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The word Flocculusis derived from the latin floccus meaning tuft of wool. Flocculi are congenital,benign,cyst like lesions present at the pupillary border of the iris.These tuft develops from the iris pigment epithelium and clinically present either as spherical or tear drop shaped lesions.
Iris flocculus has association with specific genes like ACTA2 and MYH11 . Mutations in ACTA-2 gene has an association with iris flocculi, familial TAAD (Thoracic aortic aneurysm and dissection).Iris sphincter muscles are made from smooth muscles.These muscles have a contraction-relaxation function assembly which is made up of actin and myosin filaments.Alpha actin 2 (ACTA-2 gene)regulates actin filaments function and MYH11 (Myosin heavy chain) control myosin filaments. These genes also control smooth muscles of the aorta. Mutations in these 2 genes play a significant role in the development aortic aneurysms (TAAD).ACTA-2 gene mutation accounts for 14% familial TAAD and it have also association with multisystemic smooth muscle dysfunction syndrome characterized by congenital mydriatic pupil with loss of accommodation and patent ductus arteriosus.Disabella et al studied 100 TAAD patients ,among them only 6 patients had iris focculi but they found its most common extra aortic traits in TAAD.
Role of ACTA2 gene :
Mutation of ACTA2 gene causes impaired contraction of smooth muscle cell which can produce ophthalmic manifestation like iris flocculus and congenital mydriasis with impaired accommodation and cardiac disease like nonsyndromic TAAD.
-The patient is mostly asymptomatic and rarely has vision problems.On slit lamp examination, these iris lesions present bilaterally like excrescent tufts overhanging on pupil zone. UBM and AS-OCT can be used to demonstrate finer details of these iris lesions.
1)Primary iris stromal cyst
2)Secondary iris cyst
a)Down growth epithelium cyst: Post traumatic, Post surgical
b) Drug induced cyst, intraocular tumor cyst(Medulloepithelioma)
3) Koeppe nodule
Iris Flocculus is rare and not harmful but it can be a significant ocular marker for familial TAAD which is an emergent life threatening condition.
- Guo DC, Pannu H, Tran-Fadulu V, et al. Mutations in smooth muscle alpha-actin (ACTA2) lead to thoracic aortic aneurysms and dissections [published correction appears in Nat Genet. 2008 Feb;40(2):255]. Nat Genet. 2007;39(12):1488‐1493
- Risma TB, Alward WL. Successful long-term management of iris flocculi and miosis in a patient with a strong family history of thoracic aortic aneurysms and dissections associated with an MYH11 mutation. JAMA Ophthalmol. 2014;132(6):778‐780
- Milewics DM, Ostergaard JR, Ala-Kokko LM, et al. De novo ACTA2 mutation causes a novel syndrome of multisystemic smooth muscle dysfunction. Am J Med Genet. 2010;152A:2437–43
- Disabella E, Grasso M, Gambarin FI. Risk of dissection in thoracic aneurysms associated with mutations of smooth muscle alpha-actin 2 (ACTA2). Heart. 2011;97(4):321‐326.