- Brief Report
- Open Access
Occult intraocular foreign body masquerading as panuveitis: inductively coupled mass spectrometry and electrophysiologic analysis
© The Author(s) 2011
- Received: 1 July 2011
- Accepted: 19 July 2011
- Published: 31 July 2011
- Inductively Couple Plasma Mass Spectrometry
- Sympathetic Ophthalmia
- Intraocular Foreign Body
- Couple Mass Spectrometry
Retained intraocular foreign bodies (IOFB) may rarely present as chronic uveitis, either with isolated anterior uveitis or with posterior segment inflammation. The heavy metals copper and iron may lead to both acute and chronic inflammatory processes resulting in severe inflammation, retinal degeneration, and resultant visual loss. Penetrating or perforating ocular injuries are easily recognizable in the majority of cases; however, a high index of suspicion is necessary to recognize an occult penetrating injury because of the severe visual impairment that can ensue. We describe an unusual case of a retained IOFB, which presented 6 months after a probable occult penetrating injury from metallic IOFB trauma. The severity of the patient's inflammation on presentation and retinal findings in the contralateral eye prompted further diagnostic testing including inductively coupled mass spectrometry of the IOFB and electrophysiologic testing. This rare clinical scenario, laboratory findings, and therapeutic considerations are presented.
A 19-year-old Caucasian male was referred to the Casey Eye Institute with a 3-week history of decreased vision and photophobia involving the right eye (OD). He reported hammering metal on metal 6 months prior and felt a foreign object enter his eye. The patient was evaluated at an urgent care facility where his eye was flushed, and tobramycin–dexamethasone ointment was prescribed. The patient's foreign body sensation improved, and he remained asymptomatic until 3 weeks prior to our evaluation. After ophthalmologic evaluation by another physician, he was referred to our service for suspicion of an occult IOFB.
Pars plana vitrectomy (PPV) and IOFB extraction were planned for the presumptively encapsulated IOFB. A standard three-port 20-gauge PPV was performed, taking care to dissect all of the vitreoretinal adhesions extending from the apex of the capsule surrounding the IOFB. Following vitreous dissection around the IOFB, alligator forceps were used to free the IOFB and its fibrotic capsule from the retina. Because of the dense adhesions completely surrounding the IOFB, additional dissection with the vitreous cutter was necessary to free the fibrotic adhesions extending from the IOFB capsule to the retina. After successfully liberating the IOFB from the retina, the superotemporal sclerotomy was enlarged with a microvitreoretinal blade and the IOFB was removed from the eye with alligator forceps. Next, 7-0 vicryl suture was used to close the temporal aspect of the superotemporal sclerotomy site to address the large retinal defect and associated inferotemporal retinal detachment, which were observed. The retinal defect was marked with endodiathermy; air–fluid exchange was performed, and the break was surrounded with endolaser. A 276-tire supporting the inferior 180-degree scleral bed, 240-band, and 70-Watzke sleeve secured with 5-0 Mersilene horizontal mattress sutures were used to provide additional support to the inferior retinal defect. Twenty percent SF6 gas was exchanged for air, and the sclerotomy and conjunctiva were closed in standard fashion.
Of the ferromagnetic IOFB, 4.0 mg was added to 1.5 ml of aqua regia (3:1 parts HNO3:HCl, Fisher, Metals Grade) and heated under reflux for 3 h during which the metal fragment completely dissolved. The resulting bright-yellow solution was brought up to exactly 10 ml with 1% HNO3. The solution was diluted into 1% HNO3 to fall within the range of the standard curve (the sample was measured a total of four times at dilutions of 100×, 1,000×, 100×, and 2,000×).
Inductively coupled plasma mass spectrometry analysis
Inductively coupled plasma mass spectrometry (ICP-MS) analysis was performed using an Agilent 7700× system equipped with an ASX-250 Autosampler. The system was operated at a radio frequency power of 1,550 W, an argon flow rate of 15 L/min, carrier gas flow rate of 1.04 L/min, and helium (He) gas flow rate of 4.3 ml/min (only in He mode). To evaluate which elements were present in the dissolved fragment, count rates for most common elements (∼50) were monitored using a constant spray of the sample. During this qualitative portion of the analysis, only iron showed an extremely high count rate, while few elements gave slightly elevated count rates that were ∼103× less than those for iron.
For the subsequent quantitative analysis, a method was set up for all elements that had shown elevated count rates. Data were quantified using a seven-point (0, 1, 10, 100, 1,000, 2,000, and 5,000 ppb (ng/g)) calibration curve with external standards for Mg, Al, Ca, Fe, Cu, Zn, and Pb. All data were acquired in He mode to remove interference from oxides, argides, and chlorides. For each sample, run data were acquired in triplicate and averaged. Internal standards introduced with the sample were used to correct for plasma instabilities. The National Institute of Standards and Technology standard reference material was used to ensure elemental recovery of >90%.
Composition of metallic IOFB using inductively coupled mass spectrometry
A full-field electroretinogram (ERG) was performed 2 months following surgery, as the patient's vision remained 20/50 despite successful anatomic reattachment and a normal foveal contour. Photoreceptor responses were severely abnormal for the right eye. Rods and dark-adapted cone responses were severely subnormal. The scotopic bright flash a-wave responses were moderately subnormal, whereas the b-wave amplitudes were markedly subnormal, creating an electronegative configuration consistent with siderosis.
At the final 9-month follow-up, the patient's visual acuity improved to 20/30 OD and remained 20/20 OS. Slit lamp examination showed no evidence of anterior chamber or vitreous inflammation. The retina remained attached with good chorioretinal scarring at the IOFB impact site, which was supported by the scleral buckle. The retinal hemorrhage OS resolved, and no inflammation was observed. The ERG was repeated and the right eye again demonstrated decreased amplitudes and prolonged timing of both rod- and cone-driven responses, though these were improved compared to the initial ERG.
Occult penetrating globe injuries with retained IOFBs are a relatively infrequent occurrence [1–6] and may rarely present with chronic anterior or posterior segment inflammation [2, 5, 6]. Besides meticulous ophthalmic examination, B-scan ultrasound, ultrasound biomicroscopy, and CT scans are extremely useful in the diagnosis of occult IOFB injuries. ERG changes have been characterized in the context of siderosis associated with IOFB injuries [1, 3]. In addition, retained copper IOFBs may result in acute  or chronic chalcosis [7–9]. In both siderosis and chalcosis, ERG changes may be partially reversible in some patients [10, 11].
Following PPV/IOFB extraction and retinal detachment repair, our patient's visual acuity was decreased despite a successful surgical outcome. Because of the mild anterior chamber inflammation and retinal hemorrhage observed OS, there was also suspicion for early sympathetic ophthalmia. For these reasons, electrophysiology was performed and revealed a reduction in rod and dark-adapted cone responses in both eyes, albeit to a much greater degree OD.
The ERG findings were most consistent with siderosis OD and were partially reversible with repeat testing. Contralateral ERG abnormalities have not been reported in the context of siderosis, but fortunately, these changes completely reversed on repeat testing. For this reason, the patient was treated only with routine postoperative medications, and systemic immunosuppression was deferred. Prior reports analyzing the heavy metal content of IOFBs have used diagnostic X-ray spectrometry [12, 13] and the percentage copper content of an IOFB likely plays a role in the degree of copper dissemination and associated toxicity.
In one prior patient reported with a copper IOFB, an undiluted vitreous sample showed an inflammatory reaction consisting of CD3+ T lymphocytes and polymorphonuclear leukocytes . Our patient demonstrated moderate inflammation prior to PPV/IOFB removal and the low-grade inflammation in the contralateral eye was suspicious for an autoimmune reaction. It is not clear whether this represented early sympathetic ophthalmia, but the inflammation OS completely resolved without medical therapy. We hypothesize that, following the initial IOFB injury, the intraocular inflammation was due to the toxic effects of the iron fragment. IOFB extraction led to a decrease in localized ocular inflammation and a resultant improvement in the ERG findings. The etiology of the contralateral eye inflammation is not clear; however, the mild anterior chamber inflammation in the contralateral eye had resolved at final follow-up.
ICP-MS is an extremely sensitive technique capable of detecting metal fragments approaching 1 part in 1012 (parts per trillion) and was extremely valuable in identifying iron as the predominant heavy metal in the IOFB; copper was found in minimal quantities. Reversal of ERG abnormalities has been described previously following IOFB extraction, and based on the patient's clinical course, the patient's visual prognosis remains favorable. He is under surveillance for the development of sympathetic ophthalmia given his occult penetrating globe injury.
In summary, ICP-MS and ERG accompanied PPV/IOFB retinal detachment repair in the successful management of this patient. The combination of these techniques was also instrumental in documenting the resolution of retinal changes, providing prognostic information, and may be valuable in the medical and surgical management of these complex cases.
This research was supported by an unrestricted grant from the Research to Prevent Blindness (New York, NY) to the Casey Eye Institute, Oregon Health and Science University, and Emory Eye Center, Emory University School of Medicine.
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