Cellulitis
Cellulitis is a common infection caused by bacteria that affects the dermis and
subcutaneous tissue of the skin. It is frequently caused
by Staphylococcus aureus and Streptococcus pyogenes
. The skin infection presents as an erythematous and edematous area with warmth and
tenderness. The borders are not clearly delineated. The lower extremities are the most
frequent site of infection, but cellulitis can occur anywhere on the body. Diagnosis is
usually clinical, and management involves oral and/or parenteral antibiotics. Coverage
for MRSA may be added, depending on the presence of risk factors.
Last update:
                       March 4, 2021
                       7:17 am
Table of Contents
   Overview
                       Pathophysiology and Clinical Presentation
                       Diagnosis
                       Management and Complications
                       Differential Diagnosis
                       References
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Overview
Definition
Cellulitis is inflammation of the skin and subcutaneous tissues. It is
often due to infection.
Epidemiology and etiology
     Incidence: 200 cases per 100,000 patient-years
     More common in middle-aged and older populations
     Lower extremities: most common site
     Most common agents:
        o   Staphylococcus aureus:
                 MSSA
                 MRSA
        o   Group A Streptococcus (Streptococcus pyogenes)
     Less common agents:
        o   Pasteurella multocida (from animal bites)
        o   Aeromonas hydrophila and Vibrio vulnificus (after water
            exposure)
        o   Clostridium species (myonecrosis)
        o   Pseudomonas aeruginosa (in immunocompromised
            patients)
        o   Erysipelothrix rhusiopathiae (occupational exposure in
            butchers, slaughterhouse workers, farmers, veterinarians)
Risk factors
     Breach of the skin barrier (wounds, ulcers, insect/animal bites)
      Skin inflammation (psoriasis, eczema)
      Injuries contaminated with dirt or seawater
      Preexisting infection (tinea, varicella)
      Previous history of cellulitis
      Crush injuries
      Second- and third-degree burns
      Frostbite
      Lymphedema or any obstruction of lymphatic drainage
      Immunodeficiency
      Diabetes mellitus
      Obesity
      Venous insufficiency
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Pathophysiology and Clinical Presentation
Pathophysiology
      Bacteria enter disrupted skin barrier:
          o   Through minor cuts or injuries
          o   May be secondary to a distant site or systemic infection
          o   In some cases, portal of entry is not evident.
      Invasion of dermis and subcutaneous tissue triggers cytokine
       release, recruiting neutrophils and other inflammatory cells to the
       site.
     Intrinsic bacterial factors allow the pathogen to evade initial host
      defenses, leading to erythema, pain, and local swelling of
      the skin (edema).
     In immunocompromised patients, infection is limited eventually
      to the area of invasion.
     If the pathogen overcomes the immune defenses, further spread
      (deeper and/or contiguous infection and bacteremia in
      immunodeficiency) occurs.
     Reduced control of infection occurs in:
        o   Decreased tissue vascularity and oxygenation
        o   Increased peripheral fluid stasis
        o   Poor ability to combat infections (e.g., diabetes)
Clinical findings
     Prodromal systemic symptoms:
        o   May have signs of toxicity (fever > 100.5℉ (38℃), chills,
            and tachycardia)
        o   Muscle and joint pain
        o   Headache
     Local features:
        o   Indurated lesions or edematous area with erythema and
            poorly defined borders
        o   Spreading redness or lesions
        o   Pain and tenderness in the affected area
        o   Tight, glossy, swollen skin or dimpling (noted
            in edema surrounding hair follicles)
        o   May present with purulent exudate (usually associated
            with S. aureus)
        o   An abscess may also be found (collection of pus within the
            dermis or subcutaneous layer).
   Associated signs and symptoms:
      o   Regional lymph node swelling and tenderness
          (lymphadenitis)
      o   Severe infections:
               Can present with general malaise, fatigue, dizziness,
                confusion, muscle and joint pain, and diaphoresis
               Can have blistering lesions or bullae formation
    Diagnosis
        Diagnosis of cellulitis is clinical:
            o   Edema
            o   Erythema
            o   Warmth
            o   Tenderness
            o  Associated lymphadenopathy
        Symptoms, risk factors, and progression of the skin lesion aid in
         ruling out differential diagnoses.
        Laboratory tests are nonspecific:
            o   Leukocytosis (common in all infections)
            o   ↑ Inflammatory markers:
                     Erythrocyte sedimentation rate (ESR)
                  CRP levels
      Microbiologic studies:
         o   Wound culture: used to identify pathogens and guide
             antibiotic therapy
         o   Blood culture: obtained in cases suggestive of bacteremia
             and/or in severely immunodeficient patients
      Imaging:
         o   Ultrasonography (US) is used to rule out abscess.
         o   Complicated skin and soft tissue infections need to be
             further evaluated.
                 Orbital and sinus CT to determine extent of orbital
                   cellulitis and presence of an abscess
                 MRI and/or bone scintigraphy may be performed in
                   cases of severe joint pain to confirm/rule out septic
                   arthritis or osteomyelitis.
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Localized Rashes: Impetigo, Cellulitis and Herpes Zoster
Management and Complications
Treatment approach
      Supportive care:
         o   Symptomatic treatment for fever, local pain, and aches
         o   Adequate hydration and elevation of the affected lower limb
      Empiric therapy covers group A Streptococcus and MSSA.
      Determination of risk factors and need for parenteral therapy:
         o   MRSA risk factors:
                  Recent hospitalization or surgery (≤ 2 months ago)
                Hemodialysis
                Residence in a long-term care facility
                HIV infection
                Prior episode of MRSA
                Recent antibiotic use without MRSA coverage
                Indwelling medical device
       o   Need for parenteral therapy:
                Inability to tolerate oral intake
                Systemic signs of toxicity
                Rapid progression of erythema
                Cellulitis over a medical device (vascular graft or
                 prosthetic joint)
                Failure to respond to prior oral antibiotics
Treatment regimen
    No MRSA risk factors:
       o   Oral therapy (mild infection):
                Dicloxacillin
                Amoxicillin
                Cephalexin
                Clindamycin
       o   Parenteral therapy:
                Cefazolin
                Nafcillin
                Oxacillin
                Clindamycin
    With MRSA risk factors:
      o   Oral therapy:
               Trimethoprim–sulfamethoxazole
               Amoxicillin plus doxycycline
               Amoxicillin plus minocycline
               Clindamycin
      o   Parenteral therapy:
               Vancomycin
               Daptomycin
   Other considerations:
      o   Bite wounds: add anaerobic coverage
      o   Hospitalization:
               Usually required for facial lesions because of high risk
                of spread of infection to the CNS
                (meningitis, encephalitis)
               For those with concomitant conditions such as hepatic,
                renal, or cardiac failure
      o   Severe progressive infections: might require surgical
          debridement of necrotic tissue or abscesses
Cellulitis in the left lower leg and knee:
Left: Local swelling with salmon-pink skin discoloration and local warmth is evident.
Right: leg after 6 weeks of antibiotic therapy
Image: “Helicobacter cinaedi bacteremia with cellulitis in a living-donor kidney transplant recipient identified by matrix-
assisted laser desorption ionization time-of-flight mass spectrometry: a case report” by BMC Research Notes. License: CC
BY 4.0
Complications
        Abscess:
              o    Collection of pus in the dermis or subcutaneous tissue
             o   Presents as a tender, fluctuant, erythematous swelling or
                 discrete nodule
             o   Treatment: incision and drainage of drainable abscess
                 detected on exam or US
      Necrotizing fasciitis:
             o   Deep infection associated with rapid destruction and
                 necrosis of the fascia and subcutaneous tissues
             o   Life-threatening
      Septic arthritis:
             o   Infection in a joint, frequently secondary to bacteria
             o   Develops from hematogenous seeding but can also arise
                 from extension of infection from the skin/soft tissue
      Osteomyelitis:
            Infection of the bone
             o
         o Poorly healing skin and soft tissue infections are at risk.
      Sepsis:
             o   Potentially life-threatening organ dysfunction caused by a
                 dysregulated host response to infection
             o   Presentation can include fever, tachycardia,
                 tachypnea, hypotension, and/or altered mentation.
             o   Immunocompromised patients with skin infections are at
                 risk for this condition.
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Cellulitis
Differential Diagnosis
      Erysipelas: an acute superficial infection of the upper dermis
       and lymphatics, usually caused by group A beta-
       hemolytic Streptococcus: This condition presents as a sharply
    demarcated, raised skin lesion, with erythema, edema, and
    warmth.
   Necrotizing fasciitis: a rapidly progressive infection resulting in
    extensive necrosis of subcutaneous tissue, fascia, and
    muscle: Necrotizing fasciitis is most commonly caused by group
    A Streptococcus but often involves other types of bacteria in a
    mixed infection. The condition presents with necrosis, crepitus,
    bullae, and purple skin discoloration.
   Dermatitis: general term for edematous skin rash caused by an
    allergic reaction, irritant, or infection
   Folliculitis: a localized inflammation of the hair follicle or
    sebaceous glands that is primarily caused by S. aureus:
    Presentation includes erythema, papules, pustules, and
    tenderness of the affected area.
   Impetigo: a highly contagious skin infection of the upper
    epidermis: Impetigo commonly affects children < 5 years of age
    and is caused by S. aureus or group A Streptococcus. Patients
    present with an erythematous area covered in small vesicles,
    pustules, and/or honey-colored crusts.
   Staphylococcal scalded skin syndrome                  Staphylococcal
     Scalded Skin SyndromeStaphylococcal scalded skin syndrome (SSSS),
     also known as Ritter disease and staphylococcal epidermal necrolysis, is a
     toxin-mediated condition caused by Staphylococcus aureus. The exfoliative
     toxin produced disseminates and cleaves desmoglein 1 in the epidermis,
     causing separation and detachment of the skin.Staphylococcal Scalded
     Skin Syndrome (SSSS)       : a toxin-mediated blistering skin disorder
    caused by S. aureus. Presentation includes diffuse cutaneous
    erythema, tenderness, bullae formation, and superficial
desquamation (sloughing off of the superficial layer of skin,
leaving a red “scalded” appearance). The mucous membranes
are spared.