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Ординатура / Офтальмология / Английские материалы / Ocular Differential Diagnosis 7th edition_Roy_2002

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22. Sex-linked recessive trait

23. Sturgeâ??Weber syndrome (meningocutaneous syndrome)

Arffa RC. Grayson's diseases of the cornea, 3rd ed. St. Louis: Mosbyâ??Year Book, 1991.

Frydman M, et al. Megalocornea, macrocephaly, mental and motor retardation (MMMM). Clin Genet 1990;38:149â??154.Bibliographic Links

Roy FH. Ocular syndromes and systemic diseases, 3rd ed. Philadelphia: Lippincott Williams & Wilkins, 2002.

Verloes A, et al. Heterogeneity versus variability in megalocornea-mental retardation (MMR) syndromes: report of new cases and delineation of probable types. Am J Med Genet 1993;46:132â??137.Bibliographic Links

P.256

P.257

Diagnostic table

Megalocornea (cornea having a horizontal diameter of more than fourteen millimeters)

View Table

P.258

Corneal Opacification in Infancy (See Conditions Simulating Congenital Glaucoma, p. 305)

1. *Birth trauma, such as Descemet membrane rupture 2. Chromosomal aberrations

A.Mongolism (Down syndrome)â??trisomy 21

B.Trisomy 13 (Patau syndrome)

3. Congenital malformations

A.Amyloidosis (Lubarschâ??Pick syndrome)

B.Anterior chamber cleavage syndromes

1. Axenfeld anomaly

2. Congenital central anterior synechiae

3. Congenital anterior staphyloma

4. *Peter anomaly

5. Rieger anomaly

C.Bilateral corneal dermis-like choristomas

D.Congenital glaucoma

E.De Barsy syndrome

F.*Dermoid tumors

G.*Sclerocornea

H.Xanthomas

4. Corneal dystrophy

A.*Congenital hereditary endothelial dystrophy

B.Congenital hereditary stromal dystrophy

C.Posterior polymorphous dystrophy

5. Idiopathic

6. Inborn errors of metabolism

A.*Mucopolysaccharidoses (MPS)

1. Hurler syndrome (MPS IN)

2. Maroteauxâ??Lamy syndrome (MPS VI)

3. Morquioâ??Brailsford syndrome (MPS IV)

4. Scheie syndrome (MPS IS)

B.Lowe syndrome (oculocerebrorenal syndrome)

C.von Gierke disease (glycogen disease)

D.Corneal lipoidosisâ??later

E.Mucolipidosis

1. Generalized gangliosidosis (GM1-gangliosidosis I and II) 2. ML I (lipomucopolysaccharidosis)

3. ML III (pseudo-Hurler polydystrophy)

F.Rileyâ??Day syndrome (congenital familial dysautonomia) 7. Inflammatory processes

A.Corneal ulceration

B.Herpes simplex and herpes zoster

C.Interstitial keratitis

D.Rubella syndrome (German measles)

E.Savin syndrome

Kolker AE, Hetherington I. Becker-Shaffer's diagnosis and therapy of glaucoma, 6th ed. St. Louis: CV Mosby, 1989.

Roy FH. Ocular syndromes and systemic diseases, 3rd ed. Philadelphia: Lippincott Williams & Wilkins, 2002.

Topilow HW, et al. Bilateral corneal dermis-like choristomas. Arch Ophthalmol 1981;99:1387.Bibliographic Links

P.259

Band-Shaped Keratopathy

This type of corneal opacification extends horizontally over the cornea, at the level of the Bowman membrane, in the exposed part of the palpebral aperture.

1. Anterior mosaic dystrophy, primary type

A.Episkopi (sex-linked recessive)

B.Labrador keratopathy

2. Chemical fume related as mercury vapor or calcium bichromate vapor 3. Cyclosporine as eyedrops

4. De Barsy syndrome

5. Discoid lupus erythematosus

6. Dysproteinemia

7. Gout (hyperuricemia)

8. High levels of visible electromagnetic radiation, such as xenon arc photocoagulation and laser causing acute severe anterior uveitis

9. Hypercalcemia

A.Excessive vitamin D as with oral intake, Boeck sarcoid with liver involvement, acute osteoporosis, Heerfordt syndrome, and Schaumann syndrome

B.Hyperparathyroidism

C.Hypophosphatasia (phosphoethanolaminuria)

D.Idiopathic hypercalcemia

E.Milk-alkali syndrome

F.Paget syndrome (osteitis deformans)

G.Renal failure, such as that associated with Fanconi syndrome (cystinosis)

10. Ichthyosis vulgaris

11. *Local degenerative diseases, including chronic uveitis, phthisis bulbi, absolute glaucoma,

infantile polyarthritis (Still disease), rheumatoid arthritis, interstitial keratitis, Felty syndrome, and juvenile rheumatoid arthritis

12. Long-term miotic therapy

13. Long-term steroid phosphate preparations

14. Progressive facial hemiatrophy (Parryâ??Romberg syndrome)

15. Rothmund syndrome (ectodermal syndrome)

16. Silicone oil in anterior chamber

17. Traumaticâ??chronic exposure to irritants, such as mercury fumes, calomel, calcium bichromate vapor, and hair

18. Tuberous sclerosis (Bourneville syndrome)

19. Tumoral calcinosis

20. Viscoat usage

21. Wagner syndrome (hyaloideoretinal degeneration)

22. X-linked recessive ocular dystrophy

Aldave AJ, et al. Congenital corneal opacification in De Barsy syndrome. Arch Ophthalmol 2001;119:285â??288.Bibliographic Links

Beekhuis WH, et al. Silicone oil in the anterior chamber of the eye. Arch Ophthalmol 1986;104:793.Bibliographic Links

Feist RM, et al. Transient calcific band-shaped keratopathy associated with increased serum calcium. Am J Ophthalmol 1992;113:459â??461.Bibliographic Links

Gutt L, et al. Band keratopathy and calcific lid lesions in tumoral calcinosis. Arch Ophthalmol 1988;106:725â??726.Bibliographic Links

Kachi S, et al. Unusual corneal deposit after the topical use of cyclosporine as eyedrops. Am J Ophthalmol 2000;130:667â??670.Bibliographic Links

Roy FH. Ocular syndromes and systemic diseases, 3rd ed. Philadelphia: Lippincott Williams & Wilkins, 2002.

Schlotzer-Schrehardt U, et al. Corneal stromal calcification after topical steroid-phosphate therapy. Arch Ophthalmol 1999;117:1414â??1416.Bibliographic Links

P.260

Corneal Keloids

1. Lowe syndrome (oculocerebrorenal syndrome)

2. Trauma, usually with perforation of the iris

Cibis GW, et al. Corneal keloid in Lowe's syndrome. Arch Ophthalmol 1982;100:1795.Bibliographic Links

Punctate Keratitis or Keratopathy

1. Alimentary disorders

A.Mouth

1. *Dry mouth, as in Sjögren syndrome

2. Ulcers, such as primary herpes, ocular cicatricial pemphigoid, and erythema multiforme

B.Lower alimentary tract

1. Ulcerative colitis as in Sjögren disease

2. Mild colitis, such as that due to an adenovirus

C.Stomach

1. Indigestion as in Sjögren syndrome and acne rosacea

2. Articular diseases

A.Psoriasis arthropathica

B.Reiter disease (polyarthritis enterica)

C.Rileyâ??Day syndrome (congenital familial dysautonomia)

D.Sjögren syndrome (secretoinhibitor syndrome)

3. Conjunctival discharge

A.Mucoid

1. Other types of keratoconjunctivitis sicca

2. Sjögren disease (secretoinhibitor syndrome)

B.Mucopurulent (see p. 186)

1. Angular blepharoconjunctivitis

2. Erythema multiforme (Stevensâ??Johnson syndrome)

3. Gonococcal

4. Inclusion conjunctivitis (acute stage)

5. Meningococcal

6. Reiter disease (polyarthritis enterica)

7. Trachoma

8. Vernal conjunctivitis

C.Serous

1. Adenovirus

2. Herpes simplex

3. Herpes zoster

4. Inclusion conjunctivitis (later)

5. Molluscum contagiosum

6. Trachoma (later)

7. Warts

4. Conjunctival inflammation

A.Cicatrizing (see p. 194)

1. *Ocular cicatricial pemphigoid

2. Chemical burns

3. *Erythema multiforme (Stevensâ??Johnson syndrome)

4. Diphtheria

P.261

5. Fuchsâ??Salzmannâ??Terrien syndrome (allergic reactions from drugs)

6. Radiation burns

7. *Sjögren keratoconjunctivitis sicca

8. Thermal burns

9. Trachoma

B.Diffuse catarrhal 1. Adenovirus

2. Bacterial conjunctivitis

3. Erythema multiforme (Stevensâ??Johnson syndrome)

4. Onchocerciasis syndrome (river blindness)

5. Reiter disease (polyarthritis enterica)

6. Superior limbic keratoconjunctivitis

7. Vaccinia

C.Follicular (see p. 192, 193)

1. Adenovirus

2. Herpes simplex

3. Herpes zoster

4. Inclusion conjunctivitis

5. Molluscum contagiosum

6. Trachoma

D.Giant papillary, such as in vernal and atopic conjunctivitis, and related to contact users, prosthesis, and exposed sutures

E.Papillary

1. Sjögren syndrome (secretoinhibitor syndrome)

2. Trachoma

5. Corneal conditions

A.Deep keratitis, disciform or irregular

1. *Herpes simplex

2. Herpes zoster and other viral diseases

3. Corneal dystrophy (e.g., lattice)

4. Harlequin syndrome

B.Thinned facets because of previous ulcerative or other lesions

1. Acne rosacea (ocular rosacea)

2. Erythema multiforme (Stevensâ??Johnson syndrome)

3. Gorlinâ??Chaudhryâ??Moss syndrome

4. Herpes simplex

5. Sjögren keratoconjunctivitis sicca

C.Vascularization

1. Acne rosacea (ocular rosacea)

2. Molluscum contagiosum

3. Ocular cicatricial pemphigoid

4. Phlyctenular disease (see p. 214)

5. Sjögren keratoconjunctivitis sicca

6. Trachoma

7. Vaccinia

D.Trauma

1. Chemical injury

2. Contact lens related

3. Foreign body under upper eyelid P.262

4. Mild, such as eye rubbing

5. Ultraviolet photokeratopathy

E. Thygeson superficial punctate keratitis (SPK) 6. Diseases of the lids

A.Dermatitis

1. Psoriasis

2. Seborrheic blepharitis

B.Ectropion (see p. 78â??79)

1. Exposure keratopathy

2. Neuroparalytic keratopathy

C.Folliculitis (see p. 94)

1. Blepharitis due to Demodex folliculorum

2. Seborrheic blepharitis

3. Staphylococcal blepharitis

D.Lid retraction (see p. 62â??64)

1. Endocrine exophthalmos

2. *Exposure keratopathy

E.Madarosis, such as that associated with leprosy (stiff immobile lids)

F.Nodules

1. Acne rosacea (ocular rosacea)

2. Molluscum contagiosum

3. Papilloma

4. Warts

G.Trichiasis or entropion with traumatic keratitis

H.Vesicles or ulcers

1. Herpes simplex

2. Herpes zoster

3. Ocular cicatricial pemphigoid

4. Vaccinia

I.Floppy eyelid syndrome

7. Diseases of the skin associated with punctate keratitis

A.Acne rosacea (ocular rosacea)

B.CRST (calcinosis, cutis, Raynaud phenomenon, sclerodactyly, and telangiectasia syndrome (calcinosis)

C.Erythema multiforme (Stevensâ??Johnson syndrome)

D.Follicular hyperkeratosis of the palms and soles

E.Hypertrichosis

F.Ichthyosis

G.Incontinentia pigmenti

H.Leprosy (Hansen disease)

I.Melkerssonâ??Rosenthal syndrome (Melkersson idiopathic fibroedema)

J.Ocular cicatricial pemphigoid

K.Psoriasis

8. Genitourinary diseases associated with punctate keratitis

A.Erythema multiforme (Stevensâ??Johnson syndrome)

B.Inclusion blennorrhea

C.Ocular cicatricial pemphigoid

D.Reiter disease (polyarthritis enterica)

9. Keratitis associated with use of drugs, including the following: P.263

acebutolol

cytarabine

isoniazid

acetophenazine

deslanoside

isotretinoin

acetyldigitoxin

dexamethasone

labetalol

acyclovir

dexbrompheniramine

lanatoside C

adenine arabinoside

dexchlorpheniramine

levobunolol

adrenal cortex

dextran

lidocaine

injection

 

 

aldosterone

dibucaine

medrysone

alcohol

diclofenac

mepivacaine

allopurinol

diethazine

mesoridazine

amantadine

diethylcarbamazine

methdilazine

amphotericin B

digitoxin

methimazole

antazoline

digoxin

methotrexate

antipyrine

dimethindene

methotrimeprazine

aspirin

dipivefrin

methoxsalen

atenolol

dorzolamide

methylprednisolone

auranofin

dipivalyl epinephrine (DPE)

methylthiouracil

aurothioglucose

dyclonine

metipranolol

aurothioglycanide

emedastine difumarate

metoprolol

bacitracin

emetine

minoxidil

benoxinate

epinephrine

nadolol

benzalkonium

ether

naphazoline

betamethasone

ethopropazine

neomycin

betaxolol

etidocaine

niacin

botulinum A toxin

etretinate

ofloxacin

brimonidine tartrate

F3T

oral contraceptives

brinzolamide

firaxetine hydrochloride

ouabain

brompheniramine

floxuridine

oxprenolol

bupivacaine

fluprednisolone

oxyphenbutazone

butacaine

flumethasone

paramethasone

butaperazine

fluorometholone

penicillamine

capecitabine

fluorouracil

perazine

carbimazole

fluphenazine

pericyazine

carphenazine

flurbiprofen

perphenazine

chloramphenicol

fluvoxamine maleate

phenacaine

chlorambucil

framycetin

pheniramine

chlorhexidine

gold sodium thiosulfate

phenylbutazone

chloroform

gentamicin

phenylephrine

chloroprocaine

gitalin

pilocarpine

chlorpheniramine

gold Au 198

pindolol

chlorpromazine

gold sodium thiomalate

piperacetazine

chlorprothixene

guanethidine

piperocaine

chlortetracycline

hexachlorophene

polymyxin B

chrysarobin

hydrocortisone

prednisolone

ciprofloxacin

idoxuridine

prilocaine

cocaine

IDU

procaine

colchicine

indomethacin

propofol

cortisone

iodide and iodine solutions and

prochlorperazine

 

compounds

 

cyclopentolate

 

promazine

promethazine

sulfamethizole

thioridazine

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