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Topical insulin in pediatric neurotrophic keratopathy associated with CIPA syndrome
Taher Eleiwa1, Mohamed F Farid1, Abdelrahman M Elhusseiny2
1Department of Ophthalmology, Benha University, Benha, Egypt.
Insights
Topical insulin effectively managed neurotrophic keratopathy in a child with congenital insensitivity to pain with anhidrosis (CIPA). This treatment led to corneal ulcer healing and stability over a 2-year follow-up.
Area of Science:
- Ophthalmology
- Genetics
- Regenerative Medicine
Background:
- Neurotrophic keratopathy is a serious corneal condition characterized by a loss of corneal sensation.
- Congenital insensitivity to pain with anhidrosis (CIPA) is a rare genetic disorder that affects pain and temperature sensation, increasing the risk of corneal damage.
- Corneal perforation and ulceration are severe complications that require prompt and effective management.
Abstract:
We present a case, with a 2-year follow-up, of the use of topical insulin in managing neurotrophic keratopathy in a 3-year-old boy diagnosed with congenital insensitivity to pain with anhidrosis (CIPA). Initially, the patient had a corneal perforation in the right eye, for which he underwent tectonic amniotic membrane transplantation. On examination, a central corneal ulcer with stromal infiltration was identified in the left eye, accompanied by a complete absence of corneal sensation in both eyes. Systemic features consistent with CIPA, such as the absence of a normal response to pain stimuli, anhidrosis, and self-injurious behavior, were also observed. Topical insulin, along with preservative-free lubricants (PF-L) and prophylactic antibiotics, was prescribed for both eyes. Within 2 weeks, the left corneal ulcer had healed, and treatment with topical insulin and PF-L was continued. After a 2-year follow-up, the left cornea exhibited a stable small paracentral nebula, whereas the right cornea showed a central non-adherent leucoma. No recurrence of corneal ulceration occurred.
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