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Annals of Clinical Cytology and Pathology

First Report of Autochthonous Visceral Leishmaniosis in Humans in foz Do Iguaçu, Paraná State, Southern Brazil

Case Report | Open Access

  • 1. Hospital Ministro Costa Cavalcanti
  • 2. Prefeitura do Município de Foz do Iguaçu - Centro de Controle de Zoonoses
  • 3. Acadêmico do Curso de Medicina da Universidade Federal de Santa Catarina;
  • 4. Prefeitura do Município de Foz do Iguaçu - Vigilância Epidemiológica é o que consta no site da prefeitura
  • 5. Secretaria de Saúde do Estado do Paraná
  • 6. 6 Programa de Pós-Graduação em Engenharia de Bioprocessos e Biotecnologia, Universidade Federal do Paraná, Curitiba, Paraná, Brasil
  • 7. Universidade Federal da Integração Latino Americana, Foz do Iguaçu, Paraná, Brasil UNILA
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Corresponding Authors
Vanete Thomaz Soccol, Programa de Pós-Graduação em Engenharia de Bioprocessos e Biotecnologia, Universidade Federal do Paraná, Curitiba, Paraná Brazil
Abstract

This is the first report of autochthonous visceral leishmaniosis in humans in Foz do Iguaçu city, Parana, Brazil, bordering Argentina and Paraguay. During his physical examination, a 28-year-old man from Foz do Iguaçu, showed good general health, a slightly bleached, discrete bilateral cervical lymphadenopathy, 38°C fever, confirmation of weight loss and no other symptoms About 15 days after the first visit, he presented with discrete hepatomegaly and splenomegaly palpation of the abdomen. Amyelogram, stained by May-Grunwald-Giemsa, showed normocellular bone marrow for age and presence of Leishmania amastigotes in macrophages and extracellularly. The parasite was isolated by bone marrow aspiration and cultured in Novy, Mac Neal-Nicolle medium. Serological exams by enzyme-linked immunosorbent assay and DPP were positive. Polymerase chain reaction (PCR) with primers RV1/RV2 was performed on DNA extracted from bone marrow aspirate and showed an identical pattern to the Leishmania infantum reference strain.The species of the parasite, isolated in culture, was confirmed by PCR using primers for the ITS-1 region followed by restriction fragment length polymorphism (RFLP) pattern analysis and sequencing. RFLP verified the parasite showed a very similar pattern to L. infantum and the forward and reverse sequences presented 99% identity with L. infantum. An epidemiological survey in dogs, in the house of the patient’s home and neighborhood showed 13.3% positivity. Lutzomyia longipalpis was present in the perdomestic environment of the patient’s home.

Citation

Pina Trench FJ, Ritt AG, Gewehr TA, de Souza Leandro A, Chiyo L, et al. (2016) First Report of Autochthonous Visceral Leishmaniosis in Humans in foz Do Iguaçu, Paraná State, Southern Brazil. Ann Clin Cytol Pathol 2(6): 1041.

Keywords

•    Visceral leishmaniosis
•    Human
•    Parana state
•    Southern brazil

INTRODUCTION

Visceral leishmaniosis (VL) is responsible for over 50,000 deaths per year, with an estimated average of half a million new cases annually [1]. In Brazil, VL has an effect of close to 3000 cases and approximately 200 deaths per year [2]. Over the past 20 years, there has been a transition in the epidemiological profile of VL, with an increase in the proportion of cases in the south west region and movement from rural to urban areas. In the Southern Cone, the triple borders of Argentina, Brazil and Paraguay, work has been conducted under the coordination of the Pan American Health Organization for research vectors and reservoirs of visceral leishmaniosis since 2012. In 2012 Lutzomyia longipalpis was confirmed in Foz do Iguaçu [3], and from 2012-2013, Thomaz-Soccol et al., [4] showed dog samples positive by serological tests and the parasites isolated were identified as L. infantum [5].

Here we report the first case of a patient diagnosed with visceral leishmaniosis with autochthonous transmission in Foz do Iguaçu city, Paraná State, in southern Brazil.

First Report of Vl in a man from Foz Do Iguaçu

The first report of VL in Foz do Iguaçu, Paraná, Brazil 25°32‘49“S, 54°35’18”W was a 28-year-old, brown man who worked for the military police. He attended outpatient consultation with a complaint of 30 days of daily fever of 38-39ºC and night sweats accompanied by weight loss of 3 kg. He denied travelling to any other locations in the preceding 12 months and reported that he had been tested for tuberculosis two years previously, and the results were negative after extensive research with a pulmonologist.

A physical examination showed good general health, a slightly bleached, discrete bilateral cervical lymphadenopathy, and fever of 38° C, the confirmation of weight loss, and no other signs or symptoms. An initial blood examination showed data compatible with acute infection or inflammatory disease (Table 1). The patient showed negative blood and urine cultures, an X-ray chest indicated injury, with a scar on the right apex, and an abdominal ultrasound was normal. About 15 days after the first visit, he presented discrete hepatomegaly and splenomegaly palpation of the abdomen, which were absent in the initial physical examination. The patient was referred to a hematologist to assess hematologic disease in the bone marrow. The results of samples stained by the May-Grunwald-Giemsa method and data are shown in Table (1). The myelogram showed normocellular bone marrow for the patient’s age. The myeloid series showed elements at all stages of maturation. The erythroid component presented numerous hyperplasic cells (42%) without gross changes in shape. The megakaryocytic component presented amastigotes of leishmania sp. in the macrophages and extracellularly (Table 1, Figure 1). ELISA and DPP® serology using L. infantum antigen were reactive. The parasite was isolated by bone marrow aspiration and was cultured in Novy, Mac Neal-Nicolle medium. Species identification was performed by PCR using primers RV1 and RV2 [5]. In addition, amplification of the internal transcribed spacer 1 (ITS-1) was performed, followed by RFLP, as proposed by Schönian et al. (2003) [6]. RFLP showed an identical pattern to the reference strain of L. infantum (Figure 1). The forward and reverse sequences showed 99% identity with L. infantum (MHOM/BR/74/PP75; Gene Bank access number AF103739).

The patient was treated with deoxycholate of amphotericin B at a dose of 50 mg daily for a total period of 15 days, nonsequentially. He became asymptomatic, and blood count recovery was achieved after the seventh dose of medication. He presented complications of lung disease four days after the use of amphotericin, but showed excellent clinical response with the use of trimethoprim-sulfamethoxazole. After being attended at our service for six months, he has undergone complete clinical and blood count recovery. No marrow aspiration was performed for control of cure.

Here, we report the first patient with clinical and laboratorial confirmation of VL; in the Foz do Iguaçu city, Paraná State.

Epidemiological Research in the Address of the Patient

Serological evaluation in dogs: A serological study was performed, using TR-DPP® as screening and the ELISA test for confirmation, on 165 dogs in the patient’s house and the surrounding neighborhood. Twenty-two of these samples were positive (13.3%), 142 were negative (85%) and one had an indeterminate ELISA result (1.6%). The two dogs owned by the patient had negative results. Among the positive animals, 18 were euthanatized with the owner’s consent. Four owners, who did not agree to the removal of their positive dogs, signed a term of responsibility for rejecting the euthanasia of a positive dog.

Investigating the presence of Phlebotominae: Sand flies were captured with automatic CDC light traps, used for sampling the Phlebotominae in peridomestic environments and inside the patient’s home. The traps were active from approximately 6:30 p.m. to 7:30 a.m., for three consecutive rainless nights. They were placed 1.5 m above the ground. The study was conducted from July 16th to 18th 2015. One female of Lu. longipalpis was found in the patient’s residence. Two males of the same species were captured at another residential address in the vicinity.

Using the same methodology, 12 traps were installed where the patient worked, from August 3rd o 5th 2015. In this environment, one female Lutzomyia sp. was captured.

Table 1: Results of Hematological Parameters.

First Exam Hemogram    
  Hemoglobin (g/dL ) 10.9    
  Hematocrit (%) 34.9    
  Leukopenia (cells/mcL) 2,600    
  Platelets/mcL 107,000    
  Enzymes AST and ALT (U/L of serum) 50.6 and 71.5    
  LDH -283    
  PCR 13* Shows acute disease or inflammatory syndrome
Second Exam Hemogram Myelogram  
  Hemoglobin (g/dL) -11.8 Myeloid Erythroid Megakaryocytic
  Hematocrit (%) - 36.1 4% -promyelocytes Present and numerous hyperplastic cells (42%) without gross changes 7%- lymphocytes
  RBCs (/mm³) - 4.62 16% - myelocytes   1% - monocytes
  Mean corpuscular volume - 78.1 fl 20% - metamyelocytes   4% - blasts
  WBC (/mm³) - 2,400 4% - segmented rods   2% - plasma cells
  43% neutrophils/
8% lymphocytes 
(1% eosinophils/
8% monocytes)
     
  Platelets(/mm³)- 109,000      

 

DISCUSSION

The southern regions of Brazil were not considered an important area for VL until the beginning of 2008, when a dog was diagnosed with the disease in São Borja County, in the State of Rio Grande do Sul. In the same year, Lu. longipalpis were captured and autochthonous canine cases were confirmed [7,8] followed by the first human case registered in 2009 [9]. In Santa Catarina, Steindel et al., (2013) [10] described an outbreak of autochthonous canine VL (CVL), and in 2014, Maziero et al., [11] reported dogs with serology positive for VL in São Miguel do Oeste. Neighbouring countries Paraguay and Argentina have also recorded VL in recent years [12,13]. This prompted further research and the vector Lu. longipalpis was confirmed in areas of Foz do Iguaçu near Argentina [3]. However, the real distribution of the vector, in Foz do Iguaçu city remains unknown. Autochthonous transmission of L. infantum in dogs has been verified in regions near Argentina and Paraguay [14]. Again, the real CVL distribution in Foz do Iguaçu city (is not known) has yet to be determined. These data suggest a time sequence in the establishment of the disease in a given geographic area. Thus, the stage is set for the development of the disease in humans. In anticipation of diagnosing human cases, anyone who has had a fever for over a week or who reports rapid weight loss is being including in the differential diagnosis of VL.

With this first case of human VL, it was essential to determine whether this case was autochthonous or imported, because nowadays people travel within and to different regions very quickly and easily. The serological survey showed sero reactive dogs and the presence of the vector confirmed local transmission.

From a clinical perspective, this case was a typical manifestation of visceral leishmaniosis in the initial phase. We chose to prescribe amphotericin B, using a cumulative dose for a total period of 15 non-sequential days. The increased creatinine levels and hypokalemia were controlled during hospitalization. At the end of the therapy, the patient’s splenomegaly was reduced by approximately 60%, the fever had ceased, and the pancytopenia was completely reversed.

Diagnostic tests for VL have certain limitations, for example, the serological tests can remain positive for a long time after patient treatment, thus they do not allow health professionals to evaluate the effect of the therapy and they have been known to cross-react with other diseases. Since subclinical infections occur, a positive test does not necessarily indicate active disease. Clinicians and epidemiologists always request serological tests to confirm the diagnoses, because parasitological methods are invasive. They expect the results to be reliable, with high specificity and sensitivity and as fast as possible, to enable them to treat preventable disease. However, no method provides 100% of sensitivity and the clinical features of this disease render the diagnosis difficult and complex. It is therefore important that the different specialties talk to each other and the laboratory to make decisions on patient referrals.

From now on, in Paraná state, physicians need consider a potential diagnosis of visceral leishmaniosis when a patient has fever for more than 10 days, and people traveling to Foz do Iguaçu need to know that this region is now endemic for visceral leishmaniosis.

ACKNOWLEDGEMENT

We acknowledge Prof. Philip Sidney Pacheco Badiz for English correction.

REFERENCES

1. Organización Mundial de La Salud. Control de lasleishmaniasis: informe de una reunióndel Comité de Expertos de la OMS sobre El Control e lasLeishmaniasis. Ginebra 22 a 26 de marzo de. 2010.

2. Brasil. Ministério da Saúde . Óbitos de Leishmaniose Visceral, Brasil, Grandes Regiões e Unidades Federadas (1990 a 2013). 2014.

3. Santos DR, Ferreira AC, Bisetto-Jr A. The first record of Lutzomyia longipalpis (Lutz & Neiva, 1912) (Diptera: Psychodidae: Phlebotominae) in the State of Paraná, Brazil. Rev Soc Bras Med Trop. 2012; 45: 643-645.

4. Thomaz-Soccol V. Cutaneous and Visceral leishmaniasis in the Parana state, Brazil border with Argentina and Paraguay. FIFTH WORLD CONGRESS ON LEISHMANIASIS - WORLDLEISH 5-13th to May 17th, at the Convention Center ENOTEL RESORTS, Porto de Galinhas, PE, Brazil. 2013.

5. Lachaud L, Marchergui-Hammami S, Chabbert E, Dereure J, Dedet JP, Bastien P. Comparison of six PCR methods using peripheral blood for detection of canine visceral leishmaniasis. J Clin Microbiol. 2002; 40: 210-215

6. Schönian G, Nasereddin A, Dinse N, Schweynoch C, Schallig HD, Presber W, et. al. PCR diagnosis and characterization of Leishmania in local and imported clinical samples. Diagn Microbiol Infect Dis. 2003; 47: 349-358.

7. Brasil, Ministério da Saúde. Nota técnica conjunta da Secretaria de Vigilância em Saúde do Ministério da Saúde e da Secretaria de Estado da Saúde Pública do Rio Grande do Sul sobre a situação da Leishmaniose Visceral na fronteira do Estado do Rio Grande do Sul com a Argentina. 2010.

8. Deboni SC, Barbosa M, Ramos RR 2011. Leishmaniose Visceral no Rio Grande do Sul: Vigilância Epidemiológica de casos humanos. Bol Epidemiol-Centro Estadual de Vigilância em Saúde. 2011; 13:3.

9. Souza GD, Santos E, Andrade Filho JD 2009. The first report of the main vector of visceral leishmaniasis in America, Lutzomyia longipalpis (Lutz & Neiva) (Diptera: Psychodidae: Phlebotominae), in the state of Rio Grande do Sul, Brazil. Mem Inst Oswaldo Cruz. 104: 1181-1182.

10. Steindel M, Menin A, Evangelista T, Stoco PH, Marlow MA, Fleith RC, et al. Outbreak of autochthonous canine visceral leishmaniasis in Santa Catarina, Brazil. Pesq Vet Bras. 2013; 33: 490-496.

11. Maziero N, Thomaz-Soccol V, Steindel M, Link JS, Rossini D, Alban SM, et al. Rural-urban focus of canine visceral leishmaniosis in the far western region of Santa Catarina State, Brazil. Vet Parasitol. 2014; 205: 92-95.

12. Salomon OD, Sinagra A, Nevot MC, Barberian G, Paulin P, Estevez J, et al . First visceral leishmaniasis focus in Argentina. Mem Inst Oswaldo Cruz. 2008; 103: 109-111.

13. Canese A. Leishmaniosis visceral canina em elarea metropolitana de la “Gran Asunción”, Paraguay. Medicina (Buenos Aires) 60 (Supl. III). 2000; 65.

14. Bisetto-JR A, Thomaz-Soccol V, Navarro IT. Leishmaniose Visceral no Estado do Paraná. 5ª. Revista do Conselho Regional de Medicina Veterinária do Paraná. 2014; 41: 6-7.

Received : 09 Aug 2016
Accepted : 15 Sep 2016
Published : 11 Oct 2016
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