All about leprosy in short note for microbiology 6 marks question

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Leprosy (Hansen's Disease) - Short Note

Definition

Leprosy is a chronic infectious granulomatous disease caused by Mycobacterium leprae, primarily affecting the skin, peripheral nerves, upper respiratory mucosa, and eyes - Harrison's Principles of Internal Medicine 22E, p.1447.

Causative Organism - Mycobacterium leprae

  • Obligate intracellular, rod-shaped, acid-fast bacillus (AFB)
  • Dimensions: 1-8 µm length, 0.3 µm diameter
  • Weakly acid-fast - best visualized with the Fite stain (not standard Ziehl-Neelsen)
  • Cannot be cultured in vitro (no artificial medium supports growth)
  • Slow-growing - doubling time ~12-14 days (longest of any known bacterium)
  • Infects Schwann cells of peripheral nerves and macrophages
  • Grows best in cooler tissues (skin, superficial nerves, nasal mucosa)
  • Organisms arranged in parallel arrays within macrophages called globi (lepra cells)
  • A second species, M. lepromatosis, causes diffuse lepromatous leprosy (mainly Mexico/Central America)

Epidemiology

  • Neglected tropical disease; 174,087 new cases from 182 countries reported in 2022
  • India accounts for ~78% of global burden; other endemic countries: Brazil, Nepal, Mozambique, Myanmar
  • Non-human reservoir: 9-banded armadillo (Dasypus novemcinctus) in the southern USA
  • People with HIV do not appear to have increased susceptibility to M. leprae
  • Source: Bailey & Love's Short Practice of Surgery 28E; Red Book 2021

Transmission

  • Spread via respiratory droplets/nasal secretions from untreated lepromatous patients
  • Requires prolonged close contact (years); not highly contagious
  • Household contacts of untreated patients are at increased (but still low) risk
  • Incubation period: 2-5 years (can range up to 20 years)

Classification

Ridley-Jopling Classification (1962)

Based on host immunity and bacillary load - a spectrum of 5 types:
TypeAbbreviationImmunityBacilliGranuloma
TuberculoidTTStrongFew (paucibacillary)Epithelioid + giant cells
Borderline TuberculoidBTGoodFewEpithelioid
Mid-BorderlineBBUnstableModerateMixed
Borderline LepromatousBLWeakManyMacrophage
LepromatousLLAbsentAbundant (multibacillary)Macrophage/globi
Early indeterminate leprosy (IL) - initial form with lymphocyte infiltration only.

WHO Simplified Classification

  • Paucibacillary (PB): 1-5 skin lesions, negative slit-skin smear
  • Multibacillary (MB): 6+ skin lesions and/or >1 peripheral nerve involved, positive smear

Clinical Features

  • Skin: Hypopigmented or erythematous macules/patches with loss of sensation; nodules (lepromas) in LL
  • Nerve involvement: Thickened, palpable peripheral nerves - ulnar, median, radial, lateral popliteal, posterior tibial; cranial nerves (trigeminal, facial)
  • Anesthesia leading to painless injuries, ulcers, bone resorption, and deformity
  • Leonine facies, madarosis (loss of lateral eyebrows), saddle-nose deformity in LL
  • Eye: corneal scarring, lagophthalmos, iridocyclitis
  • Leprosy is the leading cause of permanent physical disability among infectious diseases

Leprosy Reactions (Acute Exacerbations)

  • Type 1 - Reversal Reaction (LR-1): Seen in borderline (BT/BB/BL) types; sudden increase in cell-mediated immunity; acute swelling and tenderness of skin/nerve lesions
  • Type 2 - Erythema Nodosum Leprosum (ENL/LR-2): Seen in BL/LL; systemic immune complex-mediated inflammation; tender red nodules, fever, polyarthralgia, lymphadenopathy, iridocyclitis

Diagnosis

  • Clinical: Hypesthetic/anesthetic skin patch + nerve thickening + AFB on smear = triad
  • Slit-skin smear (SSS): AFB stained with Fite stain; Bacteriological Index (BI) = log-scale 0 to 6+ for bacillary density; Morphological Index (MI) = % viable solid-staining bacilli
  • Skin biopsy: Granuloma type helps classify on Ridley-Jopling scale
  • Lepromin test (Mitsuda test): Tests cell-mediated immunity - positive in TT (strong immunity), negative in LL; NOT diagnostic, used for classification only
  • M. leprae cannot be cultured; molecular PCR available in reference labs
  • Demonstration of AFB in peripheral nerves is pathognomonic

Treatment - WHO Multidrug Therapy (MDT)

DrugPaucibacillary (PB)Multibacillary (MB)
Dapsone100 mg/day100 mg/day
Rifampicin600 mg/month (supervised)600 mg/month (supervised)
ClofazimineNot included50 mg/day + 300 mg/month
Duration6 months12 months
  • WHO provides MDT free of charge worldwide via blister packs
  • Treatment failure rates are very low when therapy is completed
  • Source: Harrison's 22E, p.1454 (WHO MDT Table)

Key Points for Exam

  1. Only bacterium known to infect Schwann cells - explains nerve damage
  2. Cannot be cultured in vitro - diagnosis is clinical/histological
  3. Tissue damage is inversely proportional to immune response (more damage in TT despite fewer bacilli)
  4. Lepromin test - not diagnostic; used for prognosis/classification
  5. India accounts for majority of global burden
  6. MDT has made leprosy curable; WHO target for elimination (<1 case/10,000 population)

Give flow charts of it

Generating Image

Medical flowchart titled "LEPROSY - Pathogenesis & Classification" on white background. Clean, professional medical diagram style with boxes and arrows. Flow starts at top: [M. leprae enters via nasal mucosa/skin] → [Incubation: 2-20 years] → [Host Immune Response - KEY BRANCH POINT] Then splits into TWO main branches: LEFT BRANCH (Strong CMI): [Strong Cell-Mediated Immunity] → [Tuberculoid Leprosy (TT)] → Features box: "Few bacilli, Epithelioid granulomas, Giant cells, Many lymphocytes, Nerve destruction, Anaesthesia, Lepromin +ve" RIGHT BRANCH (Weak CMI): [Weak/Absent Cell-Mediated Immunity] → [Lepromatous Leprosy (LL)] → Features box: "Abundant bacilli (globi), Macrophage infiltration, Leonine facies, Madarosis, Saddle nose, Lepromin -ve" MIDDLE SPECTRUM (between the two branches): [BORDERLINE SPECTRUM] with three sub-boxes in a row: BT (Borderline Tuberculoid) | BB (Mid-Borderline) | BL (Borderline Lepromatous) Label under: "Unstable - can upgrade or downgrade" At bottom, a horizontal bar labeled: "← IMMUNITY STRONG | BACILLARY LOAD ↑ → " Color coding: Left side green, middle yellow, right side red

Generating Image

Medical flowchart titled "LEPROSY - Diagnosis Flowchart" on white background. Clean professional style. Start box at top center: [Suspected Leprosy Patient] ↓ [Clinical Triad Assessment] → box: "1. Hypopigmented/anaesthetic skin patch 2. Thickened peripheral nerve 3. AFB on slit-skin smear" ↓ [Any ONE feature present → Diagnose Leprosy] ↓ [WHO Classification] Splits into TWO branches: LEFT: [Paucibacillary (PB)] → "1-5 skin lesions, Negative smear (BI=0), ≤1 nerve involved" RIGHT: [Multibacillary (MB)] → "6+ skin lesions, Positive smear (BI 1-6+), >1 nerve involved" Below each branch, add: PB → [Ridley-Jopling: IL, TT, BT] MB → [Ridley-Jopling: BB, BL, LL] Bottom section - separate box: [Investigations] → Slit-Skin Smear (SSS): Fite stain, BI & MI → Skin Biopsy: Granuloma typing → Lepromin Test: Classification (not diagnosis) → PCR: Reference labs only → Nerve biopsy: Pathognomonic if AFB in nerve Use blue color scheme, arrows between all boxes

Generating Image

Medical flowchart titled "LEPROSY - WHO Multidrug Therapy (MDT) & Reactions" on white background. Two sections. TOP SECTION - Treatment: [Confirmed Leprosy] ↓ splits into two paths LEFT PATH - [Paucibacillary (PB)]: Box: "RIFAMPICIN 600mg/month (supervised) + DAPSONE 100mg/day" ↓ [Duration: 6 MONTHS (6 blister packs)] RIGHT PATH - [Multibacillary (MB)]: Box: "RIFAMPICIN 600mg/month (supervised) + DAPSONE 100mg/day + CLOFAZIMINE 50mg/day + 300mg/month" ↓ [Duration: 12 MONTHS (12 blister packs)] Both paths converge to: [CURED - Low relapse rate] BOTTOM SECTION - Leprosy Reactions (separate colored box, yellow background): Title: "Acute Reactions During/After Treatment" TWO COLUMNS: LEFT: TYPE 1 - REVERSAL REACTION - Borderline types (BT/BB/BL) - Sudden increase in CMI - Swelling/tenderness of lesions - New nerve damage - Treatment: PREDNISOLONE RIGHT: TYPE 2 - ENL (Erythema Nodosum Leprosum) - BL and LL types - Immune complex mediated - Tender red nodules + fever - Arthralgia, iridocyclitis - Treatment: THALIDOMIDE / Prednisolone Clean arrow design, color-coded boxes

Here are 3 comprehensive flowcharts covering all major aspects of leprosy:

Flowchart 1 - Pathogenesis & Classification (Ridley-Jopling Spectrum)

Leprosy Pathogenesis & Classification
Key concept: Host immunity determines where on the spectrum the patient falls. Strong CMI = Tuberculoid (few bacilli, more damage). Weak CMI = Lepromatous (abundant bacilli, less local destruction but systemic spread).

Flowchart 2 - Diagnosis Flowchart

Leprosy Diagnosis Flowchart
Key concept: Clinical triad + WHO simplified classification (PB vs MB) drives both diagnosis and treatment choice. The Lepromin test classifies, does NOT diagnose.

Flowchart 3 - WHO MDT Treatment & Reactions

Leprosy Treatment & Reactions
Key concept: MDT is the backbone - 2 drugs for PB (6 months), 3 drugs for MB (12 months). Reactions can occur during or even after treatment and must be managed separately.

Quick Summary Table for Exam

FeatureTuberculoid (TT)Lepromatous (LL)
ImmunityStrongAbsent
BacilliFewAbundant (globi)
Skin lesionsFew, well-definedMany, diffuse
Nerve damageSevere, earlyMild, late
Lepromin testPositiveNegative
InfectivityLowHigh
TreatmentPB regimen (6m)MB regimen (12m)
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