Leprosy is an infectious disease attributed to Mycobacterium leprae, with review literature also identifying Mycobacterium lepromatosis as a causative agent [1][3]. It is characterized in the source material as a neurological and dermatological disease, reflecting involvement of peripheral nerves and skin [3]. The disease is presented as a neglected tropical disease with substantial morbidity in marginalized communities [1].
Disease Profile
BacterialLeprosy
麻风病
Leprosy is a bacterial infectious disease caused by Mycobacterium leprae and, in the cited review literature, Mycobacterium lepromatosis [1]. It is also known as Hansen’s disease and is described as a curable infection that remains endemic in more than 140 countries [2]. Surveillance summaries indicate a persistent global burden, with annual new case detection plateauing at roughly 200,000 cases before the COVID-19 pandemic [1][2].
The clinical phenotype of leprosy is described as a spectrum that tracks host immune response, ranging from paucibacillary disease with vigorous pro-inflammatory immunity and few bacteria to multibacillary disease with large bacterial loads and high levels of apparently non-protective anti-M. leprae antibodies [1]. The literature also lists indeterminate, tuberculoid, borderline tuberculoid, mid-borderline, borderline lepromatous, and lepromatous forms, as well as type 1, 2, and 3 reaction states [3]. M. leprae infects Schwann cells of the peripheral nervous system, supporting the neurological component of disease [3]. The source material notes that diagnosis remains clinical, so asymptomatic infection may be missed [1].
Leprosy remains endemic in more than 140 countries and was still reporting approximately 200,000 new cases worldwide in 2017 [2]. A more recent review states that, before the COVID-19 pandemic, annual new case detection had plateaued for more than a decade at about 200,000 cases [1]. The disease causes significant morbidity in marginalized communities [1], and migration may introduce cases into nonendemic areas such as North America [2]. The sources also note reports of autochthonous transmission in parts of the United States among people without foreign exposure history [2].
The provided sources do not give a detailed transmission mechanism for leprosy beyond noting that autochthonous person-to-person transmission has been reported in the United States [2]. They also indicate that persons with infection may remain asymptomatic and therefore undetected, which has implications for ongoing spread [1]. Source-backed detail on specific routes, environmental persistence, or reservoir ecology is not yet available in the supplied snippets [1][2].
The sources identify marginalized communities as experiencing substantial morbidity [1]. They also indicate risk related to close contact with affected persons, since post-exposure prophylaxis is specifically suggested for such contacts [1]. Additional source-backed detail on age, occupation, or other high-risk groups is not yet available in the supplied snippets [1][2].
The reviewed literature emphasizes early case detection and consideration of post-exposure prophylaxis for close contacts of affected persons [1]. It also frames these measures as important for interrupting transmission and improving patient outcomes [1]. Beyond this, source-backed detail on specific prevention schedules or broader exposure-control measures is not yet available in the supplied material [1].
Leprosy surveillance should be interpreted in the context of long incubation, with the cited review giving an incubation period of 2 to 6 years and noting that longer periods have been described [1]. Because diagnosis remains clinical and asymptomatic infection may go undetected, routine case counts likely underestimate the full infection burden [1]. The literature also suggests that declining clinical expertise and nonendemic introductions can affect recognition and reporting, particularly in regions receiving migration from endemic settings [1][2].
- 1 Grijsen ML et al. Leprosy. Nat Rev Dis Primers. 2024 Nov 28. PMID: 39609422. doi: 10.1038/s41572-024-00575-1. PubMed: https://pubmed.ncbi.nlm.nih.gov/39609422/
- 2 Maymone MBC et al. Leprosy: Clinical aspects and diagnostic techniques. J Am Acad Dermatol. 2020 Jul. PMID: 32229279. doi: 10.1016/j.jaad.2019.12.080. PubMed: https://pubmed.ncbi.nlm.nih.gov/32229279/
- 3 Mungroo MR et al. Mycobacterium leprae: Pathogenesis, diagnosis, and treatment options. Microb Pathog. 2020 Dec. PMID: 32931893. doi: 10.1016/j.micpath.2020.104475. PubMed: https://pubmed.ncbi.nlm.nih.gov/32931893/
- 4 Leprosy. BMJ. 1946. doi: 10.1136/bmj.2.4475.544-b. DOI: https://doi.org/10.1136/bmj.2.4475.544-b
- 5 Leprosy. The Boston Medical and Surgical Journal. 1904. doi: 10.1056/nejm190412221512502. DOI: https://doi.org/10.1056/nejm190412221512502
- 6 Leprosy. Organization and Practice in Tuberculosis Bacteriology. 1985. doi: 10.1016/b978-0-407-00296-8.50015-7. DOI: https://doi.org/10.1016/b978-0-407-00296-8.50015-7
- A30
- 1B20
Figure 1 | Full historical trajectories across all reporting countries.
Figure 2 | Year-over-year monthly comparison for seasonality and structural shifts.
Dataset Archive
Supplementary Data | Multi-country disease dataset
Machine-readable multi-country disease dataset (JSON/CSV) with source metadata.
Source Register
Official sources and update cadences used to construct the downloadable dataset.
Australia
Australian national notifiable diseases surveillance dashboard.
Official sourceBrazil
Brazil Ministry of Health DATASUS/SINAN public DBC microdata aggregated to national monthly notification counts.
Official sourceChina
Monthly notifiable infectious disease reports published by China CDC.
Official sourceChina
Official China public health bulletin and query portal.
Official sourceChina
Biomedical literature discovery feed used as supplementary context.
Official sourceHong Kong, China
Hong Kong, China CHP annual notifiable infectious disease CSVs normalized to national monthly totals
Official sourceSouth Korea
Korea KDCA notifiable infectious disease OpenAPI or portal/KOSIS downloads aggregated to national monthly notification counts.
Official sourceUnited States
CDC National Notifiable Diseases Surveillance System provisional data.
Official source