University of Iowa Health Care

Ophthalmology and Visual Sciences

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Iris Cyst:

38-year-old female with iris lesion and gradual decrease in vision

Jordan Rixen, MD, Wallace L M Alward, MD

May 11, 2011

Chief Complaint: Iris lesion and vision loss of the left eye

History of Present Illness: The patient was a 38-year-old female who was referred by her local ophthalmologist for an iris lesion and gradual decrease in vision of the left eye. As a child, she had suffered a penetrating injury with a pencil to the left eye that was surgically repaired. She had been stable until about 3 weeks ago, when vision in her left eye started to decrease. She was seen by her ophthalmologist, who noted an obvious iris lesion and sent the patient to the University of Iowa for further evaluation.

Slit Lamp Exam Photo, caption below elaborates

Figure 1: Slit lamp exam photo, left eye. The cornea is thin and almost perforated inferiorly with iris directly beneath the corneal defect. There is a mass that appears to be originating from the posterior iris causing anterior bowing of the iris and iridocorneal touch. The pupil is almost completely obstructed by the mass. (click image for enlargement)

B-scan echography. caption below elaborates)

Figure 2: B-scan echography of the anterior chamber OS shows a 4 x 10 mm round, sonolucent lesion occupying the anterior chamber. (click image for enlargement)

Past Ocular History: Penetrating injury with a pencil to the left eye as a child

Medical History: Noncontributory

Medications: None

Allergies: No known drug allergies

Family History: Noncontributory

Social History: Noncontributory

Review of Systems: All negative

OCULAR EXAMINATION

Best Corrected Visual Acuity (BCVA):

    • Right eye (OD): 20/20
    • Left eye (OS): 20/160

Ocular motility: Full, both eyes (OU)

Intraocular pressure (IOP): 14 mmHg OU

Slit lamp exam (OS): See Figure 1

Course:

Based on history, clinical exam and echography, the patient was felt to have an iris epithelial inclusion cyst. The cyst was considered to be too large to resect. Three days after initial evaluation, there was spontaneous drainage of the cyst. A tectonic corneal graft was placed in the area of the corneal defect. Histopathology of the host corneal button showed epithelial cells overlying the corneal endothelium further supporting the diagnosis. The cyst returned 6 months later. It was again felt to be too large to resect. The cyst was treated with intracystic ethanol irrigation. At postoperative week 7, the patient had 20/20 vision OS with pinhole correction, and the cyst was no longer visible at the slit lamp (Figure 3). On echography there was recurrence of a posterior cyst, although it was smaller than previously noted.

Figure 3: Slit lamp photos before (3a) and after (3b) intracystic ethanol irrigation of the epithelial iris cyst. The pupillary opening is no longer obstructed and there is no visible evidence of the cyst. Note the tectonic corneal graft that had been placed previously to repair the corneal defect. (click on image for enlargement)
3a 3b
Figure 3a, described in capption above) Figure 3b, described in caption above)

Discussion

Iris cysts can be classified as primary or secondary. Primary cysts have no known cause and arise from the iris pigment epithelium or stroma. They tend to have a benign natural course, and visual disturbance is uncommon. Pigment epithelial cysts are darkly pigmented and can arise anywhere from the central pupillary margin to the peripheral iris. Pigment epithelial cysts are the most common lesions mistaken for iris melanoma. Ultrasound biomicroscopy is essential in narrowing the differential diagnosis if this is suspected. Pigment epithelial cysts can also dislodge and appear along the anterior iris, in the angle or free-floating in the anterior chamber. Stromal cysts are much less common than pigment epithelial cysts. These cysts are lined with non-keratinized squamous epithelium and have a translucent appearance. They are usually observed in infants and children.

Secondary iris cysts can form as a result of epithelial inclusion, as a response to medications such as prostaglandin analogues or indirect acting cholinergic agonists or from cysticercus infection. Our patient was thought to have an epithelial inclusion cyst. Following surgery or penetrating ocular trauma, epithelium from the cornea, conjunctiva, or skin can implant into the iris, which provides an environment for further cellular proliferation and formation of an epithelial inclusion cyst. Further risk factors include incarceration of the iris or lens capsule, prolonged postoperative hypotony or poor wound closure. Compared to primary iris cysts, epithelial inclusion cysts tend to have a more aggressive clinical course and can result in decreased acuity, glaucoma, uveitis and cataracts. The presence of any of these complications should prompt treatment consideration. Many treatment options have been described in the literature including surgical excision, endodiathermy, cryotherapy, laser photocoagulation and injection of chemicals. Behrouzi and Khodadoust demonstrated the use of intracystic ethanol irrigation for the treatment of epithelial iris cysts (Behrouzi, 2003). This involves inserting a needle into the base of the cyst, aspirating the cyst fluid, replacing the volume of the cyst with absolute ethyl alcohol and removing the ethanol after 1 minute. Risks of all treatment options include bleeding, endophthalmitis, cataract formation and cyst recurrence. Perhaps the most concerning risk in treating an epithelial inclusion cyst is the possibility of spilling epithelial cells outside the cyst, which could result in epithelial downgrowth.

Diagnosis: Iris epithelial inclusion cyst (secondary iris cyst)

EPIDEMIOLOGY

  • Previous perforating ocular trauma or surgery
  • Risk factors include incarceration of iris or lens capsule or poor wound closure

SIGNS

  • Iris mass or elevation
  • Scars or other signs of previous surgery or trauma
  • Decreased visual acuity (if blocks visual axis)
  • Elevated IOP (possible)
  • Anterior chamber cell/flare (possible)
  • Cataracts
  • Echography: Round or elliptic with thick walls and sonolucent or septate cavity contents. The cavity can have dense fluctuating particles. (Pigment epithelial cysts tend to have thin walls and sonolucent cavity contents)

SYMPTOMS

  • Often asymptomatic
  • May have decreased vision
  • Eye pain if uveitis or angle closure glaucoma

TREATMENT

  • Observation
  • Surgical excision
  • Intracystic ethanol irrigation
  • Endodiathermy
  • Cryotherapy
  • Laser photocoagulation

Differential Diagnosis for iris cyst

  • Primary iris cyst
  • Iris epithelial inclusion cyst
  • Iris melanoma
  • Choroidal or ciliary body melanoma
  • Iris nevus
  • Medulloepithelioma
  • Metastatic lesion

References

  1. Shields, JA. Primary cysts of the iris. Trans Am Ophthalmol Soc. 1981;79:771-809
  2. Lois, N et al. Primary cysts of the iris pigment epithelium. Clinical features and natural course in 234 patients. Ophthalmology 1998;105(10):1879-85
  3. Lois N et al. Primary iris stromal cysts. a report of 17 cases. Ophthalmology 1998;105(7):1317-22
  4. Marigo FA, Finger PT. Anterior segment tumors: current concepts and innovations. Surv Ophthalmol. 2003;48(6):569-93
  5. Lee BL et al. Epithelial downgrowth following phacoemulsification through a clear cornea. Arch Ophthalmol. 1999;117(2):283
  6. Alward, WL. Glaucoma: The Requisites in Ophthalmology. Mosby Inc. 2000
  7. Behrouzi Z, Khodadoust A. Epithelial iris cyst treatment with intracystic ethanol irrigation. Ophthalmology. 2003;110(8):1601-5
  8. Marigo FA et al. Differential diagnosis of anterior segment cysts by ultrasound biomicroscopy. Ophthalmology. 1999;106(11):2131-5

Suggested Citation Format: Rixen J, Alward WLM. Iris Cyst: 38-year-old female with iris lesion and gradual decrease in vision. EyeRounds.org. May 11, 2011; Available from: http://EyeRounds.org/cases/131-iris-cyst.htm

last updated: 05-11-2011
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