LE 1 - Randoms Flashcards
(84 cards)
A newborn presents with tiny white bumps on the face, primarily on the nose, cheeks, and chin. The pediatrician diagnoses the condition as milia. Which of the following statements is true?
a. Milia are large, fluid-filled cysts that require surgical removal.
b. Milia typically resolve within a few days after birth.
c. Milia are seen in approximately 33% of infants.
d. Milia are a sign of underlying infectious disease.
c. Milia are seen in approximately 33% of infants
π§ Rationale:
β¨ Milia are tiny white keratin-filled cysts from retained sebaceous material.
π Commonly on nose, cheeks, chin
β³ Seen in ~33% of newborns, resolve spontaneously within weeks
π« Why not the others:
β a. Milia are small, not large, donβt need surgery
β b. Resolve in weeks, not just days
β d. Not infectious
A 2-week-old infant presents with a persistent diaper rash characterized by erythematous plaques with sharply demarcated edges. The pediatrician suspects Candida albicans infection. Which of the following statements is true?
a. The rash is typically contained within the diaper area and does not involve skin folds.
b. The condition is best treated with frequent diaper changes and keeping the area dry.
c. Skin folds are usually spared in this type of diaper rash.
d. Antifungal treatment is often required to resolve the rash.
d. Antifungal treatment is often required to resolve the rash
π§ Rationale:
π Candida diaper dermatitis:
π₯ Beefy red plaques, sharp borders
π Involves skin folds
π― Needs topical antifungal like nystatin
π« Why not the others:
β a/c. Fungal rash does involve skin folds
β b. Keeping dry helps, but antifungal is essential
A newborn is found to have vesicopustules that rupture, leaving behind a scaling halo and eventually hyperpigmented macules. The diagnosis is transient neonatal pustular melanosis. Which of the following statements is true?
a. The condition typically requires intensive antibiotic therapy.
b. It is a benign and self-limiting condition requiring no specific therapy.
c. Lesions are often concentrated on the infantβs limbs only.
d. Hyperpigmentation following the lesions does not resolve and is permanent.
b. It is a benign and self-limiting condition requiring no specific therapy
π§ Rationale:
π Vesicopustules rupture β scaling with hyperpigmented macules
πΆ Seen in newborns, especially with darker skin
β No treatment needed, resolves in weeks to months
π« Why not the others:
β a. Not bacterial β no antibiotics
β c. Commonly on neck, forehead, limbs, back, not limited to limbs
β d. Pigmentation fades over time
An infant presents with comedones and papules on the cheeks, chin, and forehead, diagnosed as acne neonatorum. Which of the following statements is true?
a. The condition is usually severe and requires aggressive treatment with oral antibiotics.
b. Acne neonatorum often results in significant scarring.
c. The condition is usually benign and self-resolving, with severe cases possibly requiring mild keratolytic agents.
d. Treatment with topical steroids is the first-line therapy.
c. The condition is usually benign and self-resolving, with severe cases possibly requiring mild keratolytic agents
π§ Rationale:
πΆ Neonatal acne due to maternal androgens
β³ Appears around 2β4 weeks, resolves by 4 months
π§΄ May use topical benzoyl peroxide or keratolytics if persistent
π« Why not the others:
β a. Usually mild, no oral meds
β b. Rarely scars
β d. Steroids not first-line, can worsen acne
A newborn exhibits a vesicular rash in areas where a fetal scalp monitor was placed during delivery. The pediatrician is concerned about herpes simplex infection. Which of the following statements is true?
a. The rash typically resolves on its own without antiviral treatment.
b. Lesions are most commonly found in the abdominal area.
c. Antiviral treatment is necessary due to the risk of systemic involvement.
d. Herpes simplex infection in newborns is typically acquired postnatally.
c. Antiviral treatment is necessary due to the risk of systemic involvement
π§ Rationale:
𧬠HSV in newborns = serious risk of CNS or disseminated disease
π Immediate IV acyclovir required
β οΈ Can be acquired during delivery via maternal shedding
π« Why not the others:
β a. Must be treated, high morbidity if untreated
β b. Lesions usually on scalp, face, eyes, mucosa
β d. Most HSV infections are perinatal, not postnatal
During a routine check-up, a parent expresses concern about pink patches on their infantβs neck and eyelids. Which of the following statements is true regarding macular hemangiomas, commonly known as βStork Bitesβ?
a. They are a collection of dilated blood vessels that will persist throughout life.
b. They are commonly located on the limbs and torso and increase in size with age.
c. They typically resolve spontaneously within the first year of life.
d. They often require surgical removal due to medical complications.
c. They typically resolve spontaneously within the first year of life.
π§ Rationale:
πΆ Macular hemangiomas (aka nevus simplex) are benign capillary malformations
π Commonly found on glabella, eyelids, nape (βstork biteβ)
β³ Most fade by 1 year (especially facial ones)
π« Why not the others:
β a. They do not persist for life (nape ones may remain faint)
β b. Found on head/neck, not limbs/torso
β d. No surgery needed β totally benign
A newborn presents with a flat, red to purple lesion on their face that does not blanch when pressed. Which statement is correct about Port-Wine Stains (Nevus Flammeus)?
a. They are likely to disappear by the age of 2.
b. They are highly responsive to topical treatments and usually resolve within months.
c. They do not blanch with pressure and do not disappear with time.
d. They are usually indicative of underlying neurological abnormalities.
c. They do not blanch with pressure and do not disappear with time.
π§ Rationale:
𧬠Capillary malformation that is congenital and permanent
π§ͺ Do not fade or blanch
π‘ May be associated with Sturge-Weber syndrome if on the trigeminal nerve distribution
π« Why not the others:
β a. They do not disappear by age 2
β b. Not responsive to topical meds; require laser if treatment is needed
β d. Only sometimes linked with neurological conditions, not always
A pediatrician examines a child with dark blue patches on the lower back. What is true about Mongolian Spots?
a. They are most commonly found on the face and neck and are indicative of metabolic disease.
b. They often persist into adulthood, requiring cosmetic treatment.
c. They are present in nearly 90% of Black and Asian infants and typically fade by 4 years of age.
d. They are a form of malignant melanoma and require immediate intervention.
c. They are present in nearly 90% of Black and Asian infants and typically fade by 4 years of age.
π§ Rationale:
π¨ Due to dermal melanocytosis
π Seen over sacrum and lower back
π Common in Black, Asian, and Hispanic infants
β³ Fade spontaneously over years
π« Why not the others:
β a. Found on lower back, not face/neck; not metabolic
β b. Fade, no treatment needed
β d. Not melanoma, completely benign
An infant is brought to the clinic with a large, raised, red lesion on the back. Which statement about cavernous hemangioma is accurate?
a. They are superficial vascular lesions that are always present at birth.
b. They are typically a cosmetic concern and do not regress.
c. The majority of these lesions regress with age and do not require treatment.
d. They are primarily found in the mucous membranes of the mouth and nose.
c. The majority of these lesions regress with age and do not require treatment.
π§ Rationale:
π©Έ Deep vascular malformation
πΆ May be present at birth or shortly after
β³ Most involute spontaneously by age 9β10
π¬ Treatment only if ulceration, obstruction, or rapid growth
π« Why not the others:
β a. Often appear after birth
β b. They do regress
β d. Not limited to mucous membranes
A baby is noted to have a bright red, sharply demarcated lesion on their cheek. What is true about Strawberry Hemangiomas?
a. They typically darken and thicken over time, eventually turning into deep vascular nodules.
b. They are flat vascular malformations that will likely require laser removal.
c. The lesions are most common on the torso and usually require corticosteroid treatment.
d. Spontaneous regression is common, with most disappearing by the age of 7.
d. Spontaneous regression is common, with most disappearing by the age of 7.
π§ Rationale:
π Strawberry hemangiomas are superficial capillary hemangiomas
π Appear after birth, grow rapidly for months, then involute
β 90% resolve by age 7, leaving little or no trace
π« Why not the others:
β a. They donβt always deepen/thicken or become nodules
β b. Not malformations; laser is only used in specific cases
β c. Common on face/head, and most donβt require corticosteroids
During a pediatric rotation, you notice a newborn with a swollen scalp that crosses suture lines. In discussing this observation with your attending, you note that this swelling can be differentiated from other scalp conditions by which of the following characteristics?
a. The swelling is limited to the area above one cranial bone and does not cross suture lines.
b. The swelling is a result of blood collected beneath the periosteum of the cranial bone.
c. The swelling is a soft, diffuse, edematous area on the scalp that may cross suture lines.
d. The swelling is associated with a high risk of jaundice in the newborn.
c. The swelling is a soft, diffuse, edematous area on the scalp that may cross suture lines.
π§ Rationale:
π This describes caput succedaneum
β¨ Key feature: crosses suture lines
π§ Due to serosanguinous fluid in subcutaneous tissue from birth pressure
π« Why not the others:
β a/b β Describe cephalohematoma, which is limited by suture lines
β d β Jaundice is more strongly associated with cephalohematoma (due to RBC breakdown)
You are examining a newborn with a well-defined, fluctuant swelling on the head. To determine whether this is a cephalohematoma, which characteristic would you expect to find?
a. The swelling crosses the cranial suture lines.
b. The swelling fluctuates significantly with crying.
c. The swelling is confined to the surface of one cranial bone and does not cross suture lines.
d. The swelling typically resolves within the first few hours after birth.
c. The swelling is confined to the surface of one cranial bone and does not cross suture lines.
π§ Rationale:
π©Έ Cephalohematoma = subperiosteal blood collection
π¬ Bound by periosteum, so does not cross sutures
β³ May take weeks to resolve and can lead to jaundice
π« Why not the others:
β a β Caput succedaneum crosses sutures
β b β Fluctuation with crying is not a key feature
β d β Cephalohematoma resolves over weeks, not hours
A newborn has an unusual contour of the skull that you are evaluating. What finding on physical examination would suggest the presence of βstep-offsβ in the skull?
a. A smooth, rounded contour of the skull without abrupt changes.
b. An abrupt change in the contour that feels like an edge or step in the skull bones.
c. A diffuse swelling that extends across the suture lines of the skull.
d. A soft, boggy mass that changes in size with palpation.
b. An abrupt change in the contour that feels like an edge or step in the skull bones.
π§ Rationale:
β οΈ Step-offs suggest skull fracture or abnormal overlap from trauma
β Detected by palpating along suture lines and bony ridges
π« Why not the others:
β a β Describes a normal skull
β c β Describes caput succedaneum
β d β Suggests soft tissue swelling, not a bony abnormality
When assessing the skull of a newborn, you notice that the sutures are more palpable and wider than usual. Which of the following could be a potential implication of widely-spaced sutures?
a. They are indicative of normal intracranial pressure and healthy skull development.
b. They could signify increased intracranial pressure or a genetic syndrome.
c. They are typically associated with a smaller than average head circumference.
d. They usually suggest premature closure of the cranial sutures.
b. They could signify increased intracranial pressure or a genetic syndrome.
π§ Rationale:
𧬠Could indicate hydrocephalus, Down syndrome, or hypothyroidism
β οΈ Increased ICP causes sutures to separate
π« Why not the others:
β a β Wide sutures are not a sign of healthy pressure
β c β Often associated with macrocephaly, not microcephaly
β d β Premature closure = craniosynostosis, opposite finding
During a routine checkup, a parent expresses concern about their infantβs head shape, noting a flattening on one side. You understand that this condition, known as plagiocephaly, is often due to:
a. Genetic factors leading to asymmetric growth of the skull.
b. Frequent and prolonged time spent on the infantβs back.
c. An early closure of the cranial sutures.
d. A vitamin D deficiency in the infant.
b. Frequent and prolonged time spent on the infantβs back.
π§ Rationale:
π€ Positional plagiocephaly common in babies who sleep supine for long periods
πΆ More noticeable with limited tummy time
π‘ Managed with repositioning, supervised prone time, sometimes helmeting
π« Why not the others:
β a β Genetic causes are rare in positional plagiocephaly
β c β That would be craniosynostosis
β d β Not linked to vitamin D deficiency
Youβre observing infants in the NICU and note that some have elongated head shapes. You recognize this as dolichocephaly, which can be caused by:
a. Habitual sleeping on the stomach.
b. Consistently turning the head to one side while lying in the NICU.
c. Premature closure of the sagittal suture.
d. Excessive growth of the coronal sutures.
b. Consistently turning the head to one side while lying in the NICU.
π§ Rationale:
ποΈ Dolichocephaly = long, narrow head shape
π Common in preterm NICU infants due to positional molding
π€ Often from consistent positioning in sidelying or lateral rotation
π« Why not the others:
β a β Stomach sleeping may cause brachycephaly, not dolichocephaly
β c β Premature sagittal suture closure causes pathologic dolichocephaly, not positional
β d β Coronal suture overgrowth isnβt a real mechanism
A pediatrician examines an infant with an abnormally shaped head and suspects premature suture closure. Which condition is often associated with this finding?
a. Plagiocephaly
b. Craniosynostosis, as seen in conditions like Apertβs syndrome.
c. Dolichocephaly, due to NICU positioning.
d. Caput succedaneum, due to birth trauma.
b. Craniosynostosis, as seen in conditions like Apertβs syndrome.
π§ Rationale:
π Craniosynostosis = premature fusion of cranial sutures
𧬠Can be syndromic (e.g., Apert, Crouzon syndrome)
π Causes abnormal skull growth due to compensatory expansion elsewhere
π« Why not the others:
β a β Plagiocephaly = positional, not suture fusion
β c β Dolichocephaly can be positional or pathologic, not always syndromic
β d β Caput = soft tissue swelling, not bone/suture pathology
In a newborn exam, you note that gentle pressure on the parietal bones elicits a βping-pong ballβ effect. This finding is known as craniotabes and may be:
a. A normal variant in a newbornβs skull.
b. Always indicative of hydrocephalus.
c. Typically associated with a high risk of intracranial hemorrhage.
d. A sign of rickets, congenital syphilis, or hydrocephalus if other symptoms are present.
d. A sign of rickets, congenital syphilis, or hydrocephalus if other symptoms are present
π§ Rationale:
π§Έ Craniotabes = soft skull bones that indent like a ping-pong ball
π May be benign in newborns (esp. occiput), but if persistent or with other findings:
𦴠Think rickets
π¦ Think congenital syphilis
π§ Possibly hydrocephalus
π« Why not the others:
β a β Only normal if isolated
β b β Not always linked to hydrocephalus
β c β Does not predict ICH
A pregnant woman has elevated levels of MSAFP at 19 weeks of gestation. This finding most strongly suggests an increased risk for which of the following conditions in the fetus?
a. Neural tube defects
b. Congenital heart disease
c. Gastrointestinal malformations
d. Trisomy 13 (Patau syndrome)
a. Neural tube defects
π§ Rationale:
π High MSAFP is most commonly linked to:
π§ Open neural tube defects (e.g., spina bifida, anencephaly)
π©Έ Also seen in abdominal wall defects (e.g., gastroschisis)
π« Why not the others:
β b/c β Not strongly associated
β d β Trisomy 13 usually has normal or low AFP
In prenatal screening, elevated levels of Ξ²-HCG are most commonly associated with an increased risk for which chromosomal abnormality?
a. Trisomy 18 (Edwards syndrome)
b. Trisomy 21 (Down syndrome)
c. Turner syndrome (45, X)
d. Klinefelter syndrome (47, XXY)
b. Trisomy 21 (Down syndrome)
π§ Rationale:
π In Down syndrome, second-trimester triple/quad screens show:
β¬οΈ Ξ²-hCG
β¬οΈ MSAFP
β¬οΈ Estriol
π« Why not the others:
β a β Trisomy 18: β¬οΈ hCG
β c/d β Turner & Klinefelter donβt classically elevate Ξ²-hCG in screening
A quad screen reveals low levels of unconjugated estriol in a pregnant woman. This result is most suggestive of an increased risk for:
a. Neural tube defects
b. Trisomy 21 (Down syndrome)
c. Fetal adrenal hyperplasia
d. Ovarian dysgenesis
b. Trisomy 21 (Down syndrome)
π§ Rationale:
π Quad screen pattern for Trisomy 21:
β¬οΈ MSAFP
β¬οΈ Unconjugated estriol (uE3)
β¬οΈ Ξ²-hCG
β¬οΈ Inhibin A
π« Why not the others:
β a. Neural tube defects β β¬οΈ MSAFP
β c. Fetal adrenal hyperplasia β no characteristic uE3 drop
β d. Ovarian dysgenesis β unrelated to estriol levels
High levels of inhibin A in a maternal serum screen are most indicative of an increased risk for which condition?
a. Trisomy 13 (Patau syndrome)
b. Trisomy 18 (Edwards syndrome)
c. Trisomy 21 (Down syndrome)
d. Monosomy X (Turner syndrome)
c. Trisomy 21 (Down syndrome)
π§ Rationale:
π Inhibin A is elevated in Down syndrome pregnancies
π― Best interpreted with the other quad markers
π« Why not the others:
β a. Trisomy 13 β No clear inhibin A pattern
β b. Trisomy 18 β All markers tend to be low
β d. Turner syndrome β May affect nuchal translucency and other findings, but not typically inhibin A alone
Low levels of MSAFP, Ξ²-HCG, unconjugated estriol, and inhibin A together would most likely suggest an increased risk for:
a. Trisomy 18 (Edwards syndrome)
b. Trisomy 21 (Down syndrome)
c. Trisomy 13 (Patau syndrome)
d. Neural tube defects
a. Trisomy 18 (Edwards syndrome)
π§ Rationale:
π Trisomy 18 screening pattern:
β MSAFP
β Ξ²-hCG
β Estriol
β Inhibin A
π« Why not the others:
β b. Down syndrome β β Ξ²-hCG and inhibin A
β c. Trisomy 13 β Variable screen, not consistent
β d. Neural tube defects β β MSAFP
A fetal heart rate consistently above 160 bpm could indicate several conditions. Which of the following is a possible cause of fetal baseline tachycardia?
a. Maternal hypothyroidism
b. Fetal complete heart block
c. Maternal use of sympathomimetic medication
d. Fetal bradycardia
c. Maternal use of sympathomimetic medication
π§ Rationale:
β οΈ Baseline fetal tachycardia (>160 bpm) may be caused by:
π€ Maternal fever/infection
β¬οΈ Sympathomimetic drugs (e.g., decongestants, Ξ²-agonists)
β¬οΈ Thyroid hormone (maternal hyperthyroidism)
π« Fetal hypoxia
π« Why not the others:
β a. Maternal hypothyroidism β no tachycardia
β b. Fetal complete heart block β causes bradycardia
β d. Fetal bradycardia β opposite condition