Abstract
Localized cutaneous leishmaniasis (LCL), known as "chiclero's ulcer" in southeast Mexico, was described by Seidelin in 1912. Since then, the sylvatic region of the Yucatan peninsula has been identified as an endemic focus of LCL. The purpose of the present work was to describe the clinical picture of LCL caused by Leishmania (Leishmania) mexicana in the Yucatan peninsula. A total of 136 cases of LCL, based on isolation and characterization of L. (L.) mexicana by isoenzymes and/or monoclonal antibodies, were selected. Some variability of clinical features regarding number, type, size, form, location and time of evolution of the lesions was observed. The most frequently observed presentation was a single, ulcerated, rounded small lesion, located on the ear, with an evolution time of less than three months, with neither cutaneous metastases nor lymphatic nor mucosal involvement. This picture corresponds to previous studies carried out in the same endemic area where an organism of the L. mexicana complex has been incriminated as a major aetiological agent of classical "chiclero's ulcer", confirming that in the Yucatan peninsula LCL due to L. (L.) mexicana when located on the pinna of the ear is a remarkable characteristic.
Leishmania (L.) mexicana; "chiclero's ulcer"; Yucatan peninsula
Clinical Picture of Cutaneous Leishmaniases Due to Leishmania (Leishmania) mexicana in the Yucatan Peninsula, Mexico
Vol. 96(2): 163-167, February 2001
Fernando J Andrade-Narváez+ + Corresponding author. Fax: +52-9-923-6120. E-mail: anarvaez@tunku.uady.mx Received 16 March 2000 Accepted 29 November 2000 , Alberto Vargas-González, Silvia B Canto-Lara, Alma G Damián-Centeno
Universidad Autónoma de Yucatán, Centro de Investigaciones Regionales "Dr. Hideyo Noguchi", Laboratorio de Inmunología, Avenida Itzáes No. 490x59, Código Postal 97000, Mérida, Yucatán, México
Localized cutaneous leishmaniasis (LCL), known as "chiclero's ulcer" in southeast Mexico, was described by Seidelin in 1912. Since then, the sylvatic region of the Yucatan peninsula has been identified as an endemic focus of LCL. The purpose of the present work was to describe the clinical picture of LCL caused by Leishmania (Leishmania) mexicana in the Yucatan peninsula. A total of 136 cases of LCL, based on isolation and characterization of L. (L.) mexicana by isoenzymes and/or monoclonal antibodies, were selected. Some variability of clinical features regarding number, type, size, form, location and time of evolution of the lesions was observed. The most frequently observed presentation was a single, ulcerated, rounded small lesion, located on the ear, with an evolution time of less than three months, with neither cutaneous metastases nor lymphatic nor mucosal involvement. This picture corresponds to previous studies carried out in the same endemic area where an organism of the L. mexicana complex has been incriminated as a major aetiological agent of classical "chiclero's ulcer", confirming that in the Yucatan peninsula LCL due to L. (L.) mexicana when located on the pinna of the ear is a remarkable characteristic.
Key words: Leishmania (L.) mexicana -"chiclero's ulcer"- Yucatan peninsula
Human leishmaniases include a spectrum of diseases of variable severity ranging from cutaneous ulcer to a fatal visceral disease, all of them caused by intracellular protozoan parasites of the genus Leishmania Ross, 1903. Cutaneous leishmaniases in the New World are zoonoses caused by at least ten species of Leishmania, of the mexicana and braziliensis complexes (Marinkelle 1980, Dedet 1999). The disease is polymorphic in its clinical presentation and evolution. Differences may be due to Leishmania species or strains, host's genetic background and immune response. Localized cutaneous leishmaniasis (LCL) known as "chiclero's ulcer" (collector of natural chewing gum) in southern Mexico, was described by Seidelin (1912).Since then,the sylvatic region of the Yucatan peninsula has been considered an endemic focus of LCL (Shattuck 1933, Beltran & Bustamante 1942, Biagi et al. 1957, Andrade-Narváez et al. 1988, 1990, 1992). Clinical picture of "chiclero's ulcer" is characterized by cartilage involvement of the pinna of the ear (Martínez 1951, Biagi 1953, Lainson & Strangways-Dixon 1963, Walton 1987). Very recently, we have demonstrated that Leishmania (Leishmania) mexicana Biagi, 1953, emend. Garnham, 1962, is the main agent causing LCL in this focus, although, Leishmania (Viannia) braziliensis Vianna 1911, emend. Matta, 1916, has also been isolated from a few cases (Canto-Lara et al. 1998, 1999). Moreover, L. (V.) braziliensis has been predominantly isolated from LCL cases occurring in Belize (Evans et al. 1984) and in Guatemala (Herwaldt et al. 1992), both recognized endemic areas of LCL attributed to the Leishmania mexicana complex (Zeledón 1985). Hence, we decided to report in here the clinical findings of LCL cases caused by L. (L.) mexicana in the Yucatan peninsula.
In the present study, L. (L.) mexicana isolated from 136 patients suffering of LCL ("chiclero's ulcer") in southeast Mexico was identified by molecular methods. It was confirmed that "chiclero's ulcer" - LCL caused by L. (L.) mexicana in the Yucatan peninsula - is a clinical polymorphic disease characterized by predominantly single ulcerative lesions, located mainly on the ears and with no tendency to produce either cutaneous metastases or lymphatic or mucosal involvement.
MATERIALS AND METHODS
Patient population - Patients from the Yucatan peninsula, Mexico, with a suggestive clinical picture of LCL, who sought treatment between January 1990 and December 1995, were evaluated in a long-term clinical-epidemiological study to define dynamics of transmission of L. (L.) mexicana in that focus. This study was reviewed and approved by the Ethical Committee of the Universidad Autónoma de Yucatán, in agreement with international ethical guidelines for biomedical research involving human subjects (Ley General de Salud, Mexico). Written informed consent to participate was obtained from each patient. Eligibility for this study included a confirmed diagnosis of LCL based on visualization of the parasite by smear, biopsy, and/or isolation-culture (Garcia-Miss et al. 1990). A complete clinical history was performed in all cases recording age, sex, occupation, as well as clinical presentation through dermatological examination (number, size, form, and location of lesion(s), suggestive signs of secondary infection, time of evolution prior to diagnosis and metastases), and searching for lymphatic involvement. Mucosal were examined by means of direct examination of oropharynx with a frontal light and a tongue depressor.
Characterization of parasites - Parasites isolated by needle aspirates from the edge of the lesion were inoculated into a tube of Senekjie's modified medium and kept at 22ºC.After initial growth in culture tubes, the parasites were mass cultivated for isoenzyme electrophoresis and analyses with monoclonal antibodies as described previously in Chablé-Santos et al. (1995) and Canto-Lara et al. (1998, 1999).
RESULTS
Between January 1990 and December 1995, a total of 683 patients with cutaneous lesions suggestive of LCL were studied. Parasite demonstration by smear, biopsy, and/or isolation-culture was positive in 445 of them (65.1%). From these, L. (L.) mexicana was successfully isolated, cultured, and identified by isoenzyme characterization and/or monoclonal antibodies in 136/445 cases (30.5%). Males (128/136, 94.1%) between 10 to 40 years old (116/136, 85.3%) were mainly affected. The most common lesions were single (84.5%), rounded (52.6%), ulcerated (72.5%), and located on the ear (39.9%). However a great variability in clinical presentations was observed (Table). Four patients had 3 lesions and only three men had 4, 7, and 8 lesions respectively. Time of evolution varied from seven days to 30 years (average=9.9 months). The average area of the lesions was 2.6 cm2 (ranging from 0.03-29.6 cm2). Secondary infection was observed in 43/136 lesions (31.6%). There was no cutaneous metastases and lymphatic involvement as so mucosal involvement was not observed in any of the 136 cases even after ten years of monthly follow-up.
Table I
This paper is the first report in which clinical presentation of LCL, related to L. (L.) mexicana identified by molecular methods, is offered in southeast Mexico. The clinical picture was polymorphic but characterized by a predominantly single, painless, small rounded, ulcerative, ear-located lesion, without cutaneous metastases, lymphatic or mucosal involvement, confirming "chiclero's ulcer" clinical presentation attributed to L. mexicana complex described in previous studies carried out in the same endemic area.
In the Yucatan peninsula, previous studies (Seidelin 1912, Shattuck 1933, Biagi 1953) reported the typical "chiclero's ulcer" but precise identification techniques of species of Leishmania were not available yet. Seidelin (1912) was the first to describe the disease in the Yucatan peninsula in "two young natives, chicleros, with extensive ulcers located on the upper part of the helix of one ear, with somewhat elevated irregular borders, granular surface beset with minute vesicles, considerable destruction of the tissues and beginning deformation due to cicatricial retraction". Laymen knew the affection as a typical one, the ear "ulcer of the chiclero". Shattuck (1933) described 17 cases reporting for the first time the affection in two women and two children. Single lesion (88.2%) located on the ear (76.5%) was the most common clinical presentation. He mentioned that "such lesions persist for years and ultimately heal leaving a well-marked scar". Biagi (1953) working in Escárcega, Campeche, southwest of the Yucatan peninsula, studied 70 cases of LCL. Male were predominantly affected (94.3%). Clinical picture was characterized by a single (76.2%), nodular subcutaneous ulcerated lesion (67.5%), located predominantly on the ear (48.4%), where it usually became chronic with a time of evolution of more than 12 years. Walton (1987) pointed out that in the Yucatan peninsula, cartilage involvement of the pinna of the ear is such a common occurrence that it might be considered as a special feature of "chiclero's ulcer".
In Belize, Lainson and Strangways-Dixon (1963) in a three-years study on the epidemiology of dermal leishmaniases, studied in detail a total of 46 human cases. They found that the disease was characterized by a single dermal lesion commonly located on the ear (40%), without evidence of any cutaneous dissemination of infection or visceral involvement. Moreover, they highlighted that lesions on the ears were a particular characteristic due to their extreme chronic destruction of the cartilage and overlying tissues. The parasite was isolated in 27 instances and cultured in NNN media. It was identified as L. mexicana based on the behaviour of strains isolated in cultures and in hamsters.
In Guatemala, Herwaldt et al. (1992) evidenced the importance of species of Leishmania identification. In their study on the natural history of LCL caused by L. (L.) mexicana, 22 of the 25 lesions (88%) completely re-epithelialized in 14 weeks. In contrast, only 2/32 (6%) lesions caused by L. (V.) braziliensis cured spontaneously. They concluded that the species of Leishmania is the primary determinant of both the clinical course and the outcome of untreated lesions. It is interesting to point out that the most common location of lesions was not the ear, but the upper limbs (43%).
In Texas, McHugh et al. (1996) studied 27 cases of LCL in which the clinical presentation was characterized by a single lesion (74.1%) with an area less than 3 cm2 (96.3%), located on the head predominantly (96.3%), and from these only 6/20 (30%) were located on the ear. The parasite was isolated in eight cases and was identified by isoenzymes as L. (L.) mexicana.
All these studies demonstrate the variability of the clinical presentation of LCL caused by L. (L.) mexicana regarding the number, form, size, and location of lesions as it has been described in other species of Leishmania (Louzir et al. 1998). Various hypotheses have been proposed to explain such variability: (a) differences in parasite's virulence; (b) differences in skin permeability; (c) individual variation in the host's genetic susceptibility; (d) individual human differences of attraction for phlebotomine sand flies (Llanos-Cuentas & Campos 1988). Inter- and intraspecific variations of parasite virulence have been demonstrated (Chang et al. 1990) and human susceptibility is likely to have a genetic basis (Lara et al. 1991). The skin permeability hypothesis to the sand fly bite was evaluated by Esterre et al. (1987), however, they did not show convincingly that the differences between the patients and controls were significant. Louzir et al. (1998) studying the immunologic determinants of disease evolution in LCL due to L. major, found that an unfavorable clinical outcome was not related to an inadequate Th1 cell response, and suggested that the macrophage-activating effect of IFN-gamma may be inhibited by the concomitant expression of IL-10. Finally, McHugh et al. (1996) pointed out that although the Leishmania parasites infesting humans in Texas share a high genetical similarity with L. (L.) mexicana isolates from southeast Mexico, the epidemiology and ecology of the disease in Texas and Mexico are different. This emphasizes the importance of dynamics of transmission on the clinical presentation.
The most remarkable characteristic of "chiclero's ulcer" [LCL caused by L. (L.) mexicana in the Yucatan peninsula] is the predominant location of lesions on the ears. Lainson and Strangways-Dixon (1963) proposed that it was "simply owing to the almost constant exposure of this part of the body, day and night, to the bite of the vector. Moreover, they mentioned, according to Professor Adler, that extensive sweating of the face compared with that of the ears might be an important factor. Finally, the slightly lower temperature of the ears conceivably might lead to a faster development of L. (L.) mexicana on that site.
On the other hand, it is important to consider the possible role of the vector in determining the biting site selection. Although variability of attractiveness of human hosts has been shown for several species of mosquito (Brouwer 1960, Khan et al. 1965), at present little is known about the biting site selection of sand flies and human attractants for sand flies. Very recently, biting site distribution of three members of the Lutzomyia longipalpis complex (Diptera: Psychodidade: Phleobotominae) was documented on a male human volunteer aged 29. Female sand flies from Jacobina, State of Bahia, Brazil, displayed a marked preference for biting on the ears. Biting selection behaviour seemed to be odour-mediated as revealed by female sand fly responses to ear extracts (Rebollar-Tellez 2000). The possible role of odour-mediated biting selection behaviour of Lu. olmeca and Lu. cruciata - incriminated vectors of L. (L.) mexicana - is under study in order to explain the frequency of ear lesions.
In summary, the clinical outcome and evolution of the infection by Leishmania parasites depends on multiple factors. The study of these factors is of paramount importance to identify markers for population at risk that could be used as targets for a direct intervention leading to a better control of the disease.
To the personnel of the "Programa Solidaridad" of the "Instituto Mexicano del Seguro Social" and to the "Secretaría de Salud", from the State of Campeche, for their collaboration in case detection and notification; to Nicole R Van Wynsberghe and Eduardo A Rebollar-Tellez, for their careful editing of the manuscript.
This investigation received financial support from the UNDP/World Bank/WHO Special Programme for Tropical Diseases Research: RCS/TDR/WHO ID 900248.
- Andrade-Narváez FJ, Albertos-Alpuche NE, Canto-Lara SB, Vargas-González A, Valencia-Pacheco G, Palomo-Cetina A 1992. Risk factors associated with CL infection and disease in the State of Campeche, Yucatan Peninsula. In P Wijeyaratne, T Goodman (eds), Leishmaniasis Control Strategies. A Critical Evaluation of IDRC-supported Research, International Development Research Center MR 322e, p. 193-205.
- Andrade-Narváez FJ, Simmonds-Díaz EB, Aguilar-Rico S, Andrade-Narváez M, Palomo-Cetina A, Canto-Lara SB, García-Miss MR, Madera-Sevilla M, Albertos-Alpuche NE 1990. Incidence of localized cutaneous leishmaniasis (Chiclero's ulcer) in Mexico. Trans R Soc Trop Med Hyg 84: 219-220.
- Andrade-Narváez FJ, Simmonds-Díaz EB, Canto-Lara SB, García-Miss MR, Cruz-Ruiz AL, Palomo-Cetina A, Rico-Aguilar S, Andrade-Narváez M 1988. Current situation regard to cutaneous leishmaniasis (chiclero's ulcer) in Mexico. In BC Walton, P Wijeyaratne, F Moddaber (eds), Research on Control Strategies for the Leishmaniasis. Proceedings of an International Workshop, International Development Research Center (IDRC) MR 184e, p. 119-127.
- Beltrán F, Bustamante ME 1942. Datos epidemiológicos acerca de la "úlcera de los chicleros" (leishmaniasis americana) en México. Rev Inst Salub Enferm Trop 3: 1-28.
- Biagi F 1953. Sintesis de 70 historias clínicas de leishmaniasis tegumentaria en México (úlcera de los chicleros). Medicina 33: 385-396.
- Biagi F, Marroquin F, Gonzalez M 1957. Distribución geográfica de la leishmaniasis en Mexico. Medicina 37: 444-446.
- Brouwer R 1960. Variations in human body odour as a cause of individual differences of attraction for malaria mosquitoes.Trop Geog Med 2: 186-196.
- Canto-Lara SB, Cárdenas-Marrufo MF, Vargas-Gonzalez A, Andrade-Narváez FJ 1998. Isoenzyme characterization of Leishmania isolated from human cases with localized cutaneous leishmaniasis from the State of Campeche, Mexico. Am J Trop Med Hyg 58: 444-447.
- Canto-Lara SB, Van Wynsberghe NR, Vargas-Gonzalez A, Ojeda-Farfán FF, Andrade-Narváez FJ 1999. Use of monoclonal antibodies for the identification of Leishmania spp. isolated from humans and rodents in the State of Campeche, Mexico. Mem Inst Oswaldo Cruz 94: 305-309.
- Chablé-Santos JB, Van-Wynsberghe NR, Canto-Lara SB, Andrade-Narváez FJ 1995. Isolation of Leishmania (L.) mexicana from wild rodents and their possible role in the transmission of localized cutaneous leishmaniasis in the State of Campeche, Mexico. Am J Trop Med Hyg 53: 141-145.
- Chang KP, Chaudhari G, Fong D 1990. Molecular determinants of Leishmania virulence. Ann Rev Microbiol 44: 499-529.
- Dedet JP 1999. Leishmanioses tégumentaires. In Les Leishmanioses, Ellipses Univerisités Francophones, p. 173-175.
- Esterre P, Ridel PR, Jamet D, Dedet JP 1987. Cutaneous factors in susceptibility to American cutaneous leishmaniasis Trans R Soc Trop Med Hyg 81: 160.
- Evans DA, Lanham SM, Baldwin CI, Peter W 1984. The isolation an isoenzyme characterization of Leishmania braziliensis subspecies from patients with cutaneous leishmaniasis acquired in Belize. Trans R Soc trop Med Hyg 78: 35-42.
- García-Miss MR, Andrade-Narváez FJ, Esquivel-Vińas RE, Simmonds-Díaz EB, Canto-Lara SB, Cruz-Ruiz AL 1990. Sensitivity and specificity of ELISA for IgG antibodies to Leishmania mexicana mexicana Trans R Soc Trop Med Hyg 84: 356-358.
- Herwaldt BL, Arana BA, Navin TR 1992. The natural history of cutaneous leishmaniasis in Guatemala. J Inf Dis 165: 518-527.
- Khan AA, Maibach HI, Strauss WG, Fenley WR 1965. Screening humans for degrees of atractiveness to mosquitoes. J Econ Entomol 58: 694-697.
- Lainson R, Strangsway-Dixon J 1963. Leishmania mexicana: the epidemiology of dermal leishmaniasis in British Honduras. Trans R Soc Trop Med Hyg 57: 242- 265.
- Lara ML, Larysse Z, Scorza JV 1991. Immunogenetics of human american cutaneous leishmaniasis: study of HLA haplotypes in 24 families from Venezuela. Human Immunol 30: 129-135.
- Llanos-Cuentas A, Campos M 1988. Identification and quantification of risk factors associated with New World cutaneous leishmaniasis. In BC Walton, P Wijeyaratne, F Modabber (eds), Research on Control Strategies for the Leishmaniasis. Proceedings of an International Workshop, International Development Research Center, MR 184e, p. 252-260.
- Louzir H, Melby PC, Ben Salah AB, Marrakchi H, Aoun K, Ben Ismail R, Dellagi K 1998. Immunologic determinants of disease evolution in localized cutaneous leishmaniasis due to Leishmania major. J Inf Dis 177: 1687-1695.
- Marinkelle CJ 1980.The control of leishmaniases. Bull WHO 58: 807-818.
- Martínez E 1951. Leishmaniasis en Yucatán. Rev Méd Yucatán 26: 294-296.
- McHugh C, Melby PC, LaFon SG 1996. Leishmania in Texas: epidemiology and clinical aspects of human disease. Am J Trop Med Hyg 55: 547-555.
- Rebollar-Tellez EA 2000. Kairomone-mediated Behaviour of Members of the Lutzomyia longipalpis complex (Diptera: Psichodidae), PhD Thesis, Keele University, Staffordfshire, UK, 244 pp.
- Seidelin H 1912. Leishmaniasis and babesiasis in Yucatan. Ann Trop Med Parasitol 6: 295-299.
- Shattuck GC 1933. Leishmania, Trachoma and Foliculosis. In GC Shattuck, The Peninsula of Yucatan Medical, Biological, Meteorological and Sociological Studies, Carnegie Institution of Washington, p. 318-327.
- Walton BC 1987. American cutaneous and mucocutaneous leishmaniasis. In W Peters, R Killick-Kendrick (eds), The Leishmaniases in Biology and Medicine, Clinical Aspects and Control, Vol. II, Academic Press, p. 642-644.
- Zeledón R 1985. Leishmaniasis in North America, Central America and the Caribbean Islands. In KP Chang, RS Bray (eds), Leishmaniasis, Elsevier Science Publishers BV (Biomedical Division), p. 313-351.
Publication Dates
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Publication in this collection
28 Mar 2001 -
Date of issue
Feb 2001
History
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Accepted
29 Nov 2000 -
Received
16 Mar 2000