Diseases of the Retina — MCQs
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What is the primary cause of exudative retinal detachment?
What is the typical appearance of a subhyaloid hemorrhage in the eye?
Purtscher's retinopathy is associated with -
A 30 year old man presents to the clinic with pain in the eye, watering, redness, and photophobia. Examination of his eyes shows circumcorneal congestion and keratic precipitates. Assertion: Keratic precipitates (KPs) are proteinaceous deposits that can occur in various patterns on the corneal endothelium. Reason: Mutton fat KPs are seen in granulomatous iridocyclitis and are composed of epithelioid cells and macrophages.
What is the cause of glaucoma in retinoblastoma?
All of the following are true for retinopathy of prematurity except which of the following?
A 44-year-old woman presents with sudden painless loss of vision with a history of previous similar episodes. Fundoscopy shows no glow. What could be the possible diagnosis?
Sudden loss of vision without pain - Which of the following is NOT a cause?
Most common age related change in vitreous?
All of the following are true for sympathetic ophthalmitis except which of the following?
Diseases of the Retina Indian Medical PG Practice Questions and MCQs
Question 541: What is the primary cause of exudative retinal detachment?
- A. Traction on the retina causing detachment.
- B. Retinal tear leading to fluid accumulation.
- C. Fluid accumulation due to Coats' disease.
- D. Inflammation and vascular abnormalities leading to fluid accumulation beneath the retina. (Correct Answer)
Explanation: **Correct Answer: Inflammation and vascular abnormalities leading to fluid accumulation beneath the retina** - **Exudative retinal detachment** occurs when fluid accumulates beneath the retina due to compromised vascular integrity, often from inflammation, tumors, or systemic conditions. - This fluid is rich in protein and inflammatory mediators, leaking from choroidal or retinal vessels. - Common causes include uveitis, posterior scleritis, Vogt-Koyanagi-Harada disease, choroidal tumors, and conditions like central serous chorioretinopathy. *Incorrect: Traction on the retina causing detachment* - This describes **tractional retinal detachment**, where fibrous or fibrovascular membranes pull the retina away from the underlying retinal pigment epithelium. - It is often seen in conditions like **proliferative diabetic retinopathy** or due to prior retinal inflammatory conditions. *Incorrect: Retinal tear leading to fluid accumulation* - This is the primary mechanism of **rhegmatogenous retinal detachment**, where a break in the retina allows liquefied vitreous to pass into the subretinal space. - It is distinct from exudative detachment, which does not involve a retinal break. *Incorrect: Fluid accumulation due to Coats' disease* - While **Coats' disease** does cause exudative retinal detachment due to abnormal retinal vessels and lipid accumulation, it is a *specific disease* causing exudation, not the overarching primary cause of all exudative detachments. - The more general cause for exudative detachment involves **inflammation and vascular abnormalities**, of which Coats' disease is one example.
Question 542: What is the typical appearance of a subhyaloid hemorrhage in the eye?
- A. Boat shaped (Correct Answer)
- B. Crescent shaped
- C. Round
- D. Flame shaped
Explanation: ***Boat shaped*** - A subhyaloid hemorrhage is located beneath the **hyaloid membrane** (the posterior vitreous cortex), which is attached to the retina. - The collected blood often assumes a **dependent, gravity-influenced shape**, appearing flat on top and curved underneath, resembling a boat. *Crescent shaped* - This shape is not characteristic of a typical subhyaloid hemorrhage; it might be seen in other types of hemorrhages or detachment patterns. - **Crescentic shapes** are more commonly associated with certain types of **retinal detachments** or tears where fluid accumulation takes on a curved boundary. *Round* - While hemorrhages can be round, a subhyaloid hemorrhage typically spreads out due to gravity within the confined space, resulting in a more distinct shape. - A **perfectly round hemorrhage** is less common in the subhyaloid space as blood tends to layer out rather than remain as a sphere. *Flame shaped* - **Flame-shaped hemorrhages** are typically found in the **nerve fiber layer** due to the orientation of nerve fibers. - These hemorrhages are shallower and follow the linear arrangement of nerve fibers, unlike the larger, more globular subhyaloid bleeds.
Question 543: Purtscher's retinopathy is associated with -
- A. Head trauma (Correct Answer)
- B. Diabetes Mellitus
- C. Wilson's disease
- D. Rheumatoid arthritis
Explanation: ***Head trauma*** - **Purtscher's retinopathy** is a rare occlusive microvasculopathy characterized by sudden vision loss and specific retinal findings, classically associated with **head or chest trauma**. - The condition occurs due to **fat embolization** and **leukoembolization** with complement activation, leading to occlusion of retinal precapillary arterioles. - Classic findings include **cotton wool spots**, intraretinal hemorrhages, and **Purtscher flecken** (polygonal areas of retinal whitening between the optic disc and macula). - The term "Purtscher's retinopathy" specifically refers to trauma-induced cases, while "Purtscher-like retinopathy" describes similar findings from non-traumatic causes (acute pancreatitis, fat embolism syndrome, amniotic fluid embolism). *Diabetes Mellitus* - **Diabetic retinopathy** is associated with chronic hyperglycemia causing microvascular damage, characterized by microaneurysms, dot-blot hemorrhages, hard exudates, and venous beading. - It involves gradual progressive changes over years, not acute embolic occlusion from trauma. - Advanced stages include **proliferative diabetic retinopathy** with neovascularization and diabetic macular edema. *Wilson's disease* - **Wilson's disease** is an autosomal recessive disorder of copper metabolism affecting the liver, brain, and eyes. - Ocular manifestations include **Kayser-Fleischer rings** (copper deposition in Descemet's membrane) and sunflower cataracts. - It does not cause acute retinal vascular occlusion or the specific findings of Purtscher's retinopathy. *Rheumatoid arthritis* - **Rheumatoid arthritis** is a chronic autoimmune inflammatory disease primarily affecting joints. - Ocular manifestations include **keratoconjunctivitis sicca** (dry eyes), **episcleritis**, **scleritis**, and peripheral ulcerative keratitis. - It is not associated with Purtscher's retinopathy, which is specifically linked to traumatic or embolic events.
Question 544: A 30 year old man presents to the clinic with pain in the eye, watering, redness, and photophobia. Examination of his eyes shows circumcorneal congestion and keratic precipitates. Assertion: Keratic precipitates (KPs) are proteinaceous deposits that can occur in various patterns on the corneal endothelium. Reason: Mutton fat KPs are seen in granulomatous iridocyclitis and are composed of epithelioid cells and macrophages.
- A. Both Assertion and Reason are true, and Reason is the correct explanation for Assertion
- B. Both Assertion and Reason are true, and Reason is not the correct explanation for Assertion (Correct Answer)
- C. Assertion is true, but Reason is false
- D. Assertion is false but reason is true
Explanation: ***Both Assertion and Reason are true, and Reason is not the correct explanation for Assertion*** **Why both statements are true:** - The **Assertion** is correct: Keratic precipitates (KPs) are inflammatory cell and protein deposits that adhere to the **corneal endothelium** and can present in various patterns including fine dusty KPs, medium-sized KPs, and large mutton fat KPs. - The **Reason** is also correct: **Mutton fat KPs** are characteristic of **granulomatous anterior uveitis** (granulomatous iridocyclitis) and consist of aggregations of **epithelioid cells and macrophages**, appearing as large, greasy, white deposits. **Why Reason does NOT explain Assertion:** - The Reason describes a **specific type** of KP (mutton fat) and its cellular composition in one particular form of inflammation (granulomatous). - The Assertion makes a **general statement** about KPs occurring in various patterns. - The Reason does not explain **why** KPs can occur in various patterns or what determines these different patterns - it only describes one specific pattern. *Incorrect: Both true with Reason explaining Assertion* - The Reason is too specific and only describes one type of KP, not the general mechanism of pattern variation. *Incorrect: Assertion true, Reason false* - Both statements are medically accurate and well-established in ophthalmology literature. *Incorrect: Assertion false, Reason true* - KPs are well-documented deposits on the corneal endothelium in various forms of uveitis, making the Assertion true.
Question 545: What is the cause of glaucoma in retinoblastoma?
- A. Neovascularisation (Correct Answer)
- B. Mass effect of the tumour
- C. Blockage of trabecular network
- D. Lysis of the lens
Explanation: ***Neovascularisation*** - Retinoblastoma leads to **neovascularization of the iris (NVI)** and **angle structures** due to tumor necrosis, ischemia, and release of **angiogenic factors (VEGF)**. - The **neovascular membrane** grows over and obstructs the **trabecular meshwork** and anterior chamber angle, causing **secondary neovascular glaucoma**. - This is the **most characteristic and common mechanism** of glaucoma in advanced retinoblastoma. - Neovascular glaucoma in retinoblastoma is typically **refractory to medical treatment** and indicates poor prognosis. *Blockage of trabecular network* - While tumor cells can directly seed into the anterior chamber and block the trabecular meshwork, this mechanism is **less common** than neovascularization. - This option is also **less specific** as it doesn't identify the underlying pathophysiological process (neovascularization) that is characteristic of retinoblastoma-associated glaucoma. - Direct trabecular blockage by tumor cells typically occurs in advanced disease and often coexists with neovascularization. *Mass effect of the tumour* - The tumor mass itself rarely causes glaucoma through direct mechanical compression of outflow pathways. - Retinoblastoma causes glaucoma primarily through **secondary mechanisms** such as inflammation, neovascularization, or cellular seeding, not simple bulk effect. - Massive tumors may cause angle closure, but this is uncommon compared to neovascular mechanisms. *Lysis of the lens* - **Phacolytic glaucoma** from lens protein leakage is rare in retinoblastoma. - While lens damage can occur with advanced tumors, it is **not a typical or characteristic cause** of glaucoma in retinoblastoma. - The primary mechanisms involve the **tumor-angle-trabecular meshwork axis**, not lens pathology.
Question 546: All of the following are true for retinopathy of prematurity except which of the following?
- A. Due to hypoxia there occurs neovascularization followed by fibroproliferation
- B. Occurs in premature infants due to abnormal retinal blood vessel development.
- C. End result is bilateral blindness (Correct Answer)
- D. Blindness can be prevented by early diagnosis and ablation of avascular peripheral retina with cryotherapy or photocoagulation
Explanation: ***End result is bilateral blindness*** - While retinopathy of prematurity (ROP) can lead to severe vision loss or blindness, it is not always a bilateral end result, especially with early diagnosis and treatment. The severity can vary between eyes, and some cases resolve spontaneously. - Modern screening and intervention strategies, such as laser photocoagulation or anti-VEGF injections, are often successful in preventing complete blindness in one or both eyes. *Due to hypoxia there occurs neovascularization followed by fibroproliferation* - This statement accurately describes the pathogenesis of ROP. The initial phase involves delayed normal retinal vascularization, followed by a proliferative phase characterized by **neovascularization** in response to hypoxia in the avascular retina. - These new, abnormal vessels are fragile and prone to bleeding, and their associated **fibrovascular proliferation** can lead to retinal detachment. *Blindness can be prevented by early diagnosis and ablation of vascular premature retina with cryotherapy or photocoagulation* - This is a true statement. **Early diagnosis** through ophthalmologic screening of premature infants is crucial, and treatments like **laser photocoagulation** or **cryotherapy** are effective in ablating the avascular peripheral retina to halt the progression of abnormal vessel growth. - These interventions reduce the hypoxic drive that fuels neovascularization, thereby preventing severe retinal detachment and subsequent blindness. *Occurs in premature infants due to abnormal retinal blood vessel development.* - This statement is correct. ROP is a disease primarily affecting **premature infants** because their retinal blood vessels have not completed development by the time of birth. - Postnatal factors, including oxygen fluctuations and low birth weight, further disrupt this critical development, leading to **abnormal vascularization**.
Question 547: A 44-year-old woman presents with sudden painless loss of vision with a history of previous similar episodes. Fundoscopy shows no glow. What could be the possible diagnosis?
- A. Vitreous Hemorrhage (Correct Answer)
- B. Rhegmatogenous Retinal Detachment
- C. Acute Angle-Closure Glaucoma
- D. Fungal Keratitis
Explanation: ***Vitreous Hemorrhage*** - **Painless vision loss** is a hallmark symptom, and **previous similar episodes** suggest a recurrent condition, characteristic of vitreous hemorrhage from fragile vessels. - The **"no glow"** on fundoscopy indicates that light from the ophthalmoscope is unable to reflect off the retina due to something obstructing the clear media, such as blood in the vitreous cavity. *Rhegmatogenous Retinal Detachment* - While it causes **painless vision loss**, patients often report **floaters** or **flashes of light** preceding the detachment, which are not mentioned here. - Fundoscopy in rhegmatogenous retinal detachment would typically show a **grayish, elevated retina**, often with folds, not a complete loss of red reflex or ''no glow.'' *Acute Angle-Closure Glaucoma* - Characterized by **sudden, severe eye pain**, blurred vision, and often a **red eye** with a fixed, mid-dilated pupil. - Fundoscopy would typically reveal a **cupped optic disc** in advanced stages, but the primary finding is elevated intraocular pressure, with a clear vitreous, thus allowing an initial glow. *Fungal Keratitis* - This is an **infection of the cornea** that typically presents with pain, redness, photophobia, and a visible corneal ulcer or infiltrate. - Vision loss is gradual, and fundoscopy would still show a **normal red reflex** unless the corneal opacity is extremely dense, which is not implied by "no glow."
Question 548: Sudden loss of vision without pain - Which of the following is NOT a cause?
- A. CRAO
- B. CSR
- C. Acute congestive glaucoma (Correct Answer)
- D. Vitreous Hemorrhage
Explanation: ***Acute congestive glaucoma*** - This condition is characterized by **sudden, severe eye pain** along with blurred vision, redness, and a fixed, mid-dilated pupil. - The pain arises from abrupt elevation of **intraocular pressure**, which differentiates it from painless vision loss. *CRAO* - **Central Retinal Artery Occlusion** (CRAO) typically presents as **sudden, profound, painless monocular vision loss**. - Funduscopic examination often reveals a **cherry-red spot** in the fovea with generalized retinal whitening. *CSR* - **Central Serous Retinopathy** (CSR) causes **sudden, painless blurred vision** or a scotoma, often described as a "watery" or "shimmering" effect. - It involves leakage of fluid under the retina, typically in the macula. *Vitreous Hemorrhage* - Presents as **sudden, painless loss of vision** or a shower of floaters, often described as cobwebs or clouds. - It results from bleeding into the **vitreous cavity**, which can obscure the retina.
Question 549: Most common age related change in vitreous?
- A. Anterior vitreous detachment
- B. Vitreous hemorrhage
- C. Vitritis
- D. Posterior vitreous detachment (PVD) (Correct Answer)
Explanation: ***Posterior vitreous detachment (PVD)*** - As we age, the **vitreous body** undergoes liquefaction and shrinkage, leading to its separation from the **retina**, most commonly posteriorly. - This is a very common and usually benign age-related phenomenon, often presenting with **floaters** and **flashes of light**. *Anterior vitreous detachment* - **Anterior vitreous detachment** is much less common than PVD and not typically considered the most frequent age-related change. - It often occurs secondary to **trauma** or specific surgical procedures rather than spontaneous aging alone. *Vitreous hemorrhage* - **Vitreous hemorrhage** is a pathological condition involving bleeding into the vitreous humor, often due to **diabetic retinopathy**, retinal tears, or trauma. - It is not a normal age-related change but a complication of underlying disease. *Vitritis* - **Vitritis** refers to inflammation of the vitreous humor, commonly associated with **uveitis** or infections. - It is an inflammatory disease process, not a physiological age-related degeneration of the vitreous.
Question 550: All of the following are true for sympathetic ophthalmitis except which of the following?
- A. Mostly results from a penetrating wound
- B. Autoimmune etiology
- C. Dalen-Fuchs nodules may be seen
- D. Affects the injured eye (Correct Answer)
Explanation: ***Affects the injured eye*** - Sympathetic ophthalmia is a **bilateral, granulomatous panuveitis** that characteristically affects the **fellow, uninjured eye** (sympathizing eye) following trauma or surgery to the other eye (exciting eye). - The disease involves an immune response directed against ocular antigens, typically from the uveal tissue, in the uninjured eye. *Mostly results from a penetrating wound* - This statement is true; **penetrating ocular trauma** (e.g., from surgery or injury) is the most common trigger for sympathetic ophthalmia. - The exposure of uveal antigens from the injured eye initiates an autoimmune response. *Autoimmune etiology* - This statement is true; sympathetic ophthalmia is an **autoimmune disease** mediated by T-lymphocytes against uveal antigens. - The condition is characterized by a delayed hypersensitivity reaction against exposed uveal proteins. *Dalen Fuch's nodules may be seen* - This statement is true; **Dalen-Fuchs nodules** are characteristic histopathological findings in sympathetic ophthalmia. - These are accumulations of epithelioid cells and lymphocytes located between the retinal pigment epithelium and Bruch's membrane.
Practice by Chapter
Retinal Anatomy and Physiology
Practice Questions
Age-Related Macular Degeneration
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Diabetic Retinopathy
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Retinal Vascular Diseases
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Retinal Detachment
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Hereditary Retinal Dystrophies
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Inflammatory Retinal Diseases
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Retinal Tumors
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Retinopathy of Prematurity
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Retinal Imaging Techniques
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Intravitreal Pharmacotherapy
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Vitreoretinal Surgery
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