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Cellulitis

Cellulitis: Excerpt from The 5-Minute Pediatric Consult

Nicholas Tsarouhas, MD

Cellulitis - BASICS

Cellulitis - description

  • Cellulitis is an acute, spreading pyogenic inflammation of the dermis and subcutaneous tissue, often complicating a wound or other skin condition.
  • Cellulitis may be further classified by the unique area of the body it affects (e.g., periorbital or orbital cellulitis, peritonsillar cellulitis, etc.).

Cellulitis - general prevention

  • Good wound care can prevent most cases.
  • All wounds should be cleaned with soap and water, then covered with a clean, dry cloth.
  • Topical antibiotic ointment is optional.

Cellulitis - epidemiology

  • The most common cause of cellulitis in children is Staphylococcus aureus or Streptococcus pyogenes infection, which develops secondary to local trauma of the integument.
  • Bacteremic disease, previously seen commonly when Haemophilus influenzae type b (HIB) was prevalent, has now been surpassed by Streptococcus pneumoniae.
  • Clinical failures with penicillin-resistant S. pneumoniae have not yet become a significant problem in cases of uncomplicated cellulitis.

Cellulitis - incidence

Community-acquired methicillin-resistant S. aureus (CA-MRSA) infections continue to rise dramatically, and have become commonplace in the general population.

Cellulitis - prevalence

  • MRSA is a worldwide problem; consistently high prevalence rates are found in the US, South America, Japan and southern Europe.
  • Adult studies of hospitalized patients report prevalences of >30–40% of CA-MRSA among MRSA isolates.
  • The prevalence of CA-MRSA is pediatric patients is much higher.
  • CA-MRSA has predominantly been isolated from skin and soft tissue infections, such as cellulitis, abscesses, folliculitis and impetigo.

Cellulitis - pathophysiology

Most commonly due to local trauma with breaches in the integument (abrasions, lacerations, bite wounds, excoriated dermatitis, varicella, etc.)

  • May develop secondary to local invasion or infection (e.g., sinusitis leading to orbital cellulitis)
  • Hematogenous dissemination (rarely)

Cellulitis - etiology

  • S. aureus
  • Group A—hemolytic streptococci (S. pyogenes)
  • S. pneumoniae: Less common since the advent of childhood vaccination with heptavalent pneumococcal conjugate vaccine (Prevnar)
  • Group B streptococci (GBS), Gram-negative rods (GNR’s): neonates
  • HIB: Rare, due to childhood immunization
  • Pseudomonas aeruginosa, anaerobic bacteria: Immunocompromised children
  • Pasteurella species: From cat and dog bites
  • Eikenella corrodens: From human bites

Cellulitis - associated conditions

  • Periorbital:
    • Usually from local trauma (scratch, impetigo, eczema, excoriated Varicella, etc.)
    • Hematogenous spread is very uncommon
    • Rarely with infectious conjunctivitis
  • Orbital:
    • Commonly associated with severe sinusitis
    • Less commonly: Dental abscess, trauma, hematogenous spread
  • Buccal: Very similar to periorbital cellulitis
  • Peritonsillar:
    • Commonly secondary to severe group A— hemolytic streptococcal pharyngitis
    • Cellulitis may progress to a peritonsillar abscess
  • Extremity: Usually secondary to local trauma
  • Breast: Usually with mastitis (neonates)
  • Perianal:
    • Seen in infants and young children
    • Etiology: Group A streptococcus
    • Perianal pain, pruritus, and erythema; sometimes associated with bloody stools
  • Cellulitis–adenitis syndrome:
    • Uncommon infection of neonates and infants
    • Etiology: GBS, S. aureus, GNR’s
    • Bacteremia/meningitis commonly associated

Cellulitis - DIAGNOSIS

Cellulitis - signs & symptoms

Cellulitis - history

  • An expanding, red, painful area of swelling is the most common presentation.
  • Mild constitutional symptoms (with or without fever) are commonly associated with cellulitis.
  • A history of local trauma to the integument is the clue to the portal of bacterial entry.
  • Visual changes, proptosis, or painful or limited eye movements are worrisome for orbital cellulitis.
  • Painful swallowing, pain with opening the mouth (trismus), muffled (“hot-potato”) voice are classic presenting symptoms of peritonsillar cellulitis/abscess

Cellulitis - physical exam

  • Erythema, edema, tenderness, and warmth: Classic clinical findings of cellulitis
  • Distinct demarcation of raised erythema: Classic description of erysipelas, a superficial cellulitis usually associated with S. pyogenes
  • A red streak extending proximally from the extremity: Lymphangitis, which usually implies more serious involvement
  • Regional adenopathy: Commonly associated with minor cellulitis; occasionally complicated by lymphadenitis

Cellulitis - tests

Cellulitis - lab

  • WBC: Normal or elevated
  • Blood culture: Rarely positive. Ill-appearing children and children with extensive areas of cellulitis may warrant a blood culture.
  • Wound culture: As resistance continues to rise (especially MRSA), wound cultures are useful.

Cellulitis - imaging

  • Radiography: Sometimes helpful to rule out complications such as arthritis or osteomyelitis. Also useful in cases of suspected foreign bodies
  • Head CT scan: Important in orbital cellulitis to delineate extent of disease; also when distinction from periorbital cellulitis is clinically difficult

Cellulitis - diag proced-surgery

In many cases, a cutaneous biopsy, examined by an experienced pathologist, may be needed to identify the correct diagnosis.

Cellulitis - differencial diagnosis

  • Allergic angioedema can be excluded by its lack of tenderness and the absence of fever.
  • Red giant urticaria lesions, similarly, may masquerade as cellulitis.
  • Allergic reactions to insect stings are usually pruritic, and may present with mild to severe local erythema; a bite history should be sought.
  • Contact dermatitis, is distinguished by its painlessness, pruritus, and the Koebner phenomenon (appearance of isomorphic lesions in the lines of scratching).
  • A traumatic contusion may be mistaken for cellulitis, but the history should be confirmatory.
  • Severe conjunctivitis presents with conjunctival injection, chemosis, and discharge.
  • Popsicle panniculitis,” a cold-induced fat injury to the cheeks of infants, mimics buccal cellulitis; a history of cold weather exposure or ice or popsicle sucking should be sought.
  • Erythema nodosum, a panniculitis, consists of raised, tender lesions that are frequently over the shins; it may present as a single erythematous lesion. It is associated with systemic disorders, including inflammatory bowel disease.
  • Superficial thrombophlebitis is distinguished by a tender cord palpable along the course of the affected superficial vein.
  • An eye malignancy (retinoblastoma), invasive tumor (rhabdomyosarcoma), or metastatic disease (neuroblastoma, leukemia, lymphoma) may simulate periorbital or orbital cellulitis.

Cellulitis - TREATMENT

Cellulitis - general measures

Local care of cellulitis involves elevation and immobilization of the limb to reduce swelling, and cool sterile saline dressings to remove purulence from open lesions.

Cellulitis - medication

  • Most cases of uncomplicated, superficial cellulitis may be treated with oral antibiotics active against Staphylococcus and Streptococcus (e.g., amoxicillin–clavulanate, cephalexin, and erythromycin).
  • Isolates resistant to erythromycin may be cross-resistant to clindamycin, as well.
  • Abscesses, (in which S. aureus is a likely pathogen), should be treated with clindamycin, after appropriate incision and drainage; trimethoprim–sulfamethoxazole is an alternative.
  • Ill-appearing children or those with extensive cellulitic lesions require IV antibiotics.
  • As MRSA infections continue to rise, many experts now recommend clindamycin as initial parenteral therapy.
  • Oxacillin, nafcillin, cefazolin, and ampicillin–sulbactam are reasonable alternatives when MRSA is not strongly suspected.
  • Vancomycin is used as empiric therapy in severe or rapidly progressive infections.
  • Linezolid, a newer antibiotic, is very effective against MRSA, but it is expensive and should mostly be reserved for multiresistant organisms.
  • If hematogenous dissemination is a strong possibility, an agent active against HIB also should be added (e.g., ceftriaxone, cefotaxime).
  • The duration of antibiotics (IV and PO) should generally be 7–10 days.
  • Bite wounds should have tetanus and rabies prophylaxis issues addressed.

  • Remember to consider the possibility of MRSA in all deep, invasive, or persistent infections (i.e., consider clindamycin).
  • Penicillin and amoxicillin are never good empiric choices for even superficial cellulitis (poor S. aureus coverage).

Cellulitis - surgery

Abscesses should be surgically drained.

Cellulitis - FOLLOW UP

  • Steady improvement should be expected.
  • If daily improvement is not noted, inappropriate antimicrobial coverage, a deeper infection or abscess, or some other complication should be suspected (e.g., foreign body).

Cellulitis - prognosis

The prognosis for complete recovery is good as long as appropriate antimicrobials are administered in a timely fashion.

Cellulitis - complications

  • Local or distant spread of infection is possible.
  • Suppuration and abscess formation may occur (e.g., peritonsillar abscess).
  • Extremity cellulitis may extend into the deep tissues to produce an arthritis or osteomyelitis, or it may extend proximally as a lymphangitis.
  • Orbital cellulitis may be complicated by visual loss and/or cavernous sinus thrombosis.
  • Prior to widespread immunization against HIB, the bacteremia associated with facial cellulitis was associated with pneumonia, meningitis, pericarditis, epiglottitis, arthritis and osteomyelitis.

Cellulitis - bibliography

  1. Eady EA, Cove JH. Staphylococcal resistance revisited: Community-acquired methicillin resistant Staphylococcal aureus—an emerging problem for the management of skin and soft tissue infections. Curr Opin Infect Dis. 2003;16:103–124.
  2. Falagas ME. Vergidis PI. Diseases that masquerade as infectious cellulitis. Annals of Internal Medicine. 2005;142(1):47–55.
  3. Kluytmans-Vandenbergh MF, Kluytmans JA. Community-acquired methicillin-resistant Staphylococcus aureus: Current perspectives. Clin Microbiol Infect. 2006;12(Suppl 1):9–15.
  4. Ladhani S, Garbash M. Staphylococcal skin infections in children: Rational drug therapy recommendations. Paediatric Drugs. 2005;7(2):77–102.
  5. Lee MC, Rios AM, Aten MF, et al. Management and outcome of children with skin and soft tissue abscesses caused by community-acquired methicillin resistant Staphylococcal aureus. Pediatr Infect Dis J. 2004;23:123–127.
  6. Roberts S, Chambers S. Diagnosis and management of Staphylococcus aureus infections of the skin and soft tissue. Int Med J. 2005;35 Suppl 2:S97–S105.
  7. Swartz MN. Clinical practice. Cellulitis. N Engl J Med. 2004;350(9):904–912.
  8. Wald ER. Periorbital and orbital infections. Pediatr Rev. 2004;25(9):312–320.

Cellulitis - CODES

Cellulitis - icd9

682.9 Cellulitis and abscess, unspecified site

Cellulitis - FAQ

  • Q: Should MRSA be considered only in patients with risk factors such as recent hospitalization, chronic illness, health care worker contact, and recent antibiotic use?
  • A: No. MRSA is commonly isolated now from patients with no identified risk factors.
  • Q: Is ophthalmology consultation necessary in all cases of periorbital cellulitis?
  • A: Ophthalmology consultation is not necessary in simple, uncomplicated cases of periorbital cellulitis that clearly have no associated proptosis, limitation in extraocular eye movement, or visual impairment that would suggest a more serious orbital cellulitis.

Book Source Details

  • Book Title: The 5-Minute Pediatric Consult
  • Author(s): M. William Schwartz MD; et al.
  • Year of Publication: 2008
  • Copyright Details: The 5-Minute Pediatric Consult, Copyright © 2008 Lippincott Williams & Wilkins.

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Copyright notice for book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.




More About This Book:
Title: The 5-Minute Pediatric Consult
Authors: M. William Schwartz MD; et al.
Publisher: Lippincott Williams & Wilkins
Copyright: 2008
ISBN: 0-7817-7577-9

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