Dermatology Flashcards

1
Q

1–2 mm papules and pustules are distributed on the face and scalp.
Lesions are present at birth or within the first 2–4 weeks of life.
Comedones are absent.
What disorder has these findings?

A

Neonatal acne
Explanation
Neonatal acne typically resolves spontaneously within the first 2–3 months of life. The etiology is controversial. Some consider it to be a hypersensitivity reaction to Malassezia furfur. Neonatal acne is sometimes confused with miliaria rubra or cutaneous candidiasis. Treatment consists only of daily cleansing with soap and water. The condition does not scar and usually resolves spontaneously within 3 months. Note that there is a difference between neonatal and infantile acne

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2
Q

A child presents with the following:

Dandy-Walker syndrome
Hemangioma that is large, involving the cervicofacial area, including CN 5 (1)
Intracerebral arterial anomalies
Coarctation of the aorta
Microphthalmia
What is the syndrome presented here?

A

Answer
PHACE(S) syndrome
Explanation
PHACE(S) syndrome occurs with large, segmental facial hemangiomas.
P—posterior fossa abnormalities (Dandy-Walker)
H—hemangioma (generally large, cervicofacial lesions involving cranial nerve 3 distribution)
A—arterial anomalies (typically intracerebral arterial anomalies)
C—cardiac defects, especially coarctation of the aorta
E—eye abnormalities (microphthalmia)
S—sternal defects/supraumbilical raphe

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3
Q

Infants with port-wine stains of the lower extremities are at risk for what syndrome?

A

Klippel-Trenaunay syndrome (KTS)
Explanation
KTS presents with a vascular malformation (often mixed capillary-venous-lymphatic) of an extremity, with soft tissue and/or limb overgrowth and varicose veins. Limb overgrowth is generally progressive in nature.

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4
Q

A 9-year-old girl with a history of atopic dermatitis now presents with areas of hypopigmentation with a fine scale, mostly affecting the cheeks and extensor extremities.

What is the most likely diagnosis?

A

Pityriasis alba
Explanation
Pityriasis alba is common in school-age children with atopic dermatitis and presents as described. It is more apparent on children with darker skin and during summer because the affected skin does not tan normally. It usually affects the cheeks and extensor extremities. The face is the only area affected in up to 50% of cases. Patches vary from 1 cm to 4 cm in size and usually range between 5 and 20 in number. Treatment of pityriasis alba is primarily symptomatic and consists of appropriate general skin care, education about the benign nature of the disorder, and low-potency topical corticosteroid creams and emollients. Sun protection can help prevent tanning of the surrounding skin, which makes the condition more apparent

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5
Q

Is poison ivy spread by fluid contained in the vesicular or bullous lesions?

A

No
Explanation
Poison ivy can only be spread by contact with the plant resin. If the patient or their clothes have not been washed and still contain the poison ivy resin, then it can spread that way!

Treatment of allergic contact dermatitis, such as poison ivy, consists of removal of the antigen, cool compresses (Burow compress [aluminum acetate] is helpful for weepy lesions), topical glucocorticoids, and emollients. If severe, such as extensive poison ivy dermatitis on the face, give systemic glucocorticoids for 14 days. Shorter courses can lead to rebound flaring

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6
Q

A newborn presents with 1–2 mm firm, white papules that appear on the surface of pilosebaceous units on the face.

What is the most likely diagnosis?

A

Milia
Explanation
Milia are 1–2 mm firm, white papules, most commonly on the face. These tiny epidermal inclusion cysts generally resolve spontaneously over several months and require no treatment

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7
Q

What causes Stevens-Johnson syndrome (SJS)?

A

Severe drug reactions
Explanation
SJS presents with skin sloughing and mucous membrane involvement. The most common culprits are sulfa antibiotics and the aromatic antiseizure medications (phenytoin, phenobarbital, or carbamazepine). Treatment consists of discontinuing the offending drug, monitoring for internal organ involvement, and supportive care in a hospital setting with skilled nursing, often in burn units.

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8
Q

A child has a herpes simplex skin infection and develops target-like lesions on the palms and soles. He now has mild mucous membrane involvement as well.

What is the most likely diagnosis?

A

Erythema multiforme (EM)
Explanation
EM consists of well-defined lesions that evolve into target shapes. Palms and soles are frequently involved and mucous membranes may be affected. The target-shaped lesions are pathognomonic for EM and are characterized by a central blister or zone of necrosis/crusting. EM is further subdivided into EM minor and EM major. Both forms have the target lesions; however, in contrast to EM minor, EM major has mucosal involvement and patients can be systemically ill. The fixed target lesions last for several days (a minimum of 7 days) before resolving spontaneously

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9
Q

Fine, white scales without redness on the extensor surfaces of the extremities
Improvement to rash in hot, humid climates and during the summer
Hyperlinear palms and soles
Caused by loss-of-function mutations in the gene encoding filaggrin
Autosomal dominant
What disease has these characteristics?

A

Answer
Ichthyosis vulgaris
Explanation
Ichthyosis vulgaris is the most common ichthyosis, occurring in 1/250 people. It is transmitted in an autosomal dominant fashion. Most commonly, the condition first manifests after 3 months of age. Treatment is irritant avoidance and use of emollients and keratolytic products.

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10
Q

What virus is the most common cause of erythema multiforme (EM)?

A

Herpes simplex virus (HSV)
Explanation
EM is typically a reactive process to a viral illness, classically HSV Type 1. HSV Type 1 ( herpes labialis) is the most common culprit. EM is subdivided into EM minor and EM major, the difference being that EM major has mucosal involvement and patients can be systemically ill. Mycoplasma pneumoniae, other viruses (e.g., Epstein-Barr virus, adenovirus, HIV, CMV), medications, and autoimmune diseases have also been linked to EM.

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11
Q

You diagnose a boy in the 1st few weeks of life with X-linked recessive ichthyosis.

What is associated with this disorder, and what should you check for in this boy?

A

Answer
Undescended testes with underdeveloped penis and scrotum
Explanation
X-linked recessive ichthyosis occurs in 1/2,000–6,000 boys and generally is apparent at birth or during the 1st few months of life. The scales are more pronounced compared to the autosomal dominant form. The trunk is involved, but not the palms and soles. It is caused by the absence of the microsomal enzyme steroid sulfatase. These genitourinary (GU) abnormalities are common in this disorder, with an associated increased risk of testicular cancer. Perinatally, this disorder can cause prolonged labor. Affected boys can have cryptorchidism, with an associated increased risk of testicular cancer. If this diagnosis is suspected, patients need a thorough GU exam. Treatment of the ichthyosis consists of regular bathing and using emollients and keratolytics.

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12
Q

In a patient with extremely severe seborrhea, what diagnosis should you consider?

A

Answer
Langerhans cell histiocytosis
Explanation
Consider this particularly if atrophy, ulceration, or petechiae are present. Send for skin biopsy to diagnose.

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13
Q

What skin condition consists of red, tender, warm nodules that appear on the shins and is associated with infection (e.g., TB, β-hemolytic streptococcal, deep fungal), drugs (e.g., oral contraceptives, sulfas, penicillins), Behçet disease, sarcoidosis, and inflammatory bowel disease in children?

A

Answer
Erythema nodosum (EN)
Explanation
EN is associated with sarcoidosis, but in children, it is more commonly due to infection, drugs, or inflammatory bowel disease. It is often idiopathic, but the most common identifiable cause is streptococcal pharyngitis. EN is a reactive process—removal or treatment of the inciting trigger often results in resolution of the EN. Other treatments include rest, elevation, and NSAIDs

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14
Q

According to the American Academy of Pediatrics 2021 Red Book, should children be excluded from school or sent home early from school because of head lice?

A

No
Explanation
The child does not need to be sent home early. They can stay at school till the end of the day and can return once treatment has begun. “No-nit” policies requiring children to be free of nits before returning to school are not effective in preventing the spread of head lice. They are explicitly discouraged by the 2021 Red Book.

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15
Q

Papules and pustules with open and closed comedones distributed over the face:

Absent at birth
Appear at 2–4 months of age
More common in boys
Identify the disorder that includes these characteristics.

A

Answer
Infantile acne
Explanation
Infantile acne can be contrasted with neonatal acne based on the timing (infantile acne has a later onset) and the lesions (comedones are present in infantile acne). Infantile acne, unlike other lesions, generally requires therapy with topical benzoyl peroxide or antibiotics. It is caused by androgenic stimulation of the sebaceous glands. Infantile acne is potentially persistent and severe cases cause scarring. The condition usually resolves over 6–12 months. Rarely, infantile acne is due to pathologic states of androgen excess, such as congenital adrenal hyperplasia, adrenal tumors, or precocious puberty. If these conditions are suspected, appropriate blood work must be done to further evaluate the cause of infantile acne (e.g., measure 17-hydroxyprogesterone levels

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16
Q

What cancer do you worry about in a child who has a large, congenital melanocytic nevus?

A

Answer
Melanoma
Explanation
The lifetime risk of developing melanoma within a large, congenital melanocytic nevus is 6–8%, with the highest risk during the first 5 years of life. The future risk of melanoma within small or medium congenital melanocytic nevi appears to be small, and malignant change is rare before puberty.

17
Q

A 16-year-old boy presents with:

History of a round ringworm–like lesion 1 week ago
Subsequent development of small, oval, minimally pruritic plaques that run parallel to skin folds and rib lines
What is the most likely diagnosis?

A

nswer
Pityriasis rosea
Explanation
Pityriasis rosea is common in children and adolescents. It often presents with the “herald patch” 1–2 weeks before the pruritic rash appears on the trunk. The latter rash commonly is described as a “Christmas tree” pattern. Treat the symptoms (i.e., itching). Do not confuse this with pityriasis versicolor (a.k.a. tinea versicolor), which is a fungal infection due to Malassezia and requires antifungal therapy. Consider guttate psoriasis and secondary syphilis in the differential diagnosis for adolescents

18
Q

A 1-month-old infant presents with erythema of the scalp with a greasy scale.

What is the most likely diagnosis?

A

swer
Seborrhea
Explanation
Seborrhea is common in infants, typically beginning within the first 2 months of life. Seborrheic dermatitis occurs in infants due to lingering effects of exogenous, maternal hormones on sebaceous glands, and it improves as these hormones dissipate. Gentle shampooing with a selenium sulfide or ketoconazole preparation helps with milder presentations. Emollient use can also help remove scale. Cradle cap is a mild presentation of seborrheic dermatitis on the vertex scalp. Seborrheic dermatitis can be striking and involve the face or even the trunk and diaper area. Most cases are asymptomatic and resolve in several weeks to months

19
Q

Rash that is:

Well-defined, brown-to-reddish plaque with some slight scaling in the axillae, groin, and toe webs
Seen under the breasts of adolescent females with obesity
Caused by Corynebacterium minutissimum
Fluorescent bright red when illuminated with a Wood’s lamp
What is this disorder?

A

Answer
Erythrasma
Explanation
Erythrasma is common in adolescents, especially in those with obesity. Treat localized erythrasma with a topical erythromycin/clindamycin or an “-azole” antifungal cream. Treat extensive erythrasma with oral clarithromycin/erythromycin.

20
Q

A newborn presents with small, whitish-yellow masses on either side of the raphe on the hard palate.

What are these masses?

A

Epstein pearls
Explanation
Epstein pearls are essentially intraoral milia that resolve without treatment.

21
Q

Acrodermatitis enteropathica is due to the deficiency of what mineral?

A

Zinc
Explanation
Acrodermatitis enteropathica (zinc deficiency) can be an acquired or inherited disorder. The genetic form is an autosomal recessive disorder with impaired absorption of zinc from the intestine. Cutaneous manifestations include red, scaly patches in a periorificial distribution (i.e., mouth, anus). Patients also present with alopecia, failure to thrive, and diarrhea

22
Q

A child presents with a nevus of Ota.

What future complications do you worry about in this child?

A

Answer
Ocular and cutaneous melanoma
Explanation
Nevus of Ota (oculodermal melanocytosis) is most commonly seen in Black infants or Asian infants. It presents as unilateral, irregularly speckled areas of bluish-gray discoloration on the face, specifically the periorbital area, temple, forehead, cheek, nose, or sclera. Malignant transformation of the lesion is rare. More common complications include glaucoma, uveitis, and cataracts. Perform periodic eye and skin exams because of the rare complications of cutaneous and ocular melanoma.

23
Q

A 5-year-old has an eczematous rash in the antecubital fossa, popliteal fossa, and back of the neck. He also has double creases under the lower eyelids.

What condition most likely affects these skin areas?

A

Atopic dermatitis
Explanation
Atopic dermatitis has different presentations in different age groups. Infants and young children (0–2 years) have lesions most commonly on the cheeks and extensor surfaces of the extremities, with scalp and trunk involvement as well. Older children (2–16 years), who can scratch more, tend to present like the child described here. Adolescents present with continued flexural and chronic hand/foot dermatitis.

Other clues to diagnosis: double or triple creases under the lower eyelid (Dennie-Morgan lines); obvious sparing around the nose (“headlight sign”); small fissures at the base of the ear lobe; increased skin markings on palms and soles; dry skin (xerosis

24
Q

A newborn presents with an area of absent skin on her head.

What is the most likely diagnosis?

A

Aplasia cutis
Explanation
Aplasia cutis congenita is a congenital absence of skin that usually occurs only in a small, localized area, most commonly on the scalp. ∼ 20% will have underlying skull abnormalities. If it occurs in multiple places on the scalp, look for trisomy 13. Aplasia cutis can also be found in 15% of cases of deletion of the short arm of chromosome 4, the Wolf-Hirschhorn syndrome

25
Q

What are the white blood cells found in the pustules of transient neonatal pustular melanosis (TNPM)?

A

Neutrophils
Explanation
After the pustules rupture, the skin develops scaly, hyperpigmented macules of uniform size that may persist for months before resolving on their own. TNPM is seen in 2–5% of Black neonates.

26
Q

X-linked dominant
Patterned blistering that follows the lines of Blaschko (the routes of embryonic cell migration)—on the extremities most prominent
Delayed eruption of teeth with peg- or cone-shaped teeth; commonly missing teeth as well
Strabismus
Scarring (cicatricial) alopecia, without the potential for hair regrowth
What disorder has these findings?

A

nswer
Incontinentia pigmenti
Explanation
Incontinentia pigmenti is an X-linked dominant disorder that is usually lethal in males. It often presents as a rash on an otherwise healthy baby girl. Boys with this condition usually do not survive. There are 4 different stages of skin findings, but all 4 stages may or may not appear. Some patients have lesions of different stages concurrently. The blistering described is most commonly asked about on exams. Delayed eruption of teeth with peg- or cone-shaped teeth is a classic finding! 7% of affected children become blind due to retinal neovascularization and detachment. Skin biopsy and molecular genetic studies can help confirm the clinical diagnosis. Refer all patients to dentists, ophthalmologists, and neurologists.

27
Q

What syndrome should you suspect in an infant born with a large facial port-wine stain (a.k.a. nebus flammeus)?

A

Sturge-Weber syndrome (SWS)
Explanation
SWS consists of an ipsilateral cerebral vascular malformation that can cause neurologic complications, including seizures, intellectual disabilities, contralateral hemiplegia, choroidal vascular anomalies, and glaucoma.

Traditionally, persons with port-wine stains along the CN 5 (1) distribution were felt to be at the highest risk for SWS. Several studies confirm the GNAQ gene mutation is responsible for SWS capillary malformations.

The majority of facial port-wine stains are not associated with SWS.

28
Q

What presents as a ringworm-like lesion but is not scaly and usually appears on the distal portion of the extremities

A

nswer
Granuloma annulare (GA)
Explanation
GA is a benign skin disorder with an unknown cause. It resembles tinea corporis, but there is no scale on the surface of the lesion as you would see with tinea corporis. It is generally asymptomatic and self-limited, disappearing within months to a few years. If a patient desires treatment, topical corticosteroids are indicated.

29
Q

What are the white blood cells found in the pustules of erythema toxicum neonatorum?

A

Eosinophils
Explanation
Erythema toxicum neonatorum is a common, self-limited condition occurring in the 1st few days of life; rarely is it present at birth. Increased levels of immunological and inflammatory mediators suggest it is an immunological reaction. It consists of small, pink pustules filled with eosinophils. It typically resolves spontaneously within the 1st week of life

30
Q

What is the recommended treatment for a very large congenital dermal melanocytosis on the buttocks area in a Black infant?

A

None
Explanation
Congenital dermal melanocytosis (formerly mongolian spots) are present at birth and are seen in > 60% of Black babies. They disappear or fade over 7–13 years. No therapy is necessary

31
Q

A patient presents with small, grouped, freckle-like, café au lait spots measuring 1–4 mm in the axilla.

What disease should you consider?

A

Neurofibromatosis Type 1 (NF1)
Explanation
The lesions described are known as the Crowe sign, which occurs in the axilla or groin. Crowe sign is among the major diagnostic criteria of NF1. Other major diagnostic criteria of NF1 are ≥ 6 café au lait spots (must be > 5 mm prepubertal and > 15 mm postpubertal). Other associations with café au lait spots are Legius syndrome, McCune-Albright syndrome (irregular border, like the “coast of Maine”), and Watson syndrome.

32
Q

A 5-month-old presents with a hemangioma that involves the orbit.

What is the risk (high or low) of ocular complications?

A

Answer
High
Explanation
Periorbital hemangiomas have ~ 80% risk of ocular complications, including astigmatism, amblyopia, refractive errors, and occasionally blindness

33
Q

10-year-old presents with well-defined, erythematous skin lesions with distinctive, mica-like (silvery) scales that are symmetrical on the knees, elbows, sacral area, and scalp. She has ice pick–like pitting of her nails. Additionally, she has thickened nails and onycholysis (separation of the distal nail from the nail bed).

What is the most likely diagnosis?

A

Psoriasis
Explanation
~ 35% of people with psoriasis experience onset < 20 years of age. Guttate psoriasis is common in children and involves small, scaly papules and plaques of the face, trunk, and extremities. The nail changes are not pathognomonic of psoriasis, but they are commonly seen.