemangioma (see attached image).

typically appear before 4 weeks of age.

93
Q

An infantile hemangioma (IH) that usually arises before 4 weeks of age may proliferate until ____ age, after which the growth plateaus and then regresses which continues and completes by ___ years of age.

A

-proliferates during the first 5-8 months of age, f/by

-plateau of growth between 6-12 months of age, f/by

-regression/involution that may be completed by 4 years of age.

94
Q

Infantile hemangiomas (IHs) are not present at birth but may arise from several types of precursor lesions (present at birth) such as _____ (list all).

A

-pale area of blanching (vasoconstriction)
-an erythematous macule
-a telangiectatic red macule
-blue bruise-like patches.

95
Q

What are the differential diagnoses in a child p/with a red/pink skin lesion?

A
  1. Infantile hemangiomas (IHs):
    -not present at birth but may arise from an area of blanching or macular erythema that is present at birth.
    -appears within 4 wks. after birth.
    -proliferate in the first 5-8 mo. of age.
    -Regression after 6-12 months that is completed by age 4 years.
  2. Port-wine stain:
    -pink patch but does not proliferate into a red plaque.
  3. Pyogenic granuloma
    -papule/nodule on a narrow base
    -rarely occurs before 1 year of age.
  4. Arteriovenous malformation: pulsatile with bruit.
  5. Kaposiform hemangio-endothelioma: a/w aggressive growth, and often nodular.
96
Q

Infantile Hemangiomas (IHs) most commonly occur on _____locations followed by ___ and ___.

A

-head & neck (in 60% cases) f/by
-trunk (25% of cases), and
-extremities (15% of cases).

97
Q

Superficial infantile hemangiomas (IHs) involve ____ skin layers, and appear raised, lobulated, and bright red.

A

superficial dermis

98
Q

Deep hemangiomas are also called _____ hemangiomas that arise from ____ skin layers, and appear as a bluish-hued nodule, plaque, or tumor.

A

also called subcutaneous hemangiomas;

arise from the reticular dermis and/or the subcutis layer.

*Mixed hemangiomas have features of both superficial and deep hemangiomas.

99
Q

Complicated infantile hemangiomas include ______ .

A
  1. Ulcerated IHs ( in ~10%):
    -esp. in anogenital region, lower lip, axilla, and neck regions.
  2. Ophthalmologic complications include amblyopia, astigmatism, myopia, retrobulbar involvement, and tear duct obstruction.
  3. Airway obstruction in nasal, subglottic, and laryngeal passages.
  4. Difficulties with feeding with perioral or lip hemangiomas.
  5. Visceral hemangiomatosis:
    -esp. with multifocal hemangiomas (≥ 5 lesions),
    -may be a/w liver or GI involvement.
  6. Cosmetic disfigurement with large IHs involving the face, perioral area, ears, or nasal tip (Cyrano nose).
  7. PHACES syndrome:
    -posterior fossa malformations,
    -hemangioma: large segmental cervico-facial hemangioma (≥ 5 cm),
    -arterial anomalies,
    -cardiac anomalies,
    -eye anomalies, and
    -Sternal or abdominal clefting.
  8. LUMBAR syndrome:
    -lumbosacral hemangioma,
    -urogenital anomalies,
    -myelopathy,
    -bony deformities,
    -anorectal/arterial anomalies
    -renal anomalies.
100
Q

True/False?
Most infantile hemangiomas do not require treatment because they resolve on their own.

A

true

101
Q

_____ are the first-line agents used in the m/m of complicated Infantile Hemangiomas (IHs); _____ can be used as alternative agents.

A

beta blockers, e.g. oral propranolol (2mg/kg/day);

alternative agents: oral prednisone (2-4mg/kg/day).

102
Q

Topical beta blocker such as timolol, may be used to t/t ___ type of IH.

A

small, superficial, and uncomplicated IH.

*topical timolol which may prevent proliferation and hasten regression.

103
Q

Pulsed dye laser (PDL) is indicated for resolution of _____ in patients with IH.

A

residual erythema and telangiectasias in lesions that have involuted.

104
Q

Parental consent is usually required if a patient is ____ years of age. Exceptions include patients who have children of their own, are married, or are financially independent of their parents.

A

<18 years of age.

105
Q
A