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Trypanosoma cruzi infection associated with atypical clinical manifestation during the acute phase of the Chagas disease

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Abstract

Background

Chagas disease (CD) is caused by the protozoan parasite Trypanosoma cruzi and is transmitted by triatomine insects. Clinical manifestations vary according to the phase of the disease. Cutaneous manifestations are usually observed in the acute phase (chagoma and Romaña’s sign) or after reactivation of the chronic phase by immunosuppression; however, a disseminated infection in the acute phase without immunosuppression has not been reported for CD. Here, we report an unusual case of disseminated cutaneous infection during the acute phase of CD in a Mexican woman.

Methods

Evaluation of the patient included a complete clinical history, a physical exam, and an exhaustive evaluation by laboratory tests, including ELISA, Western blot and PCR.

Results

Skin biopsies of a 50-year-old female revealed intracellular parasites affecting the lower extremities with lymphangitic spread in both legs. The PCR tests evaluated biopsy samples obtained from the lesions and blood samples, which showed a positive diagnosis for T. cruzi. Partial sequencing of the small subunit ribosomal DNA correlated with the genetic variant DTU II; however, serological tests were negative.

Conclusions

We present a case of CD with disseminated skin lesions that was detected by PCR and showed negative serological results. In Mexico, an endemic CD area, there are no records of this type of manifestation, which demonstrates the ability of the parasite to initiate and maintain infections in atypical tissues

.

Background

CD is an anthropozoonosis caused by the protozoan parasite Trypanosoma cruzi and is transmitted by various species of blood-sucking triatomine insects (kissing bugs). Trypanosoma cruzi originates in the Americas, where it is considered a major social and public health problem [1, 2]. CD has become a concern in the developed world because of human migration; thus, physicians worldwide are familiar with this disease [3, 4], and global warming and other factors further increase vector distribution [5].

CD has three phases: acute, indeterminate and chronic. The acute phase occurs immediately following infection, and only 5% of individuals show symptoms during this phase. Symptoms during this phase can include malaise and fever, which may conclude between four and eight weeks later. Cutaneous manifestations are frequent during the acute phase and may include localized inflammation at the site of inoculation (chagoma), unilateral palpebral edema (Romaña’s sign) and a generalized morbilliform eruption (schizotrypanides). In this phase, the presence of parasites in the blood is observed, which makes diagnosis by PCR highly sensitive, whereas serological tests are not conclusive [1, 2, 6].

Individuals in the indeterminate phase are asymptomatic, and 20–40% of infected individuals will progress to the chronic phase, which is characterized by cardiovascular (heart failure, arrhythmia and thromboembolism) or digestive (megacolon and megaesophagus) complications [1,2,3,4,5,6]. Cutaneous manifestations in the chronic phase are extremely rare and have been observed only as a result of reactivation of the infection in immunocompromised individuals (HIV/AIDS) or in infected individuals undergoing immunosuppressive treatment for an organ transplant [7,8,9,10,11,12,13,14,15]. This reactivation is characterized by the presence of amastigotes in skin biopsies, fever and positive serological tests for T. cruzi infection. However, a disseminated infection has not been observed in the acute or chronic phase of the disease to date.

In this report, we present an unusual case of cutaneous disseminated CD in Mexico, highlighting that this type of parasite reaction is extremely rare.

Methods

Serological diagnosis

ELISAs and Western blots were performed to determine the presence of antibodies against T. cruzi. In both cases, the total protein extract of the Ninoa strain (MHOM/MX/1994/Ninoa) was used as the antigen. Both tests were performed as indicated by Rangel-Flores et al. [16]. Control sera that were positive and negative for T. cruzi infection were evaluated previously in a routine checkup by the blood bank at the General Hospital Dr Manuel Gea Gonzalez. For the ELISA, each sample was evaluated in triplicate, and the cut-off point (CO) was calculated according to the equation CO = m + 2.5δ, where m is the average absorbance of the negative samples and δ is the standard deviation.

DNA isolation and PCR

DNA was extracted from biopsy samples that were embedded in paraffin. Briefly, the samples were dewaxed with 100% xylol and incubated at 55 °C for 30 min and then centrifuged at 18,800×g for 5 min. The supernatant was then removed, and the samples were hydrated in 1 ml sequential steps with ethanol (100, 90, 80 and 70%) [17]. The samples were then placed in 1 ml of lysis solution (50 mM Tris-HCl; 50 mM EDTA, pH 8; 50 mM NaCl; 1% SDS and 20 μg/ml proteinase K), macerated with a homogenizer (Pro Scientific, pro200, Oxford, USA) and incubated at 55 °C overnight. The phenol-chloroform technique was used to extract DNA [18].

Universal primers designed in the laboratory were used to amplify a region of conserved sequences of small subunit ribosomal DNA (SSU rDNA) of the family Trypanosomatidae; the forward primer Trypanosomatidae18SF 5ʹ-ATC TGG TAA AGT TCC CCG TG-3ʹ and the reverse primer Trypanosomatidae18SR 5ʹ-CCG TTT CGG CTT TTG TTG GT-3ʹ were used to amplify a fragment of 830 bp. In addition, a diagnostic PCR assay using a DNA satellite of T. cruzi was performed using the primers TCZ_F (5ʹ-GCT CTT GCC CAC AMG GGT GC-3ʹ) and TCZ_R (5ʹ-CCA AGC AGC GGA TAG TTC AGG-3ʹ), which amplify a region of 188 bp; the satellite DNA PCR conditions were set according to Elias et al. [19]. To discard the presence of other related parasites, such as Leishmania, the following primers were used: LM9 (5ʹ-GGA CGA GCT CAT GGC GCC-3ʹ) and LM12 (5ʹ-CTG GCA CAC CTC CAC GTA C-3ʹ), and for the L. mexicana complex, IR1 (5ʹ-GCT GTA GGT GAA CCT GCA GCA GCT GGA TCA TT-3ʹ) and LM17 (5ʹ-CCC CTC TCC TCC TCC CC-3ʹ); the PCR conditions were performed according to Berzunza et al. [20].

PCR amplifications for small subunit ribosomal DNA (SSU rDNA) were carried out in a final volume of 25 μl, containing 10 pmol of each primer, 1× PCR buffer (8 mM Tris-HCl, pH 8; 20 mM KCl), 1.5 mM MgCl2, 0.5 mM dNTPs, and 2 U of Taq DNA Polymerase (Promega, Madison, WI, USA). Approximately 500 to 1000 ng of DNA was used as a template to amplify genomic sequences. The amplification conditions were 1 cycle at 94 °C for 5 min, 35 cycles including denaturation, annealing and extension steps at 94 °C for 30 s, 54 °C for 1 min and 72 °C for 30 s, respectively, and a final extension step at 72 °C for 7 min. The presence of amplicons was observed by electrophoresis in a 1.5% agarose gel, after which the band was purified using an AxyPrep PCR clean-up kit (Axigen Biosciences, Union City, CA, USA) and sequenced on both strands by a commercial supplier (Instituto de Biologia, Universidad Nacional Autonoma de Mexico).

Phylogenetic reconstruction and network tree

The sequences obtained in this study were subjected to a BLAST search in the GenBank database and were submitted with the number MK640442. Multiple alignments were performed using the CLUSTAL W and Muscle programs and manually adjusted with MEGA 5.05 software [21]. The best-fit model of nucleotide substitution was the Hasegawa-Kishino-Yano model with gamma distribution and invariable sites, as determined using the Akaike information criterion in Modeltest software, version 3.7 [22]. Phylogenetic reconstruction was performed using Mr Bayes 3.1.2 software [23]. The analysis was performed over 10 million generations, with trees sampled every 100 generations. Trees with scores lower than those at the stationary phase (‛burn-inʼ) were discarded. The trees that reached the stationary phase were collected and used to build consensus trees. Other sequences were collected from GenBank and used as DTU references and for population genetics analysis (Additional file 1: Table S1). Median-joining network [24] was constructed using NETWORK 4.611 (http://fluxusengineering.com) with the default settings and assumptions.

Results

A 50-year-old woman from Mexico City presented with cutaneous non-healing ulcers affecting the lower extremities, which had been treated with multiple antibiotics. The present illness initiated with erythematous subcutaneous nodules that suddenly appeared in both thighs. Over one week, the nodules increased in size and developed central necrosis, after which some of them ulcerated (Fig. 1a, b). The patient had stayed in Baja California, Mexico, where she received multiple bites from different insects a few days before the initiation of the current dermatosis.

Fig. 1
figure1

Subcutaneous nodules (a), ulcer (b), scars and subcutaneous nodules in both legs (c). d Photomicrograph of deep dermis with inflammatory infiltrate and infected cell (Giemsa staining; 400×). e Photomicrograph showing intracellular amastigote nests (Giemsa staining; 1000×). f Photomicrograph showing intracellular amastigote nests (H&E straining; 1000×). Scale-bars: d, 100 µm; e, f, 50 µm

The relevant medical background includes cholecystectomy, hysterectomy, hypothyroidism, systemic arterial hypertension and dyslipidemia treated with liothyronine/levothyroxine, olmesartan/hydrochlorothiazide and atorvastatin, respectively. A diagnosis of viral myocarditis was made the previous year after, with negative results for other parasites, including T. cruzi infection.

Physical examination revealed diffuse subcutaneous nodules with lymphangitic spread in both legs (Fig. 1c); nevertheless, the vital signs, complete blood count (CBC) and blood chemistry remained within the normal parameters.

Additionally, two skin biopsies were obtained, one from a subcutaneous nodule and the other from an ulcerated lesion. Histopathological analysis revealed an epidermis with irregular acanthosis, a deep dermis and adipose tissue with dense inflammatory infiltrate (Fig. 1d); macrophages were observed whose cytoplasm contained numerous round or ovoid microorganisms with a central nucleus and kinetoplast, which were morphologically compatible with amastigotes (Fig. 1e, f).

Considering the histopathological results and the dissemination of the cutaneous lesions, a leishmaniasis diagnosis was suggested; therefore, treatment with itraconazole together with an antimonial for local infiltration was started. Despite some initial clinical improvement, the lesions evolved to erythematous fibrous scars. Approximately 12 weeks later, a group of new disseminated lesions appeared (Fig. 1c), which resembled the original nodular lesions and displayed lymphangitic spread. At this time, bacterial, mycobacterial and fungal cultures, as well as, Leishmania evaluation by PCR tests were negative. Thus, a PCR was performed to determine the presence of Trypanosomatidae with DNA isolated from the biopsies and blood; with a positive result, and the partial SSU rDNA sequences obtained showed an identity of 99% with the T. cruzi Y30 clone (GenBank: JN942610). Bayesian phylogenetic analysis (Additional file 2: Figure S1) showed high posterior probability values (1.00) for DTU II and DTU VI; however, the network trees (Fig. 2) showed a clear association with the DTU II of T. cruzi, while satellite DNA sequences (Additional file 3: Text S1) showed a 98% (180/183) of identity to T. cruzi isolates from southern Texas (GenBank: LT220305).

Fig. 2
figure2

Haplotype network constructed with SSU ribosomal DNA sequences from different Trypanosoma cruzi DTUs sequences available on GenBank. The numbers refer to mutational changes; the sizes of circles are proportional to haplotype frequencies and the color indicates the geographical distribution; the black arrow indicates the sequences obtained in the present study (GenBank: MK640442)

A complete cardiovascular evaluation (electrocardiogram, transthoracic echocardiogram and barium swallow) was performed with normal results; thereafter, cardiovascular follow-up was recommended. The serological ELISA and WB tests were negative for the presence of antibodies against T. cruzi; the ELISA value was 0.12 of absorbance, below the CO point (0.18), and no specific antigens were detected in the WB test (data not shown).

Discussion

Here, we present a case of CD characterized by subcutaneously disseminated skin lesions that displayed lymphangitic spread in both legs; the lesions appeared two weeks after a trip to Baja California, Mexico. In this region of Mexico, the presence of six species of triatomine insects has been reported, and serological tests have indicated a high prevalence of T. cruzi infection [25, 26]. Based on the patient’s description, we hypothesized that the transmission route was vectorial and that the infection was acquired in northern Mexico; nevertheless, we do not dismiss other possible routes and areas of infection.

The clinical diagnosis was erythema nodosum, which is classified as a form of panniculitis (subcutaneous hypersensitivity reaction). Different forms of panniculitis have been reported during the reactivation of CD in the chronic phase [7,8,9,10,11,12,13,14,15], in which the presence of parasites was observed in the lesions but not in the blood. In this study, the diagnosis of T. cruzi was made in samples obtained from both blood and histopathological skin examination, with negative serological tests, so we suggest an acute infection. To the best of our knowledge, this is the first reported case of a disseminated cutaneous infection in the acute phase, at least among the cases registered in Mexico.

Due to the disseminated skin lesions, different diagnoses were considered, among them the presence of Leishmania spp. infections; however, the PCR analyses did not show specific amplifications for any Leishmania species, including the L. mexicana complex, suggesting that the disseminated skin lesions were produced exclusively by T. cruzi. Interestingly, the T. cruzi SSU rDNA sequence obtained in this work corresponds to DTU II, which is also a novel finding, considering that the genotype circulating in humans, reservoirs and vectors in Mexico is predominantly DTU I [27, 28]. The presence of DTU II has not been reported in northern Mexico, and there is only one report in southern Mexico corresponding to infections in reservoirs [29]. The satellite DNA sequences showed 98% of identity to isolates from southern Texas, which were associated with rodents, and the high identity suggests that similar genetic variants of these parasites are circulating between Mexico and the USA. This last finding agrees with the hypothesis that the patient was infected in northern Mexico.

Regarding the patient’s medication intake before infection, some reports have evaluated the relationship between the medications and T. cruzi infection. Zhao et al. [30] observed that in murine models, atorvastatin resulted in the overexpression of low-density lipoprotein (LDL) receptors, enhancing the number of parasites in tissues, inflammation and heart tissue damage, associated with high mortality rates during acute T. cruzi infection. Furthermore, Nagajyothi et al. [31] observed that LDL receptors play an important role in the internalization of the parasite. On the other hand, olmesartan decreases IL-1β and TNF-α and increases IL-10 [32], which could help the parasite establish an infection by decreasing the levels of proinflammatory cytokines [33]. Liothyronine has been associated with decreased immunoglobulins in the plasma of birds, but this effect is unknown in humans [34]. The combination of atorvastatin, liothyronine and olmesartan may have created a unique environment for T. cruzi, suggesting that perturbation of the immune system rather than immune suppression may affect the clinical presentation and infection development. Further studies should be conducted to determine the real impact of these drugs on T. cruzi infection and whether the administration of these drugs can induce a disseminated infection.

Finally, this type of report is important because characterization of this disease is difficult due to its similarity to other diseases; likewise, skin lesions caused by T. cruzi are scarcely reported in the literature, probably because the parasite is associated with tropism to other tissue types. However, these findings demonstrate the ability of the parasite to infect and maintain atypical lesions.

Conclusions

We present a case of disseminated skin lesions that were induced by T. cruzi, characterized by the presence of parasites in both the blood and lesions as detected by PCR, with negative serological diagnoses. This is the first case reported of a disseminated cutaneous infection in the acute phase without apparent immunosuppression in the patient.

Availability of data and materials

Data supporting the conclusions of this article are included within the article and its additional files. The datasets used and/or analyzed during the present study are available from the corresponding author upon request.

Abbreviations

CD:

Chagas disease

SSU rDNA:

18S small subunit ribosomal DNA

PCR:

polymerase chain reaction

DTU:

discrete typing units

DTUI:

discrete typing unit I

DTUII:

discrete typing unit II

References

  1. 1.

    Rassi A Jr, Rassi A, Marin-Neto JA. Chagas disease. Lancet. 2010;375:1388–402.

  2. 2.

    Perez-Molina JA, Molina I. Chagas disease. Lancet. 2018;391:82–94.

  3. 3.

    Castillo-Riquelme M. Chagas disease in non-endemic countries. Lancet Glob Health. 2017;5:e379–80.

  4. 4.

    Requena-Méndez A, Bussion S, Aldasoro E, Jackson Y, Angheben A, Moore D, et al. Cost-effetiveness of Chagas disease screening in Latin American migrants at primary health-care centres in Europe: a Markov model analysis. Lancet Glob Health. 2017;5:e439-37.

  5. 5.

    Villalobos G, Nava-Bolaños A, De Fuentes-Vicente JA, Téllez-Rendón JL, Huerta H, Martínez-Hernández F, et al. A reduction in ecological niche for Trypanosoma cruzi-infected triatomine bugs. Parasites Vectors. 2019;16(12):240.

  6. 6.

    WHO, Control of Chagas disease. Report of a WHO Expert Committee. Technical Report Series No. 811. Geneva: World Health Organization; 1991.

  7. 7.

    Gallerano V, Consigli J, Pereyra S, Gómez Zanni S, Danielo C, Gallerano R, Guidi A. Chagas’ disease reactivation with skin symptoms in a patient with kidney transplant. Int J Dermatol. 2007;46:607–10.

  8. 8.

    Prestes de Campos F, Mor Pansard H, Cláudio Arantes L, Teixeira Rodrigues A, Falster Daubermann M, Azambuja MF, et al. A case of Chagas’ disease panniculitis after kidney transplantation. J Bras Nefrol. 2016;38:127–31.

  9. 9.

    Riganti J, Guzzi Maqueda M, Baztan Piñero MC, Volonteri VI, Galimberti RL. Reactivation of Chagas’ disease: cutaneous manifestations in two immunosuppressed patients. Int J Dermatol. 2012;51:829–34.

  10. 10.

    Sartori AM, Sotto MN, Braz LM, da Cruz Oliveira O Jr, Patzina RA, Barone AA, Shikanai-Yasuda MA. Reactivation of Chagas disease manifested by skin lesions in a patient with AIDS. Trans R Soc Trop Med Hyg. 1999;93:631–2.

  11. 11.

    Altclas J, Sinagra A, Jaimovich G, Salgueira C, Luna C, Requejo A, et al. Reactivation of chronic Chagas’ disease following allogeneic bone marrow transplantation and successful pre-emptive therapy with benznidazole. Transpl Infect Dis. 1999;1:135–7.

  12. 12.

    La Forgia MP, Pellerano G, de las Mercedes Portaluppi M, Kien MC, Chouela EN. Cutaneous manifestation of reactivation of Chagas disease in a renal transplant patient: long-term follow-up. Arch Dermatol. 2003;139:104–5.

  13. 13.

    Tomimori-Yamashita J, Deps PD, Almeida DR, Enokihara MM, De Seixas MT, Freymüller E. Cutaneous manifestation of Chagas’ disease after heart transplantation: successful treatment with allopurinol. Br J Dermatol. 1997;137:626–30.

  14. 14.

    Hall CS, Fields K. Cutaneous presentation of Chagas’ disease reactivation in a heart-transplant patient in Utah. J Am Acad Dermatol. 2008;58:529–30.

  15. 15.

    Hemmige V, Tanowitz H, Sethi A. Trypanosoma cruzi infection: a review with emphasis on cutaneous manifestation. Int J Dermatol. 2012;51:501–8.

  16. 16.

    Rangel-Flores H, Sánchez B, Mendoza-Duarte J, Barnabe C, Breniere FS, Ramos C, Espinoza B. Serologic and parasitologic demonstration of Trypanosoma cruzi infections in an urban area of central Mexico: correlation with electrocardiographic alterations. Am J Trop Med Hyg. 2001;65:887–95.

  17. 17.

    Sepp R, Szabó I, Uda H, Sakamoto H. Rapid techniques for DNA extraction from routinely processed archival tissue for use in PCR. J Clin Pathol. 1994;47:318–23.

  18. 18.

    Sambrook J, Fritsch EF, Maniatis T. Molecular cloning: a laboratory manual. Cold Spring Harbor: Cold Spring Harbor Laboratory Press; 2001.

  19. 19.

    Elias MCQB, Vargas N, Tomazi L, Pedroso A, Zingales B, et al. Comparative analysis of genomic sequences suggests that Trypanosoma cruzi CL Brener contains two sets of non-intercalated repeats of satellite DNA that correspond to T. cruzi I and T. cruzi II types. Mol Biochem Parasitol. 2005;140:221–7.

  20. 20.

    Berzunza-Cruz M, Bricaire G, Salaiza Suazo N, Pérez-Montfort R, Becker I. PCR for identification of species causing American cutaneous leishmaniasis. Parasitol Res. 2009;104:691–9.

  21. 21.

    Tamura K, Peterson D, Peterson N, Stecher G, Nei M, Kumar S, et al. MEGA5: Molecular Evolutionary Genetics Analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol Biol Evol. 2011;28:2731–9.

  22. 22.

    Posada D, Crandall KA. Modeltest: testing the model of DNA substitution. Bioinformatics. 1998;14:817–8.

  23. 23.

    Ronquis F, Huelsenbeck JP. MrBayes 3: Bayesian phylogenetic inference under mixed models. Bioinformatics. 2003;19:1572–4.

  24. 24.

    Bandelt HJ, Forster P, Rohl A. Median-joining networks for inferring intraspecific phylogenies. Mol Biol Evol. 1999;16:37–48.

  25. 25.

    Ibarra-Cerdeña C, Sánchez-Cordero V, Townsend Peterson A, Ramsey JM. Ecology of North American triatominae. Acta Trop. 2009;110:178–86.

  26. 26.

    Velasco-Castrejón O, Valdespino JL, Tapia-Conyer R, Salvatierra B, Guzmán-Bracho C, Magos C, et al. Seroepidemiology of Chagas disease in Mexico. Salud Publica Mex. 1992;34:186–96.

  27. 27.

    Bosseno M, Barnabé C, Magallón-Gastélum E, Lozano-Kasten F, Ramsey J, et al. Predominance of Trypanosoma cruzi lineage I in Mexico. J Clin Microbiol. 2002;40:627–32.

  28. 28.

    Zingales B, Miles MA, Campbell DA, Tibayrenc M, Macedo AM, Teixeira MM, et al. The revised Trypanosoma cruzi subspecific nomenclature: rationale, epidemiological relevance and research applications. Infect Genet Evol. 2012;12:240–53.

  29. 29.

    López-Cancino SA, Tun-Ku E, De la Cruz-Felix HK, Ibarra-Cerdeña CN, Izeta-Alberdi A, Pech-May A, et al. Landscape ecology of Trypanosoma cruzi in the southern Yucatan Peninsula. Acta Trop. 2015;151:58–72.

  30. 30.

    Zhao D, Lizardo K, Cui MH, Ambadipudi K, Lora J, Jelicks L, et al. Antagonistic effect of atorvastatin on high fat diet induced survival during acute Chagas disease. Microbes Infect. 2016;18:675–86.

  31. 31.

    Nagajyothi F, Weiss LM, Zhao D, Koba W, Jelicks LA, et al. High fat diet modulates Trypanosoma cruzi infection associated myocarditis. PLoS Negl Trop Dis. 2014;8:e3118.

  32. 32.

    de Araújo RF, Jr Reinaldo MP, Brito GA, de França Cavalcanti P, Freire MA, de Medeiros CA, de Araújo AA. Olmesartan decreased levels of IL-1β and TNF-α, down-regulated MMP-2, MMP-9, COX-2, RANK/RANKL and up-regulated SOCs-1 in an intestinal mucositis model. PLoS ONE. 2014;2014(9):e114923.

  33. 33.

    González F, Villar S, D’Attilio L, Leiva R, Marquez J, Lioi S, et al. Dysregulated network of immune, endocrine and metabolic markers is associated to more severe human chronic Chagas cardiomyopathy. Neuroimmunomodulation. 2018;25:119–28.

  34. 34.

    McNabb FMA. Thyroid hormones, their activation, degradation and effects on metabolism. J Nutr. 1995;125(Suppl. 6):S1773–6.

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Author information

LLG, FMS and IHU performed the surgery and clinical following up of the patient. LLG and MEVM performed the histological analysis. NMB, GV and FMH performed the PCR, the phylogenetic analysis and serological test. LRG, MRV and AOD, contributed with relevant and critical comments. GV and FMH formulated the idea and contributed reagents and materials. All authors contributed to drafting the manuscript. All authors read and approved the final manuscript.

Correspondence to Guiehdani Villalobos or Fernando Martínez-Hernández.

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Rangel-Gamboa, L., López-García, L., Moreno-Sánchez, F. et al. Trypanosoma cruzi infection associated with atypical clinical manifestation during the acute phase of the Chagas disease. Parasites Vectors 12, 506 (2019) doi:10.1186/s13071-019-3766-3

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Keywords

  • Cutaneous disseminated infection
  • Trypanosoma cruzi
  • Acute phase of the Chagas disease

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