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Pediatric Ophthalmology & Strabismus

Orbital Cellulitis

Orbital cellulitis is a bacterial infection of the soft tissues within the orbit posterior to the orbital septum (a fibrous membrane at the front of the eyelid). It is considered an ophthalmic emergency.

The severity of orbital infection is assessed using the Chandler classification (1970).

Chandler I–III

Grade I (periorbital cellulitis): Edema of the eyelids and surrounding soft tissues, limited to the area anterior to the orbital septum.

Grade II (orbital cellulitis): Spread of infection to intraorbital fat tissue, with proptosis and ophthalmoplegia.

Grade III (subperiosteal abscess): Abscess formation between the orbital periosteum and the orbital wall.

Chandler IV–V

Grade IV (orbital abscess): Abscess formation within the orbital fat, with severe proptosis and complete restriction of eye movement. Vision loss is prominent.

Grade V (cavernous sinus thrombosis): Infection spreads intracranially. The most severe type with bilateral findings and impaired consciousness.

This disease commonly occurs in children and also affects young adults. Due to the anatomical relationship around the orbit, it is closely associated with sinusitis (especially ethmoid sinusitis). Compared to adults, children have a different immune response, and infection easily spreads to the orbit through the thin lamina papyracea adjacent to the ethmoid sinus. To confirm the association with the paranasal sinuses, early imaging is recommended if suspected.

Q What is the difference between preseptal cellulitis (eyelid cellulitis) and orbital cellulitis?
A

Preseptal cellulitis is an infection localized anterior to the orbital septum (eyelid side) and does not involve proptosis, ophthalmoplegia, or vision loss. Orbital cellulitis is an infection that extends posterior to the septum into the orbit, and these findings are present. CT is useful for differentiating between the two.

  • Eyelid swelling and redness: The earliest symptom, often rapidly progressive.
  • Eye pain and headache: Due to increased intraorbital pressure and inflammation.
  • Diplopia (double vision): Occurs with ophthalmoplegia.
  • Vision loss: Caused by compression or vascular compromise of the optic nerve. A serious sign.
  • Fever: As a systemic inflammatory response.

Clinical findings (findings confirmed by physician examination)

Section titled “Clinical findings (findings confirmed by physician examination)”

In a study of 9 cases of orbital cellulitis due to MRSA (methicillin-resistant Staphylococcus aureus), eyelid edema 88.9%, pain 88.9%, proptosis 66.7%, ophthalmoplegia 66.7%, and fever 55.5% were recorded. 1)

  • Proptosis: Due to increased orbital contents from abscess or edema. Greater degree indicates more severe disease.
  • Ophthalmoplegia: Due to direct inflammatory infiltration of extraocular muscles or nerve involvement. Recovery of ocular motor palsy is the slowest, with some cases requiring 18 months. 3)
  • Eyelid edema and conjunctival chemosis: Due to venous and lymphatic drainage impairment.
  • Elevated intraocular pressure and optic disc edema: Signs that threaten visual function due to increased orbital pressure.
  • Eyelid retraction in neonates: In neonatal orbital cellulitis, eyelid retraction is an important early sign. 2)

Laboratory values include a median CRP of 178 mg/L and median WBC of 17.9×10⁹/L. 1)

Q Does vision loss require emergency surgery?
A

Vision loss is a dangerous sign indicating optic nerve compression and may require urgent intervention. However, surgical indication is not based solely on vision loss but on a comprehensive assessment of abscess size and location on CT, age, and response to antibiotic therapy. See “Standard Treatment” section for details.

Orbital cellulitis develops through three main routes.

  • Direct extension from sinusitis: The most common route. In children, 91% of orbital infections originate from sinusitis (especially ethmoid sinusitis). 7) Infection spreads easily into the orbit through the thin lamina papyracea. Direct hematogenous spread via valveless veins also contributes. 7)
  • Hematogenous infection (bacteremia): In immunocompromised individuals and neonates, infection can occur via the bloodstream.
  • Exogenous infection: Trauma around the orbit, ophthalmic surgery, or direct extension from surrounding tissues.
  • Main pathogens: Staphylococcus aureus, Streptococcus pyogenes, and Streptococcus pneumoniae are typical causative organisms.
  • MRSA: Increasing in recent years. In Taiwan, the proportion of MRSA rose from 14.5% to 37.5%, and in Australia it is reported as 28.6%. 1) Strains producing Panton-Valentine leukocidin (PVL) toxin are strongly associated with abscess formation. 1)
  • Immunocompromised patients (HOC; hematogenous orbital cellulitis): Various pathogens such as Candida, MRSA, Klebsiella, Enterococcus, and Zygomycetes are involved. 3)
  • Neonates: MSSA (methicillin-sensitive Staphylococcus aureus) is common, but bacteremia and meningitis are often complicated. 2)

Upper respiratory tract infection, sinusitis, facial trauma, odontogenic infection, and immunocompromised status (including HIV infection) are the main risk factors. 8)

Q Why does infection spread from sinusitis to the eye?
A

The medial wall of the orbit (lamina papyracea) is very thin and adjacent to the ethmoid sinus. In addition, valveless veins run between the paranasal sinuses and the orbit, allowing infection to spread bidirectionally. 7) Therefore, ethmoid sinusitis can easily spread directly into the orbit.

TestUse/Features
CT (with contrast)First choice. Evaluates the presence, size, and location of subperiosteal abscess.
MRI (STIR sequence)Detailed evaluation of soft tissue, osteomyelitis, and intracranial lesions
B-scan ultrasoundAuxiliary test when radiation exposure should be avoided

CT scan is the basic diagnostic tool, and imaging with a slice thickness of 3 mm or less including coronal views is recommended for the orbit. Contrast-enhanced CT allows identification of subperiosteal abscess and orbital abscess, as well as evaluation of associated sinusitis.

MRI (especially STIR sequence) provides excellent soft tissue contrast and can detect osteomyelitis even within 12 days of onset when CT may not. 4) It is also essential for evaluating intracranial complications (epidural abscess, brain abscess). DWI (diffusion-weighted imaging) is useful for confirming abscess formation. 1)

  • Blood tests: Evaluate WBC, CRP, and procalcitonin (PCT). In a report by Coleombe et al., WBC 17700/μL, CRP 107 mg/L, and PCT 5.04 ng/mL were recorded. 7)
  • Blood culture: The positive rate in typical orbital cellulitis is only about 2–7.9%, but in immunocompromised patients (HOC) it is as high as 75%. 3)
  • Next-generation sequencing (NGS): Can identify pathogens within 48 hours and is useful even in cases where conventional culture methods are difficult. 3)

Diseases requiring differentiation include the following:

  • Preseptal cellulitis (eyelid cellulitis): Limited to the area anterior to the septum, lacking proptosis and ophthalmoplegia. 8)
  • Idiopathic orbital inflammation (pseudotumor): Non-infectious orbital inflammation. Responds well to steroids.
  • Orbital tumor/lymphoma: In recurrent treatment-resistant cases, tumor must be excluded. In culture-negative recurrent cases, consider the possibility of malignant lymphoma. 9)
  • Thyroid eye disease / orbital pseudotumor: Bilateral, chronic course, no fever, helpful for differential diagnosis.

Orbital cellulitis is generally treated with intravenous antibiotics after hospitalization. Collaboration with an otolaryngologist is essential, and surgical drainage is performed as needed.

Initial empirical treatment is based on the following:

  • Ceftriaxone (100 mg/kg/day) + Vancomycin: Broad coverage including MRSA and Gram-negative bacteria. Essential for severe cases with subperiosteal abscess or in areas with high MRSA prevalence. 4)
  • Cefotaxime/Ceftriaxone + Flucloxacillin → Vancomycin: Switch to vancomycin (± clindamycin) after MRSA is confirmed. 1)
  • Add Metronidazole: Used when anaerobic infection (intracranial extension via frontal sinus) is suspected. 4)
  • Ceftazidime + Clindamycin: When coverage for Pseudomonas is needed. 6)
  • Neonates (Vancomycin 15 mg/kg + Meropenem 40 mg/kg three times daily): Covers both MSSA and Gram-negative bacteria. Requires at least 3 weeks of administration; discontinuation before 3 weeks increases risk of failure. 2)

Transition to outpatient parenteral antibiotic therapy (OPAT) is considered after clinical stability, and switching to oral antibiotics may require a long period (up to 7 weeks). 4)

Indications for Surgery

Large abscess: Active drainage is considered for large subperiosteal abscesses (e.g., ≥20 mm).

Visual impairment: If there is decreased visual acuity or afferent pupillary defect, it may be an emergency indication.

Antibiotic resistance: If there is worsening or no improvement after appropriate antibiotic therapy.

Intracranial extension: If there is spread to epidural abscess or brain abscess.

Surgical Procedure

FESS (Functional Endoscopic Sinus Surgery): Drainage of sinusitis. Performed in 88.9% of MRSA cases. 1)

External orbital drainage: Drainage of abscess via external incision. Combined approach with endoscopic surgery is also performed. 4)

Multidisciplinary collaboration: Collaboration among otorhinolaryngology, ophthalmology, and neurosurgery is essential in severe cases. 4)

The usefulness of dexamethasone as an adjunctive therapy has been reported.

AlQahtani et al. reported a dramatic improvement in a 3-year-old patient with MRSA and Pseudomonas aeruginosa infection (subperiosteal abscess 6.6 mm) treated with ceftazidime plus clindamycin and three courses of dexamethasone 6 mg (q12h, 3 days). 6)

Heri-Kovacs et al. reported that IV dexamethasone 250 mg/day for 4 days was effective in a case of orbital cellulitis after COVID-19 vaccination without sinusitis. 5)

The use of steroids requires judgment based on individual clinical circumstances, and a standard administration protocol has not been established.

Q Is surgery always necessary for subperiosteal abscess (SPA)?
A

Not all SPAs require surgical drainage. If the abscess is small, visual function is preserved, and there is a good response to antibiotic therapy, conservative treatment may be attempted. However, if there is vision loss, elevated intraocular pressure, or lack of response to antibiotics, prompt surgical drainage should be considered.

6. Pathophysiology and Detailed Mechanisms

Section titled “6. Pathophysiology and Detailed Mechanisms”

The lamina papyracea, which forms the interface between the orbit and the paranasal sinuses, is a bony plate that constitutes the medial orbital wall. It is extremely thin and prone to perforation. This anatomical feature facilitates the spread of infection from ethmoid sinusitis to the orbit.

Between the paranasal sinuses and the orbit, there are valveless veins that allow infection to spread hematogenously in both directions. 7) Frontal sinusitis can also lead to direct extension to the epidural space and intracranial cavity. 4)

  • Panton-Valentine leukocidin (PVL): A toxin produced by community-acquired MRSA, strongly associated with leukocyte damage and abscess formation. 1)
  • Intracranial spread via valveless veins: The infection from the frontal sinus can extend to the orbit and further to the epidural space and brain. 7)
  • Severe disease in immunocompromised patients (HOC): In immunocompromised individuals, hematogenous orbital cellulitis (HOC) can develop, involving multiple opportunistic pathogens. 3) Recovery of ocular motor palsy may take up to 18 months. 3)

7. Latest Research and Future Perspectives (Research-stage Reports)

Section titled “7. Latest Research and Future Perspectives (Research-stage Reports)”

Increasing trend of MRSA and treatment strategies

Section titled “Increasing trend of MRSA and treatment strategies”

In a retrospective study of 9 cases by Ang et al., the median hospital stay for MRSA orbital cellulitis was 13.7 days, and 100% of cases required surgical intervention. 1) The proportion of MRSA in orbital cellulitis varies by region, rising from 14.5% to 37.5% in Taiwan. 1)

Optimization of antibiotic selection and establishment of initial treatment protocols considering PVL-producing MRSA are future challenges.

Diagnostic application of next-generation sequencing (NGS)

Section titled “Diagnostic application of next-generation sequencing (NGS)”

Tang et al. reported 4 cases of HOC in immunocompromised patients and emphasized that NGS can identify pathogens within 48 hours. 3)

Heri-Kovacs et al. reported a 72-year-old man who developed orbital cellulitis (5 mm proptosis, ophthalmoplegia) without sinusitis 9 days after the second dose of VeroCell (inactivated COVID vaccine). 5) It resolved within 4 days after IV dexamethasone 250 mg/day for 4 days. The pathogenesis is unknown.

Ishak et al. reported a case repeatedly treated as culture-negative “orbital cellulitis” that was ultimately found to be B-cell lymphoma. 9) In treatment-resistant or recurrent orbital cellulitis, early suspicion of tumors or granulomatous diseases and thorough examination including biopsy are essential.


  1. Ang T, Smith JEH, Maqsood N, et al. Orbital cellulitis caused by methicillin-resistant Staphylococcus aureus: a case series. Int Ophthalmol. 2023;43:2925-2933.
  2. Kulkarni V, Gopinath A, Goswami S, et al. Orbital cellulitis with cerebral abscess and temporal abscess in a neonate. BMJ Case Rep. 2023;16:e252390.
  3. Tang X, Li H. Hematogenous orbital cellulitis: a report of four cases. BMC Infect Dis. 2023;23:522.
  4. Kotwal T, Lee A, Kapoor S, et al. Orbital cellulitis with subperiosteal abscess complicated by osteomyelitis and epidural abscess: a case report. Global Pediatr Health. 2021;8:1-5.
  5. Heri-Kovacs A, Eibenberger K, Tausch MK, et al. Orbital cellulitis following SARS-CoV-2 vaccination: a case report. Case Rep Ophthalmol. 2022;13:210-214.
  6. AlQahtani DS, Alshahrani OA, Abu AlOla MA, et al. Refractory orbital cellulitis: a management challenge. Saudi J Ophthalmol. 2021;35:261-262.
  7. Colombe MM, Djoubeir M, Pierre-Jean M, et al. Orbital cellulitis with cerebral empyema as a complication of ethmoiditis in a 14-year-old child: a case report. Clin Case Rep. 2023;11:e6984.
  8. Vanga S, Madhivanan K, Kooner KS, et al. Preseptal and orbital cellulitis: a review. Cureus. 2023;15(11):e48439.
  9. Ishak F, Siddiqa A, Chaudhry M, et al. B-cell lymphoma masquerading as recurrent orbital cellulitis. Cureus. 2024;16(10):e70759.

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