Bacterial Rashes












CHAPTER 12
BACTERIAL RASHES

 


Scarlet Fever







































Synonym Scarlatina.
Inheritance n/a
Prenatal Diagnosis n/a
Incidence Actual numbers of cases are not tracked but ~10% of patients who contract pharyngitis because of group A beta-hemolytic streptococcus (GABHS) will develop SF.
Age at Presentation M = F; no racial predilection; typically seen in ages 4 to 15 years and most commonly in children of 4 to 8 years of age; rare under 1 to 3 years of age owing to protective maternal anti-exotoxin antibodies; by 10 years of age, ~80% of children have developed lifelong protective antibodies to causative streptococcal pyrogenic exotoxins; recurrences are rare due to cross reactivity of antibodies to exotoxins.
Pathogenesis Associated with streptococcal pharyngitis though can rarely occur due to infection at other sites; cutaneous reaction to erythrogenic toxins A, B, and C produced by streptococci but most commonly group C.
Key Features

Often presents as a syndrome of exudative pharyngitis, fever, and bright-red exanthem (rash on skin).



  • Oropharynx/tonsillopharynx: ~1- to 4-day incubation period for strep throat then abrupt onset of fever and sore throat; nausea, vomiting, headache, and abdominal pain are possible, particularly in younger children; beefy-red, enlarged tonsils with possible petechiae present on soft palate; white strawberry tongue on first 2 days then and red strawberry tongue; often tender anterior cervical adenopathy.
  • Skin: 1 to 2 days after fever onset can see erythematous patches develop on neck and upper trunk; by ~day 4 classic erythematous, rough, sandpaper-like rash rapidly develops on trunk and extremities; circumoral pallor also possible; accentuation often occurs in skin folds with some linear purpura referred to as Pastia lines; rash lasts ~4 to 5 days then will see desquamation that resolves over 1 to 2 weeks but can sometimes take a month to clear and often dramatic peeling of the palms and soles.
  • Gastrointestinal: Mesenteric lymphadenopathy can mimic “acute abdomen.”
Differential Diagnosis Some toxin producing staphylococci may produce an identical skin eruption, pityriasis rosea, rubeola (measles), rubella (German measles), erythema infectiosum (parvo B-19 infection), staphylococcal scalded skin syndrome (SSSS), erythema toxicum neonatorum, infectious mononucleosis (Epstein-Barr virus infection), Kawasaki disease, toxic shock syndrome (TSS), perianal streptococcal dermatitis, other viral exanthems, and drug eruptions.
Laboratory Data Throat culture or rapid streptococcal antigen testing to identify organism and direct treatment.
Management

10- to 14-day course of oral antibiotics indicated, generally rapid clinical improvement.



  • Penicillins are the drugs of choice unless documented allergy; penicillin VK 250 mg bid in children, 500 mg bid for adolescents; intramuscular penicillin (benzathine penicillin G) is an option if necessary (<27 kg 600,000 units IM ×1 dose; >27 kg 1.2 million units IM ×1 dose); amoxicillin 25 to 30 mg/kg/day based on weight divided bid, if >40 kg then 500 mg bid.
  • First-generation cephalosporins may be effective; cephalexin 25 to 50 mg/kg/day divided q6-8h (max 4 g/day).
  • Clindamycin and macrolides are also effective options though some GABHS resistance can be seen to the latter; erythromycin has also been used but resistance and GI toleration issues are also possible.
  • Simple emollients for desquamation.
Prognosis Generally excellent if identified and treated promptly. Treatment is indicated to prevent both the nonsuppurative (eg, acute rheumatic fever [ARF], poststreptococcal glomerulonephritis) and suppurative (eg, peritonsillar abscess, mastoiditis, and adenitis) complications of streptococcal infection, and to reduce the symptoms from strep pharyngitis.

image PEARL/WHAT PARENTS ASK


Be sure to warn parents of the desquamation that occurs 1 to 2 weeks after the rash resolves and the dramatic peeling that may occur on the hands and feet.











Skin | Associated Findings
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12.1. Scarlatina.

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12.2. Scarlatina.


Erythema Marginatum (Rheumatic Fever)







































Synonym Erythema marginatum rheumatica and erythema annulare.
Inheritance n/a
Prenatal Diagnosis n/a
Incidence/Prevalence 6% to 10% of patients with ARF; incidence of ARF following streptococcal pharyngitis is ~0.5% to 3% of infected patients (0.23-1.88 patients per 100,000 population).
Age at Presentation ARF occurs most often in patients aged 6 to 20 years and rarely occurs after the age of 30.
Pathogenesis Complication of GABHS pharyngitis (not cellulitis), exact pathophysiologic pathway is not known; erythema marginatum is not a diagnosis but a sign underlying ARF.
Key Features

  • Skin: Short-lived, erythematous, annular lesions with raised edges and central clearing over time; adjacent lesions expand and meet and tend form larger annular and polycyclic lesions (rings of various sizes); can also form rings within rings, commonly on abdomen, chest, and limbs but almost never on face; usually appears at the onset of acute attack of ARF or relapse; frequently is present when there are no other signs of active infection and ESR is normal, will often come and go and can last from 1 or 2 days to months or years.
  • Systemic: Five major clinical criteria for ARF (Jones criteria):

    1. Carditis and valvulitis (pancarditis) clinical or subclinical (50%-70%).
    2. Migratory polyarthritis involving the large joints (35%-66%).
    3. Central nervous system involvement/Sydenham chorea (10%-30%).
    4. Subcutaneous nodules (up to 10%).
    5. Erythema marginatum (6%-10%).

Minor criteria:



  1. Arthralgia.
  2. Fever.
  3. Elevated acute phase reactants (ESR and C-reactive protein).
  4. Prolonged PR interval on electrocardiogram.

To make the diagnosis of ARF, a patient needs 2 major criteria or 1 major plus 2 minor criteria.

Differential Diagnosis Drug reactions, urticaria, hereditary angioedema, streptococcal infections without rheumatic fever, erythema multiforme, urticaria multiforme and other viral exanthems, Kawasaki syndrome, and juvenile idiopathic arthritis.
Laboratory Data High index of suspicion, throat culture is gold standard in diagnosis acute streptococcal pharyngitis; rapid streptococcal antigen test (RST) very high sensitivity, negative RST cannot exclude GABHS so culture should be obtained to confirm the negative RST; clinical diagnosis of streptococcal pharyngitis without a positive culture has a very low sensitivity.
Management

Treat the underlying streptococcal infection to reduce nonsuppurative complications; risk of rheumatic fever recurrence is greatest during the first 3 to 5 years; prophylaxis is recommended indefinitely in patients with established heart disease or if frequently exposed to streptococci.



  • Standard treatment of GABHS: Penicillin VK (oral), benzathine penicillin G (intramuscular).Patients with a nonanaphylactic allergy to penicillin may be treated with a first-generation cephalosporin; those with anaphylactic reactions should be treated with clindamycin; oral macrolides may also be used.
  • Treatment of ARF: Aspirin: Often for 6 to 8 weeks (until symptoms of ARF resolving and erythrocyte sedimentation rate [ESR]/CRP are normal), benzathine penicillin G 1.2 million units IM every 4 weeks (oral therapy is less reliable), oral cephalosporins in penicillin allergic patients; management of heart failure symptoms as recommended by a cardiologist.
Prognosis Prognosis is related to underlying ARF complications. Erythema marginatum (as a sign of ARF) will resolve with time though it can recur or remain present for months to years.

image PEARL/WHAT PARENTS ASK


Just as it is important to emphasize the importance of immunizations to avoid the potentially serious complications of vaccine preventable diseases, it is important to encourage evaluation of children with sore throat with or without fever to exclude streptococcal pharyngitis. When symptoms of strep pharyngitis occur, it is important to confirm the diagnosis and treat early to nonsuppurative complications.











Skin | Associated Findings
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Staphylococcal Scalded Skin Syndrome (SSSS)



































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Aug 17, 2025 | Posted by in PEDIATRICS | Comments Off on Bacterial Rashes

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Synonym Ritter von Ritterschein disease, Ritter disease, and staphylococcal epidermal necrolysis.
Inheritance n/a
Prenatal Diagnosis n/a
Incidence ~8 cases per million children, 45 cases per million in children <2 years.
Age at Presentation Generally appears before 6 years of age.
Pathogenesis Bacterial toxin-mediated from strains of S. aureus (SA) phage group 2 strains 55 and 71; less commonly types 3A, 3B, 3C, and ST121; toxins cleave desmoglein 1 (keratinocyte-to-keratinocyte adhesion molecule in upper epidermis of nonmucosal skin); predisposing infection or bacterial colonization; renal immaturity and lack of antibodies prevents excretion of toxins leading to clinical findings; site of entry/source of infection is often not identified; may be from mild bacterial infections as impetigo, conjunctivitis, and minor wounds; rarely from more severe illnesses as pneumonia, sepsis, and endocarditis.
Key Features

Frequent prodrome of nonspecific upper respiratory symptoms, irritability, and occasionally low grade fever; high fever may indicate serious infection; 1- to 10-day incubation period.



  • Skin: Early painful erythema in flexural areas (eg, skin folds of neck, axillae, inguinal and gluteal areas); spares mucosa; erythema may be difficult to detect in darker skinned patients; can become generalized within ~48 hours; erythema progresses to flaccid blisters and bullae with wrinkling; erosions and desquamation are possible from minor trauma to the skin (Nikolsky sign); crusting and fissuring around mouth, nose, and eyes.
Differential Diagnosis Bullous impetigo, cellulitis, irritant/allergic contact dermatitis, burns, Stevens-Johnson syndrome, toxic epidermal necrolysis, child abuse/neglect, scarlet fever, TSS, and pemphigus foliaceus.
Laboratory Data Bacterial culture of any suspected sites of cutaneous infection or (if none are found) other common sites of colonization (eg, nares, conjunctivae, and nasopharynx) to determine susceptibilities; is helpful to confirm diagnosis though are not always positive; almost all are MSSA, rarely MRSA; clindamycin resistance is rising (~30%-40% in recent studies); ESR often elevated; biopsy not generally necessary though will see subcorneal blister formation with possible acantholysis (loss of intercellular attachments), and inflammation not a typical feature.
Management