Dexamethasone intravitreal implants in the management of tubercular multifocal serpiginoid choroiditis
© The Author(s). 2016
Received: 25 June 2016
Accepted: 22 August 2016
Published: 30 August 2016
Continuous progression of lesions despite an adequate treatment has been described in tubercular multifocal serpiginoid choroiditis. Reported treatments for this paradoxical response include systemic steroids, immunosuppressive drugs, and intravitreal methotrexate. We describe the use of dexamethasone intravitreal implants in a patient presenting with this condition.
A 46-year-old woman sought medical attention for scotomas in her left eye. Tests suggested multifocal serpiginoid choroiditis associated with latent tuberculosis infection, and hence, she was started on anti-tuberculosis drugs in combination with corticosteroids. Given that lesions progressed despite this treatment, we began treatment with dexamethasone intravitreal implants. After injection of the second implant, we succeeded in inactivating the inflammatory process.
Dexamethasone intravitreal implants may be a suitable alternative to systemic steroids or immunosuppressive therapy in the management of continuous progression of lesions in tubercular multifocal serpiginoid choroiditis.
KeywordsOZURDEX Dexamethasone intravitreal implant Uveitis Multifocal serpiginoid choroiditis Tuberculous uveitis
Multifocal serpiginoid choroiditis (MSC) is a rare entity producing chronic recurrent progressive inflammation of the retinal pigment epithelium and choriocapillaris that is associated with latent tuberculosis infection . Treatment consists of anti-tuberculosis antibiotics and corticosteroids. A paradoxical response to treatment has been described in some patients with MSC, consisting of progression of the disease despite appropriate treatment. We describe the case of a patient with this condition who was treated with dexamethasone intravitreal implants to manage this paradoxical response.
Requests were made for the following: serologies for syphilis, Borrelia burgdorferi, hepatitis B and C, and HIV, for which results were normal; quantiFERON (Cellestis, Victoria, Australia) and Mantoux tests, which were positive; and a chest X-ray, which produced no abnormal findings.
MSC is a type of posterior uveitis characterised by recurrent and chronic inflammation of the retinal pigment epithelium and choriocapillaris, associated with latent tuberculosis infection . The usual treatment consists of administering anti-tuberculosis antibiotics together with oral corticosteroids. It has been reported, however, that lesions progress in some patients, despite appropriate treatment for tuberculosis. This paradoxical response has been attributed to an elevated immune response to the release of tubercular antigens; antibiotics may trigger the release of these antigens as the mycobacteria are lysed . A remarkable point is that rifampicin, a commonly used anti-tuberculosis drug, decreases bioavailability of corticosteroids; hence, this may contribute to the progression of inflammation. In fact, the dose of corticosteroids needs to be doubled when patients are treated with rifampicin .
Gupta et al.  described the progression of the disease in 12 out of 84 patients (14 %) with MSC. The continued progression was managed by increasing the dosage of oral prednisolone in nine patients (two of them receiving also intravenous metilprednisolone) while in four patients, immunosuppressive agents (cyclophosphamide or azathioprine) were given to control the condition. In the other three patients, the dosage of oral corticosteroid was not increased further. Basu et al.  described the progression of the disease in 26 out of 106 patients (24.5 %) with different types of presumed tuberculous uveitis; 24 patients had MSC, and of these, seven showed progression of the disease; all of these patients were effectively managed by increasing the dose of corticosteroids and continued antibiotics. Julian et al.  described the use of intravitreal methotrexate in patients with MSC with active disease despite treatment with systemic antibiotics. In their series of three eyes from two patients, choroidal lesions healed within the first month after the injection. Since dexamethasone intravitreal implants have been shown to be very effective in managing intraocular inflammation both in non-infectious  and infectious uveitis , and a local approach has the advantage of reducing the risk of activating tubercular systemic disease, we considered this treatment a suitable option for our patient.
The treatment was effective, though two injections were required. For 5 months after the first injection, we observed healing of the lesions and no new ones appeared. After this period, when the effect of the implant would be expected to have worn off, recurrence was observed, and this was effectively managed with a second dexamethasone intravitreal implant. Though a paradoxical response is more frequent early after initiating antibiotic treatment, cases developing after as long as 5 months have been described . The second flare-up we observed falls into this category of late recurrences.
We believe that in such cases of MSC with a paradoxical recurrence of inflammation, use of a dexamethasone intravitreal implant, to our knowledge, not previously described for this condition, may be a suitable alternative to systemic immunosuppressive therapy. Local management of the condition would avoid inducing severe immunosuppression in patients with a latent tuberculosis infection and hence, the associated risk of developing active tuberculosis. On the other hand, serpiginoid inflammatory lesions in the posterior segment of the eye (serpiginous-like choroiditis) may be caused by infectious aetiologies other than tuberculosis so they should be ruled out before giving a dexamethasone intravitreal implant to treat this condition .
Multifocal serpiginoid choroiditis
Human immunodeficiency virus
We are grateful to the editors of Ideas Need Language Services for help in improving the use of English in the manuscript.
AF, JA, and IRA saw the patient and collected the data from the medical history. SV and JA prepared the outline and figures for the manuscript. SV and AF have prepared the manuscript. All authors have read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Consent was obtained from the patient for the publication of this report.
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