Skip directly to site content Skip directly to page options Skip directly to A-Z link Skip directly to A-Z link Skip directly to A-Z link
Volume 27, Number 9—September 2021
Dispatch

Disseminated Cutaneous Leishmaniasis and Alcohol Misuse, Northeast Brazil, 2015–2018

Author affiliations: Hospital São José for Infectious Diseases, Fortaleza, Brazil (A.Q. Sousa); Federal University of Ceará, Fortaleza (A.Q. Sousa, P.D.T. Sindeaux Filho, D.I.M. Cavalcante, M.S. Frutuoso, F.F. Pereira, L.P.S. Santos, J.A.N. Queiroz, M.M.L. Pompeu); S; tate University of Ceará, Fortaleza (J.W.O. Lima); Harvard University, Boston, Massachusetts, USA (J.H. Maguire); University of Virginia, Charlottesville, Virginia, USA (R.D. Pearson)

Cite This Article

Abstract

Disseminated cutaneous leishmaniasis (DCL) is an uncommon form of Leishmania braziliensis infection. It remains unknown why some people develop this clinical condition. We describe 14 DCL patients in Northeast Brazil during 2015–2018. These patients regularly drank large amounts of alcohol, possibly increasing their risk for DCL.

Leishmaniasis is a parasitic disease caused by infection with Leishmania parasites, which are transmitted by the bites of phlebotomine sand flies. Localized cutaneous leishmaniasis (LCL), disseminated cutaneous leishmaniasis (DCL), and mucosal leishmaniasis are clinical manifestations of L. braziliensis infection. DCL was initially described in the 1980s (1,2); in 2002, Turetz et al. (2) defined DCL as ≥10 cutaneous lesions (papular, nodular, acneiform, crusted, or ulcerated) on ≥2 anatomic regions of the body (i.e., the head, trunk, upper, and lower extremities). L. guyanensis, L. panamensis, and L. peruviana parasites also cause DCL in the New World, whereas L. tropica and L. major cause DCL in the Old World (3). DCL is distinct from anergic diffuse cutaneous leishmaniasis caused by L. amazonensis, L. mexicana, and L. aethiopica infections; anergic diffuse cutaneous leishmaniasis causes multiple nonulcerating, nonhealing lesions in immunocompromised persons (3).

In Ceará, a state in Northeast Brazil, only L. braziliensis has been isolated from persons who have LCL or DCL (4). We observed that many DCL patients in this region report heavy alcohol use. An excessive intake of alcohol can impair the immune response and increase susceptibility to viral and bacterial infections (5). Carvalho et al. (1) postulated that DCL patients might have a weaker cellular immune response to Leishmania spp. than LCL patients. We assessed the association of DCL with heavy alcohol consumption in a region to which L. braziliensis is endemic.

The Study

We conducted the case–control study in an outpatient clinic in the Baturité region, Ceará state, Northeast Brazil, during 2015–2018, when 358 LCL and DCL cases were diagnosed. We identified 18 DCL patients and 38 LCL patients matched by sex, age (within ±5 years), and time of diagnosis. All DCL cases fulfilled the criteria set by Turetz et al. (2). Patients with known causes of immunosuppression and pregnant or lactating women were excluded from the study. We collected data on the duration of skin lesions, number and type of lesions, mucosal involvement, underlying conditions (e.g., diabetes, hypertension, etc.) and diagnostic method (i.e., culture, smears, histopathology, or immunohistochemical [IHC] assay). Our histopathological diagnoses were based on inflammatory cell infiltrate patterns and the presence of granulomas and amastigotes. For IHC assays, we used the EnVision FLEX HRP Magenta, High pH (Dako Omnis) kit (Agilent Technologies, https://www.agilent.com) with murine hyperimmune serum from mice infected with Leishmania braziliensis. We defined parasite load as the number of intracellular and extracellular amastigotes in 15 high-powered fields (×40) using IHC assays. This work was approved by the Human Ethics Committee of the Federal University of Ceará (Fortaleza, Brazil) (protocol no. 1.552.232 e CAAE 53919816.2.0000.5054).

Figure

Lesions of patients with disseminated cutaneous leishmaniasis, Baturité region, Ceará State, Northeast Brazil, 2015–2018. Patient numbers match those given in Table 1. A) Ulcerated, acneiform, and papular lesions on the back of patient 1. B) Ulcerated lesions on the genitalia of patient 2. C–D) Crusted and crusted-horny lesions on the face of patient 3. E) Papular, crusted, and ulcerated lesions on the trunk of patient 3. F) Crusted, ulcerated, and papular lesions on the back of patient 6. G) Ulcer surrounded by zosteriform and papular lesions on the back of patient 11. H) Papular, crusted, and ulcerated lesions on the face as well as an ulcerated and crusted-horny lesion on the superior right eyelid of patient 12.

Figure. Lesions of patients with disseminated cutaneous leishmaniasis, Baturité region, Ceará State, Northeast Brazil, 2015–2018. Patient numbers match those given in [[ANCHOR###T1###Table 1###Anchor]]. A) Ulcerated, acneiform, and papular lesions...

Participants completed a standardized questionnaire (i.e., the Alcohol Use Disorder Identification Test) to estimate the amount of alcohol intake in grams per day (6). We considered ≥28 g/d to be a high level of alcohol consumption (7). Most DCL patients were men 19–77 years of age with a duration of disease ranging from 5–36 weeks at diagnosis of leishmaniasis. Each patient had 13–720 lesions on their trunk, limbs, scalp, face, eyelids, conjunctivae, lips, ears, palms, soles of the feet, or genitalia (Figure). Most (56.3%) patients had lesions in the nasal mucosa. Seventeen patients had ≥1 ulcerated lesion; in patient 5, all lesions were ulcerated (Table 1).

DCL and LCL patients were well-matched by sex and age (Table 2). DCL patients had longer durations of disease before diagnosis than LCL patients (p<0.01). All LCL lesions were ulcerated and found predominantly in exposed skin areas: lower limbs (50%), upper limbs (25%), head (10%), and trunk (5%). In total, 36 (92%) LCL patients had 1–2 lesions; the other 3 (8%) patients had 3, 5, and 6 lesions. We observed nasal mucosa involvement in only 1 LCL patient.

In total, 14 (78%) DCL patients drank alcohol in the form of cachaça, a popular beverage made by distilling fermented sugar cane juice (8). Cachaça has an alcohol content of 40%, similar to that of other distilled spirits such as whiskey, tequila, and vodka. One liter of cachaça or whiskey contains 400 g of pure alcohol. For the 14 patients who drank cachaça, alcohol intake ranged from 45–800 g/d. Twelve (67%) DCL patients drank >350 mL of cachaça (140 g of alcohol) daily. The other 4 (22%) DCL patients did not drink alcohol, including 3 patients who had diabetes. LCL patients had a significantly lower alcohol intake than DCL patients (p<0.01). In total, 25 (64%) LCL patients did not drink alcohol. Fourteen (36%) LCL patients reported alcohol consumption, including 4 who had alcohol intakes >28 g/d, 3 who had intakes of 28–50 g/d, and 1 who had an intake of 400 g/d. In addition, 3 LCL patients had diabetes. We found an association between alcohol intake and parasite load (Spearman ρ = 0.482; p = 0.03).

Conclusions

The clinical manifestations of DCL in these patients did not differ substantially from those reported previously (2,9). However, we observed 1 patient who had only ulcerated lesions and another with crusted-horny lesions, both uncommon forms of this rare disease (Figure). The duration of skin lesions before diagnosis was longer in persons with DCL than LCL, similar to the observations of Turetz et al. (2). Most DCL lesions were identified by histopathological assays. Our results suggest that DCL is associated with alcohol misuse.

Alcohol causes dysregulation of the innate and adaptive immune responses (10). Persons who misuse alcohol have decreased tissue recruitment of neutrophils during bacterial infections and substantial defects in neutrophil function. In addition, these persons have dendritic cells that are fewer in number and have impaired differentiation and function (11), possibly causing an imbalance toward a Th2 profile (12,13). Persons who misuse alcohol produce macrophages with decreased phagocytic and microbicidal activity as well as reduced adherence to other cells in the lesion, which increases their migration to the circulatory system (5,13). These immune anomalies could explain the correlation between alcohol misuse and parasite load in DCL patients. Vitamin and micronutrient deficiencies are also common in persons who misuse alcohol (14) and might also contribute to risk for DCL.

Other risk factors might also contribute to the pathogenesis of DCL. For example, younger age and male sex are associated with DCL (2); we controlled for these variables in our analysis. Different strains of L. braziliensis might also account for the differential manifestations of LCL and DCL. Cardoso et al. (15) showed that neutrophils from healthy persons had decreased microbicidal activity when infected with parasites from DCL patients compared with LCL patients.

In summary, we found an association between DCL and heavy alcohol use. Excessive alcohol intake impairs the human immune system. We postulate that alcohol misuse is a risk factor for DCL in persons infected with L. braziliensis. Additional studies are needed to determine whether this association is causal, and if so, to elucidate the mechanism(s) of immune dysregulation responsible for development of DCL in persons infected with L. braziliensis. Health officials should consider campaigns focused on preventing sand fly bites in persons who misuse alcohol.

Dr. Sousa is head of the department of Clinical Medicine at the Federal University of Ceará in Fortaleza, Brazil. His primary research interests are leishmaniasis and other emerging infectious diseases in Northeast Brazil.

Top

References

  1. Carvalho  EM, Barral  A, Costa  JM, Bittencourt  A, Marsden  P. Clinical and immunopathological aspects of disseminated cutaneous leishmaniasis. Acta Trop. 1994;56:31525. DOIPubMedGoogle Scholar
  2. Turetz  ML, Machado  PR, Ko  AI, Alves  F, Bittencourt  A, Almeida  RP, et al. Disseminated leishmaniasis: a new and emerging form of leishmaniasis observed in northeastern Brazil. J Infect Dis. 2002;186:182934. DOIPubMedGoogle Scholar
  3. Hashiguchi  Y, Gomez  EL, Kato  H, Martini  LR, Velez  LN, Uezato  H. Diffuse and disseminated cutaneous leishmaniasis: clinical cases experienced in Ecuador and a brief review. Trop Med Health. 2016;44:2. DOIPubMedGoogle Scholar
  4. Sousa  AQ, Parise  ME, Pompeu  MML, Coelho Filho  JM, Vasconcelos  IAB, Lima  JWO, et al. Bubonic leishmaniasis: a common manifestation of Leishmania (Viannia) braziliensis infection in Ceara, Brazil. Am J Trop Med Hyg. 1995;53:3805. DOIPubMedGoogle Scholar
  5. Szabo  G, Saha  B. Alcohol’s effect on host defense. Alcohol Res. 2015;37:15970.PubMedGoogle Scholar
  6. World Health Organization. AUDIT: The Alcohol Use Disorders Identification Test: guidelines for use in primary health care. 2001 [cited 2021 Mar 25]. https://apps.who.int/iris/handle/10665/67205
  7. US Centers for Diseases Control and Prevention. Alcohol use and your health. 2021. [cited 2021 Mar 25]. https://www.cdc.gov/alcohol/fact-sheets/alcohol-use.htm
  8. Alcarde  AR, Souza  PA, Belluco  AES. Chemical profile of sugarcane spirits produced by double distillation methodologies in rectifying still. Food Sci Technol (Campinas). 2011;31:35560. DOIGoogle Scholar
  9. Machado  PR, Rosa  MEA, Costa  D, Mignac  M, Silva  JS, Schriefer  A, et al. Reappraisal of the immunopathogenesis of disseminated leishmaniasis: in situ and systemic immune response. Trans R Soc Trop Med Hyg. 2011;105:43844. DOIPubMedGoogle Scholar
  10. Pasala  S, Barr  T, Messaoudi  I. Impact of alcohol abuse on the adaptive immune system. Alcohol Res. 2015;37:18597.PubMedGoogle Scholar
  11. Parlet  CP, Waldschmidt  TJ, Schlueter  AJ. Chronic ethanol feeding induces subset loss and hyporesponsiveness in skin T cells. Alcohol Clin Exp Res. 2014;38:135664. DOIPubMedGoogle Scholar
  12. Franchi  S, Sacerdote  P, Moretti  S, Gerra  G, Leccese  V, Tallone  MV, et al. The effects of alcoholism pharmacotherapy on immune responses in alcohol-dependent patients. Int J Immunopathol Pharmacol. 2010;23:84755. DOIPubMedGoogle Scholar
  13. Molina  PE, Happel  KI, Zhang  P, Kolls  JK, Nelson  S. Focus on: Alcohol and the immune system. Alcohol Res Health. 2010;33:97108.PubMedGoogle Scholar
  14. Fuchs  J. Alcoholism, malnutrition, vitamin deficiencies, and the skin. Clin Dermatol. 1999;17:45761. DOIPubMedGoogle Scholar
  15. Cardoso  T, Bezerra  C, Medina  LS, Ramasawmy  R, Scheriefer  A, Bacellar  O, et al. Leishmania braziliensis isolated from disseminated leishmaniasis patients downmodulate neutrophil function. Parasite Immunol. 2019;41:e12620. DOIPubMedGoogle Scholar

Top

Figure
Tables

Top

Cite This Article

DOI: 10.3201/eid2709.203714

Original Publication Date: August 08, 2021

Table of Contents – Volume 27, Number 9—September 2021

EID Search Options
presentation_01 Advanced Article Search – Search articles by author and/or keyword.
presentation_01 Articles by Country Search – Search articles by the topic country.
presentation_01 Article Type Search – Search articles by article type and issue.

Top

Comments

Please use the form below to submit correspondence to the authors or contact them at the following address:

Anastácio Q. Sousa, Department of Clinical Medicine, School of Medicine, Federal University of Ceará. Rua Prof. Costa Mendes, 1608–4o. andar–Rodolfo Teófilo, CEP 60.430-140, Fortaleza, Ceará, Brazil

Send To

10000 character(s) remaining.

Top

Page created: June 28, 2021
Page updated: August 18, 2021
Page reviewed: August 18, 2021
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
file_external