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Anais Brasileiros de Dermatologia

Print version ISSN 0365-0596

An. Bras. Dermatol. vol.86 no.5 Rio de Janeiro Sept./Oct. 2011

http://dx.doi.org/10.1590/S0365-05962011000500024 

CASO CLÍNICO

 

Report of three new leprosy cases in children under fifteen in the municipality of Itaguai, Rio de Janeiro - event alert for epidemiological investigation*

 

 

Vivian Fichman Monteiro de SouzaI; Roberto Souto da SilvaII; Claudia Lucia Paiva e ValleIII; Daniel Lago ObadiaII; Egon Luiz Rodrigues DaxbacherII

IPhysician with a degree in Medicine from the State University of Rio de Janeiro (Universidade do Estado do Rio de Janeiro - UERJ) - Resident at the Dermatology Service of the Teaching Hospital Pedro Ernesto, State University of Rio de Janeiro (Hospital Universitário Pedro Ernesto, Universidade do Estado do Rio de Janeiro - HUPE - UERJ) - Rio de Janeiro (RJ), Brazil
IIPreceptor of the Dermatology Service of the Teaching Hospital Pedro Ernesto, State University of Rio de Janeiro (Hospital Universitário Pedro Ernesto, Universidade do Estado do Rio de Janeiro - HUPE - UERJ) - Rio de Janeiro (RJ), Brazil
IIIPostgraduate degree in Public Health - Physician and Coordinator of the Hansen's Disease program at the city of Itaguaí - RJ and physician of the state Hansen's Disease program of the State Health and Civil Defense Department - Rio de Janeiro (SESDEC-RJ) - Rio de Janeiro (RJ), Brazil

Mailing address

 

 


ABSTRACT

Leprosy is an infectious disease with an average incubation period of two to five years. It is caused by Mycobacterium leprae, mainly affecting skin, mucous membranes and peripheral nerves. When it occurs in children under fifteen, it reflects an intense and long contact period, with a high bacillary load. Therefore, it is considered an important alert sign that points to the challenge of controlling the disease. The authors report three cases of leprosy in children under fifteen that occurred in the Itaguaí district, Rio de Janeiro. The epidemiologic implications of new cases detected at this age and the fundamental role of examining the patients' close contacts and the possible identification of source cases as an effort for leprosy control are discussed.

Keywords: Child; Epidemiology; Leprosy


 

 

INTRODUCTION

Hansen's Disease, hansenosis or leprosy is an infectious illness of slow evolution and great incapacitating potential. 1,2,3 Its agent, Mycobacterium leprae or Hansen's bacillus was discovered by Hansen in Norway, in 1873, but the first records mentioning hansenosis were written between 400 and 600 B.C., in India. 3,4

The incubation period varies from 06 months to 21 years. The upper airways are considered the main transmission route and primary entry route for the bacillus into the body.1,2,3 The transmission sources seem to be carriers of multibacillary forms.5 Individual conditions, factors related to endemic levels and unfavorable social conditions influence the risk of becoming infected with Hansen's disease. 6 As it is a highly infectious illness of low pathogenicity, most of the infected people do not become sick, revealing a protective role of innate immunity. Despite that, in endemic areas continuous exposure to the bacillus may lead to illness, even in resistant people; consequently the great number of tuberculoid leprosy cases constitute an indicator of high endemicity and of the presence of hidden transmission focuses. 3,6

The intervention in the transmission chain is done through the earliest possible diagnosis, by means of active and passive detection, and treatment of sources of infection.7

Studies about historical evolution of leprosy in developed countries demonstrated a positive relationship between decline of new cases and increase of age at the onset of disease. In areas of high prevalence and detection, such as Brazil, the high number of cases in younger than fifteen years of age indicates, therefore, active and recent transmission, assisting in monitoring the endemic disease.8

 

CASE REPORTS

CASE 1

Female, black, eight-year-old patient was referred to the Sanitary Dermatology (SD) service with a hyperchromic papule located on the forehead since two years before, which evolved to plaque with elevated hyperchromic borders, measuring two centimeters in diameter and with a hypochromic center (Figure 1), during the previous year. She reported that, in the last three months, a satellite papule appeared. The physical examination revealed thermal anesthesia at the center of the lesion and absence of nervous trunks thickening, which led to clinical diagnosis of Hansen's disease, suggesting the borderline-tuberculoid form due to the morphology of the lesion associated with the satellite papule. A physical examination of contacts was performed.2 No bacilloscopy (which would be negative in this case), histopathological test or Mitsuda test were performed. In the evaluation of all seven household contacts, there was suspicion regarding the ten-year-old sister and the six-year-old cousin.

 

 

CASE 2

The above mentioned six-year-old cousin of the patient had a hypochromic macule that progressed to hypochromic plaque one year ago, three centimeters in diameter, with microtubercula in its interior, localized on left forearm, with thermal anesthesia (Figure 2). Absence of nervous trunks thickening. She denied pruritus or desquamation.

 

 

CASE 3

The patient's 10-year-old sister presented a 2 cm hypochromic macule, that progressed to hypochromic plaque with microtubercula on the lesion borders during the previous two years, slightly sparing the center. It is located on the left shoulder, with thermal anesthesia within the lesion (Figure 3). Absence of nervous trunks thickening. The lesion did not present desquamation or pruritus.

 

 

Cases 2 and 3 had clinical diagnosis of tuberculoid Hansen's disease and a supplementary histological test was done for documentation and counterreferral for the city of residence. No bacilloscopy nor Mitsuda tests were performed.

The histopathological tests of both contacts demonstrated the tuberculoid form of Hansen's disease (Figures 4 and 5).

 

 

 

 

DISCUSSION

Hansen's disease, in Brazil, still presents high coefficients of detection, despite the drop in the coefficient of prevalence in the last few years. The detection rate - an indicator of disease transmissibility - of 20.56 cases/100,000 inhabitants is considered as a very high endemicity level.9

As the incubation period of leprosy is long (two to five years), its occurrence in those younger than fifteen reflects early and intense exposure to a high bacillary load that leads to illness, in spite of an apparently adequate immunity. Detection of new cases in this age bracket is, therefore, considered an event alert for active and recent transmission, pointing to the need for epidemiological surveillance activities and immediate investigation to search for the source case.7,10

In our case, this investigation, consisting of examination of the seven household contacts recorded, led to two other new cases diagnosed in children who, besides having family ties, studied in the same school. The Ministry of Health defines household contact as each and every person who resides or has resided with the Hansen's disease patient in the last five years.11 It is important to emphasize that especially in cases where patients are younger than fifteen years of age, the identification of household contacts should include, in addition to family members, possible caregivers who do not necessarily live in the same house. The increased risk of illness among contacts may be related to genetic family susceptibility and the physical distance of the index case.12

Besides the examination of household contacts, other strategies that may be used are information, education and communication (IEC) activities, aiming at stimulating spontaneous demand, and examinations of the collectivity in schools, which represent active search. In this case, the city health secretariat of Itaguaí, after IEC activities and offer of dermatologicalneurological examination to those with signs and symptoms, did not identify other cases in the school where the children study. The probable origin of the source patient is Minas Gerais, where the three girls had close and prolonged contact with a family member diagnosed with the multibacillary form who was identified, according to information provided by the children caregivers, due to the information on health education and communication transmitted to family members during the examination of contacts. Therefore, contagion was probably the result of a migratory movement. In such situations, the investigation becomes even more complex and, besides the knowledge about the geographic distribution of Hansen's disease, we should take into account the population flows that may be responsible for the onset of new cases outside the epidemiological context of the area of residence.13

In the new World Health Organization (WHO)'s global strategic plan for control of Hansen's disease 2011 - 2015, the detection of new cases in patients younger than fifteen years of age is an important indicator, having already been elected by the Ministry of Health (MH) as endemic monitoring indicator since 14,15 WHO recommends diagnostic validation of new cases on a routine basis, an activity that the Ministry of Health has been carrying out and encouraging, mainly in this age bracket, considered by many of difficult diagnosis when made merely on clinical basis by the basic health units.14,16 This sanitary dermatology health unit (SD), a state leprosy reference, contributes to the diagnosis and validation, as described in the cases above.

According to Decree nº 125/2009 of MH, the coefficient of detection in patients younger than 15 years of age is considered hyperendemic when presenting a value higher than 10 per 100,000 inhabitants. The city of Itaguaí presented a population of 29,200 inhabitants in 2008, year when the three new cases here reported were detected (Table 1).7

Our conclusion is, therefore, that the detection of only three new cases raises the coefficient of detection in patients younger than 15 years of age, in the above mentioned municipality, to a value considered as hyperendemic (Table 1). This fact alerts us to the need to increase surveillance activities in this area, both for resident and imported cases. The report here presented illustrates and emphasizes the importance of a reference unit in the diagnosis of cases in this age bracket and points to the need for identification of contagion sources in the context of epidemiological surveillance, in an attempt to control Hansen's disease.

 

REFERENCES

1. Burns T, Breathnach S, Cox N, Griffiths C, editors. Rook's textbook of dermatology. 7th edition. New York: Blackwell Publishing; 2004. (Lockwood DNJ. Leprosy; vol. 2, chapter 29). p.1347-1368.         [ Links ]

2. Talhari S, Neves RG. Hanseníase: Dermatologia Tropical. 4 ed. Manaus: Gráfica Tropical; 2006. p. 15-16        [ Links ]

3. de Oliveira MLWR. Infecções por micobactérias. In: Ramos-e-Silva M, Castro MCR. Fundamentos de dermatologia. Rio de Janeiro: Editora Atheneu; 2009. p. 907-27.         [ Links ]

4. Argens LM. The discovery of the leprosy bacillus. Tidsskr Nor Laegeforen. 2002;122:708-9.         [ Links ]

5. Klatser PR, van Beers S, Madjid B, Day R, de Wit MY. Detection of Mycobacterium leprae nasal carriers in populations for which leprosy is endemic. J Clinic Microbiol. 1993;31:2947-51.         [ Links ]

6. Richardus JH, Habbema JDF. The impact of leprosy control on the transmission of M. leprae: is elimination being attained? Lepr Rev. 2007;78:330-7.         [ Links ]

7. Ministério da Saúde. Portaria Conjunta. Nº 125/2009. Define ações de controle da hanseníase. [acesso 08 Maio 2010]. Disponível em: http://bvsms.saude.gov.br/bvs/saudelegis/svs/2009/poc0125_26_03_2009.html        [ Links ]

8. Meima A, Irgens LM, van Oortmarsen GJ, Richardus JH, Habbema JD. Disappearance of leprosy from Norway: an exploration of critical factors using an epidemiological modelling approach. Int J Epidemiol. 2002;31:991-1000.         [ Links ]

9. Ministério da Saúde. Secretaria de Vigilância em Saúde. Departamento de Vigilância Epidemiológica. Hanseníase no Brasil: dados e indicadores epidemiológicos selecionados. Brasília: Ministério da Saúde; 2009. [acesso 09 Mar. 2010]. Disponível em: http://portal.saude.gov.br/portal/arquivos/pdf/caderno_de_indicadores_hanse_brasil_01_a08_atual.pdf        [ Links ]

10. Imbiriba EB, Hurtado-Guerrero JC, Garnelo L, Levino A, Cunha Mda G, Pedrosa V. Perfil epidemiológico da hanseníase em menores de quinze anos de idade, Manaus (AM), 1998-2005. Rev Saúde Pública. 2008;42:1021-6        [ Links ]

11. Ministério da Saúde. Secretaria de Atenção à Saúde. Departamento de Atenção Básica. Cadernos de Atenção Básica. Vigilância em Saúde: Dengue, Esquistossomose, Hanseníase, Malária, Tracoma e Tuberculose. Série A. Cadernos de Atenção Básica n. 21. Brasília: Ministério da Saúde; 2007. 199 p.         [ Links ]

12. Durães SMB, Guedes LS, Cunha MD, Magnanini MMF, Oliveira MLWDR. Estudo epidemiológico de 107 focos familiares de hanseníase no município de Duque de Caxias - Rio de Janeiro, Brasil. An Bras Dermatol. 2010;85:339-45.         [ Links ]

13. Penna MLF, de Oliveira MLWdR, Penna G. Spatial distribution of leprosy in the Amazon region of Brazil. Emerg Infect Dis. 2009;15:650-2.         [ Links ]

14. World Health Organization. Enhanced Global Strategy for Further Reducing the Disease Burden Due to Leprosy (plan period 2011-2015), 2009. [cited 2010 Mar 09]. Available from: http://portal.saude.gov.br/portal/arquivos/pdf/op_guidelines_2011_2015.         [ Links ]

15. Ministério da Saúde. Secretaria de Vigilância em Saúde - Nota técnica No.10 / 2007 sobre indicadores de monitoramento do comportamento da Hanseníase 21/08/07. Brasília: Departamento de Vigilância Epidemiológica, 2007.         [ Links ]

16. Daxbacher ELR. Acurácia diagnóstica na atenção básica: proposta de validação em menores de 15 anos - Projeto piloto em 5 estados das regiões norte, nordeste e centro-oeste. Hansen Int. 2008;33:41-62.         [ Links ]

 

 

Mailing address:
Vivian Fichman Monteiro de Souza
Rua cinco de Julho nº108, apt 1001, Copacabana
CEP: 22051030 - Rio de Janeiro - RJ, Brazil
E-mail: vivianfichman@terra.com.br

Received on 11.06.2010.
Approved by the Advisory Board and accepted for publication on 06.08.2010.
Conflict of interest: None
Financial funding: None

 

 

* Work carried out at the Dermatology Service of the Teaching Hospital Pedro Ernesto, State University of Rio de Janeiro (Hospital Universitário Pedro Ernesto, Universidade do Estado do Rio de Janeiro - HUPE - UERJ) - Rio de Janeiro (RJ), Brazil.