Epidermal parasitic skin diseases: a neglected category of poverty-associated plagues
Hermann Feldmeier a & Jorg Heukelbach b
a. Institute of Microbiology and Hygiene, Charité University Medicine Berlin, Campus Benjamin Franklin, Berlin, Germany.
b. School of Medicine, Federal University of Ceará, Fortaleza, Brazil.
Correspondence to Hermann Feldmeier (e-mail: firstname.lastname@example.org).
(Submitted: 30 August 2007 – Revised version received: 22 February 2008 – Accepted: 25 February 2008 – Published online: 28 November 2008.)
Bulletin of the World Health Organization 2009;87:152-159. doi: 10.2471/BLT.07.047308
Epidermal parasitic skin diseases (EPSD) occur worldwide and have been known since ancient times. Despite the considerable burden caused by EPSD, this category of parasitic diseases has been widely neglected by the scientific community and health-care providers. This is illustrated by the fact that in the recent edition of The Communicable disease control handbook, a reference manual for public health interventions, only one EPSD (scabies) is mentioned.1 EPSD fulfil the criteria defined by Ehrenberg & Ault (2005) for neglected diseases of neglected populations, but are not listed on national or international agendas concerning disease control priorities.2,3 This probably explains why efforts to control EPSD at the community level have very rarely been undertaken.4
Six EPSD are of particular importance: scabies, pediculosis (head lice, body lice and pubic lice infestation), tungiasis (sand flea disease) and hookworm-related cutaneous larva migrans (HrCLM). They are either prevalent in resource-poor settings or are associated with important morbidity. In this paper we focus on these diseases, summarize the existing knowledge on the epidemiology and the morbidity in resource-poor settings and focus on the interactions between EPSD and poverty.
We use the term “underprivileged population” to designate a typical resource-poor setting in low-income countries, in contrast to the socioeconomic characteristics of affluent communities in high-income countries. The expressions “hot-climate country” and “cold-climate country” are used when we refer to climatic restrictions on the occurrence of EPSD.
Searches of PubMed and LILACS using keywords “parasitic skin disease”, “scabies”, “pediculosis”, “tungiasis”, “cutaneous larva migrans” and their synonyms were used as a source of references. Searches were made without time limitations. In addition, we used references retrieved by the authors during previous work on EPSD. Articles in English, French, Portuguese and Spanish were reviewed and analysed where quantitative data were provided, the study design was sound and the study had been performed in a resource-poor setting in a low-income country. Of 95 articles identified by these criteria, 50 were selected and cited in the reference list.
The six major EPSD differ considerably in their biological and epidemiological characteristics and life cycles (Table 1). Scabies is caused by a mite (Sarcoptes scabiei), pediculosis by lice, tungiasis by sand fleas (Tunga penetrans) and HrCLM by nematode larvae. Although HrCLM and tungiasis are self-limiting diseases, the parasites may persist for months and can cause long-lasting sequels. S. scabiei and lice propagate continuously and cause persisting symptoms if the infestation remains untreated.5
In EPSD, host-parasite interactions are restricted to the stratum corneum, the upper layer of the epidermis, which is where the ectoparasites complete their life-cycles, in part or entirely. In other parasitic skin diseases, such as leishmaniasis, loiasis or onchocerciasis, other layers of the dermis are also affected. Whereas S. scabiei and lice accomplish their life-cycle within or on top of the epidermis, T. penetrans needs the host only for the production of eggs and completes its other developmental stages off-host. In contrast, animal hookworm larvae that have penetrated into the epidermis find themselves at a biological impasse and cannot develop further.
Scabies, pediculosis capitis and pediculosis pubis occur worldwide but pediculosis corporis is restricted to cold-climate countries and is virtually absent in the tropics (Table 1). HrCLM is very rare in industrialized parts of the world but is ubiquitously present in developing countries.6 Tungiasis is geographically restricted to the Caribbean, sub-Saharan Africa and South America.7
Except in epidemic circumstances, data on EPSD are not recorded so there is no reliable information available on global disease occurrence, changes in incidence over time, and spatial distribution in endemic areas. Hengge et al.8 suggested that 300 million cases of scabies exist worldwide, with many more individuals being at risk at any point in time. Similarly, in resource–poor settings, virtually all individuals are permanently at risk for head-lice infestation, i.e. several billion people globally. As tungiasis and HrCLM are climatically and spatially restricted, the number of people at risk is lower, although still sufficient to merit attention.
The distribution of EPSD is irregular, and incidence and prevalence vary in relation to area and population studied. A study in a resource-poor community in urban Bangladesh, for example, showed that virtually all children aged less than 6 years developed scabies within a period of 12 months.9 In a rural village in the United Republic of Tanzania, the overall prevalence was 6%, in rural and urban Brazil 8–10%, and in rural India 13%.10–12 In Egyptian children, the prevalence was estimated to be 5% but in Australian Aboriginal communities the prevalence in this age group approached 50%.13,14 Of 5–9-year-olds children living in a displacement camp in Sierra Leone, 86% were found to be infested with S. scabiei.15
In some native populations in the Amazon lowland, head-lice infestation is present in virtually all inhabitants, while it is quite rare among adults in affluent societies.16 In an urban slum in Fortaleza, Brazil, girls experienced 19 new head-lice infestations per year, and boys 15 (authors’ unpublished data, 2008). In contrast, in Germany the incidence was estimated at 1500 per 10 000 children per year.16
During peak transmission, the prevalence of tungiasis in children living in resource-poor rural and urban communities in Brazil and Nigeria reached more than 60%.7,17 In contrast, in high-income communities in these same countries, tungiasis is restricted to single cases that typically occur when people visit local beaches.18 The situation is similar for HrCLM, with prevalence in children as high as 15% during the rainy season and an incidence of 1.840 cases per 10 000 individuals per year.19
EPSD usually show considerable seasonal variation of disease occurrence (Table 1).20–23 In the tropics, the cyclical changes are particularly evident in tungiasis and HrCLM; prevalence of tungiasis is highest in the dry season and of HrCLM in the rainy season.19,20
The factors responsible for the high burden of EPSD in resource-poor communities are complex and have not been clarified. It has been suggested that crowding, sharing of beds, frequent population movements, poor hygiene, lack of access to health care, inadequate treatment, malnutrition and social attitudes contribute to the high burden of scabies in these settings.24 It is difficult to disentangle the relative importance of economic, environmental and behavioural factors, since they frequently coexist.25 There is, however, circumstantial evidence that extreme poverty and its economic and social consequences play a pivotal role (Fig. 1).9,25
Fig. 1. Typical setting in a resource-poor neighbourhood in north-eastern Brazil in which EPSD are prevalent and the exposure risk for tungiasis and cutaneous larva migrans is high
Tungiasis is a paradigmatic example for this complex web of causation. Sand flea disease is a zoonosis affecting a broad spectrum of animals, with pigs, dogs, cats and rats as the principal reservoirs. In resource-poor settings, stray dogs and cats are common and organic waste frequently litters the soil. Rats are attracted if garbage is not collected, sewage not disposed of properly and food stored inadequately. The risk for infestation is high if feet are not protected by shoes and socks, either because people cannot afford them or if wearing shoes is not part of local custom.26,27 In resource-poor rural and indigenous populations in the hinterland of Brazil, the transmission of T. penetrans occurred almost exclusively indoors.7 Dwellings in these settings typically do not possess a solid floor, or the ground is covered with rough concrete or broken tiles with many crevices, thus providing an ideal habitat for the off-host development of T. penetrans. In an urban environment it spreads in slums, where roads and paths are not paved, waste litters the area and yards consist of sand or mud.
Atypical paths of transmission in resource-poor settings are another epidemiological characteristic of EPSD. When laundry is dried on the ground, instead of using clothes lines, there is a high risk of contamination from dog and cat faeces containing hookworm larvae. In resource-poor settings, the high frequency of lesions of HrCLM on the upper part of the body, including the face, probably reflects this particular type of transmission.28
Another epidemiological peculiarity in poor settings is the observation that deficient sanitation is a significant risk factor for scabies.9 So far, it seems that scabies is not influenced by hygienic practices or the availability of water, since the prevalence of scabies is very high in the Kuna Indians in Panama and among children in the Solomon Islands, where individuals take frequent baths and where careful daily personal hygiene is traditional.29,30 We suggest that deficient sanitation is a characteristic of poor households and that poor hygiene does not by itself increase the odds of acquiring scabies. Interestingly, in rural Egypt, high prevalence of scabies was associated with households receiving their water supply from a hand pump, which the authors considered an indicator of low socioeconomic status rather than of deficient hygiene.13 In resource-poor settings, scabies is usually not a sexually transmitted disease, while this seems to be a common mode of transmission in high-income countries.25
Poverty also plays a role in the transmission dynamics of head lice. In children living in a poor urban neighbourhood in north-eastern Brazil, the infestation rate depended significantly on the income of the household: the lower the family’s income, the more head-lice episodes a child experienced per unit of time. In high-income countries, children of all socioeconomic groups are at similar risk for infestation with Pediculus humanus var. capitis.16
Within a resource-poor population, certain groups are at a particularly high risk for disease occurrence and severe morbidity. These may be girls and women (head-lice infestation), children (head-lice infestation, scabies, HrCLM, tungiasis), the elderly (scabies, tungiasis) or displaced or homeless people (scabies, pediculosis corporis, pediculosis pubis).7,11,31,32
A peculiar epidemiological characteristic of EPSD is the concomitant presence of several ectoparasites on the same individual. In a fishing community in Brazil, for instance, 9% of the inhabitants were simultaneously infested with two or more ectoparasites.33 Not surprisingly, individuals with EPSD also tend to be co-infected with intestinal helminths.33
Although the morbidity associated with EPSD is significant, a systematic assessment of the severity of the burden is still lacking. Engels & Savioli34 suggested that EPSD may represent a considerable subjective burden, although disability-adjusted life years (DALYS) have not yet been calculated.
According to its pathophysiological basis, pathology can be schematically divided into two patterns, namely inflammation-related and itch-related. In tungiasis, the predominant morbidity is the result of heavy inflammation surrounding the lesions, together with secondary bacterial infection (Fig. 2 and Fig. 3).35 Superinfection reinforces the inflammatory process. Persistent inflammation and superinfection frequently lead to long-lasting sequelae – i.e. secondary morbidity – such as suppuration, ulceration, gangrene, necrosis of surrounding tissue, deformation and loss of nails, resulting in physical disability.7,36 Tungiasis has also been associated with tetanus in non-vaccinated individuals. In a study in São Paulo, Brazil, tungiasis was identified as the port of entry for 10% of tetanus cases.37 All heavily infested individuals living in a resource-poor neighbourhood in north-eastern Brazil showed signs of acute and chronic inflammation: 19% had fissures; 50% presented with ulcers; deformation and/or loss of nails occurred in 69%,36 resulting in walking difficulty in all patients and difficulty in gripping in half of the patients with lesions at the fingers. A broad host of pathogenic microorganisms has been isolated from superinfected lesions, such as Staphylococcus aureus, Streptococcus pyogenes, enterobacteriaceae, Bacillus spp., Enterococcus faecalis, Pseudomonas spp., as well as various anaerobic pathogens.35,38
Fig. 2. Tungiasis-associated pathology at the heel
Fig. 3. Multiple sand flea lesions at the fingertips
Body lice are vectors of a host of pathogenic bacteria, such as Rickettsia prowazekii (the agent of epidemic typhus), Borrelia recurrentis (the agent of relapsing fever), Bartonella quintana (the agent of trench fever and bacillary angiomatosis) and Yersinia pestis (the agent of plague), and can cause important secondary morbidity through life-threatening infections.39 Head lice can transfer Y. pestis during blood sucking.40 Lice can passively carry staphylococci, streptococci, Acinetobacter spp. and Serratia marcescens and transfer them from infected lesions to other areas of the skin.41
Morbidity related to itching (pruritus) is best studied in scabies as it is such a common symptom that patients scratch their lesions almost constantly. Repeated scratching of a lesion causes excoriation and denudation of the skin thus creating portals of entry for pathogenic bacteria. The clinical consequences of secondary bacterial infection, especially with group A streptococci, result in significant, frequently unrecognized illnesses, such as cellulitis, boils, pyomyositis, lymphangitis and generalized lymphadenopathy.42 Streptococci and staphylococci bacteria have been isolated from skin burrows as well as from faecal pellets of the ectoparasite, suggesting that the mites themselves may contribute to the spread of pathogenic bacteria.43 Moreover, secondary infection of scabies lesions with group A streptococci is a major precipitant of post-streptococcal glomerulonephritis and possibly also of rheumatic fever.44
The debilitating impact of persistent itch has repeatedly been stressed for a variety of non-infectious diseases but remains to be assessed for EPSD. In neurophysiology it is known that chronic itch leads to persistent firing of specialized A and C itch fibres in the skin. As a consequence, pain fibres in the neighbourhood are transformed into itch fibres, eventually leading to a sensitization of spinal neurons. A similar consequence can be anticipated to occur in EPSD. Since the pruritus intensifies at night, disturbance of sleep is to be expected. Recently, alterations of sleep have been confirmed in 84% of patients with HrCLM21 and in 72% patients with scabies.42 Tungiasis has also been shown to cause considerable sleep alterations.38
An aspect of morbidity which has been completely neglected is the psychological impact of EPSD. Since lesions on the skin can be seen by the naked eye, in the case of HrCLM and tungiasis even from a distance, the fact that an individual is infested with ectoparasites does not go unnoticed and can be a source of mental strain and distress. The unhealthy aspect of the skin in EPSD and constant scratching of lesions could influence self-esteem and affect the ability to adjust socially. In north-eastern Brazil, mothers of children with tungiasis are faced with societal notions linking the presence of this ectoparasitosis to neglect. The resulting stigma discouraged mothers from bringing their children to the health centre.45 If patients with scabies are treated with a topical acaricide, the compound has to be applied to the whole body surface. Unfortunately, acaricides, such as sulfur in petrolatum, have a strong odour and so may reinforce stigmatization.
In resource-poor communities in Brazil, the severity of tungiasis was directly related to the economic status of the household in which the affected individuals lived.9,46 A similar observation has been made in individuals with scabies in urban Bangladesh. Morbidity also depends on the duration of disease which means that the longer the infestation progresses, the higher the intensity of clinical signs and symptoms. This is of importance where access to health care is limited, delaying diagnosis and limiting availability of drugs for treatment. Finally, infection with HIV and human T-lymphotropic virus type 1, frequent in many resource-poor communities in the tropics, induces an exceptionally severe form of scabies, namely crusted or “Norwegian” scabies.47
Although several characteristics should make interventions against EPSD cost-effective, control has rarely been attempted. First, the diagnosis of EPSD is relatively easy and can usually be done by the affected individual with a high degree of certainty.48 Second, five of the six major EPSD can be effectively treated with topically applicable insecticides/acaricides or with oral ivermectin. Third, since there is a considerable overlap in the spatial distribution of EPSD and because these diseases cluster in similar population groups, interventions against different EPSD could be performed simultaneously.
Control of scabies by mass treatment with topical permethrin has been achieved in hyperendemic indigenous communities in Australia and Panama.29,30 The interventions resulted in a significant reduction in prevalence of scabies and severity of pyoderma without concomitant use of antibiotics. In a low-income fishing community in Ceará State, Brazil, where scabies, pediculosis, tungiasis and HrCLM were endemic, mass treatment with ivermectin was performed (2 doses of 200 μg/kg body weight 10 days apart) and the population was followed up for a period of 9 months. Prevalence 30 days after treatment dropped by 97% for active pediculosis and 82% for scabies.49 Tungiasis and HrCLM also decreased, although, due to the seasonal variation of these ectoparasitoses, the reduction of disease occurrence could not be quantified. Nine months after mass treatment, the prevalences of pediculosis and scabies were reduced by a factor of 2.1 and 2.6, respectively, when compared to pre-intervention.
A plant-based repellent based on coconut oil was used to prevent infestation with sand fleas in an area with extremely high transmission. The twice-daily application of the repellent on the skin of the feet decreased the infestation rate by 86% and reduced intensity of infestation by 90% despite ongoing transmission.50 At the same time, tungiasis-associated pathology declined to an insignificant level.
Measures to reduce poverty in vulnerable populations could be a universal approach to reducing the prevalence and morbidity of EPSD because this category of illness is so intricately related to extreme poverty.
Future goals and strategies
Since major knowledge gaps currently impede the calculation of the global burden of EPSD, it is important to assess disease occurrence and morbidity in a systematic manner. This would lead to an adjustment of the global burden of neglected diseases because existing data suggest that EPSD have a more substantial impact on health than previously thought.34 Looking at EPSD as a coherent family of infectious skin diseases will make sense in different ways: they tend to cluster in the same populations, they share similar animal reservoirs/ways of transmission and, to make progress in controlling them, they have to be addressed in an integrated manner.
What is needed?
First, sound epidemiological research should be encouraged. We urgently need reliable data on the spatial distribution, incidence, prevalence, seasonal variation, clustering of different EPSD in the same population and on risk factors for development of severe disease. Second, clinical and epidemiological methods have to be combined to determine primary and secondary morbidity associated with EPSD. The association of skin lesions with pathogenic micro-organisms, particularly group A streptococci, warrants indepth investigations. The possible relationship between EPSD, pyoderma and debilitating sequels such as post-streptococcal glomerulonephritis has to be scrutinized.
What can be done?
Since EPSD are so intricately linked with poverty, it seems unlikely that they can be eradicated as long as people continue to live in extreme poverty. Since prevalence, intensity of infestation and morbidity are correlated, a reduction in prevalence will presumably be followed by a decrease in morbidity. This can be achieved by repeated mass treatment with ivermectin. Alternatively, interventions could be targeted at the most vulnerable groups in a defined setting. In both cases it would be essential to make ivermectin available in all endemic areas. A different approach suitable for scabies, pediculosis and tungiasis is based on the prevention of infestation by the reduction of exposure. By this line of thought, the combat of tungiasis and HrCLM could be integrated in existing schemes of zoonosis control.
Based on experiences from north-eastern Brazil and the Solomon Islands, it seams feasible and practical to integrate control of EPSD, pyoderma, filariasis and intestinal nematodes.29,49 Ehrenberg & Ault2 have advocated this approach in their previous analysis of possible interventions for “neglected diseases of neglected populations” in the Caribbean and Latin America. Measuring the effect of such integrated control is likely to reveal the real impact of EPSD on human health and well-being.
A distinction needs to be made between developing interventions that address the needs of poor people and methods of actually reaching those people. In the case of EPSD, control measures will only be successful if communities are committed to participating and members of the community actively engage themselves during planning, implementation and execution. However, it is the responsibility of the society to provide arenas and resources where those on the lowest incomes can commit themselves and contribute actively.
EPSD are more than just irritations of the skin or bearable nuisances. They have a substantial impact on the health of people living in extreme poverty. EPSD are widespread, polyparasitism is common and significant primary and secondary morbidity is obvious. The epidemiology is characterized by inequality: the disease burden is very high in impoverished communities and the very poor are disproportionately affected. Within this vulnerable group, children, women, the elderly, homeless and displaced persons bear an exceptionally high burden of disease.
Poverty influences the epidemiology of EPSD in many ways. It favours the presence of animal reservoirs, ensures ongoing transmission, facilitates atypical ways of spreading the infectious agent and increases the chances of exposure. This results in an extraordinarily high prevalence and intensity of infestation and significant morbidity of EPSD. Stigma, lack of access to health care and deficient behaviour in seeking health care are the reasons why EPSD frequently progress untreated.
Inequality and neglect seem to be the major driving forces that keep the disease burden at an intolerably high level. Health-care stakeholders and political decision-makers must acknowledge that EPSD are debilitating and merit much more attention from health professionals than hitherto given.
The ongoing uncontrolled urbanization in many developing countries makes it likely that EPSD will remain the overriding parasitic diseases for people living in extreme poverty and remain indicators of neglect by societies and particularly public health policies. ■
We thank Ingela Krantz (Skövde, Sweden) and Dirk Engels (Geneva, Switzerland).
Funding: Travel grants were made available by DAAD (Bonn, Germany) and CAPES (Brasília, Brazil) through the PROBRAL German-Brazilian Academic Exchange Programme.
Competing interests: None declared.
- Hawker J, Begg M, Blair L, Reintjes R, Weinberg J. Communicable disease control handbook. 2nd ed. Oxford: Blackwell; 2006.
- Ehrenberg JP, Ault SK. Neglected diseases of neglected populations: thinking to reshape the determinants of health in Latin America and the Caribbean. BMC Public Health 2005; 5: 119- doi: 10.1186/1471-2458-5-119 pmid: 16283932.
- Hotez P, Ottesen E, Fenwick A, Molyneux D. The neglected tropical diseases: the ancient afflictions of stigma and poverty and the prospects for their control and elimination. Adv Exp Med Biol 2006; 582: 23-33 doi: 10.1007/0-387-33026-7_3 pmid: 16802616.
- Heukelbach J, Mencke N, Feldmeier H. Cutaneous larva migrans and tungiasis: the challenge to control zoonotic ectoparasitoses associated with poverty. Trop Med Int Health 2002; 7: 907-10 doi: 10.1046/j.1365-3156.2002.00961.x pmid: 12390594.
- Heukelbach J, Walton SF, Feldmeier H. Ectoparasitic Infestations. Curr Infect Dis Rep 2005; 7: 373-80 doi: 10.1007/s11908-005-0012-2 pmid: 16107235.
- Heukelbach J, Feldmeier H. Epidemiological and clinical characteristics of hookworm-related cutaneous larva migrans. Lancet Infect Dis 2008; 8: 302-9 doi: 10.1016/S1473-3099(08)70098-7 pmid: 18471775.
- Tungiasis HJ. Rev Inst Med Trop Sao Paulo 2005; 47: 307-13 pmid: 16553319.
- Hengge UR, Currie BJ, Jager G, Lupi O, Schwartz RA. Scabies: a ubiquitous neglected skin disease. Lancet Infect Dis 2006; 6: 769-79 doi: 10.1016/S1473-3099(06)70654-5 pmid: 17123897.
- Stanton B, Khanam S, Nazrul H, Nurani S, Khair T. Scabies in urban Bangladesh. J Trop Med Hyg 1987; 90: 219-26 pmid: 3669122.
- Henderson CA. Skin disease in rural Tanzania. Int J Dermatol 1996; 35: 640-2 doi: 10.1111/j.1365-4362.1996.tb03688.x pmid: 8876290.
- Heukelbach J, Wilcke T, Winter B, Feldmeier H. Epidemiology and morbidity of scabies and pediculosis capitis in resource-poor communities in Brazil. Br J Dermatol 2005; 153: 150-6 doi: 10.1111/j.1365-2133.2005.06591.x pmid: 16029341.
- Sharma RS, Mishra RS, Pal D, Gupta JP, Dutta M, Datta KK. An epidemiological study of scabies in a rural community in India. Ann Trop Med Parasitol 1984; 78: 157-64 pmid: 6742927.
- Hegazy AA, Darwish NM, Abdel-Hamid IA, Hammad SM. Epidemiology and control of scabies in an Egyptian village. Int J Dermatol 1999; 38: 291-5 doi: 10.1046/j.1365-***************.x pmid: 10321946.
- Currie BJ, Carapetis JR. Skin infections and infestations in Aboriginal communities in northern Australia. Australas J Dermatol 2000; 41: 139-43 doi: 10.1046/j.1440-0960.2000.00417.x pmid: 10954983.
- Terry BC, Kanjah F, Sahr F, Kortequee S, Dukulay I, Gbakima AA. Sarcoptes scabiei infestation among children in a displacement camp in Sierra Leone. Public Health 2001; 115: 208-11 doi: 10.1016/S0033-3506(01)00445-0 pmid: 11429717.
- Feldmeier H. Pediculosis capitis - Die wichtigste Parasitose des Kindesalters. Kinder- und Jugendmedizin 2006;6:211-214.
- Ugbomoiko US, Ofoezie IE, Heukelbach J. Tungiasis: High prevalence, parasite load and morbidity in a rural community in Lagos State, Nigeria. Int J Dermatol 2007; 46: 475-81 doi: 10.1111/j.1365-4632.2007.03245.x pmid: 17472674.
- Heukelbach J, Gromide M, Araújo F, Pinto NSR, Santana RD, Brito JRM, et al., et al. Cutaneous larva migrans and tungiasis in international travelers exiting Brazil: an airport survey. J Travel Med 2007; 14: 374-80 doi: 10.1111/j.1708-8305.2007.00156.x pmid: 17995532.
- Heukelbach J, Wilcke T, Meier A, Saboia Moura RC, Feldmeier H. A longitudinal study on cutaneous larva migrans in an impoverished Brazilian township. Travel Med Infect Dis 2003; 1: 213-8 doi: 10.1016/j.tmaid.2003.10.003 pmid: 17291920.
- Heukelbach J, Wilcke T, Harms G, Feldmeier H. Seasonal variation of tungiasis in an endemic community. Am J Trop Med Hyg 2005; 72: 145-9 pmid: 15741550.
- Jackson A, Heukelbach J, Calheiros CM, Soares VL, Harms G, Feldmeier H. A study in a community in Brazil in which cutaneous larva migrans is endemic. Clin Infect Dis 2006; 43: e13-8 doi: 10.1086/505221 pmid: 16779735.
- Downs AM. Seasonal variation in scabies. Br J Dermatol 2004; 150: 602-3 doi: 10.1046/j.1365-2133.2004.05823.x pmid: 15030355.
- Mimouni D, Ankol OE, Gdalevich M, Grotto I, Davidovitch N, Zangvil E. Seasonality trends of Pediculosis capitis and Phthirus pubis in a young adult population: follow-up of 20 years. J Eur Acad Dermatol Venereol 2002; 16: 257-9 doi: 10.1046/j.1468-3083.2002.00457.x pmid: 12195566.
- Green MS. Epidemiology of scabies. Epidemiol Rev 1989; 11: 126-50 pmid: 2509232.
- Heukelbach J, Feldmeier H. Scabies. Lancet 2006; 367: 1767-74 doi: 10.1016/S0140-6736(06)68772-2 pmid: 16731272.
- Ugbomoiko US, Ariza L, Ofoezie IE, Heukelbach J. Risk factors for tungiasis in Nigeria: identification of targets for effective intervention. PLoS Negl Trop Dis 2007 pmid: 18160986.
- Heukelbach J, de Oliveira FA, Hesse G, Feldmeier H. Tungiasis: a neglected health problem of poor communities. Trop Med Int Health 2001; 6: 267-72 doi: 10.1046/j.1365-3156.2001.00716.x pmid: 11348517.
- Heukelbach J, Wilcke T, Feldmeier H. Cutaneous larva migrans (creeping eruption) in an urban slum in Brazil. Int J Dermatol 2004; 43: 511-5 doi: 10.1111/j.1365-4632.2004.02152.x pmid: 15230890.
- Taplin D, Porcelain SL, Meinking TL, Athey RL, Chen JA, Castillero PM, et al., et al. Community control of scabies: a model based on use of permethrin cream. Lancet 1991; 337: 1016-8 doi: 10.1016/0140-6736(91)92669-S pmid: 1673175.
- Lawrence G, Leafasia K, Sheridan J, Hills S, Wate J, Wate C, et al., et al. Control of scabies, skin sores and haematuria in children in the Solomon Islands: another role for ivermectin. Bull World Health Organ 2005; 83: 34-42 pmid: 15682247.
- Estrada B. Ectoparasitic infestations in homeless children. Semin Pediatr Infect Dis 2003; 14: 20-4 doi: 10.1053/spid.2003.127213 pmid: 12748918.
- Heukelbach J, Jackson A, Ariza L, Feldmeier H. Prevalence and risk factors of hookworm-related cutaneous larva migrans in a rural community in Brazil. Ann Trop Med Parasitol 2008; 102: 53-61 doi: 10.1179/136485908X252205 pmid: 18186978.
- Heukelbach J, Wilcke T, Winter B, Sales de Oliveira FA, Saboia Moura RC, Harms G, et al., et al. Efficacy of ivermectin in a patient population concomitantly infected with intestinal helminths and ectoparasites. Arzneimittelforschung 2004; 54: 416-21 pmid: 15344847.
- Engels D, Savioli L. Reconsidering the underestimated burden caused by neglected tropical diseases. Trends Parasitol 2006; 22: 363-6 doi: 10.1016/j.pt.2006.06.004 pmid: 16798088.
- Feldmeier H, Heukelbach J, Eisele M, Sousa AQ, Barbosa LM, Carvalho CB. Bacterial superinfection in human tungiasis. Trop Med Int Health 2002; 7: 559-64 doi: 10.1046/j.1365-3156.2002.00904.x pmid: 12100437.
- Feldmeier H, Eisele M, Saboia-Moura RC, Heukelbach J. Severe tungiasis in underprivileged communities: case series from Brazil. Emerg Infect Dis 2003; 9: 949-55 pmid: 12967492.
- Litvoc J, Leite RM, Katz G. Aspectos epidemiológicos do tétano no estado de São Paulo (Brasil). Rev Inst Med Trop Sao Paulo 1991; 33: 477-84 pmid: 1844978.
- Heukelbach J, Jackson A, Ariza L, Calheiros CM, Soares VL, Feldmeier H. Epidemiology and clinical aspects of tungiasis (sand flea infestation) in Alagoas State, Brazil. J Infect Developing Countries 2007; 1: 202-9.
- Fournier PE, Ndihokubwayo JB, Guidran J, Kelly PJ, Raoult D. Human pathogens in body and head lice. Emerg Infect Dis 2002; 8: 1515-8 pmid: 12498677.
- Houhamdi L, Lepidi H, Drancourt M, Raoult D. Experimental model to evaluate the human body louse as a vector of plague. J Infect Dis 2006; 194: 1589-96 doi: 10.1086/508995 pmid: 17083045.
- Meinking TL, Taplin D. Infestations: pediculosis. Curr Probl Dermatol 1996; 24: 157-63 pmid: 8743266.
- Jackson A, Heukelbach J, da Silva Filho AF, de Barros Campelo Jr E, Feldmeier H. Clinical features and associated morbidity of scabies in a rural community in Alagoas, Brazil. Trop Med Int Health 2007; 12: 493-502 pmid: 17445140.
- McCarthy JS, Kemp DJ, Walton SF, Currie BJ. Scabies: more than just an irritation. Postgrad Med J 2004; 80: 382-7 doi: 10.1136/pgmj.2003.014563 pmid: 15254301.
- Currie BJ, Brewster DR. Rheumatic fever in Aboriginal children. J Paediatr Child Health 2002; 38: 223-5 doi: 10.1046/j.1440-1754.2002.00850.x pmid: 12047686.
- Heukelbach J, van Haeff E, Rump B, Wilcke T, Moura RC, Feldmeier H. Parasitic skin diseases: health care-seeking in a slum in north-east Brazil. Trop Med Int Health 2003; 8: 368-73 doi: 10.1046/j.1365-3156.2003.01038.x pmid: 12667157.
- Muehlen M, Feldmeier H, Wilcke T, Winter B, Heukelbach J. Identifying risk factors for tungiasis and heavy infestation in a resource-poor community in northeast Brazil. Trans R Soc Trop Med Hyg 2006; 100: 371-80 doi: 10.1016/j.trstmh.2005.06.033 pmid: 16297946.
- Blas M, Bravo F, Castillo W, Castillo WJ, Ballona R, Navarro P, et al., et al. Norwegian scabies in Peru: the impact of human T cell lymphotropic virus type I infection. Am J Trop Med Hyg 2005; 72: 855-7 pmid: 15964976.
- Heukelbach J, Kuenzer M, Coulthard M, Speare R, Feldmeier H. Correct diagnosis of current head lice infestation made by affected individuals from a hyperendemic area. Int J Dermatol 2006; 45: 1437-8 doi: 10.1111/j.1365-4632.2006.03097.x pmid: 17184249.
- Heukelbach J, Winter B, Wilcke T, Muehlen M, Albrecht S, Oliveira FA, et al., et al. Selective mass treatment with ivermectin to control intestinal helminthiases and parasitic skin diseases in a severely affected population. Bull World Health Organ 2004; 82: 563-71 pmid: 15375445.
- Feldmeier H, Kehr JD, Heukelbach J. A plant-based repellent protects against Tunga penetrans infestation and sand flea disease. Acta Trop 2006; 99: 126-36 doi: 10.1016/j.actatropica.2006.05.013 pmid: 17010927.