NEET-PG 2012 - Dermatology PYQs Practice Questions

Q: Raindrop pigmentation is caused by?

Arsenic. ***Arsenic*** - Chronic **arsenic** exposure can lead to characteristic skin manifestations, including **raindrop pigmentation**, which appears as small, scattered hypopigmented macules surrounded by hyperpigmented skin, particularly on the trunk and extremities. - This pigmentation is a result of altered **melanin distribution** and **keratinocyte damage** due to arsenic toxicity. *Clofazimine* - **Clofazimine** is an anti-leprosy drug that can cause **reddish-brown to bluish-black skin discoloration**, which is a diffuse pigmentation, not "raindrop" in nature. - The pigmentation associated with clofazimine is due to drug deposition in tissues and is usually reversible. *Dapsone* - **Dapsone** is primarily known for causing **methemoglobinemia** and **hemolytic anemia**, especially in patients with G6PD deficiency. - While it can cause some dermatological side effects, **pigmentation** is not a characteristic feature, and it does not produce a "raindrop" pattern. *Minocycline* - **Minocycline** can cause various types of pigmentation, including **blue-gray discoloration** in scars, shins, and mucous membranes, as well as diffuse brown pigmentation. - However, the pigmentation caused by minocycline is typically diffuse or localized to specific areas, and it does not present as "raindrop pigmentation." [Practice more Dermatology PYQs on OnCourse]

Q: Which of the following pairs of conditions is incorrectly matched?

Erythema chronicum migrans - malignancy. ***Erythema chronicum migrans - malignancy*** - **Erythema chronicum migrans** is the characteristic skin lesion of **Lyme disease**, caused by the bacterium *Borrelia burgdorferi*, transmitted by ticks. - It is not associated with malignancy; rather, its presence indicates a **bacterial infection** requiring antibiotic treatment. *Erythema marginatum - rheumatic fever* - **Erythema marginatum** is a **major diagnostic criterion** for **rheumatic fever**, a post-streptococcal inflammatory disease. - The rash is characterized by non-itchy, pink or red macules with raised, serpiginous borders that spread outwards, often transient. *Erythema gyratum repens - malignancy* - **Erythema gyratum repens** is a rare **paraneoplastic dermatosis** strongly associated with various internal malignancies, most commonly lung cancer. - It presents as a characteristic **wood-grain-like pattern** of concentric, migratory erythematous bands. *Necrotic acral erythema - HCV* - **Necrotic acral erythema** is a skin condition that predominantly affects the hands and feet and has a strong association with **hepatitis C virus (HCV) infection**. - It presents with violaceous plaques that can ulcerate and become necrotic, often in patients with chronic HCV. [Practice more Dermatology PYQs on OnCourse]

Q: Muir–Torre syndrome shows

Sebaceous gland tumors. ***Sebaceous gland tumors*** - **Muir-Torre syndrome** is a genetic condition characterized by the presence of at least one **sebaceous gland tumor** (adenoma, epithelioma, or carcinoma) and at least one internal malignancy. - It is considered a variant of **Lynch syndrome (hereditary nonpolyposis colorectal cancer - HNPCC)**, stemming from germline mutations in **DNA mismatch repair genes**. *Intestinal polyps (associated with familial adenomatous polyposis)* - While Lynch syndrome (to which Muir-Torre is related) does involve an increased risk of colorectal cancer, **multiple intestinal polyps** are the hallmark of **Familial Adenomatous Polyposis (FAP)**. - FAP is caused by a mutation in the **APC gene**, distinct from the mismatch repair gene mutations seen in Muir-Torre syndrome. *Lisch nodules (associated with Neurofibromatosis type 1)* - **Lisch nodules** are benign **iris hamartomas** typically found in patients with **Neurofibromatosis type 1 (NF1)**. - NF1 is a neurocutaneous disorder caused by a mutation in the **NF1 gene**, presenting with café-au-lait spots, neurofibromas, and optic gliomas, which are unrelated to Muir-Torre syndrome. *Hyperelastic joints (associated with Ehlers-Danlos syndrome)* - **Hyperelasticity of joints** and skin is a characteristic feature of **Ehlers-Danlos syndrome (EDS)**, a group of heritable disorders affecting connective tissue. - EDS is caused by defects in **collagen synthesis or processing**, and its clinical manifestations are distinct from the mucocutaneous and internal malignancies seen in Muir-Torre syndrome. [Practice more Dermatology PYQs on OnCourse]

Q: Richner-Hanhart syndrome is characterized by which of the following?

Ocular and cutaneous features. ***Ocular and cutaneous features*** - **Richner-Hanhart syndrome**, also known as **Tyrosinemia type II**, is characterized by the classic triad of **painful hyperkeratotic plaques** on the palms and soles (cutaneous features), **corneal ulcers** or **dendritic keratitis** (ocular features), and **variable neurological involvement**. - These features arise from the accumulation of **tyrosine** due to a deficiency of the enzyme **hepatic tyrosine aminotransferase (TAT)**. - The **ocular and cutaneous manifestations** are the hallmark features that define this syndrome. *Autosomal dominant* - Richner-Hanhart syndrome is inherited in an **autosomal recessive** pattern, meaning two copies of the defective gene (TAT gene on chromosome 16) are required for the condition to manifest. - An **autosomal dominant** inheritance pattern would mean only one copy of the defective gene is sufficient to cause the disorder. *Associated with abnormality in lipid metabolism* - The syndrome is an inborn error of **amino acid metabolism**, specifically involving **tyrosine**, not lipid metabolism. - Diseases associated with abnormality in **lipid metabolism** include conditions like Gaucher disease, Niemann-Pick disease, or Fabry disease. *Never associated with neurological involvement* - This is **incorrect**. **Neurological involvement** including intellectual disability, developmental delay, seizures, and behavioral problems occurs in **30-50% of cases**. - The accumulation of **tyrosine** and its metabolites (particularly tyrosine crystals) can be **neurotoxic**, leading to varying degrees of neurological impairment. - Early dietary restriction of tyrosine and phenylalanine can prevent or minimize neurological complications. [Practice more Dermatology PYQs on OnCourse]

Question 1

Which of the following statements is true regarding donovanosis?

Accepted Answer

Painless ulcerative lesions are characteristic of donovanosis

Answer

Pseudolymphadenopathy is characteristic

Answer

Penicillin is used for treatment

Answer

Painful ulcer is characteristic

Question 2

Raindrop pigmentation is caused by?

Accepted Answer

Arsenic

Answer

Dapsone

Answer

Minocycline

Answer

Clofazimine

Question 3

Which of the following pairs of conditions is incorrectly matched?

Accepted Answer

Erythema chronicum migrans - malignancy

Answer

Erythema gyratum repens - malignancy

Answer

Erythema marginatum - rheumatic fever

Answer

Necrotic acral erythema - HCV

Question 4

Muir–Torre syndrome shows

Accepted Answer

Sebaceous gland tumors

Answer

Intestinal polyps

Answer

Lisch nodules

Answer

Hyperelastic joints

Question 5

Richner-Hanhart syndrome is characterized by which of the following?

Accepted Answer

Ocular and cutaneous features

Answer

Autosomal dominant

Answer

Associated with abnormality in lipid metabolism

Answer

Never associated with neurological involvement

Question 6

Which of the following statements about spider telangiectasia is false?

Accepted Answer

More common in males

Answer

Light therapy for treatment

Answer

May be associated with liver disease

Answer

Can be caused by trauma

Question 7

What is the maximum cumulative dose of isotretinoin for acne treatment?

Accepted Answer

120-150 mg/kg

Answer

30-60 mg/kg

Answer

60-90 mg/kg

Answer

90-120 mg/kg

Question 8

Loss of intercellular cohesion between keratinocytes is referred to as?

Accepted Answer

Acantholysis

Answer

Acanthosis

Answer

Keratinolysis

Answer

Spongiosis

Question 9

Which of the following is NOT a feature of atopic dermatitis?

Accepted Answer

Darier’s Sign

Answer

Dennie-Morgan fold

Answer

Hyperlinearity of palms

Answer

Hertoghe’s sign

Question 10

What is the first symptom of leprosy?

Accepted Answer

Decreased pain

Answer

Decreased vibration & position sense

Answer

Decreased temperature

Answer

Decreased light touch

NEET-PG 2012 — Dermatology