A 28-year-old male patient, known case of Marfan syndrome, presented with complaints of low vision in both eyes since childhood. He gave a clinical history of having undergone intracapsular cataract extraction (ICCE) in the right eye 3 years previously. At presentation, the best spectacle corrected visual acuity (BCVA) was 6/12 and 1/60 in the right eye and left eye, respectively. On slit lamp examination, the right eye had an intercalary staphyloma extending from 11 to 2 o’ clock with Descemet scar in the superior cornea [Fig. 1]. The iris showed atrophic patches, a fixed and dilated pupil and aphakia with no capsular support [Fig. 2]. The left eye had iridodonesis with 8 clock hours of nasal subluxation of a clear crystalline lens [Fig. 3]. Fundus was noted to be normal on indirect ophthalmoscopy. Intralenticular lens aspiration was planned for the patient's left eye. However, the patient refused surgery.
Figure 1
Slit lamp photograph of right eye showing an intercalary staphyloma, superior descemet scar, and aphakia
Figure 2
Slit lamp photograph of right eye showing 360° iris atrophy with aphakia
Figure 3
Slit lamp photograph of left eye showing nasally subluxated lens with superotemporal stretched zonules and inferotemporal deficient zonules
Slit lamp photograph of right eye showing an intercalary staphyloma, superior descemet scar, and aphakiaSlit lamp photograph of right eye showing 360° iris atrophy with aphakiaSlit lamp photograph of left eye showing nasally subluxated lens with superotemporal stretched zonules and inferotemporal deficient zonules
Discussion
Marfan syndrome is characterized by abnormalities of the fibrillin protein that is responsible for providing strength and elasticity to the connective tissue.[12]“Ectopia lentis” is a common finding in Marfan syndrome that often requires surgery for visual rehabilitation.[3] The ectopic lens can be removed through a corneal, limbal, or scleral incision. However, there are reports in literature that suggest the risk of staphyloma formation following ocular trauma and scleral incisions in these cases.[45] Goldberg and Ryan[4] reported an intercalary staphyloma in a 5-year-old female child of Marfan syndrome following blunt ocular trauma with a stone. Seelenfreund et al.[5] reported occurrence of an incisional staphyloma following retinal detachment surgery in a case of Marfan syndrome. Therefore, this case highlights an important lesson that any form of trauma to the sclera (surgical or mechanical) should be avoided in cases of Marfan syndrome considering the pre-existing scleral thinning and risk of staphyloma formation.
Declaration of patient consent
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