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Published on: February 12, 2018
Syphilitic interstitial keratitis: treatment with immunosuppressive drug combination therapy
Jelka G Orsoni1, Laura Zavota, Francesca Manzotti
1Institute of Ophthalmology, University of Parma, Parma, Italy. jorsoni@unipr.it
Insights
A 6-year-old boy with congenital syphilitic keratitis, unresponsive to standard care, achieved successful treatment using a combination of immunosuppressive drugs. This therapy led to significant corneal healing and long-term remission of symptoms.
Area of Science:
- Ophthalmology
- Pediatrics
- Infectious Diseases
Background:
- Congenital syphilitic keratitis is a rare but serious ocular manifestation of congenital syphilis.
- Traditional treatments involving topical steroids and cycloplegics can be ineffective and lead to complications.
Observation:
- A 6-year-old boy presented with congenital syphilitic keratitis refractory to conventional therapies.
- Clinical diagnosis was confirmed by laboratory tests.
Findings:
- Systemic immunosuppressive therapy with oral cyclosporine and low-dose oral steroids was initiated.
- The patient showed significant corneal healing within the first month without renal, hepatic, or growth abnormalities.
- Long-term follow-up revealed limited recurrences and sustained remission after therapy tapering.
Implications:
- This case highlights the potential efficacy of combination immunosuppressive therapy for severe congenital syphilitic keratitis.
- This approach may offer a viable alternative to standard treatments, potentially reducing complications.
Objective:
The following is a case presentation of congenital syphilitic keratitis in a boy 6 years of age who was successfully treated with an immunosuppressive drug combination therapy.
Methods:
Congenital syphilitic keratitis was diagnosed by clinical findings and laboratory tests. The child was unresponsive to traditional treatment; thus, systemic immunosuppressive therapy, which consisted of oral cyclosporine 4 mg/kg/d, 6 days per week, and oral low-dose steroids (fluocortolone 0.8 mg/kg a week, given every other day), was initiated.
Results:
Corneal disease showed great improvement with this therapy, with progressive healing of lesions in the first month of treatment and no signs of toxic renal, hepatic, or growth abnormalities. Recurrences of uveitis have not occurred, and corneal interstitial keratitis episodes have been limited to 3 in an 8-year period. After 6 months with no recurrences, a tapering off of the systemic therapy was initiated, and the child is still asymptomatic and without flare-ups.
Conclusions:
Congenital syphilitic keratitis is usually treated with topical steroids and cycloplegic drugs, which not only can be ineffective but can also lead to complications such as cataract and glaucoma. In the present case report, a pediatric patient affected by syphilitic interstitial keratitis was treated successfully with an immunosuppressive drug combination therapy.
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