Coloboma is an embryologic ocular defect characterized by a gap or hole in ocular structures, with an incidence of 0.14% and typically bilateral occurrences. The classification of colobomas includes types based on location and completeness, with associated clinical features like visual field defects and retinal detachments being common complications. Treatment options vary depending on the severity and location of the defect, encompassing surgical interventions and management of associated conditions such as cataracts and retinal detachments.

1. Dr Shah_Noor
HassanFCPS,FRCS
Coloboma

2. Definition
 Koloboma (in Greek) – Mutilated or curtailed.
 Primarily its a embryologic defect.
 Malformation refers to a notch, gap, hole, or fissure in any of
the ocular structures.

3. Demography
 Most cases are sporadic
 Incidence – 0.14%
 Usually bilateral - 60%
 Complicated by RRD.
 RRD – 40% in lifetime.
 Congenital, developmental ocular defect – associated
with iris coloboma, microphthalmous, high myopia,
glaucoma, cataract and phthisis bulbi.

4. 3 embryonic layers:
 The neural ectoderm - optic vesicle and optic cup.
 Surface ectoderm
 Cranial neural crest
 minor contribution from the mesoderm
(striated extraocular muscles and vascular endothelia).
EMBRYOGENESIS
(RPE, the iris sphincter and dilator muscles, the posterior iris neuro-epithelium, the
pigmented and nonpigmented ciliary epithelium, and the optic nerve fibers and
glia)
The lens, the corneal epithelium, the lacrimal gland, the surface epidermis of the lids
 and the epithelium of the adnexal glands and conjunctiva .
Corneal keratocytes, endothelium and trabecular meshwork; the iris and choroidal
stroma, including pigmented and nonpigmented cells;
the ciliary smooth muscle; the fibroblasts of the sclera; and the optic nerve meninge

5. GENESIS of COLOBOMA
• 5th to 7th week of fetal life (7–14 mm
stage)
• Closure – Inferior midline from
equator
Faulty closure results in a area
with
absence of uveal tissue and
RPE.
… Coloboma

6. GENESIS of COLOBOMA

7. HISTOLOGY
 Total absence of the RPE and Choroid.
(Rarely /Occasionally choroidal
vessel may be seen to traverse the
colobomatous defect).
 The sensory retina is very thin
(Rudimentary retinal tissue -
abnormal, underdeveloped,
undifferentiated, diaphanous,
flimsy,anomalous and maldeveloped).

8. CLASSIFICATION

9. TYPES
1. TYPICAL / ATYPICAL
2. COMPLETE / INCOMPLETE
3. LENS COLOBOMA
4. POSTERIOR SEGMENT COLOBOMA

10. 1. TYPICAL
2. ATYPICAL
TYPICAL
 Inferonasal – most frequent.
 May affect any part of the globe –traversed by
the fissure from iris to the optic nerve.

11.  Located anywhere other than in inferonasal quadrant
ATYPICAL

12. 2. COMPLETE / INCOMPLETE
 Full thickness defect, involving both the pigment
epithelium and the iris stroma.
Total - Extending to the iris root and giving rise to
the “keyhole pupil.
Partial – Involving only the pupillary margin and
causing a slightly oval pupil.
COMPLETE:

13.  Partial thickness, involving either the pigment
epithelium or the iris stroma.
 Wedge shaped and best demonstrated by iris
transillumination.
 Heterochromia iridis and colobomata have
occurred simultaneously.
INCOMPLETE:

14. 3. LENS COLOBOMA
- a coloboma of the zonule and/or ciliary body
 a misnomer because there is no actual loss of lens
substance.
 Segmentally defective or absent development of the
zonules.

15. 4. POSTERIOR SEGMENT COLOBOMA
A. Choroidal coloboma
B. Optic disc coloboma
C. Macular coloboma

16. A. Choroidal coloboma
Types: Ida mann classification

17. Types: Ida mann classification
4
5
1
2
3
6
7

18.  Atypical and unrelated to choroidal fissure
closure.
 Bilateral, symmetrical, circumscribed and
excavated defects that involve both the
choroid and retina.
B. Macular colobomata

19. Classified :
1. Pigmented
2. Nonpigmented
3. Associated with abnormal vessels
B. Macular colobomata

20. B. Macular colobomata

21. C. Optic disc coloboma
• Rare, unilateral or bilateral
• Usually sporadic - occasionally dominant
• VA – decreased (Depends on severity).
• Large disc with inferior excavation
• Superior visual field defects
• Associated with other colobomas
•

22. • Optic disc involvement has been classified into six types,
increasing in severity from a normal disc outside the
chorioretinal coloboma as the mildest form to a
nonidentifiable disc shape with blood vessels
emerging from the superior border of a large chorioretinal
coloboma.
•This classification is helpful forThis classification is helpful
for predicting the degree of visual impairment in optic disc
colobomata, particularly in infants and young
children whose visual acuity can be difficult to measure.

23. Clinical Features

24.  Asymptomatic
 Leucocoria - early in life
 Loss of central vision
(useful peripheral vision may be preserved if the
lesion is small).
 Visual field defect - not noticed by the patient
 Visual loss - RD

25.  Vision depends - Involvement of the optic nerve, macula,
and papulomacular bundle.
 Bilateral cases - poor visual function and nystagmus.
 Unilateral cases - a sensory strabismus, with
superimposed “organic amblyopia.
 Asymptomatic - macula is spared and the optic nerve
and papulomacular bundle are not severely involved

26. SIGNS
 Inferonasal "key hole" pupil may be seen if iris is
involved
 Amblyopia
 Visual field defects
 Relative afferent pupillary defect (RAPD)
 Associated microphthalmia

27. Choroidal coloboma
Fundus coloboma
 Glistening white with definable borders, frequently with
irregular clumps of pigment along the rim.

28.  Margins - Variations
Choroidal coloboma

29.  Area of bare sclera devoid of overlying normally differentiated
retina or choroid.
 Undifferentiated retinal remnants may persist as a membrane,
sometimes with associated retinal vessels.
Choroidal coloboma

30.  Enlarged, white, sharply delineated,
bowl-shaped excavations
 2–8 diopters in depth
 Rim of neural tissue - preserved
superiorly
 Six types – Severity of disc
involvement
Optic disc coloboma

31. Macular colobomata
Bilateral, symmetrical, circumscribed and
excavated defects that involve both the choroid
and retina.

32. COMPLICATIONS

33. COMPLICATIONS
 Retinal detachment - most common
 Cataract and Lens subluxation
 Subretinal neovascularization causing serous macular
detachment
 Secondary glaucoma
 Amblyopia, Nystagmus
 Anisometropia, and Sensory strabismus

34. RD in Coloboma
 RRD – 40% in lifetime
 0.6–1.7% are associated with
retinochoroidal coloboma.
 Congenital RD – incomplete attachment
 Acquired RD– more common
 RRD/ Non-RRD

35. PATHOGENESIS OF DETACHMENT
Rudimentary
retinaAbnormal
preretinal tissue
Tractional process
break formation.
Extremely thin
minimal changes
Atrophic hole
retinal pigment epithelial pump - missing
Myopic
Vitreous Syneresis

36. Histologic sections – RRD in Coloboma
Inner layer break - Central
 Retinal vascular ischemia or scleral stretching could
explain the break in the inner layer.
Outer layer break - at the margin of the coloboma
 Secondary either to vitreous traction at the margin or
 Extension of an initially isolated detachment to the
margin of the coloboma, where there is less glial support.

37.  Subtle defects in the lens/zonule/ciliary body
complex.
 Fluid can gain access to the subretinal space
through a break in the nonpigmented
epithelium of the ciliary body.
PATHOGENESIS OF DETACHMENT – contd…

38. Non- RRD and Retinoschisis associated
with Choroidal & disc coloboma
 Dome-shaped macular detachment *
with an outer lamellar macular hole with irregular margins #
surrounded by a schisis-like separation between the inner and outer retina †.
 Note the optic and adjacent choroidal coloboma.

39.  Outer lamellar macular hole
may be secondary to chronic
cystoid macular oedema
KAZUKI HOTTA etal Br J Ophthalmol 1999;83:123 ( January )
PATHOGENESIS

40. Finding of breaks – Difficult d/t
(1) The rudimentary retina is extremely thin,
(2) The breaks are usually atrophic holes without the presence of
flaps or operculae
(3) The white background of the sclera
(4) The tiny breaks may be hidden under the overhanging edge of
the coloboma, and
(5) Tiny breaks may be hidden in areas of hemorrhage.

41. Cataracts
 Pigment clumping on the lens capsule at the equator.
 Subcapsular and cortical opacification, anterior and
posterior polar cataracts, and total opacification.
 Lens subluxation
 USG

42. USG

43. SRNVM causing serous macular detachment
 Develops - Superotemporal edge of the coloboma
 Comparable to the CNVM associated with high
myopia, angioid streaks, choroidal ruptures.

44.  Predisposition: Abrupt termination and abnormal
architecture of the RPE and Bruch’s membrane at
the margin.
Treatment with laser photocoagulation.
SRNVM causing serous macular
detachment

45. MANAGEMENT

46. Evaluation
 Lack of cooperation, nystagmus and micropthalmos
- EUA in children's
 SLE & Fundus Evaluation
 Accurate refraction & BCVA
 Ultrasonography
 Fields

47. TREATMENT
 Treatment of refractive error and amblyopia, if present
 Low vision (vision rehabilitation) services, if indicated
 Associated - Cataract,RD orCNV :treated accordingly

48. Iris defects
 Impose no visual defect
 cosmetic contact lens
 Surgical treatment as part of cataract extraction /
penetrating keratoplasty
 Repaired with nonabsorbable sutures.
 Iris prosthesis

49. Iris defects
 Zonular integrity is insufficient
 Haptics should be placed 90 degrees from
the defect
 Cataract and microphthalmia may be
complicated by postoperative :
uveal effusion, retinal detachment, intraocular
hemorrhage, and malignant glaucoma

50. RETINOCHOROIDAL COLOBOMA
Prophylactic
 Laser treatment – posteriorly along the edge of the coloboma
and
 Cryopexy anteriorly

51. TREATMENT of RRD
 RD Outside coloboma
- Conventional scleral buckling techniques.
- Vitrectomy + intraocular tamponade in complicated
cases.
 RD Involving Coloboma
- Buckling (Low Success rate)
- Vitrectomy + EL + SOI

52. External buckling has a low success rate (35 -57%)
- Difficulty in identifying breaks,
- Posterior location of the breaks,
- Impossible to flattened the anomalous retina
- Inability to create a surrounding retinopexy
(cryotherapy or laser photocoagulation).
TREATMENT of RRD contd…

53. Wang et al . Tr. Am. Ophth Soc. vol.
LXXXIII, 1985
Better Results:::
Radial Buckles:
- One/Two buckle/s
- Length depends on length of coloboma
Retinopexy surrounding coloboma

54. Preferred modality -Vitreous surgery
 Vitrectomy + Intraocular Gas
 Vitrectomy + SOI
 Vitrectomy + PFCL
 Encirclage + Vitrectomy + Intraocular tamponade

55. SURGICAL TECHNIQUE
 PARS PLANA VITRECTOMY
 PARS PLANA LENSECTOMY-where ever required.
 Induction of PVD and MP ( membrane peeling) wherever required.
 Use of wide angle visualisation system and magnification of
microscope

56. Vitrectomy With Cyanoacrylate
Retinopexy
 Cyanoacrylate retinopexy at regions suspected of
retinal break.
 Endophotocoagulation around the disc or at the
papillomacular bundle was avoided.
Kazuki Hotta etal . The Management of Retinal Detachments Associated With Choroidal Colobomas by Vitrectomy
With Cyanoacrylate Retinopexy Japanese J Ophthalmol Vol 42,Issue 4, July 1998, Pages 323-326 (E search)

57. DIFFERENTIAL
DIAGNOSES

58. DIFFERENTIAL DIAGNOSES
 Morning glory disk anomaly
 Chorioretinal scar
 Staphyloma (idiopathic, myopic, or associated
with connective tissue disorder).
 North Carolina macular dystrophy

59. Morning glory disk anomaly
 Paracentral defect, typically
inferior
 Annular zone of pigmentary
disturbance
 Anomalous retinal vessels and a
central glial tuft.

60. OPTIC NERVE PITS
 Crater-like holes or indentations in the
surface of the optic disk
 Frequently seen- temporal aspect of the
disk
 incidence is approximately 1:10,000
 incomplete or partial colobomata –
Atypical
 57% in the left eye and 43% in the right

61. Histologically
 Herniations of dysplastic retina into a collagen-lined
pocket, which often extends posteriorly into the
subarachnoid space through a defect in the lamina
cribrosa.
 Edema and cystoid degeneration of the outer
plexiform layer - macula
OPTIC NERVE PITS

62.  Etiology - faulty closure of an aberrant
fetal fissure
 Asymptomatic
 Associated with CSR or Serous retinal
detachment or R’Schisis
 Communication between the vitreous
and/or retina and the subretinal space may
develop.
OPTIC NERVE PITS

63. Differential diagnosis:
 healed toxoplasma choroiditis
 healed chorioretinitis secondary to Toxocara
canis
Macular colobomata

64. Toxplasmosis Scar

65. Scarred SRNVM

66. Bilateral colobomas
 Symmetric location

67. Chorioretinitis scar
 Asymmetric location

68. Iris coloboma

69. Systemic Associations of Coloboma
1. CNS malformation - basal encephalocele and cysts
2. Chromosomal anomalies - Patau syndrome (trisomy 13) and
cat-eye syndrome (trisomy 22)
3. ‘CHARGE’ - Coloboma, Heart defects, choanal Atresia,
Retarded development, Genital and Ear anomalies
4. Other syndromes - Meckel-Gruber, Goltz, Lenz microphthalmos,
Walker-Warburg and Goldenhar

70. Conclusion
 Often associated with microphthalmia.
 Isolated ocular anomaly or in association with
multisystem anomalies
 Wide variation in severity
 Treatment is dependent on location and severity
 A genetic evaluation is warranted in all cases

71. RF data
Jan 2006 to 2010
 Fourty six eyes of 45 patients with retinal detachments
related to coloboma of the choroid were analyzed. All eyes
underwent through various procedure for retinal detachment
surgery..

72. Patient characteristic N46 NO %
AGE MEAN 21.9Year
RANGE 7-40 Year
SEX MALE 31 67.4
FEMALE 15 32.6
COLOBOMATOUS EYE RE 6 13
LE 6 13
BOTH 34 74
COLOBOMATOUS EYE WITH RD RE 22 47.8
LE 18 39.2
BE 6 13

73. SURGICAL PROCEDURES NO. OF PATIENTS %
ENCIRCLAGE+BMV+SOI 18 39.1
CATRACT/LENSECTOMY+ENCIRCLAGE
+BMV+SOI
10 21.7
BMV+SOI 9 19.6
BMV+C3F8 1 2.2
RD SURGERY 8 17.4

74. SURGICAL PROCEDURES NO. OF
PATIENTS
% SOR RE RD % OF Re RD %Of Re RD
After SOR
1. ENCIRCLAGE+BMV+SOI 18 39.1 8 3 16 37.5
2. CATRACT/LENSECTOMY +
ENCIRCLAGE +BMV+SOI
10 21.7 4 2 20 50
3. BMV+SOI 9 19.6 4 1 11 25
4. BMV+C3F8 1 2.2 _ 1 100 --
5. RD SURGERY 8 17.4 _ 3 37.5 --

75. BEST CORRECTED VISUAL ACUITY AT LAST FOLLOW UP
BEST CORRECTED VISUAL ACUITY NO.OF PATIENTS %
20/20 –20/40 1 2.1
20/60—20/120 6 13.0
20/200—10/200 27 58.9
3/200—COUNTING FINGER 5 10.9
HEND MOVEMENT—PERCEPTION OF
LIGHT
6 13.0
NO PERCEPTION OF LIGHT 1 2.1
46 100

76. Thanks