Abstract
Objective
Subperiosteal orbital abscesses (SPOAs) secondary to acute sinusitis are rare occurrences in the pediatric age group, more so in the neonatal period. Here, a rare case of SPOA in a 38-day-old newborn later drained via endoscopic sinus surgery is included also. This review describes the demographic data, clinical history, treatment, microbiology results, complications, and outcome.
Methods
The admission records for all the patients who were admitted to the Pediatric Surgical Ward in Sarawak General Hospital, Kuching, Malaysia, between January 2004 and May 2009 were retrospectively reviewed. Records of patients who presented with preseptal cellulitis, orbital cellulitis, subperiosteal abscess (extraconal), orbital abscess (intraconal), and cavernous sinus thrombosis were closely studied. Ophthalmology consultations were obtained in all these cases. Ultimately, 3 patients having SPOA secondary to acute sinusitis were selected for this review.
Results
All patients were male with rapid onset of periorbital signs, absence of purulent rhinorrhea, and presence of significant thrombocytosis (exceeding 500 × 10 9 /L). The 38-day-old newborn had mixed infection of methicillin-resistant coagulase-negative Staphylococcus bacteremia and local Acinetobacter eye infection with Staphylococcus aureus in the SPOA. All had medially located SPOA that was adequately drained via endoscopic sinus surgery, resulting in full recovery.
Conclusion
Newborns with preexisting risk factors and immature immunity are at risk of severe and rare infections. Contrast-enhanced paranasal sinus computed tomographic scan is mandatory and reliable to differentiate preseptal and postseptal orbital infection, as both conditions can present similarly and rapidly deteriorate. In the contrast-enhanced computed tomography–demonstrable SPOA, endoscopic sinus surgery drainage of the abscess proved to be safe and reliable as the main treatment modality. All patients recovered well without complications.
1
Introduction
Acute sinusitis is the predominant cause of orbital infection in children. An apparent redness or swelling of the orbital region can be a harbinger of a local orbital infection, a trauma, or more ominously, a spreading infection from the neighboring paranasal sinus. The clinician needs to be aware of the possibility of the paranasal sinus infection because the clinical symptoms may be subtle or even absent. Therefore, a high index of suspicion is often needed because a missed diagnosis or delayed treatment can result in potentially catastrophic complication, that is, loss of vision, intracranial extension of the infection, or disseminated sepsis.
2
Material and methods
The admission records of all the patients who were admitted to the Pediatric Surgical Ward (pediatric admission age criteria, up to 12 years old) in Sarawak General Hospital, Kuching, Sarawak, Malaysia, between January 2004 and May 2009 were retrospectively reviewed. Records of patients who presented with the Chandler et al classification of orbital complications—preseptal cellulitis, orbital cellulitis, subperiosteal abscess (extraconal), orbital abscess (intraconal), and cavernous sinus thrombosis—were closely studied. Ophthalmology consultations were obtained in all these cases. The results are detailed in Table 1 . Ultimately, 3 patients having subperiosteal orbital abscess (SPOA) were selected for this review. Their demographic data, clinical history, treatment, microbiology results, duration of hospital stay, complications, and outcome were reviewed.
Cases | Sinusitis-related case | Non–sinusitis-related cases (trauma, eye, skin, systemic causes) | Total cases |
---|---|---|---|
Preseptal cellulitis | 3 | 14 | 17 |
Orbital cellulitis | – | 3 | 3 |
SPOA (extraconal) | 3 | – | 3 |
Orbital abscess (intraconal) | – | – | 0 |
Cavernous sinus thrombosis | – | – | 0 |
Total | 6 | 17 | 23 |
2
Material and methods
The admission records of all the patients who were admitted to the Pediatric Surgical Ward (pediatric admission age criteria, up to 12 years old) in Sarawak General Hospital, Kuching, Sarawak, Malaysia, between January 2004 and May 2009 were retrospectively reviewed. Records of patients who presented with the Chandler et al classification of orbital complications—preseptal cellulitis, orbital cellulitis, subperiosteal abscess (extraconal), orbital abscess (intraconal), and cavernous sinus thrombosis—were closely studied. Ophthalmology consultations were obtained in all these cases. The results are detailed in Table 1 . Ultimately, 3 patients having subperiosteal orbital abscess (SPOA) were selected for this review. Their demographic data, clinical history, treatment, microbiology results, duration of hospital stay, complications, and outcome were reviewed.
Cases | Sinusitis-related case | Non–sinusitis-related cases (trauma, eye, skin, systemic causes) | Total cases |
---|---|---|---|
Preseptal cellulitis | 3 | 14 | 17 |
Orbital cellulitis | – | 3 | 3 |
SPOA (extraconal) | 3 | – | 3 |
Orbital abscess (intraconal) | – | – | 0 |
Cavernous sinus thrombosis | – | – | 0 |
Total | 6 | 17 | 23 |
3
Results
3.1
Case 1
A 38-day-old newborn, with a current weight of 4.34 kg, presented to the referring hospital with right periorbital swelling of 4 days’ duration, which was increasing in size, associated with fever and yellowish eye discharge ( Fig. 1 ). Ophthalmologic examination revealed absence of rapid pupillary afferent defect and limitation of eye movement on lateral gaze. There were no upper respiratory tract infection (URTI) symptoms. The mother was well antenatally, and the baby was born with a birth weight of 2.5 kg via full-term spontaneous vaginal delivery. However, it was complicated by birth asphyxia and presumed sepsis, requiring mechanical ventilation and 7 days of intravenous cefotaxime and crystalline penicillin. He was discharged well from the ward on the eighth day of life. On presentation to the referring hospital, the total white blood cell count (TWCC) was 17.4 × 10 9 /L (reference range, 5.7–23.8 × 10 9 /L) and the platelet count was 833 × 10 9 /L (reference range, 150–400 × 10 9 /L). He was also started on intravenous ceftazidime, cloxacillin, and metronidazole. On arrival on the third day, an urgent computed tomographic (CT) scan of the orbits and paranasal sinus was performed, demonstrating proptosis with a subperiosteal abscess collection measuring 3.1 × 1.9 cm on the medial wall of the right orbit displacing the medial rectus muscle and opacification of the ipsilateral ethmoid air cells. There was also dehiscence of the medial wall of the orbit ( Fig. 2 ). A diagnosis of right SPOA secondary to acute ethmoiditis was made. He also began to develop fever of 39°C. The blood culture grew methicillin-resistant coagulase-negative Staphylococcus (CNS), and direct eye smear for Gram stain taken earlier showed Acinetobacter sp (sensitive to amikacin, ampicillin sulbactam, amoxicillin clavulanate, piperacillin, and imepenem; resistant to netilmicin, gentamicin, ceftazidime, and meropenem). Subsequently, an emergency endoscopic drainage procedure of the abscess was performed the same day. Intraoperatively, the right medial meatus area was edematous; and thick pus was drained after an opening was made through the region of lamina papyracea (LP). The pus grew Staphylococcus aureus (sensitive to penicillin, oxaxillin, vancomycin, clindamycin, and fusidic acid) . Postoperatively, the newborn recovered uneventfully and was discharged on day 5 with broad-spectrum oral antibiotics.
3.2
Case 2
A previously healthy 4-year-old boy presented with 3 days’ duration of progressively worsening left eye swelling and left ear purulent discharge with high fever of 38.5°C. There was no history of purulent rhinorrhea. On ophthalmologic examination, the left eye was proptosed, the upper eyelid was edematous, and the extraocular muscle movements were limited. Subconjuctival hemorrhage was also present on the medial aspect. Otoscopy revealed left otitis externa with inflamed dull tympanic membrane. His TWCC was 17.4 × 10 9 /L and platelet count was 959 × 10 9 /L. Paranasal sinus CT scans showed mucosal thickening in the left ethmoid air cells and bilateral maxillary antrum with a 2.2 × 0.5-cm subperiosteal collection in the left orbit displacing the medial rectus muscle with left mastoid effusion ( Fig. 3 ). He was started on intravenous ceftriaxone, cloxacillin, and metronidazole with framycetin and gramicidin (Sofradex; Sanofi-Aventis, Paris, France) ear drops. Subsequently, an emergency endoscopic decompression of the abscess with anterior ethmoidectomy was performed the same day. The pus, blood, and eye swab cultures were unremarkable. He recovered well and was discharged on day 3 with broad-spectrum oral antibiotics.
3.3
Case 3
A 9-year-old boy presented with 7 days’ duration of progressively worsening right eye swelling, headache, and fever. There was otherwise no purulent rhinorrhea. He was a known case of allergic rhinitis but was poorly compliant to treatment. On examination, the left eye was proptosed with subconjuctival hemorrhage present; and he had restricted extraocular movements. However, his visual acuity was normal. His TWCC was 17.1 × 10 9 /L and platelet count was 526 × 10 9 /L. He was started on intravenous ceftazidime and metronidazole. Paranasal sinus CT scans on day 2 showed mucosal thickening in the right ethmoid air cells and maxillary antrum with a subperiosteal abscess collection in the right orbit. He was then referred to the otorhinolaryngology unit on day 5; and subsequently, endoscopic drainage procedure of the abscess with anterior ethmoidectomy was performed the day after. There was no record of the pus sent for culture and sensitivity study. He recovered without complications, and he was discharged on the day 12 with broad-spectrum oral antibiotics.