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Published on: September 19, 2019
Mucogenic glaucoma in a child
Ta C Chang1, Linda Y Huang1,2, Kara M Cavuoto1
1Bascom Palmer Eye Institute, University of Miami Millers School of Medicine, Miami, FL, United States.
Insights
A congenital iris stromal cyst caused secondary glaucoma in a 4-year-old. Surgical removal of the mucin-producing cyst resolved the pediatric glaucoma, marking the first reported case of mucogenic glaucoma in a child.
Area of Science:
- Ophthalmology
- Pediatric Ophthalmology
Background:
- Congenital iris stromal cysts are rare ocular anomalies.
- Secondary glaucoma can arise from various intraocular conditions.
Observation:
- A 4-year-old presented with acute eye pain, redness, and elevated intraocular pressure (IOP).
- Ultrasound biomicroscopy identified mucoid material within the anterior chamber, suggestive of a mucin-producing cyst.
- The patient had a history of unilateral congenital iris stromal cyst.
Findings:
- The elevated IOP and optic nerve damage were attributed to mucin accumulation from the iris cyst.
- Pathologic examination confirmed a mucin-secreting iris cyst lined with goblet cells.
- Surgical excision of the cyst led to spontaneous normalization of IOP.
Implications:
- This case represents the first report of mucogenic glaucoma in a pediatric patient.
- Mucogenic glaucoma should be considered in the differential diagnosis of childhood glaucoma with nonacquired ocular anomalies.
- Surgical excision of the causative iris cyst can be a curative treatment for this rare condition.
Purpose:
We describe a case of secondary open-angle glaucoma due to mucin-producing congenital iris stromal cyst in a 4 year old patient.
Observations:
A 4-year old female patient with a history of unilateral congenital iris stromal cyst presented with sudden-onset eye pain and redness, with markedly elevated intraocular pressure and evidence of early optic nerve damage. During the examination under anesthesia, the anterior chamber angle was open and there was no evidence of pupillary block. Ultrasound biomicroscopy revealed mildly echogenic substance filling the anterior chamber suspicious of mucoid material, which was verified by the inability to aspirate the material through a 25 gauge needle. The iris cyst was excised, and the intraocular pressure normalized spontaneously. Pathologic examination confirmed a mucin-secreting iris cyst lined with goblet cells and confirmed the mucogenic mechanism.
Conclusions And Importance:
This is the first reported case of mucogenic glaucoma in a pediatric patient. This rare entity should remain on the differential diagnoses of childhood glaucoma associated with nonacquired ocular anomalies. Surgical excision of the iris cyst may be curative.
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