Leprosy

Original Editor - Manisha Shrestha Top Contributors - Manisha Shrestha, Kim Jackson, Nikhil Benhur Abburi and Nupur Smit Shah

Original Editor - User Name
Top Contributors - Manisha Shrestha, Kim Jackson, Nikhil Benhur Abburi and Nupur Smit Shah

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Introduction

Leprosy is a chronic infectious bacterial disease affecting the nerves, skin, eyes, and muscosa of upper respiratory tract. Leprosy was renamed Hansen’s disease after Norwegian scientist Gerhard Henrik Armauer Hansen, who in 1873 discovered the slow-growing bacterium now known as Mycobacterium leprae as the cause of the illness.

Leprosy is curable and treatment in the early stages can prevent disability. It can be cured with multidrug treatment regime, if early diagnosis is made.

Leprosy is a polymorphic infectious disease, the manifestation of which is determined by the immune system of the host.

World Leprosy Day is observed on the last Sunday of January each year. Established in 1954 by French philanthropist Raoul Follereau, it aims to raise awareness about leprosy (now called Hansen’s disease) and teach people about this ancient disease that is easily curable today.

Epidemiology

Around the world:

• The number of new cases reported globally to World Health Organization (WHO)external icon in 2019 was more than 200,000.
• Close to 15,000 children were diagnosed with Hansen’s disease in 2019, more than 40 a day.
• An estimated 2 to 3 million people are living with Hansen’s disease-related disabilities globally.
• In 2019, the countries with the highest number of new diagnoses were India, Brazil, and Indonesia.
• Over half of all new cases of Hansen’s disease are diagnosed in India, which remains home to a third of the world’s poor, a group disproportionately affected by the disease.[1]
• Among the new cases, 10 816 new cases were detected with grade- 2 disabilities (G2D) and the G2D rate was recorded at 1.4 per million population.[2]

Mycobacterium leprae

Mycobacterium leprae is

• an intracellular, pleomorphic, acid-fast, pathogenic bacterium
• an aerobic bacillus (rod-shaped bacterium)
• in size and shape, it closely resembles Mycobacterium tuberculosis
• The difficulty in culturing the organism appears to be because it is an obligate intracellular parasite that lacks many necessary genes for independent survival.
• grown in mouse foot pads and more recently in nine-banded armadillos
• It multiplies slowly. On average, the disease incubation period is 5 years but symptoms may occur within 1 year. It can also take as long as 20 years or even more to occur.
• They can be grown in the laboratory by injection into the footpads of mice.

Mode of transmission

• Two exit routes of M. leprae from the human body often described are the skin and the nasal mucosa.
• The entry route of M. leprae into the human body is also not definitively known. The skin and the upper respiratory tract are most likely; however, recent research increasingly favours the respiratory route.
• The bacillus is likely transmitted via droplets, from the nose and mouth, during close and frequent contact with untreated cases.

Clinically Relevant Anatomy

Pheripheral nervous system

Pheripheral nerve and adjacent cells( schwann cell)

Layers of Skin

Mechanism of Injury / Pathological Process

Lepra bacilli enters into the body through respiratory route. Then those bacilli migrates towards the neural tissues and binds to schwann cells ( which is the major target of the bacilli). Afterward, it invades schwann cells by specific laminin binding protein and phenolic glycolipid-1(PGL-1). Binding of M. leprae to SCs induces demyelination and loss of axonal conductance. Bacteria are also found in macrophages, muscle cells and endothelial cells of blood vessels. Bacilli start multiplying slowly within the cells and gets liberated from destroyed cells and then enter unaffected cells. As bacilli multiply ,bacterial load increases in body and thus infection is recognized by body immune system. Specific and effective cell mediated immunity provides protection to a person against leprosy.

When cell mediated immunity (CMI) is effective in controlling infection, lesions are healed spontaneously or produce paucibacillary type of leprosy. Person with good CMI may have granuloma formation in cutaneous nerve causing swelling of nerve and hence destroyed. It causes inflammation in epineurium causes compression and destruction of unmyelinated sensory and  autonomic fiber. Myelinated motor fibers are the last to get affected causing motor impairments. Good CMI limits disease to schwann cells-pure neural leprosy.

If CMI is deficient, produce multibacilary leprosy with multi system involvement. Bacilli which escapes from nerve to adjacent skin caused classical skin lesions. Bacilli liberated by schwann cells engulfed by histiocytes-wandering macrophages-travel to other tissue through blood and lymph. Phagocytosis of M. leprae by monocyte-derived macrophages can be mediated by complement receptors CR1 (CD35), CR3 (CD11b/CD18), and CR4 (CD11c/CD18) and is regulated by protein kinase.

Classification

Leprosy can be broadly classified via two classification system.

1. Ridley and Jopling classification

In the 1960s, Ridley and Jopling proposed a histological classification scheme for leprosy that ranged in severity. Leprosy is classified within two poles of the disease with transition between the clinical forms . Clinical, histopathological, and immunological criteria identify five forms of leprosy:

• Tuberculoid leprosy (TT)
• Borderline tuberculoid (BT)
• Mid borderline (BB)
• Borderline lepromatous (BL)
• Lepromatous leprosy (LL)

2. WHO classification

Initially, patients were divided into two groups for therapeutic purposes: paucibacillary (TT, BT) and multibacillary (midborderline (BB), BL, LL) . It was recommended later that the classification is to be based on the number of skin lesions, less than or equal to five for paucibacillary (PB) and greater than five for the multibacillary (MB) form.

Clinical Presentation

Clinical features of Leprosy

Characteristics	Tuberculoid	Borderline tuberculoid	Midborderline	Borderline lepromatous	Lepromatous leprosy
Number of lesions	Single or upto 3	A Few (up to 10)	Several (10–30)	Numerous, asymmetrical (>30)	Innumerable, symmetrical
Size	Variable, usually large	Variable, some are large	Variable	Small, some can be large	Small
Surface changes	Hypopigmented	Dry, scaly, look bright, and infiltrated	Dull or slightly shiny	Shiny	Shiny
Sensations	Absent	Markedly diminished	Moderately diminished	Slightly diminished	Minimally diminished
Hair growth	Nil	Markedly diminished	Moderately diminished	Slightly diminished	Not affected initially
Skin smear	Negative	Negative or 1+	1–3+	3–5+	Plenty, including globi (6+)
Lepromin test	Strongly positive	Weakly positive	Negative	Negative	Negative

Since it mainly affects skin and nerves, these are some clinical features seen in patient with leprosy:

• Hypopigmented or reddish patch/es on skin
• Diminished sensation within skin patches
• Paresthesias (tingling or numbness in hands or feet)
• Painless wounds or burns on hands or feet
• Tender, enlarged peripheral nerves

If the diseases is left untreated, it become chronic and may lead to physical deformities. Such as:

• Weakness of hands with claw fingers
• Foot drop
• Facial paralysis
• Lagopthalmos
• Lack of eyebrows and eyelashes
• Collapsed nose
• Perforated nasal septum
• Trophic ulcers

Diagnostic Procedures

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Outcome Measures

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Management / Interventions

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Differential Diagnosis

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Resources

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