Moderate to hard leprosy quiz
Questions are grouped by history, clinical features and investigations, treatment, and Government of India programmes. Answers with explanations follow each section.
A. History and basic science
1. The first effective drug used widely for leprosy was:
a) Rifampicin
b) Clofazimine
c) Promin
d) Dapsone
Answer: c) Promin
Explanation: Promin, a sulphone drug, was introduced in the 1940s and was the first major effective treatment for leprosy. Dapsone later became the more practical oral sulphone. Widespread dapsone monotherapy eventually selected resistant organisms, leading to multidrug therapy.
2. Who first identified Mycobacterium leprae in 1873?
a) Albert Neisser
b) Gerhard Armauer Hansen
c) Robert Koch
d) Charles Laveran
Answer: b) Gerhard Armauer Hansen
Explanation: Hansen demonstrated the bacillus in leprosy lesions in 1873. Leprosy is therefore also called Hansen disease.
3. Which statement best explains why M. leprae cannot be grown on ordinary artificial culture media?
a) It is an obligate intracellular organism
b) It grows only at 42°C
c) It is not acid-fast
d) It requires anaerobic media
Answer: a) It is an obligate intracellular organism
Explanation: M. leprae cannot be cultured in standard artificial media. Historically, the mouse footpad and nine-banded armadillo were important experimental models. It prefers cooler tissues, approximately 32-34°C, explaining its tropism for skin, peripheral nerves, nose, and anterior eye.
4. The major antigen implicated in the attachment of M. leprae to Schwann cells is:
a) Cord factor
b) Phenolic glycolipid-1
c) Lipoarabinomannan only
d) Mycolic acid
Answer: b) Phenolic glycolipid-1
Explanation: Phenolic glycolipid-1, or PGL-1, contributes to interaction with Schwann cells and neural involvement. This neural tropism is a key reason leprosy causes sensory loss, weakness, deformity, and disability.
5. The usual generation time of M. leprae is:
a) 18-24 hours
b) 3-4 days
c) 11-14 days
d) 6 weeks
Answer: c) 11-14 days
Explanation: M. leprae divides extremely slowly. This contributes to the long incubation period and gradual clinical progression.
6. The leprosy spectrum is primarily determined by:
a) Size of inoculum alone
b) Duration of disease alone
c) Host cell-mediated immune response
d) Bacterial genotype alone
Answer: c) Host cell-mediated immune response
Explanation: Strong cell-mediated immunity produces the tuberculoid pole, with few organisms. Poor cell-mediated immunity produces the lepromatous pole, with numerous bacilli and widespread disease.
B. Clinical features and investigations
7. Which is not a WHO cardinal sign of leprosy?
a) Definite sensory loss in a hypopigmented or reddish skin lesion
b) Thickened peripheral nerve with sensory loss or muscle weakness
c) Demonstration of acid-fast bacilli in slit-skin smear
d) Generalized pruritus with normal nerve examination
Answer: d) Generalized pruritus with normal nerve examination
Explanation: Diagnosis is clinical if at least one cardinal sign is present. Itching alone is nonspecific and is not a cardinal sign.
8. A patient has multiple symmetrical, shiny infiltrated papules and nodules, diffuse skin infiltration, bilateral nerve involvement, and a high bacillary index. The most likely diagnosis is:
a) Tuberculoid leprosy
b) Borderline tuberculoid leprosy
c) Lepromatous leprosy
d) Indeterminate leprosy
Answer: c) Lepromatous leprosy
Explanation: Lepromatous leprosy lies at the multibacillary pole. It commonly causes symmetrical lesions, diffuse infiltration, nodules, high bacillary load, and widespread nerve involvement.
9. A sharply demarcated hypopigmented anesthetic plaque with marked thickening of a nearby nerve is most typical of:
a) Borderline lepromatous leprosy
b) Tuberculoid or borderline tuberculoid leprosy
c) Histoid leprosy
d) Lucio phenomenon
Answer: b) Tuberculoid or borderline tuberculoid leprosy
Explanation: Localized, well-defined, dry, hairless, hypoesthetic or anesthetic patches with asymmetrical nerve enlargement suggest the tuberculoid end of the spectrum.
10. The preferred site for palpating the common peroneal nerve in leprosy is:
a) Behind the medial malleolus
b) At the fibular neck
c) In the carpal tunnel
d) At the radial styloid
Answer: b) At the fibular neck
Explanation: The common peroneal nerve is palpated around the neck of the fibula. Involvement may produce weakness of dorsiflexion and foot drop.
11. The earliest functional abnormality over a leprosy lesion is often:
a) Loss of sweating
b) Fixed claw hand
c) Complete anesthesia
d) Corneal opacity
Answer: a) Loss of sweating
Explanation: Autonomic nerve fibers may be affected early, causing dry skin and reduced sweating. Sensory impairment may subsequently become demonstrable.
12. Which finding best supports active neuritis?
a) Stable thickened nerve without tenderness or deficit
b) Nerve tenderness with recent sensory or motor loss
c) Old painless claw hand with no recent worsening
d) Painless healed trophic ulcer
Answer: b) Nerve tenderness with recent sensory or motor loss
Explanation: Acute nerve pain or tenderness, with new sensory loss or weakness, suggests neuritis and requires urgent assessment to prevent irreversible damage.
13. Which statement about slit-skin smear is correct?
a) A negative smear excludes leprosy
b) It is mainly useful in multibacillary disease
c) It is the preferred test for all early paucibacillary lesions
d) It identifies the exact immune-spectrum type in every case
Answer: b) It is mainly useful in multibacillary disease
Explanation: A positive slit-skin smear is a cardinal sign and indicates bacillary presence. A negative smear does not exclude PB leprosy, where organisms are often sparse or absent in smears.
14. The bacteriological index in slit-skin smears measures:
a) Viability of bacilli only
b) Number of bacilli on a logarithmic scale
c) Degree of nerve tenderness
d) Severity of deformity
Answer: b) Number of bacilli on a logarithmic scale
Explanation: The BI reflects bacillary load. The morphological index assesses the proportion of solid-staining bacilli and has historically been used as an indicator of viability.
15. A skin biopsy in lepromatous leprosy typically shows:
a) Well-formed epithelioid granulomas with no bacilli
b) Foamy macrophages packed with bacilli
c) Subepidermal blister with eosinophils
d) Pure vasculitis without organisms
Answer: b) Foamy macrophages packed with bacilli
Explanation: Lepromatous disease shows diffuse infiltrates of foamy histiocytes, often called lepra cells, with abundant acid-fast bacilli. Tuberculoid disease instead shows well-formed granulomas with scant or absent bacilli.
16. A patient with BL leprosy develops abrupt edema and erythema of pre-existing lesions, with acute ulnar nerve tenderness and weakness. This is:
a) Type 1 reaction
b) Type 2 reaction
c) Relapse
d) Lucio phenomenon
Answer: a) Type 1 reaction
Explanation: Type 1 reaction, also called a reversal reaction, is a cell-mediated inflammatory reaction seen especially in borderline disease. Acute neuritis and new nerve-function impairment are central concerns.
17. Fever, crops of painful erythematous nodules, arthritis, orchitis, and iridocyclitis in a patient with LL leprosy suggest:
a) Type 1 reaction
b) Erythema nodosum leprosum
c) Indeterminate leprosy
d) Relapse only
Answer: b) Erythema nodosum leprosum
Explanation: ENL is a type 2 reaction, usually occurring in BL or LL disease. It is systemic and may involve skin, nerves, joints, eyes, testes, kidneys, and lymph nodes.
18. Which feature favors relapse over a lepra reaction?
a) Sudden painful inflammation of existing lesions
b) Acute nerve tenderness with edema
c) Gradual appearance of new lesions after release from treatment
d) Fever with tender erythematous nodules
Answer: c) Gradual appearance of new lesions after release from treatment
Explanation: Relapse tends to be gradual, with slowly progressive lesions and sometimes a rising bacillary index. Reactions are usually acute inflammatory events. A 2025 systematic review reported that relapse risk is higher in multibacillary disease and high-bacillary-load cases, reinforcing the need for careful long-term clinical review in selected patients. See the
relapse systematic review.
C. Treatment and complications
19. WHO-recommended MDT for paucibacillary leprosy consists of:
a) Rifampicin and dapsone for 6 months
b) Rifampicin, dapsone, and clofazimine for 6 months
c) Rifampicin, dapsone, and clofazimine for 12 months
d) Ofloxacin, minocycline, and clarithromycin for 6 months
Answer: b) Rifampicin, dapsone, and clofazimine for 6 months
Explanation: WHO recommends the same three drugs for PB and MB leprosy, with different durations: 6 months for PB and 12 months for MB disease. This is the current standard referenced by
WHO.
20. WHO-recommended MDT duration for multibacillary leprosy is:
a) 3 months
b) 6 months
c) 12 months
d) 24 months in all cases
Answer: c) 12 months
Explanation: MB disease receives rifampicin, dapsone, and clofazimine for 12 months. Longer or alternative regimens may be needed in selected situations, such as drug resistance or intolerance, under specialist guidance.
21. A patient on MDT develops dark red-brown discoloration of the skin and marked dryness. The likely responsible drug is:
a) Rifampicin
b) Dapsone
c) Clofazimine
d) Prednisolone
Answer: c) Clofazimine
Explanation: Clofazimine causes red-brown to blackish discoloration and xerosis. Counseling beforehand is important because cosmetic changes can reduce adherence.
22. A patient taking dapsone develops pallor, fatigue, jaundice, and dark urine. The most likely adverse effect is:
a) Hemolysis
b) Optic neuritis
c) Tendon rupture
d) Ototoxicity
Answer: a) Hemolysis
Explanation: Dapsone may cause hemolytic anemia, particularly in people with G6PD deficiency, and may also cause methemoglobinemia. Severe rash, fever, hepatitis, and systemic features may indicate dapsone hypersensitivity syndrome.
23. A patient develops new wrist drop during MDT. The best next step is:
a) Stop MDT permanently
b) Reassure and review after treatment completion
c) Urgently assess nerve function and treat neuritis or reaction
d) Start antibiotics for cellulitis only
Answer: c) Urgently assess nerve function and treat neuritis or reaction
Explanation: New motor weakness is a nerve-function impairment emergency. MDT should generally continue, while prompt anti-inflammatory treatment and specialist referral are arranged as clinically appropriate.
24. Which drug is specifically useful in severe ENL but is contraindicated in pregnancy because of teratogenicity?
a) Clofazimine
b) Thalidomide
c) Dapsone
d) Rifampicin
Answer: b) Thalidomide
Explanation: Thalidomide can be highly effective in ENL but has extreme teratogenic risk. Its use is tightly regulated and contraindicated in pregnancy. Corticosteroids and clofazimine also have roles depending on severity and organ involvement.
25. A person with an anesthetic sole should be advised primarily to:
a) Walk barefoot to improve sensation
b) Inspect the feet daily and use protective footwear
c) Stop all physical activity permanently
d) Apply topical antibiotic daily even if no ulcer exists
Answer: b) Inspect the feet daily and use protective footwear
Explanation: Sensory loss permits repeated unnoticed trauma. Disability prevention includes daily inspection, moisturizing dry skin, safe footwear, avoidance of heat and sharp objects, early treatment of wounds, and physiotherapy where needed.
D. Government programmes and public-health questions: India
26. India achieved elimination of leprosy as a public-health problem at the national level in:
a) 1991
b) 2000
c) 2005
d) 2015
Answer: c) 2005
Explanation: India reached a national prevalence of less than 1 case per 10,000 population in 2005. This is elimination as a public-health problem, not eradication. New cases and transmission can still occur.
27. In leprosy programme terminology, elimination as a public-health problem means a prevalence of:
a) Less than 10 per 10,000 population
b) Less than 1 per 10,000 population
c) Zero new cases for one year
d) Zero disability in all treated persons
Answer: b) Less than 1 per 10,000 population
Explanation: The threshold is prevalence below 1 per 10,000 population. It does not mean transmission has stopped or that there are no new cases.
28. The National Leprosy Eradication Programme is implemented under:
a) National Health Mission
b) National AIDS Control Programme
c) National Tuberculosis Elimination Programme
d) Integrated Child Development Services only
Answer: a) National Health Mission
Explanation: NLEP is a centrally sponsored scheme functioning under the National Health Mission. It emphasizes early diagnosis, free MDT, disability prevention, contact tracing, surveillance, and stigma reduction.
29. India’s National Strategic Plan and Roadmap for Leprosy 2023-2027 aims primarily to:
a) Eradicate every mycobacterium by 2024
b) Interrupt leprosy transmission at district level by 2027
c) Stop providing MDT after 2025
d) Replace clinical examination entirely with PCR
Answer: b) Interrupt leprosy transmission at district level by 2027
Explanation: The plan targets interruption of transmission by 2027, ahead of the Sustainable Development Goal timeline. The official
NLEP programme page describes this framework and its alignment with the WHO Global Leprosy Strategy.
30. The most important purpose of post-exposure prophylaxis in leprosy contacts is to:
a) Treat established claw hand
b) Replace MDT in confirmed cases
c) Reduce risk of disease among eligible contacts
d) Diagnose all smear-negative cases
Answer: c) Reduce risk of disease among eligible contacts
Explanation: In appropriate eligible contacts, single-dose rifampicin PEP is used after screening to reduce the risk of developing leprosy. It complements, but never replaces, contact examination, active case detection, and prompt MDT for confirmed cases.
31. Under NLEP, Nikusth/Nikusth 2.0 is primarily used for:
a) Histopathological staining
b) Real-time case reporting, monitoring, and programme management
c) Manufacturing MDT blister packs
d) Measuring nerve-conduction velocity
Answer: b) Real-time case reporting, monitoring, and programme management
Explanation: Nikusth is the electronic reporting and monitoring platform used by NLEP. Nikusth 2.0 supports digital surveillance and programme operations.
32. Which activity is the most appropriate example of disability prevention and medical rehabilitation under NLEP?
a) Delaying treatment until smear results are available
b) Self-care training for anesthetic hands and feet
c) Routine isolation of every treated patient
d) Stopping MDT when discoloration occurs
Answer: b) Self-care training for anesthetic hands and feet
Explanation: Disability Prevention and Medical Rehabilitation includes early nerve-function assessment, management of reactions and neuritis, ulcer care, self-care education, protective footwear, physiotherapy, reconstructive surgery when indicated, and social rehabilitation.
33. The best explanation of why child cases are an important programme indicator is:
a) Children cannot receive MDT
b) A child case suggests recent or ongoing community transmission
c) Every child case is necessarily drug resistant
d) Child cases occur only in lepromatous disease
Answer: b) A child case suggests recent or ongoing community transmission
Explanation: Detection of leprosy in children is a warning of recent transmission. Reducing child cases is therefore central to the goal of interrupting transmission.
34. Which programme measure most directly reduces delay in diagnosis at community level?
a) Restricting services to tertiary hospitals
b) Contact tracing and active case detection with community awareness
c) Waiting for visible deformity before referral
d) Providing dapsone monotherapy
Answer: b) Contact tracing and active case detection with community awareness
Explanation: Early detection prevents disability and reduces transmission. NLEP uses awareness activities, active case detection, contact tracing, ASHA-linked surveillance approaches, and integration with primary health services.
One-line revision points
- Hansen, 1873: First identification of M. leprae.
- Three cardinal signs: sensory loss in lesion, thickened nerve with deficit, or smear positivity.
- Type 1 reaction: borderline disease, acute inflammation and neuritis.
- Type 2 reaction/ENL: BL/LL disease, painful nodules and systemic involvement.
- WHO MDT: PB 6 months, MB 12 months, both with rifampicin + dapsone + clofazimine.
- India: national elimination threshold reached in 2005, but elimination does not equal eradication.
- NLEP goal: interruption of transmission at district level by 2027.
- PEP: screening of contacts plus eligible single-dose rifampicin prophylaxis.