Diagnosis and Management of Leprosy
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Background: Leprosy is a chronic infectious disease caused by Mycobacterium leprae, which tends to attack peripheral nerves and skin. The diagnosis of leprosy is based on the presence of one of three cardinal signs. Early diagnosis of leprosy is critical and is made through clinical examination and investigation. Purpose: To discuss the diagnosis, laboratory examination, and treatment of leprosy, considering that early diagnosis and appropriate treatment are the key elements in breaking the chain of transmission and preventing leprosy patients' disabilities. Review: Leprosy is a chronic granulomatous infectious disease caused by the Mycobacterium leprae. Based on clinical appearance, histopathology findings, and immunological, leprosy is grouped into six forms using the Ridley-Jopling classification, namely Tuberculoid (TT), Borderline Tuberculoid (BT), Borderline-borderline Mid-borderline (BB), Borderline-lepromatous (BL), Subpolar Lepromatous (LLs), and Polar Lepromatous (LLp). Based on the treatment category, leprosy is grouped into paucibacillary (PB) and multibacillary (MB). Leprosy is often diagnosed clinically, and skin scraping smear remains the preferred laboratory method. The negative results of smear skin scraping may not necessarily exclude leprosy. Therefore, a higher sensitivity test might be needed to detect M. leprae. Treatment with Multi-Drug Therapy (MDT) is adjusted based on the type of leprosy, whether it belongs to the PB or MB group. Treatment of PB type, regimens are rifampicin and dapsone, while in MB type, the patients received rifampicin, dapsone, and clofazimine regimens. Conclusion: A proper diagnosis for leprosy, both through physical examination and laboratory examination, is required to determine an effective MDT treatment and break the chain of disease transmission.
Bhat RM, Prakash C. Leprosy: an overview of pathophysiology. Interdiscip Perspect Infect Dis 2012; Vol 2012(181089):1-6.
Lastória JC, Morgado de Abreu MAM. Leprosy: a review of the epidemiological, clinical, and etiopathogenic aspects – Part 1. An Bras Dermatol 2014;89(2):205-18.
World Health Organization. Weekly epidemiological record: Global leprosy update, 2015: time for action, accountability, and inclusion. WHO. Geneva; 2016, 91: 405-20.
World Health Organization. Weekly epidemiological record: global leprosy update, 2017: reducing the disease burden due to leprosy. WHO. Geneva; 2018, 93: 445-56.
Pusat Data dan Informasi Kementerian Kesehatan Republik Indonesia. 2018. Infodatin Kusta 2018. [online] Available at: <http://www.pusdatin. kemkes.go.id/download.php?file=download/pusdatin/infodatin/infoDatin-kusta-2018.pdf>
World Health Organization. Guidelines for the diagnosis, treatment and prevention of leprosy. New Delhi: WHO, Regional Office for South East Asia; 2018.
Lastória JC, Morgado de Abreu MAM. Leprosy: a review of laboratory and therapeutic aspects – Parts 2. An Bras Dermatol 2014;89(3):389-403.
World Health Organization. WHO expert committee on leprosy eight report. Geneva: WHO; 2012.
PERDOSKI. Panduan praktek klinis bagi dokter spesialis kulit dan kelamin di Indonesia. Jakarta: PERDOSKI; 2017.
Cunha C. et al. A historical overview of leprosy epidemiology and control activities in Amazonas, Brazil. Rev Sociedade Bras Me Trop 2015; 48 (Suppl I):55-62.
Lee DJ, Rea TH, & Modlin RL. In: Wolf K, Goldsmith LA, Katz SL, Gilchrest BA, Paller AS, Leffel DJ, editors, Fitzpatrick's dermatology in general medicine, 8th ed. New York : McGraw-Hill; 2013, p.4226-43.
Kementrian Kesehatan RI. Pedoman nasional program pengendalian kusta. Jakarta. 2012
Yawalkar SJ. Leprosy for medical practicioners and paramedical workers 8th revised ed. Basel: Novartis Foundation for Sustainable Development; 2009.
Lockwood DNJ. In Griffiths CEM, Barker J, Bleiker T, Chaimer R, Creeamer D, editors, Rook's Textbook of Dermatology, 9th ed, Chichester: John Wiley & Sons, Ltd; 2016, p 28.1-18.
Hastings RC. Leprosy second edition. Louisiana: Churchill Livingstone. 1994
James WD, Berger TG, Elston DM.Hansen's Disease. In: Andrews' diseases of the skin - clinical dermatology. 11th ed. Philadelphia: Elsevier; 2011. p.336–7.
Sabin TD, Swift TR, Jacobson RR: Leprosy. In: Dyck PJ, Thomas PK, eds: Peripheral neuropathy. Philadelphia: Elsevier Saunders. 2005, p.2089-90, Figure 91-4.
Mahajan VK. Slit-skin smear in leprosy: lest we forget it! Indian J Lepr 2013; 85(4):177-83.
Djuanda A. Ilmu penyakit kulit dan kelamin Edisi kelima. Jakarta : Balai Penerbit FKUI; 2007.
Maltempe FG, Baldin VP, Lopes MA, Siqueira VLD., Scodro RBL, Cardoso RF, Caleffi-Ferracioli K. R. Critical analysis: use of polymerase chain reaction to diagnose leprosy. Braz J Pharm Sci 2016; 52: 163-7.
Manandhar U, Adhikari .C, Sayami G. Clinico-histopathological correlation of skin biopsies in leprosy. J Pathol Nepal 2013; 3:452-8.
Shetty VP, Rambhia KD, Khopkar US. Descriptive pathology of nerve in leprosy. Diunduh dari https://www.internationaltextbook ofleprosy.org/sites/default/files/ITL_9_1%20FNAL.pdf. Last update 01/10/2018
Chatura KR, Sangeeths S. Utility of fite-faraco stain for both mast cell count and bacillary index in skin biopsies of leprosy patients. Indian J Lepr 2012; 84:209-15.
Tomas MM, Jacob M, Chandi SM, et al. Role of S-100 staining in differentiating leprosy from other granulomatous skin diseases. Int J Lepr 1999;67:1-5.
Indian Association of Leprologists. Indian Association of Leprolgists Textbook of Leprosy (Second ed.). New Delhi: Jaypee Brothers Medical Publishers (P) Ltd; 2017.
Rivoire BL, TerLouw S, Groathouse NA, Bennan PJ. The challenge of producing skin test antigens with minimal resources suitable for human application against a neglected tropical disease; leprosy. PLoS Negl Trop Dis 2014; 8(5): e2791 : 1-11.
Kaur A, Shirazi N, Harsh M, Roy S. Role of s-100 immunostaining in differentiation of borderline leprosy from other granulomatous diseases of skin. Indian J Lepr 2018; 90: 289 -96.
Amirudin_MD. Penyakit kusta di Indonesia; masalah penanggulangannya, MDVI 2015; Suppl 1:1-4.
Penna MLF, Penna GO, Iglesias PC, Natal S, Rodrigues LC. Anti-PGL-1 positivity as a risk marker for the development of leprosy among contacts of leprosy cases: systematic review and metaanalysis. PLoS Negl Trop Dis 2016; 10(5): 1-11.
Zenha EMR, Ferreira MAN, Foss NT. Use of anti-PGL-1 antibodies to monitor therapy regimes in leprosy patients. Braz J Med Biol Res, October 2009, Volume 42(10): 968-72.
Sengupta U. Recent Laboratory Advances in Diagnostics and Monitoring response to treatment in leprosy. Indian Dermatol Online J 2019;10(2):106-14.
Fabri ACOC, Carvalho APM, Vieira NF, Bueno IC, Rodrigues RN, Monteiro TBM, et al. Integrative literature review of the reported uses of serological tests in leprosy management. Rev Soc Bras Med Trop 2016;49(2):158-64.
Rumondor B, Prakoeswa AC, Trianita MN, Iswahyudi, Herwanto N, Listiawan MY, Agusni I, Izumi S, Duthie M, Prakoeswa CRS. Immunoglobulin AMG Anti Natural Disaccharide Octyl - Leprosy IDRI Diagnostic (NDO-LID) serologic test for leprosy diagnosis: a Pilot Study. Dermatology Reports 2019; Vol 11(s1):8025.
Soto A, Munoz PT. Leprosy diagnosis: an update on the use of molecular tools. Mol Biol 2015; 4: 139-44
Tatipally S, Srikantam A, Kasetty S. Polymerase chain reaction (pcr) as a potential point of care laboratory test for leprosy diagnosis – a systematic review. Trop. Med. Infect. Dis. 2018; 3(4): 107-20.
Siwakoti S, Rai K, Bhattarai NR, Agarwal S, Khanal B. Evaluation of polymerase chain reaction (pcr) with slit skin smear examination (sss) to confirm clinical diagnosis of leprosy in Eastern Nepal. PLoS Negl Trop Dis 2016; 10(12): 1-11.
Gurung P, Gomes CM, Vernal S, Leeflang MM. Diagnostic accuracy of tests for leprosy: a systematic review and meta-analysis. Clin Microbiol Infect 2019; 25(11):1315-27.
Penna GO, Bu ̈hrer-Se Ìkula S, Kerr LRS, Stefani MMdA, Rodrigues LC, de Arau Ìjo MG, et al. Uniform multidrug therapy for leprosy patients in Brazil (U-MDT/CT-BR): results of an open label, randomized and controlled clinical trial, among multibacillary patients. PLoS Negl Trop Dis 2017; 11(7): 1-19.
Manickam P, Mahendale SM, Nagaraju B, Katoch K, James A, et al. International open trial of uniform multidrug therapy regimen for leprosy patients: Findings & implications for national leprosy programmes. Indian J Med Res 2016; 144(4): 525–35.
Kar HK, Kumar B. IAL Textbook of leprosy. New Delhi: Jaypee Brothers Medical Publishers (P) Ltd; 2010, p.336-42.
Makino M, Matsuoka M, Goto M, Hatano K. Leprosy: science working towards dignity. Kanagawa: Tokai University Press; 2011, p.146-7.
Rao PN, Jain S. Newer management options in leprosy. Indian J Dermatol 2013; 58(1):6-11.
Cruz RCS, Penna MLF, Talhari S, Bu ̈hrer-Se Ìkula S, Penna GO. Leprosy: current situation, clinical and laboratory aspects, treatment history and perspective of the uniform multidrug therapy for all patients. An Bras Dermatol 2017;9 2(6): 761-73.
Podder I, Saha A, Bandyopadhyay D. Clinical and histopathological response to multidrug therapy in paucibacillary leprosy at the end of 6 months: a prospective observational study from Eastern India. Indian J Dermatol 2018; 63(1): 47–52.
Maymone MBC, Vankatesh S, Laughter M, Abdat R, Hugh J, Dasco MM, et al. Leprosy: treatment and management of complications. J Am Acad Dermatol 2020; 83(1):17-30.
Bhide AA, Khemani UN, Kamath RR, Vaidyanathan V, Ponathil AP, Kura MM. An alternative hepatosafe treatment in leprosy. Indian J Drugs Dermatol 2016; 2: 33-6.
Muhaira WT, Darmi M, Lubis RD. Hemolytic anemia incident in leprosy patients receiving multi-drug therapy at Haji Adam Malik Central Hospital, Medan-Indonesia. Bali Med J 2018; Vol 7( 2): 442-6.
Wang N, Parimi L, Liu H, Zhang F. A review on dapsone hypersensitivity syndrome among chinese patients with an emphasis on preventing adverse drug reactions with genetic testing. Am J Trop Med Hyg 2017; 96(5):1014-8.
Beltra Ìn-Alzate C, Lo Ìpez D Ìıaz F, Romero- Montoya M, Sakamuri R, Li W, Kimura M, et al. Leprosy drug resistance surveillance in Colombia: the experience of a sentinel country. PLoS Negl Trop Dis 2016; 10(10): 1-12.
Maia MV, Cunha CS. Adverse effects of alternative therapy (minocycline, ofloxacin, and clofazimine) in multibacillary leprosy patients in a recognized health care unit in Manaus, Amazonas, Brazil. An Bras Dermatol 2013; 88(2): 205-10.
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