Diagnosis & Treatment Flashcards

1
Q

CC: possibly trauma, transient FB sensation, mild photophobia, discomfort
Findings: Mild VA reduction, moderate bulbar injection, possible circumcorneal flush (w/ or w/o AC rxn), Corneal epithelium staining, Topical anesthetic relieves pain entirely (dull-ache is a sign of a AC rxn)

A

Superficial Epithelial Abrasion
Tx:
1. Eliminate direct/indirect cause such as removing FB, epilation of lash, refit of RGP, management of epitheliopathies.
2. Irrigate in office and apply AB ung (gentamicin or tobramycin)
3. If mild - AB gtt is optional; If moderate - severe then AB gtts QID for 2-3 days or until resolution.
4. Lubricating gtts q3-4 hours starting 2 hours after leaving office
5. Apply Heating pack q2-4 hours for the first day
6. Hypertonic gtts q3-4hrs for 2-3 days if corneal edema is present
7. Aspirin or Ibuprofen for pain relief
*Advise patient that discomfort will probably get worse before it gets better

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2
Q

The 4 Morning Syndromes

A
  1. Marginal Keratitis (toxic staph)
  2. Epithelial Basement Membrane Dystrophy
  3. Recurrent Corneal Erosion (RCE)
  4. Fuch’s Endothelial Dystrophy
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3
Q

What type of Burn (Thermal vs. Radiation vs. Acid vs. Alkali) creates more complications?

A

Alkali - because it continues to penetrate through the cornea (collagenolytic response) for hours - days after initial contact. May cause ulceration, melting, permanent stromal scarring or perforation. Reaction is directly proportional to pH (greater pH equals greater tissue reaction)

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4
Q

Hemosiderosis (Rust Ring formation) occurs how many hours after initial injury?

A

2 - 48 hours after embedding. All hemosiderotic epithelial cells must be removed to avoid chronic weakening, irritation re-erosion of epithelium and risk of infection.

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5
Q

How long does it take for the Basal Epithelial Cells to regenerate or repair EBM?

A

at least 6-8 weeks

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6
Q

Which type of Iris Nodule appears away from the pupillary border?

A

Busacca - whitish-yellow lumps representing iris stroma and always associated with granulomatous uveitis.
Koeppe - most common, round or oval masses located at the pupil border.

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7
Q

Describe the 4 types of hypersensitivity reactions

A
  1. Type I - Immediate or Anaphylactic which is mediated by IgE and the primary cell is the Mast Cell/Basophil
  2. Type II - Cytotoxicity - the antigens are typically endogenous and are mediate by IgM + IgG + complement
  3. Type III - Immune Complex - mediated by IgG and some IgM - antigen may be exogenous or endogenous and Neutrophils cause the damage
  4. Type IV - Cell Mediated or Delayed - damage occurs via sensitized T lymphocytes. Example - Tuberculin (PPD test)
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8
Q

Are males or Females more affected by Behcet’s Disease?

A
Globally = Males
USA = Females
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9
Q

HLA associated with Behcet’s?

A

HLA-B5

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10
Q

Still’s Triad?

A
  1. Iridocyclitis
  2. Band Keratopathy
  3. Cataract
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11
Q

What is the diagnosis?
Etiology: Unknown
Clinical: dermatological disease in children
Diagnosed via: Biopsy
Ocular: AAU, Epibulbar Mass, Spontaneous Hyphema

A

Juvenile Xanthogranuloma (JXG)

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12
Q

Reiter’s Triad?

A
  1. Arthritis - especially the knee joint
  2. Nongonococcal urethritis
  3. Conjunctivitis/Uveitis
    - Post venereal exposure usually chlamydial
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13
Q

Hutchinson’s Triad? - seen in congenital syphilis

A
  1. Interstitial Keratitis
  2. Notched Incisor Teeth
  3. Eighth nerve deafness
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14
Q

Aniridia may be associated with what systemic problem?

A

Wilms’ Tumor - nephroblastoma typically seen in children.

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15
Q

Whats the diagnosis?

  • Usually white females 30-40 years old
  • Unilateral
  • Development of iris holes (pseudopolycoria)
  • Progresses over 1-3 years
  • Pupil distortion/displacement caused by PAS
  • Complications: secondary glaucoma, corneal edema, pain, reduced VA
  • Mimics Chandler’s syndrome (corneal endothelial changes, iris atrophy, mild glaucoma)
A

Essential Iris Atrophy

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16
Q

Pathologic causes of Heterochromia

A

Fuch’s heterochromic iriidocyclitis, Intraocular FB hemosiderosis, Intraocular neoplasias

17
Q

Name the Systemic Syndrome:
Etiology: AD, defective formation of collagen and elastic fibers
Physical: Slender, long arms/legs/fingers, high arched palate, hyperextensible joints, floppy heart valves, aneurysmal dilation, dissecting aneurysm, ectopic lentis sup-temp, hypoplasia of the iris, zonular lysis, blue sclera

A

Marfan’s Syndrome

18
Q

Name the Systemic Situation:
Symptoms: fever, night sweats, malaise, fatigue, backache, myalgia, arthralgia, roth spot heme, Osler’s nodes (raised lesions on pads of fingers), Janeway Lesions (hemes on palms or soles), pale skin

A

Subacute Bacterial Endocarditis - occurs on damaged heart valves, artificial valves or IV drug Abusers
Etiology: Streptococcus viridens infection of a previously damaged heart valve in presence of turbulent blood flow.