Most common malignant tumour of eyelid is ?
Bilateral ptosis is seen in all except which of the following?
Which of the following statements about corneal dystrophy is true?
What is the most common complication of pars planitis?
Jack in box scotoma is seen after correction of Aphakia by?
Shaffer's sign is seen in ?
What type of deposit is commonly associated with age-related macular degeneration?
What is the term for the fusion of the palpebral and bulbar conjunctiva?
What does extraretinal fibrovascular proliferation at the ridge indicate?
Herpetic keratitis is treated by which of the following?
NEET-PG 2012 - Ophthalmology NEET-PG Practice Questions and MCQs
Question 11: Most common malignant tumour of eyelid is ?
- A. Basal cell carcinoma (Correct Answer)
- B. Malignant melanoma
- C. Squamous cell carcinoma
- D. Sebaceous gland carcinoma
Explanation: ***Basal cell carcinoma*** - **Basal cell carcinoma (BCC)** accounts for approximately 85-95% of all eyelid malignancies, making it the most common type. - It often presents as a **pearly nodule** with telangiectatic vessels, frequently affecting the lower eyelid. *Squamous cell carcinoma* - **Squamous cell carcinoma (SCC)** is the second most common eyelid malignancy, but it is significantly less frequent (5-10%) than BCC. - SCC has a **higher metastatic potential** compared to BCC. *Malignant melanoma* - **Malignant melanoma** is a rare but highly aggressive eyelid tumor, accounting for less than 1% of all eyelid malignancies. - It is characterized by its **pigmented appearance** and rapid growth pattern. *Sebaceous gland carcinoma* - **Sebaceous gland carcinoma** is a relatively uncommon, but aggressive, tumor of the eyelid, comprising about 1-5% of cases. - It often mimics benign lesions like a **chalazion** or chronic blepharitis, leading to delayed diagnosis.
Question 12: Bilateral ptosis is seen in all except which of the following?
- A. Trauma
- B. Hyperthyroidism (Graves' disease) (Correct Answer)
- C. Congenital
- D. Myotonic dystrophy
Explanation: ***Hyperthyroidism (Graves' disease)*** - **Hyperthyroidism** causes eyelid retraction, leading to a **stare** or **lid lag**, rather than **ptosis**. - **Graves' ophthalmopathy** can cause proptosis (bulging eyes) and conjunctival injection, but does not typically manifest as ptosis. *Congenital* - **Congenital ptosis** is often present at birth due to improper development of the **levator palpebrae superioris muscle**. - It can be **bilateral** and is usually isolated, without other systemic symptoms. *Trauma* - **Traumatic ptosis** can occur if the **levator muscle**, **aponeurosis**, or **third cranial nerve** is damaged. - This can be **bilateral** depending on the nature and extent of the head trauma. *Myotonic dystrophy* - **Myotonic dystrophy** is a **hereditary muscle disorder** characterized by progressive muscle weakness. - **Bilateral ptosis** is a very common early sign of **myotonic dystrophy**, often accompanied by **facial weakness** and **myotonia**.
Question 13: Which of the following statements about corneal dystrophy is true?
- A. It involves neovascularization.
- B. It is caused by inflammation.
- C. It is usually unilateral.
- D. It is typically bilateral. (Correct Answer)
Explanation: ***It is typically bilateral.*** - **Corneal dystrophies** are inherited genetic disorders that usually affect both eyes symmetrically. - This bilateral presentation is a key characteristic distinguishing them from other corneal conditions. *It is caused by inflammation.* - **Corneal dystrophies** are primarily genetic and degenerative, not inflammatory. - While inflammation can cause corneal damage (e.g., keratitis), it is not the underlying cause of dystrophy. *It involves neovascularization.* - **Neovascularization** (growth of new blood vessels) is typically a response to chronic inflammation, hypoxia, or infection in the cornea. - It is generally not a feature of primary corneal dystrophies, which are characterized by abnormal deposits or structural changes within the corneal layers. *It is usually unilateral.* - As inherited genetic conditions, **corneal dystrophies** almost always affect both eyes. - Unilateral involvement would suggest a different etiology, such as trauma, infection, or a localized acquired condition.
Question 14: What is the most common complication of pars planitis?
- A. Cataract (clouding of the lens) (Correct Answer)
- B. Retinal detachment (separation of retina)
- C. Cystoid macular edema (swelling of central retina)
- D. Glaucoma (increased intraocular pressure)
Explanation: **Cataract (clouding of the lens)** - **Cataract formation** is the most common ocular complication in patients with pars planitis, often due to chronic inflammation or steroid use. - The inflammation can disrupt lens metabolism, leading to **opacification** over time. *Retinal detachment (separation of retina)* - While possible, **retinal detachment** is a less common complication of pars planitis compared to cataract formation. - It can occur in severe cases, often due to vitreous traction on fragile peripheral retina or tears associated with **snowbanking**. *Cystoid macular edema (swelling of central retina)* - **Cystoid macular edema (CME)** is a significant cause of vision loss in pars planitis but is not the most frequent complication overall. - It results from the inflammatory compromise of the blood-retinal barrier, leading to fluid accumulation in the **macula**. *Glaucoma (increased intraocular pressure)* - **Glaucoma** can occur in pars planitis, often secondary to chronic inflammation affecting the **trabecular meshwork** or prolonged steroid use. - However, it is less common than cataracts and CME as a primary complication.
Question 15: Jack in box scotoma is seen after correction of Aphakia by?
- A. IOL
- B. Spectacles (Correct Answer)
- C. Contact lens
- D. None of the options
Explanation: ***Spectacles*** - **Jack-in-the-box scotoma** describes a visual phenomenon where objects appear to jump into and out of the field of vision. This occurs due to the **peripheral scotoma** and **ring scotoma** created by high-plus aphakic spectacle lenses. - Aphakic spectacles cause significant **magnification of the central visual field** (about 25-30%) and a corresponding minification/displacement of the peripheral field, leading to areas where objects are transiently obscured or reappear. *IOL* - An **intraocular lens (IOL)** replaces the natural lens within the eye, providing a much more stable and centered optical correction. - IOLs generally do not cause significant magnification changes or the peripheral scotoma associated with aphakic spectacles. *Contact lens* - **Contact lenses** sit directly on the cornea, offering a visual correction that is much closer to the nodal point of the eye than spectacles. - This placement results in less peripheral distortion and magnification compared to spectacles, making jack-in-the-box scotoma unlikely. *None of the options* - As **aphakic spectacles** are known to cause jack-in-the-box scotoma, this option is incorrect.
Question 16: Shaffer's sign is seen in ?
- A. Acute angle-closure glaucoma
- B. Diabetic retinopathy
- C. Age-related macular degeneration
- D. Retinal detachment (Correct Answer)
Explanation: ***Retinal detachment*** - **Shaffer's sign** refers to the presence of **pigment cells** (tobacco dust) in the **anterior vitreous**, indicating a retinal break or detachment. - This sign is due to the release of retinal pigment epithelium cells into the vitreous following a tear in the retina. *Acute angle-closure glaucoma* - This condition is characterized by a **sudden increase in intraocular pressure** due to blocked fluid outflow, causing pain, redness, and blurred vision. - It does not involve pigment cells in the vitreous, but rather changes in the **anterior chamber angle**. *Diabetic retinopathy* - This is a microvascular complication of diabetes, leading to damage to the blood vessels in the retina, causing **hemorrhages**, **exudates**, and **neovascularization**. - It does not typically present with free pigment in the vitreous as a primary diagnostic sign. *Age-related macular degeneration* - This condition affects the **macula**, often causing distorted vision and central vision loss, and is characterized by drusen and atrophy. - While it can involve retinal changes, it does not classically present with pigment cells in the vitreous as a diagnostic indicator.
Question 17: What type of deposit is commonly associated with age-related macular degeneration?
- A. Iron
- B. Drusen (Correct Answer)
- C. Lipochrome
- D. Hemosiderine
Explanation: ***Drusen*** - **Drusen** are yellow deposits of extracellular material that accumulate beneath the **retinal pigment epithelium (RPE)**. - Their presence is a hallmark sign of **age-related macular degeneration (AMD)** and can lead to vision loss by disrupting retinal function. *Iron* - While iron can accumulate in ocular tissues in conditions like **siderosis bulbi** (due to retained intraocular foreign bodies), it is not a characteristic deposit of macular degeneration. - Ocular iron deposition typically causes different pathologies, such as retinal dysfunction or glaucoma, rather than AMD. *Lipochrome* - **Lipochrome** refers to a class of pigments, including **lipofuscin**, which can accumulate in cells as a byproduct of cellular metabolism and aging. - Although lipofuscin buildup occurs in the RPE with age, **drusen** are the specific, organized extracellular deposits pathognomonic for macular degeneration. *Hemosiderine* - **Hemosiderin** is an iron-storage complex formed from the breakdown of hemoglobin, found in situations of hemorrhage or chronic bleeding. - It is not a typical deposit found in macular degeneration; its presence in the retina usually indicates a history of retinal hemorrhage.
Question 18: What is the term for the fusion of the palpebral and bulbar conjunctiva?
- A. Trichiasis (inward growth of eyelashes)
- B. Ectropion (outward turning of eyelid)
- C. Symblepharon (Correct Answer)
- D. Tylosis (thickening of skin on palms and soles)
Explanation: ***Symblepharon*** - **Symblepharon** is the term for the adhesion between the **palpebral conjunctiva** (lining the eyelid) and the **bulbar conjunctiva** (covering the eyeball). - This condition can limit eye movement and cause chronic irritation, often resulting from severe conjunctival inflammation or injury. *Trichiasis (inward growth of eyelashes)* - **Trichiasis** refers to the misdirection of eyelashes such that they rub against the cornea or conjunctiva. - It causes irritation, foreign body sensation, and can lead to corneal abrasion, but it does not involve fusion of conjunctival layers. *Ectropion (outward turning of eyelid)* - **Ectropion** is a condition where the lower eyelid turns outward or sags away from the eyeball. - This exposes the conjunctiva, causing dryness, irritation, and epiphora (excessive tearing), but it is not a fusion of conjunctival tissues. *Tylosis (thickening of skin on palms and soles)* - **Tylosis** is a medical term referring to diffuse **hyperkeratosis** or thickening of the skin, typically observed on the palms and soles. - This condition is completely unrelated to the conjunctiva or eye structures.
Question 19: What does extraretinal fibrovascular proliferation at the ridge indicate?
- A. Normal retina
- B. Stage II Retinopathy of Prematurity
- C. Stage III Retinopathy of Prematurity (Correct Answer)
- D. Stage I Retinopathy of Prematurity
Explanation: ***Stage III Retinopathy of Prematurity*** - Extraretinal fibrovascular proliferation at the ridge is the defining characteristic of **Stage III Retinopathy of Prematurity (ROP)**. - This stage signifies significant **neovascularization** extending into the vitreous, increasing the risk of **retinal detachment**. *Normal retina* - A normal retina does not exhibit **fibrovascular proliferation** or a distinct ridge, as its vascularization is fully developed and confined to the retinal plane. - Absence of any abnormal vascular growth or demarcation line indicates a healthy, mature retinal structure. *Stage II Retinopathy of Prematurity* - Stage II ROP is characterized by a **ridge** that is elevated and appears three-dimensional, but it **lacks extraretinal fibrovascular proliferation**. - This stage represents progression from Stage I, where the demarcation line becomes a prominent ridge, but without new vessel formation outside the retina. *Stage I Retinopathy of Prematurity* - Stage I ROP is characterized by a thin, flat **demarcation line** distinguishing vascularized from avascular retina, without any significant elevation or fibrovascular proliferation. - This initial stage indicates an arrested phase of retinal vascular development, but without the more severe signs of neovascularization.
Question 20: Herpetic keratitis is treated by which of the following?
- A. Analgesics
- B. Atropine
- C. Steroids
- D. Acyclovir (Correct Answer)
Explanation: ***Acyclovir*** - **Acyclovir** is an **antiviral agent** that specifically targets the **herpes simplex virus**, which is the causative agent of herpetic keratitis. - It works by inhibiting viral DNA replication, thereby reducing viral load and preventing further damage to the cornea. *Analgesics* - **Analgesics** are used to manage pain but do not address the **viral etiology** of herpetic keratitis. - While they can improve patient comfort, they are not a definitive treatment for the underlying infection. *Atropine* - **Atropine** is a **cycloplegic agent** used to paralyze the ciliary muscle and dilate the pupil, often to reduce pain from ciliary spasms in uveitis. - It does not have **antiviral properties** and is not effective against the herpes virus. *Steroids* - **Corticosteroids** can suppress inflammation but are generally **contraindicated** in active herpetic keratitis, especially in the epithelial form. - They can worsen the viral infection by compromising the immune response, potentially leading to **corneal ulceration** and perforation.