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Benign Essential blepharospasm Involuntary Femals 6th decade
Tx Botulinum toxin every few weeks |
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Excess blinking with subsequent spasm Occurs SECONDARY to ocular inflammation |
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Fasiculations of the orbicularis Typically unilateral and self-limited
CC: jumping or quivering of the lid or eye
Cause: Fatigue, Stress, Medication, Alcohol
Management: Cool compresses Topical antihisatmines
GOAL: Prolong the muscle refractory period
OTC remedy Tonic water i contains quinine |
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Aberrant Regeneration Due to trauma to the 9rd nerve
MR fibers run to the LPS Elevation when the eye is aDducted |
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AKA Jaw winking Congenital ptosis cases when patient opens mouth ptosis gets better. TX: Surgery |
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Angioedema with urticaria |
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Occurs secondary to histamine release Histamine triggers massive vasodilation
Characterizedby severe swelling and may also see hives
Associated with itching
TX: Antihistamines, Cool compress, Steroids possibly. |
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Wool Sorters Disease Infection is via contact through break of skin.
You will see Preseptal Cellulitis
eschar, black to brown ulcer on lid |
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Can have primary or secondary lid lesions
Eye signs: Conjunctival chancre, madarosis, scleritis, interstitial keratitis
Tx: Penicillin |
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Parasitic infection Characterized by hypertrophy of the lids and subcutaneous tissue
Severe edema occurs due to a surge of lymphatic fluid into the sub-q tissue
Severe allergic response to the parasite. |
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Mosst often secondary to a small pox vaccine. through direct contamination of the lid.
Can be used in warfare |
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An autoimmune response to the sun
Ocular Signs: Poliosis, uveitis, inflammatory RD Other signs: Headache, encephalopathy, seizures, vitiligo, deafness. |
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Hereditary Autosomal Recessive syndrome
Sunlight exposure has progressive pigment changes to the skin MACULES AN SCARRING Patients have increased risk of cancers, BCC,SCC,Melanoma, and conjunctibal malignancies |
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Swelling associated with a well-defined expanding red line
Skin trauma that is invaded by B hemolytic streptococcus
May lead to ectropion or entropion |
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Erythema Multifome AKA Stevens Johnson Syndrome |
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Severe type IV or delayed(DTH) hypersensitivity Causative agents are typically medication Sulfa drugs, barbituates Young Males Iatrogenic
Flu-like symptomes Severe rash with perivascular inflammation and bulls eye appearance
Ocular signs: mucous discharge, pseudomembrane formation, papillary response, bullae formation, swollen crusted lids.
Management: Electrolytes, tears, bandage contact lens, lid taping
Topical systemic steroids in high doses to reduce inflammtion and scarring
Surgery may be necessary to decrease and correct scarring |
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Ocular Cicatricial Pemphigoid |
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Auto-immune mucous membrane disorder in which bullae form in various mucous tissues and rupture causeing severe pain and scarring
Older Women
Similar to Eyrthema multifome
Keratinization of the cornea and conjunctiva |
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Cause: Staph but infrequently strep Children Macular rash on lids and face with crusted over blister like lesions (bullae) Treatment: Topical antibiotics |
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Harbored in nerves Frontal Nerve = lesions on upper lid and forehead and superior conj Pthalmic division of CN V = HZO Nasociliary involvement = Hutchinsons sign: Tip of nose involved
Tx: Oral Antivirals, acyclovir 800mg 5 times a day, topicals drying lotions, steroids, antihistamines, antidepressents, prednisone, analgesics |
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Complete absence of ocular tissue in the orbit Related to how the optic vesicle forms Surgeon places solid conformer in eye |
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Abnormal smallness of one or both eyes Pure microophthalmos: Absence of all ocular defects Nanophthalmos: Absence of ocular contents within the eye itself |
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Some or all the the sutures in the skull close too early in an infant Main concern: Increase in intercranial pressure. -Possible exophthalmos, Mesured from pt's zygomatic arch on each side. |
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Craniosynostosis Premature fusion of the sagittal suture |
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Craniosynostosis Premature fusion of metopic asuture or frontal suture High retreating forehead. From above their forehead looks like a pyramid |
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Craniosynostosis Premature fusion of coronal suture Flat-head syndrome Shortened front to back diameter of skull |
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Craniosynostosis Premature closure of coronal and lambdoidal suture Tower skull or high-head syndrome |
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Craniosynostosis Premature closure of coronal or lambdoidal suture flattening of back or side of head oblique slant |
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Increased distance between the eyes cleft palate, nose and upper lip |
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Vertical mal-alignment of the orbit (one eye is higher than the other) Causes: Congenital: Craniosynostosis, Orbital facial clefts Acqured: Facial/orbital fractures, trauma, mass/tumors |
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Vertical mal-alignment of the orbit (one eye is higher than the other) Causes: Congenital: Craniosynostosis, Orbital facial clefts Acqured: Facial/orbital fractures, trauma, mass/tumors |
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AD: Premature closure of cranial base sutures, orbit, and maxillary complex Brachycephaly Sightns/symptoms: Wide set bulging eyses, beaked nore, underdeveloped jaw, DENTAL problems (V shaped palates), Hearing loss, cleft lip/palate. Exophthalmos, Hypertelorism, V pattern exotropia, Aniridia, Blue sclera, Cataract, Ectopic lens, glaucome, megalocornea, optic nerve hypoplasia |
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AD: Acrocephosyndactly: Brachycephaly and/or oxycephaly. Severe Symemetrical syndactyly of hands and feet. Signs: proptosis, Hypertelorism, Exotropia, Corneal exposure, optic atrophy. High cleft palate, low set ears, organ anomalies, mentally handicapped. |
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Treacher Collins OR Franceeshetti-Zwahlen-Klein Syndrome Sighns: Hypoplasia of the zygomatic, maxilla & mandile bone indistinct inferior orbital margin, Conductive hearing loss. Coloboma: part of tissue is missing (of the eyelid), and ectropian |
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Incomplete development of ear, nose, soft palate, lip, and mandible usually on ONE side of the face. 99% of organs will be underdeveloped on one side of the body. SColiosis of the spine. PREAURICULAR APPENDAGE( blobs of the tissue near the ear) Lipodermoid, epibulbar dermoid cyst Hearing loss |
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Unusually small mandible (micrognathia) Posterior displacement or retraction of the tounge. Upper airway obstruction, Cleft palate, "bird face" appearance |
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Hallermanstrieff Syndrome |
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Dyscephaly, Dental anomalies, Structures are smaller, Hypotrichosis(not many eyelashes), Skin problems on head, bilateral congenital cataracts, Bilateral MICROHTHALMIA |
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CSF CYST Meninges protrude through orbit |
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Neural tube defect Sac-like protursions of the brain and meninges CSF AND GRAY MATTER Exophthalmos, pulsating proptosis (NO BUITS) Anterior Vs Posterior: Supero-medial orbit affected VS defect in sphenoid bone |
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Cause: Sinus infection, Trauma, Allergies, Tumor. Ethmoid: push eyes down Ethmoid: Push eye out Maxillary: Elevate and push in Orbital: sphenoid compress optic nerve and vision loss Symptoms: Older,l Vission loss, ephiphora, facial trauma or sinus disease....... |
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One Eye, One orbit, no vision, nose and nostrils missing |
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Paired ocular strucres in one orbit Failure of midline facial structure development, no nose |
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General inflammation/infection of the soft tissues of the orbit. BEHIND the orbital septum, caused by SINUS NFECTION, orbital fracture, dental infection, orbital trauma, post surgical Staphylococcus, streptococcus, or Haemophilus influenzae Symptoms: Very sick, FEVER, malaise, headache, rhinorrhea, prulent nasal discharge, HASPITALIZATION, Swelling, RESTRICTED PAINFUL EYE MOVEMENTS, Dark red color Raised IOP DECREASED VA's Tx: Referral out, IV antibiotics could be life threatening |
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Infection ANTERIOR to ORBITAL septum. 2o to localized infections. Normal ocular movements/ normal EOMs No exophthalmos Little to no VA reduction Small Fever, less pain the orbital cellulitus Tx: Oral antibiotic AMOXOCILLIN 500mg PO TID |
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Cavernous Sinus Thrombosis |
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Cavernous sinus that is filled with venous blood (behind the superior orbital fissures) CN 3,4,5, and 6, and carotid artery 2o to infection or trauma. Very similar to orbital cellulitus but BILATERAL, Blue area behind ears, Cranial nerve signs, altered consciousness Orbital Pain, Visual disturbances. Spreads via communicating veins, increased IOP, Can effect grey matter, seizures, unabler to stay awake. Tx: Hospitalization: Broad spectrum IV antibiotics |
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Idopathic orbital inflammatory disease. 2o to Syphilis,sarcoid, TB Unilateral, middle age, ABRUPT PAINFUL ONSET(Tellate Sign) Limitation of gaze, Exopthalmos, dry eye, Decreased VAs, diplopia Tx: Oral prednisone 60-100 mg/qqd for 2-3 weeks. benign. |
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Orbital Pseudotubor that involves EOM's Third most common orbital disorder Unilateral and often younger adults Proptosis, Chemosis EOM limited movement |
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When Orbital pseudotumor effects the orbital apex Pt presents: Pain proptosis, Vission loss, Defects with CN 3,4,5,6, +APD |
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Intermittent Exophthalmos |
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Popping Eye syndrome Non-pulsatile, no bruit Eye being pushed out of socket Varix: congenital enlargement of venous channels |
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Bulging, pulsating eye Eye pops out of socket, with a pulse Will hear Bruits Rare and painful 2o to trauma, Caused by an arteriovenous aneurysm involving the ophthalmic or internal carotid artery |
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Carotid Cavernous Fistula |
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Removal of the eyeball orbital contents remain |
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Remove entire contents of the globe leaving the scleral shell and sometimes cornea intact |
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Entire removal of the orbital contents including eyebaall, EOM, fat and connective tissue. |
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Axenfeld-Reiger's Syndrome |
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