eMedicine Specialties > Ophthalmology > Orbit

Cellulitis, Preseptal

Author: Aaron L Sobol, MD, Medical Director, Laurel Ridge Eyecare, Tulane University School of Medicine
Coauthor(s): Kelly A Hutcheson, MD, Associate Professor, Department of Ophthalmology, George Washington University School of Medicine, Children's National Medical Center,
Contributor Information and Disclosures

Updated: Apr 4, 2008

Introduction

Background

Preseptal cellulitis is a common infection of the eyelid and periorbital soft tissues characterized by acute eyelid erythema and edema. This bacterial infection usually results from local spread of adjacent upper respiratory tract infection, external ocular infection, or following trauma to the eyelids. Preseptal cellulitis tends to be a less severe disease than orbital cellulitis (postseptal cellulitis), which can present in a similar manner. Orbital cellulitis has a higher morbidity, requires aggressive treatment, and may require surgical intervention, whereas preseptal cellulitis usually is managed medically. Delineation of the exact location of inflammation is necessary for proper diagnosis and treatment.

Pathophysiology

Periorbital inflammation is classified by location and severity. One of the major anatomical landmarks in determining the location of disease is the orbital septum. The orbital septum is a thin membrane that originates from the orbital periosteum and inserts into the anterior surfaces of the tarsal plates of the eyelids. The septum separates the superficial eyelid from the deeper orbital structures, and it forms a barrier that prevents infection in the eyelid from extending into the orbit. Preseptal cellulitis differs from orbital cellulitis in that it is confined to the soft tissues that are anterior to the orbital septum. Preseptal cellulitis may spread posterior to the septum and progress to form subperiosteal and orbital abscesses. Infection in the orbit can spread posteriorly and cause cavernous sinus thrombosis or meningitis.

Upper respiratory tract infections, especially paranasal sinusitis, commonly precede preseptal cellulitis. In 2 large case series, nearly two thirds of cases of cellulitis were associated with upper respiratory tract infection. One half of these cases were from sinusitis.

The most common organisms are Staphylococcus aureus, Staphylococcus epidermidis, Streptococcus species, and anaerobes, reflecting the organisms that commonly cause upper respiratory tract infections and external eyelid infections. Blood and skin culture results tend to be negative.

Prior to the introduction of the Haemophilus influenzae type b (Hib) polysaccharide vaccine in 1985, H influenzae was the most common organism isolated in blood cultures. One study prior to the introduction of the vaccine noted that blood culture results were more likely to be positive (42%) if the patient had an upper respiratory infection and that subcutaneous aspirates were more likely to be positive (44%) if the patient had eyelid trauma or external ocular infection. Since the vaccine has come into widespread use, the rate of Haemophilus -positive blood cultures has dropped; studies report that the rate of any positive blood culture is now less than 4%. The reason that the rates for bacteremia for all organisms have dropped is unclear.

A study specifically looking at periorbital and orbital cellulitis since the advent of the vaccine likewise found that the rates of Hib-related cellulitis dropped from 11.7% to 3.5%. Total cases per year from all pathogens also declined, suggesting that H influenzae may have played a facilitative role in the pathogenesis of cellulitis.

In the era of concern about biologic warfare, it is also important to note that periorbital cellulitis has also been reported with both smallpox and anthrax.

Frequency

United States

In 1995, approximately 5000 US inpatients had an International Classification of Diseases, 9th revision (ICD-9), diagnosis of deep inflammation of the eyelid as a primary discharge diagnosis according to the NationalCenter for Disease Statistics.

Mortality/Morbidity

  • Morbidity occurs from the spread of pathogens to the orbit, which can threaten vision and result in CNS spread. Untreated orbital cellulitis can lead to the development of an orbital abscess or can spread posteriorly to cause cavernous sinus thrombosis. Systemic spread of bacteria may lead to meningitis and sepsis.
  • Earlier diagnosis, expeditious treatment, and improved antibiotics have led to a reduction of serious ocular and CNS complications.

Race

No known racial predilection exists.

Sex

No known sexual predilection exists.

Age

Preseptal cellulitis is primarily a pediatric disease with approximately 80% of patients younger than 10 years and most patients younger than 5 years. Patients with preseptal cellulitis tend to be younger than patients with orbital cellulitis.

Clinical

History

Patients may have mild-to-moderate temperature elevation. Although it has been suggested that orbital cellulitis generates a greater leukocytosis and febrile response than preseptal cellulitis, it is widely believed that these responses cannot be used to differentiate between the 2 conditions.

  • Patients may complain of the following:
    • Pain
    • Conjunctivitis
    • Epiphora
    • Blurred vision
  • Signs include periorbital erythema and edema (sometimes so severe that patients cannot voluntarily open the eye).

Physical

Because both orbital cellulitis and preseptal cellulitis can present with eyelid inflammation, it is important to perform a complete ocular examination. Be alert for signs of systemic illness, especially in children.

  • The eyelids and ocular adnexa should be inspected for signs of local trauma.  
    • Cervical, submandibular, or preauricular lymphadenopathy may be present. A tender preauricular lymph node may be suggestive of adenoviral conjunctivitis.
    • Conjunctivitis may be present, and the quality of conjunctival drainage should be noted.
    • Test both vision and pupillary reactions in all patients presenting with eyelid inflammation, as evidence of limited motility or impaired vision suggests that inflammation has spread to the orbit.
    • An afferent pupillary defect suggests optic nerve compression, and immediate surgical drainage should be performed.
    • Resistance to retropulsion and proptosis suggest orbital involvement. An eyelid speculum may be needed to examine the eye and ocular movements.
    • The ocular fundus should be examined carefully for signs of optic nerve swelling and venous engorgement.
  • Inspect for possible dacryocystitis or dacryoadenitis, which can result in the spread of inflammation to adjacent tissues. 
  • Sinus tenderness, rhinorrhea, adenopathy, and other hallmarks of upper respiratory tract infection may be present.

Causes

  • Antecedent events may include the following recent eyelid lesions:  
    • Hordeola
    • Chalazia
    • Bug bites
    • Trauma
    • Recent surgical procedures near the eyelids
    • Oral procedures
  • A concurrent or recent upper respiratory tract infection, especially sinusitis, may be present.
  • Many systemic diseases have been reported with concurrent preseptal cellulitis.
    • Varicella
    • Asthma
    • Nasal polyposis
    • Neutropenia

More on Cellulitis, Preseptal

Overview: Cellulitis, Preseptal
Differential Diagnoses & Workup: Cellulitis, Preseptal
Treatment & Medication: Cellulitis, Preseptal
Follow-up: Cellulitis, Preseptal
Multimedia: Cellulitis, Preseptal
References

References

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  2. Agarwal M, Biswas J, S K, Shanmugam MP. Retinoblastoma presenting as orbital cellulitis: report of four cases with a review of the literature. Orbit. Jun 2004;23(2):93-8. [Medline].

  3. Ambati BK, Ambati J, Azar N, Stratton L, Schmidt EV. Periorbital and orbital cellulitis before and after the advent of Haemophilus influenzae type B vaccination. Ophthalmology. Aug 2000;107(8):1450-3. [Medline].

  4. Barone SR, Aiuto LT. Periorbital and orbital cellulitis in the Haemophilus influenzae vaccine era. J Pediatr Ophthalmol Strabismus. Sep-Oct 1997;34(5):293-6. [Medline].

  5. Donahue SP, Schwartz G. Preseptal and orbital cellulitis in childhood. A changing microbiologic spectrum. Ophthalmology. Oct 1998;105(10):1902-5; discussion 1905-6. [Medline].

  6. Eustis HS, Armstrong DC, Buncic JR, Morin JD. Staging of orbital cellulitis in children: computerized tomography characteristics and treatment guidelines. J Pediatr Ophthalmol Strabismus. Sep-Oct 1986;23(5):246-51. [Medline].

  7. Hirsch M, Lifshitz T. Computerized tomography in the diagnosis and treatment of orbital cellulitis. Pediatr Radiol. 1988;18(4):302-5. [Medline].

  8. Hu G, Wang MJ, Miller MJ, Holland GN, Bruckner DA, Civen R, et al. Ocular vaccinia following exposure to a smallpox vaccinee. Am J Ophthalmol. Mar 2004;137(3):554-6. [Medline].

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  12. McCarty ML, Wilson MW, Fleming JC, Thompson JW, Sandlund JT, Flynn PM, et al. Manifestations of fungal cellulitis of the orbit in children with neutropenia and fever. Ophthal Plast Reconstr Surg. May 2004;20(3):217-23. [Medline].

  13. Molarte AB, Isenberg SJ. Periorbital cellulitis in infancy. J Pediatr Ophthalmol Strabismus. Sep-Oct 1989;26(5):232-4; discussion 235. [Medline].

  14. Reynolds DJ, Kodsi SR, Rubin SE, Rodgers IR. Intracranial infection associated with preseptal and orbital cellulitis in the pediatric patient. J AAPOS. Dec 2003;7(6):413-7. [Medline].

  15. Ruttum MS, Ogawa G. Adenovirus conjunctivitis mimics preseptal and orbital cellulitis in young children. Pediatr Infect Dis J. Mar 1996;15(3):266-7. [Medline].

  16. Schwartz GR, Wright SW. Changing bacteriology of periorbital cellulitis. Ann Emerg Med. Dec 1996;28(6):617-20. [Medline].

  17. Soysal HG, Kiratli H, Recep OF. Anthrax as the cause of preseptal cellulitis and cicatricial ectropion. Acta Ophthalmol Scand. Apr 2001;79(2):208-9. [Medline].

  18. Weiss A, Friendly D, Eglin K, Chang M, Gold B. Bacterial periorbital and orbital cellulitis in childhood. Ophthalmology. Mar 1983;90(3):195-203. [Medline].

Further Reading

Keywords

preseptal cellulitis, periorbital cellulitis, eyelid infection, eyelid erythema, eyelid edema, bacterial infection, upper respiratory tract infection, ocular infection, eyelid trauma, orbital cellulitis, postseptal cellulitis, orbital septum

Contributor Information and Disclosures

Author

Aaron L Sobol, MD, Medical Director, Laurel Ridge Eyecare, Tulane University School of Medicine
Aaron L Sobol, MD is a member of the following medical societies: American Academy of Ophthalmology and American Society of Cataract and Refractive Surgery
Disclosure: Nothing to disclose.

Coauthor(s)

Kelly A Hutcheson, MD, Associate Professor, Department of Ophthalmology, George Washington University School of Medicine, Children's National Medical Center,
Kelly A Hutcheson, MD is a member of the following medical societies: Alpha Omega Alpha, American Academy of Ophthalmology, American Association for Pediatric Ophthalmology and Strabismus, and Association for Research in Vision and Ophthalmology
Disclosure: Nothing to disclose.

Medical Editor

Brian A Phillpotts, MD, Former Vitreo-Retinal Service Director, Former Program Director, Clinical Assistant Professor, Department of Ophthalmology, Howard University College of Medicine
Brian A Phillpotts, MD is a member of the following medical societies: American Academy of Ophthalmology, American Diabetes Association, American Medical Association, and National Medical Association
Disclosure: Nothing to disclose.

Pharmacy Editor

Simon K Law, MD, PharmD, Assistant Professor of Ophthalmology, Jules Stein Eye Institute; Chief of Section of Ophthalmology Surgical Services, Department of Veterans Affairs Healthcare Center, West Los Angeles
Simon K Law, MD, PharmD is a member of the following medical societies: American Academy of Ophthalmology, American Glaucoma Society, and Association for Research in Vision and Ophthalmology
Disclosure: Nothing to disclose.

Managing Editor

Mark T Duffy, MD, PhD, Consulting Staff, Division of Oculoplastic, Orbito-facial, Lacrimal, and Reconstructive Surgery, Green Bay Eye Clinic, BayCare Clinic
Mark T Duffy, MD, PhD is a member of the following medical societies: American Academy of Ophthalmology, American Medical Association, American Society of Ophthalmic Plastic and Reconstructive Surgery, Sigma Xi, and Society for Neuroscience
Disclosure: Allergan - Botox Cosmetic Consulting fee Consulting; Quest medical - lacrimal balloons Honoraria Speaking and teaching

CME Editor

Lance L Brown, OD, MD, Ophthalmologist, Affiliated With Freeman Hospital and St John's Hospital, Regional Eye Center, Joplin, Missouri
Disclosure: Nothing to disclose.

Chief Editor

Hampton Roy Sr, MD, Associate Clinical Professor, Department of Ophthalmology, University of Arkansas for Medical Sciences
Hampton Roy Sr, MD is a member of the following medical societies: American Academy of Ophthalmology, American College of Surgeons, and Pan-American Association of Ophthalmology
Disclosure: Nothing to disclose.

 
 
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