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Topic :ophthalmic manifestation
in leukemia
By Cynthia Oloo
Bsc.comprehessive Ophthalmology and cataract surgery
Jomo Kenyatta University of Agriculture and Technology/Sabatia Eye Hospital
Ocular manifestation
• Leukemia is a group of malignant neoplasms derived from the
hematopoietic stem cells as a results of abnormal proliferations of
blood cells in the bone marrow
• Liebreich first described leukemic retinopathy in1863
• Classified into acute or chronic or lymphoid or myeloid type
• ALL is most common ocular manifestation occurs in 90% of cases
• Ophthalmic classification is categorized into 2 major
 primary or direct leukemic infiltration
Secondary or indirect leukemic infiltration
Cont ,
DIRECT
• Can have 3 patterns
1. Infiltration of the orbit mimicking orbital inflammation diseases
2. Direct infiltration of the : Ant segment, vitreous, choroid, retina
mimicking uveitis, choroiditis and retinitis
3. Infiltration of the optic nerve presenting with or without another
CN III, IV,VI
Orbit and eyelids
Primary –it more common in ALL
• Orbit infiltration – exophthalmos, diplopia
• Eyelids –edema , inflammation, chemosis, pain
Secondary –orbit can show affectation after remission
• Lacrimal glands are affected causing tears dysfunction
• Preseptal cellulitis , acute dacrocystitis in ISS pts
conjunctiva
Primary- hyperemia , edematization of lower subpalpebral conjunctiva
• Infiltrates can be seen around vessels
• In the form of a conjunctival mass
Secondary- hyperviscosity can produce vascular anomalies
• 4 stages of severity- hyperemia, chemosis, pseudomembranous with
complete loss of conjunctival epithelium , compromise of the corneal
epithelium(cook and bartley et al 1997)
• Severe DES due to Meibomian dysfunction
• Can lead to ectropion, cicatricial lagophthalm
Palpebral linchenification
ectropion LL
Sclera
Primary – scleral infiltration is common in ALL, can stimulate scleritis
Episcleritis is associated by Adult-T cell lymphocytes
• Around the episcleral vessel
• It usually asymptomatic
• Can be autopsy finding(Sharma et al, 2004)
Secondary- Opportunistic infectious scleritis in ISS pts
Cornea
Primary – is avascular structure
• It is hardly affected by direct
• Ring-shaped, corneal ulcers, subepithelial limbal infiltrates, peripheral
ulcers (Tayor et al, 1997)
Secondary- Citarabine that corneal toxicity
• Interefering with epithelium’s synthesis of DNA
• Keratoconjunctivitis sicca is most common manifestation
• Acute calcium keratopathy, corneal thining, keratitis,
ulcers(herpetic/fungal, corneal melting, perforation
Anterior chamber and iridocorneal angle
Primary – anterior uveitis, pseudohypopyon, spontaneous hyphema
• Infiltration of iris is not common
• It occurs associated with involvement of choroid and ciliary body
• Characterized by change of iris color ,pseudohypopyon ,grey /yellow
• Hpopyon estimated 2.5 to 18% relapsed cases
• IOPs may be high to show signs of acute glaucoma
Cont,
Secondary-hypopyon uveitis secondary due to anaemia
• Ischaemia of the anterior segment may cause corneal edema,
• Conjunctival chemosis, visual loss, anterior uveitis,high IOPs, eye
pain
Lens
• Subcapsular cataract
• Consequences of use of steroid,
• Chemotherapy, radiotherapy
• Ischaemic causes due to anaemia
Vitreous
• Vitreous opacities and infiltration of leukemic cells in the vitreous
body
Choroid
Primary-is most commonly affected ocular tissue
• Involvement is not clinically apparent
• Choroidal and orbital leukemic infiltration mimic advanced RB
• Diffuse or perivascular involvement
• If affected , overlying retina shows alterations such as photoreceptor
Damage, RPE atrophy,
SRD , usually bilateral, affecting posterior pole
Cont,
Secondary-much less common
• Retinochoroidal infarction detected during RX of ALL
Retina
Primary- very commonly
• 70% of pts with leukemia shows fundus changes(Alemayesh et al, 1996)
• Early –venous dilatation , tortuosity,
• Vascular sheathing, superficial and intraretinal
Hemorrhages
Cont,
• Cotton wool spots –due to ischaemic( leukemic retinopathy)
• CRAO in pt with hyperviscosity
Cont,
• Retinal hemorrhages –mainly at the posterior pole
• Inner layers with focal destruction
• May be dot or flame shaped with a white component in the center
• White component contain; leukemic cells, debris , platelet -fibrin
aggregates or septic emboli
Secondary-OI involves retina during period of neutropenia
• Susceptible to CMV, candida aspergillus(common)
• Protozoa, bacteria
Cont,
• Other viruses such as herpes, varicella, munps
• May cause necrotizing retinitis
Optic nerve
Primary- O.N usually involved in CNS
• It can happen in upto 13-18% of cases
• Symptoms depends on raised ICP and affectation of CN
• Ocular symptoms –blurred vision, loss of VA or diplopia(CN
III,IV,VI)
• Affectation of ON is asymptomatic
• Papilloedema can be found ;Due to
1. Direct infiltration by leukemic cells
2. Increased Intraocular pressure
3. Swelling due to retrolaminar leukemic invasion
Cont,
• ON can singly be affected without papilloedema
• Affectation of ON occurs during evolution of ALL
Secondary – Toxicity of chemo, radio, antibiotics
• Ischaemia after anaemia or hyperviscosity
Treatment
Intravitreal injections
1. Dexamethasone
2. Anti –VEGFs
3. Methotrexate (MTX)-400mg/0.1ml twice weekly in the first month,
Once weekly in 2 months, then once monthly
conclusion
• Ophthalmic manifestation in pts suffering ALL are very common
• Ocular involvement can be caused by directly infiltration by leukemic
cells
• Secondary to anaemia, thrombocytopenia, leukopenia, hyperviscosity
and Ois in ISS pts
• RX is difficult because the effect of chemo in the eye is very limited
• Radio is frequently used for RX
• RX with methotrexate has shown improvement according to
retrospective done at ocular oncology service at the Goldscleger Eye
institute
Referrence
• In -tech ophthalmic manifestation of lymphoblastic leukemia
• Scientific report (2020) on ocular manifestation of leukemia and
results of treatment with intravitreal methotreaxate

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OPHTHALMIC MANIFESTATION OF LEUKEMIA.pptx

  • 1. Topic :ophthalmic manifestation in leukemia By Cynthia Oloo Bsc.comprehessive Ophthalmology and cataract surgery Jomo Kenyatta University of Agriculture and Technology/Sabatia Eye Hospital
  • 2.
  • 3. Ocular manifestation • Leukemia is a group of malignant neoplasms derived from the hematopoietic stem cells as a results of abnormal proliferations of blood cells in the bone marrow • Liebreich first described leukemic retinopathy in1863 • Classified into acute or chronic or lymphoid or myeloid type • ALL is most common ocular manifestation occurs in 90% of cases • Ophthalmic classification is categorized into 2 major  primary or direct leukemic infiltration Secondary or indirect leukemic infiltration
  • 4. Cont , DIRECT • Can have 3 patterns 1. Infiltration of the orbit mimicking orbital inflammation diseases 2. Direct infiltration of the : Ant segment, vitreous, choroid, retina mimicking uveitis, choroiditis and retinitis 3. Infiltration of the optic nerve presenting with or without another CN III, IV,VI
  • 5. Orbit and eyelids Primary –it more common in ALL • Orbit infiltration – exophthalmos, diplopia • Eyelids –edema , inflammation, chemosis, pain Secondary –orbit can show affectation after remission • Lacrimal glands are affected causing tears dysfunction • Preseptal cellulitis , acute dacrocystitis in ISS pts
  • 6. conjunctiva Primary- hyperemia , edematization of lower subpalpebral conjunctiva • Infiltrates can be seen around vessels • In the form of a conjunctival mass Secondary- hyperviscosity can produce vascular anomalies • 4 stages of severity- hyperemia, chemosis, pseudomembranous with complete loss of conjunctival epithelium , compromise of the corneal epithelium(cook and bartley et al 1997) • Severe DES due to Meibomian dysfunction • Can lead to ectropion, cicatricial lagophthalm Palpebral linchenification
  • 8. Sclera Primary – scleral infiltration is common in ALL, can stimulate scleritis Episcleritis is associated by Adult-T cell lymphocytes • Around the episcleral vessel • It usually asymptomatic • Can be autopsy finding(Sharma et al, 2004) Secondary- Opportunistic infectious scleritis in ISS pts
  • 9. Cornea Primary – is avascular structure • It is hardly affected by direct • Ring-shaped, corneal ulcers, subepithelial limbal infiltrates, peripheral ulcers (Tayor et al, 1997) Secondary- Citarabine that corneal toxicity • Interefering with epithelium’s synthesis of DNA • Keratoconjunctivitis sicca is most common manifestation • Acute calcium keratopathy, corneal thining, keratitis, ulcers(herpetic/fungal, corneal melting, perforation
  • 10. Anterior chamber and iridocorneal angle Primary – anterior uveitis, pseudohypopyon, spontaneous hyphema • Infiltration of iris is not common • It occurs associated with involvement of choroid and ciliary body • Characterized by change of iris color ,pseudohypopyon ,grey /yellow • Hpopyon estimated 2.5 to 18% relapsed cases • IOPs may be high to show signs of acute glaucoma
  • 11. Cont, Secondary-hypopyon uveitis secondary due to anaemia • Ischaemia of the anterior segment may cause corneal edema, • Conjunctival chemosis, visual loss, anterior uveitis,high IOPs, eye pain Lens • Subcapsular cataract • Consequences of use of steroid, • Chemotherapy, radiotherapy • Ischaemic causes due to anaemia
  • 12. Vitreous • Vitreous opacities and infiltration of leukemic cells in the vitreous body
  • 13. Choroid Primary-is most commonly affected ocular tissue • Involvement is not clinically apparent • Choroidal and orbital leukemic infiltration mimic advanced RB • Diffuse or perivascular involvement • If affected , overlying retina shows alterations such as photoreceptor Damage, RPE atrophy, SRD , usually bilateral, affecting posterior pole
  • 14. Cont, Secondary-much less common • Retinochoroidal infarction detected during RX of ALL
  • 15. Retina Primary- very commonly • 70% of pts with leukemia shows fundus changes(Alemayesh et al, 1996) • Early –venous dilatation , tortuosity, • Vascular sheathing, superficial and intraretinal Hemorrhages
  • 16. Cont, • Cotton wool spots –due to ischaemic( leukemic retinopathy) • CRAO in pt with hyperviscosity
  • 17. Cont, • Retinal hemorrhages –mainly at the posterior pole • Inner layers with focal destruction • May be dot or flame shaped with a white component in the center • White component contain; leukemic cells, debris , platelet -fibrin aggregates or septic emboli Secondary-OI involves retina during period of neutropenia • Susceptible to CMV, candida aspergillus(common) • Protozoa, bacteria
  • 18. Cont, • Other viruses such as herpes, varicella, munps • May cause necrotizing retinitis
  • 19. Optic nerve Primary- O.N usually involved in CNS • It can happen in upto 13-18% of cases • Symptoms depends on raised ICP and affectation of CN • Ocular symptoms –blurred vision, loss of VA or diplopia(CN III,IV,VI) • Affectation of ON is asymptomatic • Papilloedema can be found ;Due to 1. Direct infiltration by leukemic cells 2. Increased Intraocular pressure 3. Swelling due to retrolaminar leukemic invasion
  • 20. Cont, • ON can singly be affected without papilloedema • Affectation of ON occurs during evolution of ALL Secondary – Toxicity of chemo, radio, antibiotics • Ischaemia after anaemia or hyperviscosity
  • 21. Treatment Intravitreal injections 1. Dexamethasone 2. Anti –VEGFs 3. Methotrexate (MTX)-400mg/0.1ml twice weekly in the first month, Once weekly in 2 months, then once monthly
  • 22. conclusion • Ophthalmic manifestation in pts suffering ALL are very common • Ocular involvement can be caused by directly infiltration by leukemic cells • Secondary to anaemia, thrombocytopenia, leukopenia, hyperviscosity and Ois in ISS pts • RX is difficult because the effect of chemo in the eye is very limited • Radio is frequently used for RX • RX with methotrexate has shown improvement according to retrospective done at ocular oncology service at the Goldscleger Eye institute
  • 23. Referrence • In -tech ophthalmic manifestation of lymphoblastic leukemia • Scientific report (2020) on ocular manifestation of leukemia and results of treatment with intravitreal methotreaxate