Childhood Infectious Diseases

   
 
Table 2-3 Childhood Infections
 Disease Exanthem Etiology/Course
 
Acute Hemorrhagic
Edema of Infancy

(Finkelstein Disease)
Large circinate painful purpuric plaques involving face, ears, distal extremities → evolve into edematous targetoid lesions
Etiology: likely infectious (viral or bacterial)

Age: 6 months–3 years; self-limited

Leukocytoclastic vasculitis seen on histology

May be hypersensitivity reaction to infection (medication/vaccination less likely)
 
Erythema Infectiosum
(‘Slapped Cheek’ or
Fifth Disease)
Bright red macular erythema over cheeks → lacy eruption mainly on the extremities
Etiology: parvovirus B19 (ssDNA) also causes hydrops fetalis; peaks in spring and winter

Age: school-age children; self-limited

Mild prodrome, 10% with arthralgias
 
Gianotti–Crosti
Syndrome
Abrupt onset of skin-colored to pink-red edematous papules to cheeks, buttocks, extremities
Etiology: likely infectious (HBV, EBV)

Age: 6 months–2 years; self-limited

May have low-grade fever and lymphadenopathy
 
Hand-Foot-Mouth
Disease
Elliptical grayish vesicles, pustules, and erosions on hands, feet, and buttocks


Oral: vesicles/erosions red base
Etiology:coxsackievirus A16 (enterovirus 71 less often)

Age: children <10 years (± adults); self-limited

Fever, sore mouth, anorexia, abdominal pain; enteroviral infection may also cause myocarditis, pneumonia, meningoencephalitis
 
Henoch–Schönlein
Purpura (HSP)
Purpuric macules and papules favoring lower extremities and buttocks
Etiology: possibly infectious (viral, strep)

Age: peaks at 4–7 years (± adults); self-limited Presents 1–2 week after upper respiratory infection

Arthralgias, GI bleeding, abdominal pain, nephritis with hematuria → IgA vasculitis
 
Herpangina
Exanthem: often absent

Oral: painful gray vesicles on
tonsillar, palate, buccal mucosa
Etiology: various enteroviruses (often coxsackie group A/B and echovirus)

Age: 3–10 years old; self-limited
 
Kawasaki Disease
(Mucocutaneous Lymph
Node Syndrome)
Polymorphous eruption (morbilliform, erythema multiforme-like or bullous); ± edema and erythema of distal extremities; can be generalized or localized (groin, LE)


Oral: red swollen or dry fissured lips; strawberry tongue; pharyngeal erythema
Etiology: unknown but likely infectious

Age: children <5 years of age

Arthritis, abdominal pain, GI symptoms

Complications: cardiac aneurysm (in ¼ of untreated patients), myocarditis, pericarditis Oral: red swollen or dry fissured lips; strawberry tongue; pharyngeal erythema

Need 5 of 6 criteria for diagnosis: rash • fever >5 days • conjunctivitis • palmoplantar erythema, edema, or desquamation • swollen lips or red tongue • cervical lymphadenopathy
 
Measles (Rubeola or
First Disease)
Erythematous macules/papules over forehead, hairline, and behind the ears → spreads downward


Oral: Koplik spots (gray papules on buccal mucosa)
Etiology: measles virus (paramyxovirus)

Age: unvaccinated children

Prodrome: fever, cough, nasal congestion, rhinorrhea, conjunctivitis; rash appears after Koplik spots

Complications:encephalitis, otitis media, pneumonia, myocarditis, ± subacute sclerosing panencephalitis
 
Infectious
Mononucleosis
Polymorphous: morbilliform (common), urticarial, petechial, or erythema multiforme-like lesions


Of note, morbilliform eruption may occur after treatment with ampicillin
Etiology: infectious (EBV)

Age: children, young adults (15–25 years); self-limited

Fever, pharyngitis, fatigue, myalgias, headaches, hepatosplenomegaly, lymphadenopathy

Complications: splenic rupture, airway obstruction, hepatitis
 
Papular Purpuric
Gloves and Socks
Syndrome
Erythema, edema, petechiae, and purpura on palms/soles (± extension to dorsal aspect), + burning and pruritus
Etiology: parvovirus B19

Age: children and young adults; self-limited

Mild prodromal symptoms, occurs mainly in young adults; peaks in spring
 
Roseola
(Exanthem Subitum
or Sixth Disease)
Circular to elliptical “rose red” macules or papules involving trunk, occasionally surrounded by white halo
Etiology: human herpesvirus 6 (HHV6)

Age: 6 months–3 years

Sudden-onset high fever; rash begins as fever subsides

Complications in healthy patient: mainly seizures
 
Rubella
(German Measles or
Third Disease)
Erythematous macules and papules on face → spreads acrally, accompanied by tender lymphadenopathy (occipital, postauricular, cervical)
Etiology: togavirus (ssRNA)

Age: unvaccinated children/adults; self-limited

Usually mild prodrome

Complications: arthralgia/arthritis, hepatitis, myocarditis, pneumonia
 
Scarlet Fever
(Second Disease)
Erythema of axilla, neck, chest → evolve to pink papules with erythematous background (sandpaper-like) → hand and foot desquamation (7–10 days later); Pastia’s lines (linear petechial streaks in body folds)

Oral: “red strawberry” tongue
Etiology: group A β-hemolytic streptococci (erythrogenic toxin A, B, C)

Age: children (1–10 years old)

Extracutaneous: sore throat, headaches, chills, fever, nausea, abdominal pain, anorexia

Treatment: PCN 10–14 days (erythromcyin in PCN- allergic pts)
 
Unilateral
Laterothoracic
Exanthem
Morbilliform or eczematous eruption in axilla and lateral trunk with unilateral dominance (± bilateral involvement)
Etiology: likely viral

Age: children (6 months–10 years); self-limited
 
Varicella (Chickenpox)
Pruritic, erythematous macules/papules of scalp, face → spreads to trunk and extremities, evolves into vesicles with narrow red halo (“dew drops on rose petal”), central crust or necrosis seen within lesions
Etiology : varicella zoster virus (VZV)

Age : children and adults; self-limited in healthy children

Complications in children: secondary bacterial infection

Adults with more severe presentation (pneumonia, 10–30% mortality if untreated)

All stages of development seen simultaneously
      
 
   


Figure 2.3 A: Dermal hematopoiesis (Courtesy of Dr. Vandana Mehta) B: Congenital syphilis (Courtesy of Dr. Paul Getz) C: Congenital syphilis (Courtesy of Dr. Paul Getz) D: Congenital syphilis (Courtesy of Dr. Paul Getz) E: Candidiasis (Courtesy of Dr. Paul Getz) F: Langerhans cell histiocytosis (Reprint from Morgan MB, Smoller BR, Somach SC. Deadly Dermatologic Diseases. New York, NY: Springer; 2007)
Figure 2.3
A: Dermal hematopoiesis
(Courtesy of Dr. Vandana Mehta)
B: Congenital syphilis
(Courtesy of Dr. Paul Getz)
C: Congenital syphilis
(Courtesy of Dr. Paul Getz)
D: Congenital syphilis
(Courtesy of Dr. Paul Getz)
E: Candidiasis
(Courtesy of Dr. Paul Getz)
F: Langerhans cell histiocytosis
(Reprint from Morgan MB, Smoller BR, Somach SC. Deadly Dermatologic Diseases. New York, NY: Springer; 2007)
 
Figure 2.4 A: Acrodermatitis enteropathica (Courtesy of Michelle B. Bain) B: Acrodermatitis enteropathica (Courtesy of Michelle B. Bain) C: Gianotti–Crosti syndrome (Courtesy of Dr. Michelle B. Bain) D: Gianotti–Crosti syndrome (Courtesy of Dr. Michelle B. Bain) E: Varicella (Reprint from Abdel-Halim AW. Passing the USMLE. New York , NY: Springer , 2009) F: Papular purpuric gloves and socks syndrome (Reprint from Burgdorf WH , Plewig G, Wolff HH, Landthaler M, eds.. Braun-Falco’s Dermatology. 3rd ed. Heidelberg: Springer; 2009)
Figure 2.4
A: Acrodermatitis enteropathica
(Courtesy of Michelle B. Bain)
B: Acrodermatitis enteropathica
(Courtesy of Michelle B. Bain)
C: Gianotti–Crosti syndrome
(Courtesy of Dr. Michelle B. Bain)
D: Gianotti–Crosti syndrome
(Courtesy of Dr. Michelle B. Bain)
E: Varicella
(Reprint from Abdel-Halim AW. Passing the USMLE. New York, NY: Springer, 2009)
F: Papular purpuric gloves and socks syndrome
(Reprint from Burgdorf WH, Plewig G, Wolff HH, Landthaler M, eds.. Braun-Falco’s Dermatology. 3rd ed. Heidelberg: Springer; 2009)