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Article

Clinical and Epidemiological Characteristics of Sporotrichosis in a Reference Center of Uruguay

1
Cathedra of Infectious Diseases, Faculty of Medicine, University of the Republic, Montevideo 11300, Uruguay
2
Mycology Laboratory, Department of Parasitology and Mycology, Institute of Hygiene, Faculty of Medicine, University of the Republic, Montevideo 11300, Uruguay
3
Department of Clinical Laboratory, Faculty of Medicine, University of the Republic, Montevideo 11300, Uruguay
*
Author to whom correspondence should be addressed.
J. Fungi 2022, 8(3), 322; https://doi.org/10.3390/jof8030322
Submission received: 20 February 2022 / Revised: 10 March 2022 / Accepted: 14 March 2022 / Published: 21 March 2022
(This article belongs to the Special Issue Fungal Infections of Implantation (Subcutaneous Mycoses))

Abstract

:
Background: Sporotrichosis is a fungal implantation disease of subacute/ chronic course caused by species of the dimorphic fungus Sporothrix spp. This infection usually develops after traumatic inoculation of contaminated soil, plants or organic material contaminated by Sporothrix spp. conidia into skin or mucosa. The objective of this work is to contribute to the knowledge of sporotrichosis in Uruguay by providing a report of a series of cases diagnosed in a reference center. Methods: We conducted a retrospective, observational, descriptive and cross-sectional study of cases of sporotrichosis diagnosed in the last 38 years. Results: In the period analyzed, 157 cases of sporotrichosis were diagnosed, 152 of those corresponded to male patients. The most frequent clinical presentation was nodular lymphatic in 120 patients. In relation to epidemiological antecedents, 128 patients had been scratched by armadillos during hunting. Conclusions: Sporotrichosis in Uruguay is a sporadic disease with a clear seasonal pattern related to particular social practices, such as hunting armadillos. Related to this practice, the affectation is greater in males and in young adults.

1. Introduction

Sporotrichosis is a fungal implantation disease of subacute/ chronic course caused by species of the dimorphic fungus Sporothrix schenckii complex [1,2,3,4]. This disease has a worldwide distribution with high incidence in Latin America, India, Japan, China and South Africa [5,6]. It is a cosmopolitan disease and particularly endemic in temperate zones with humid climates [7,8]. It is considered the most frequent subcutaneous mycosis in Latin America [9,10].
It is characterized by nodular lesions in the skin and in the subcutaneous tissue that subsequently ulcerates, mainly affecting the lymphocutaneous system, but rarely affecting other organs [1,11,12,13,14,15]. This infection usually develops after the traumatic inoculation of contaminated soil, plants, and organic material contaminated by Sporothrix spp. conidia into skin or mucosa [11,12,13,14,15,16]. Infection with this fungus is related to areas of the body exposed to trauma [17,18]. Historically, sporotrichosis was known as the “gardener’s mycosis”, classically associated with soil manipulation activities, whether due to occupational or leisure reasons [9,19,20].
Although Sapronotic transmission was historically the most common source of human sporotrichosis, zoonotic infections have become increasingly common [21]. In Uruguay, the transmission was reported to be related to armadillo hunting and more recently in Brazil and Argentina related to cats [9,22,23,24]. Species of the Sporothrix schenckii complex are highly successful mammal pathogens, including S. brasiliensis, S. schenckii sensu stricto, S. globosa, and S. luriei, agents of human and animal sporotrichosis [16]. Particularly, S. brasiliensis is reported as an emerging fungal pathogen with cat-to-human (zoonotic) and cat-to-cat/dog transmission (enzootic) and epidemic and epizootic potential [21,24]. Sporotrichosis is an emergent disease and, over the past two decades, the incidence of zoonotic sporotrichosis has risen, particularly in Brazil [16]. Scratches and bites or contact with the exudate of cutaneous lesions of infected cats transmits sporotrichosis, in the great majority of the cases by S. brasiliensis [2,3,24,25,26].
Some authors hypothesized that the cats’ infection may occur via an inhalation route, as cats have nasal mucosal lesions and the Sporothrix spp. were isolated from nasal cavity and lungs. However, healthy cats have a minor role in sporotrichosis transmission because it is believed that it is related to a low charge of spores of Sporothrix spp. in the oral cavity and claws of healthy cats [24,25,26,27,28,29].
The epidemiological profile is mainly characterized by children, elderly, and women, because these groups usually have direct and more frequent contact with these animals [9,30].
Recently, genetic sequencing studies confirmed that S. schenckii is a complex composed of cryptic species: S. albicans, S. brasiliensis, S. globosa, S. luriei, S. mexicana, and S. schenckii [17,31,32,33]. S. brasiliensis and S. schenckii are common in Brazil, S. mexicana is present in Mexico, and S. globosa is common in countries such as China, India, Japan, the USA, Spain and Italy [17,34]. Interestingly, it arises that the crypticas species have a different pathogenic potential and S. schenckii causes a benign chronic subcutaneous mycosis, S. brasiliensis is highly virulent, and S. globosa causes mainly fixed cutaneous lesions [5,35,36]. The aim of this work is to contribute to the knowledge of sporotrichosis in Uruguay by reporting of a series of cases diagnosed in a reference center.

2. Materials and Methods

We conducted a retrospective, observational, descriptive and cross-sectional study of cases of sporotrichosis diagnosed in the last 38 years (1 January 1983 to 31 December 2020), using a database of patients diagnosed in this period in the outpatient clinics of parasitic and fungal diseases of the Department of Parasitology and Mycology of the Faculty of Medicine, University of the Republic—Uruguay.
This outpatient clinic is a mycology and parasitology reference center for the public and private sub sectors of the health system, with mostly patients of the public subsector assisted here.
We highlight that the population included in this work were referred from specialist doctors and generalist doctors from different assistant centers. For this reason, the cases remitted here have a more complex diagnosis and/or in the referring center and parasitology and mycology specialists are not included. Thus, the data do not show a reflection of sporotrichosis in the general population.
This review was constructed from the records of the outpatient assistance of the parasitology and mycology and the cases were enrolled in a SPSS 22 database. The clinical and analytical data are associated with the collection of direct exams and cultures with an autogenerated number.
The diagnosis was made by direct study of the secretion of the ulcerated lesions on fresh material, by making appositional smears for Gram staining, and confirmed by culture in Sabouraud media at 28 °C of the samples obtained from the ulcerated lesions. Genus identification was performed by visualizing the micromorphology of the colonies.
All patients with a diagnosis of sporotrichosis, confirmed with cultures in Sabouraud agar medium at 28 °C, were included in this study.
In reference to the clinical data we collected, we recorded age, biological sex, epidemiological history, origin and area of residence, occupation, month of the year in which the diagnosis was made, clinical manifestations, immune status, biological sample from which the diagnosis, findings on direct mycological examination and antimicrobial treatments received.

Ethical Aspects

This case report, including the collection and evaluation of the patient’s protected medical information, was conducted in accordance to the Personal Data Protection Law N 18331 of Uruguay of 2008 and adhered to the ethical principles of the Medical World Association for medical research involving human subjects described in the Declaration of Helsinki as amended in 2013. The ethical review and approval of this study was waived because the clinical records did not present patronymic data associated with the historical database, and the patients could not be identified. We believe this report will benefit the diagnosis and management of future patients with sporotrichosis.

3. Results

In the period analyzed, 157 cases of sporotrichosis were diagnosed, 152 (97.0%) of which corresponded to male patients and only four of which (2.5%) corresponded to female patients (Table 1).
The age range was between 13 and 79 years old, with a media of 30.8 ± 12.3 years and 54.1% of the patients were between 13 and 49 years old (Figure 1).
Regarding the occupation of the patients, 63 patients had jobs not related to possible exposure to sporotrichosis (merchants, salesmen, employees, administrative), 24 patients were rural workers, six patients were gardeners, four constructors; 15 of them were high school students, seven were retired, three were military officers and occupational data is not available in 35 cases (Table 1).
In relation to the place of acquisition of sporotrichosis, the majority (n = 132, 84.1%) of the patients acquired it in the provinces, linked to rural areas. The distribution of the majority of sporotrichosis cases is concentrated in the south central region of Uruguay. The province with the highest number of cases was Durazno, with 34 cases. The following provinces in frequency were Lavalleja and Florida with 18 cases each. In the provinces of Treinta y Tres, we registered 13 cases, in Tacuarembó 10 cases, in Cerro Largo and Canelones nine cases each, five cases in Montevideo, four cases in Rocha, in Paysandú and Flores three cases were registered each, in Rio Negro and Colonia two cases were recorded for each and in the departments of Rivera, Artigas, Maldonado and Soriano one case was recorded in each province. In 20 cases, data on the place of acquisition of the sporotrichosis was not obtained. (Table 1, Figure 2).
According to the location of the entrance door, 115 patients with lesions to the upper limbs (73.2%), 16 patients to the lower limbs (10.2%) and six cases (3.8%) in other locations (neck, chest and abdomen). In 20 cases (12.7%), the anatomical site of the lesion was not recorded in the registry (Table 2).
In relation to epidemiological antecedents, 128 patients (81.5%) had scratches from armadillos obtained during hunting, while in 11 cases (7.0%) injuries from plants were reported or a different cause was identified. A total of 18 cases (11.5%) did not have a traumatic antecedent or the patient did not know how to describe it (Figure 3).
Although cases are reported throughout the year, there are concentrations of them between April and September, with 114 cases being found in this period (72.6%) (Figure 4).
The most frequent clinical presentation was nodular lymphatic in 120 patients (76.4%), fixed forms were in 30 cases (19.1%) and it was not recorded in seven cases (4.5%) (Table 2).
In a direct mycology study, asteroid bodies were found in 82 patients (52.3%), while in the other 75 patients they were not (47.7%) (Table 2). We highlight that all samples with asteroid bodies in the direct mycology study developed colonies compatible with Sporothrix spp.
At the moment of outpatient assistance, 32 patients (20.4%) received treatment with antibiotics, 17 (10.8%) with antifungals and one patient with both. The antibiotics were trimethoprim sulfamethoxazole in 12 cases and cephradine in 20 cases. All the patients treated with antifungals received itraconazole. The patient with both treatments received cephradine and itraconazole.

4. Discussion

Although the cases presented here were distributed across all age groups, there is a clear predominance among male young adults. In fact, this characteristic of the population is related to the mechanism of acquisition particularly in Uruguay by armadillo hunting [22,23,24]. In other countries, they are more often related to agriculture and floriculture tasks, and therefore predominate in women and children [25,27,30]. Since the late 1990s, sporotrichosis in Rio de Janeiro, Brazil, has become an urban endemic phenomenon, and the epidemic is linked to transmission from infected cats to humans. The high prevalence of cases from the metropolitan area of Rio de Janeiro has created a sporotrichosis belt. The majority are female patients and from poor socioeconomic backgrounds who acquire the disease through domiciliary or professional contact (bite or scratch) with cats infected with sporotrichosis [5,32,36,37].
In most of our patients, sporotrichosis was linked to scratches by armadillos, another less frequent mechanism are scratches by vegetable thorns and contaminated wood splinters. In Uruguay, the acquisition is strongly linked to armadillo hunting, in fact, this epidemiological antecedent was reported historically in our country [22]. However, it cannot be classified as a zoonotic transmission as it occurs in cat–human transmission, since armadillos do not present sporotrichosis. Thus, inoculation occurs through scratches in the manipulation of the armadillos, since the spores of Sporothrix spp. are found in their caves. Secondary to this practice, the affectation is greater in males and an average age of young adults. In this way, the anatomical involvement is greater at the level of the upper limbs than the involvement of other locations to a lesser extent.
The most frequent clinical presentation was the lymphangitic-nodular cutaneous form in the upper limbs that appears at an average of 3 months before the microbiological diagnosis. This determines that the patients presented the characteristic clinic with multiple nodules in different evolutionary stages. Fixed forms have been seen in a small number of cases, which requires more time to diagnose.
In Uruguay, the distribution of cases presents a clear predominance in the austral autumn and winter months; linked to the high frequency of armadillo hunting in March and April connected to autumn holidays.
After inoculation, the coldest months of the year arrive, which favors a progression of the disease. The etiological diagnosis is generally late, between 1 to 3 months after the onset of symptoms.
We highlight the importance of the visualization of asteroid bodies in mycological direct study, as this permits shorter times to diagnose with respect to the culture, within just a few minutes after taking of samples [38,39,40]. The observation of microscopic asteroid bodies allows for the prescription of specific treatment in the initial consultation. At the time of microbiological diagnosis, direct visualization of asteroid bodies depends on the quality of the image and the expertise of the team that performs the diagnosis; our center had a good performance in this case. In the present series, asteroid bodies were observed in 52,3% of the cases, less than those reported by other authors, which could be linked to the number of plates studied [39]. A sensitivity of the order of 90% was reported in the context of research work with the study of five live slides; this can hardly be performed in clinical diagnostic laboratories due to the high demand for time that it requires [38,40].
The diagnostic confirmation via the development of colonies compatible with Sporothrix spp. in the cultures in cases of clinical suspicion, epidemiological background and positive direct microscopy was consistent with what was expected. However, the confirmation of microbiological diagnosis is always late.
A small percentage of patients were initially treated with antibiotics, which reinforces the concept of the need for broad knowledge of the epidemiology and clinical presentation of sporotrichosis, in order to establish a correct diagnosis and treatment and avoid incorrect exposure to antimicrobials. Until 1986, the indicated treatment was potassium iodide and thermotherapy [41], in the following years itraconazole-based therapy was introduced at a dose of 200 to 400 mg/day from 4 to 6 months depending on the clinical presentation [42,43], in all cases associated with the application of local thermotherapy [41,42]. All patients who received itraconazole responded favorably to treatment at a dose of 200 mg every 12 h for up to 15 days after a resolution of the lesions.

5. Conclusions

Sporotrichosis in Uruguay is a sporadic disease with a clear seasonal pattern related to a particular social practice such as hunting armadillos. The epidemiological variation in relation to gender and transmission mechanism opens the possibility in our country of the beginning of other epidemiological mechanisms already described in other countries of the region that have not appeared so far. Regarding the late clinical forms of presentation, the importance of the diagnostic approach with direct mycological study and the confirmation of microbiological diagnosis, which is always late, we strongly recommend consultation with an infectious diseases specialist in a patient with clinical suspected sporotrichosis, with or without an epidemiological history.

Author Contributions

Conceptualization, E.C. and P.P.; methodology, E.C. and P.P.; software, E.C., A.A. and L.D.; validation, P.P., M.C. and Z.A.; formal analysis, E.C., A.A. and L.D.; investigation, E.C., P.P.; resources, P.P., M.C. and Z.A.; data curation, Z.A., M.C. and P.P.; writing—original draft preparation, E.C. and P.P.; writing—review and editing, E.C. and P.P.; visualization, E.C., A.A., L.D., M.C., Z.A. and P.P.; supervision, P.P., M.C. and Z.A. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study was carried out in accordance with the Declaration of Helsinki and the ethical review and approval for this study was waived because the clinical records did not present patronymic data associated with the historical database, and the patients could not be identified.

Informed Consent Statement

The ethical review and approval of this study was waived because the clinical records did not present patronymic data associated with the historical database, and the patients could not be identified.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Rippon, J.W. Tratado de Micología Médica; Mc Graw-Hill: Interamericana, Mexico, 1990. [Google Scholar]
  2. De Oliveira, L.C.; Almeida-Paes, R.; Pizzini, C.V.; Gutierrez-Galhardo, M.C.; Freitas, D.F.S.; Zancopé-Oliveira, R.M. Diagnostic performance of mycologic and serologic methods in a cohort of patients with suspected sporotrichosis. Revista Iberoamericana de Micología 2019, 36, 61–65. [Google Scholar] [CrossRef] [PubMed]
  3. Marimon, R.; Cano, J.; Gené, J.; Sutton, D.A.; Kawasaki, M.; Guarro, J. Sporothrix brasiliensis, S. globosa, and S. mexicana, three new Sporothrix species of clinical interest. J. Clin. Microbiol. 2007, 45, 3198–3206. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Marimon, R.; Gené, J.; Cano-Lira, J.F.; Guarro, J. Sporothrix luriei: A rare fungus from clinical origin. Med. Mycol. 2008, 46, 621–625. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  5. Chakrabarti, A.; Bonifaz, A.; Gutierrez-Galhardo, M.C.; Mochizuki, T.; Li, S. Global epidemiology of sporotrichosis. Med. Mycol. 2015, 53, 3–14. [Google Scholar] [CrossRef] [Green Version]
  6. Gutierrez-Galhardo, M.C.; Freitas, D.F.S.; Valle, A.C.F.D.; Almeida-Paes, R.; Oliveira, M.M.E.; Zancopé-Oliveira, R.M. Epidemiological Aspects of Sporotrichosis Epidemic in Brazil. Curr. Fungal Infect. Rep. 2015, 9, 238–245. [Google Scholar] [CrossRef]
  7. Sharma, R.; Mahajan, V.K.; Chauhan, P.S.; Mehta, K.S.; Sharma, A.; Sharma, J. The clinico-epidemiological characteristics and therapeutic experience of 152 patients with cutaneous sporotrichosis: A 10-year retrospective study from India. Int. J. Dermatol. 2020, 60, 99–106. [Google Scholar] [CrossRef]
  8. MacKinnon, E.J.; Conti-Díaz, A.I.; Gezuele, E.; Civila, E.; Da Luz, S. Isolation of Sporothrix schenckii from nature and considerations on its pathogenicity and ecology. Sabouraudia 1969, 7, 38–45. [Google Scholar] [CrossRef]
  9. Orofino, R.; Macedo, P.; Rodrigues, A.; Bernandes-Engemann, A.R. Sporotrichosis: An update on epidemiology, etiopathogenesis, laboratory and clinical therapeutics. An. Bras. Dermatol. 2017, 92, 606–620. [Google Scholar] [CrossRef]
  10. Conti-Diaz, I. Epidemiology of sporotrichosis in Latin America. Mycopathologia 1989, 108, 113–116. [Google Scholar] [CrossRef]
  11. Toriello, C.; Brunner-Mendoza, C.; Ruiz-Baca, E.; Duarte-Escalante, E.; Pérez-Mejía, A.; Reyes-Montes, M.D.R. Sporotrichosis in Mexico. Braz. J. Microbiol. 2021, 52, 49–62. [Google Scholar] [CrossRef]
  12. López, E.; Reyes, M.; Pérez, A.; Ruiz-Baca, E.; Villagómez-Castro, J.C.; Mora-Montes, H.M.; Flores-Carreón, A.; Toriello, C. Sporothrix schenckii complex and sporotrichosis, an emerging health problem. Future Microbiol. 2011, 6, 85–102. [Google Scholar] [CrossRef] [PubMed]
  13. Rodrigues, A.M.; Bagagli, E.; de Camargo, Z.P.; Bosco, S.D.M.G. Sporothrix schenckii sensu stricto Isolated from Soil in an Armadillo’s Burrow. Mycopathologia 2014, 177, 199–206. [Google Scholar] [CrossRef] [PubMed]
  14. Rodrigues, A.M.; De Hoog, G.S.; de Carmargo, Z.P. Sporothrix Species Causing Outbreaks in Animals and Humans Driven by Animal–Animal Transmission. PLOS Pathog. 2016, 12, e1005638. [Google Scholar] [CrossRef] [PubMed]
  15. Conti-Díaz, I. Esporotricosis, Micetomas, Cromomicosis. In Micosis que Afectan Piel y Mucosas; Torres-Rodriguez, J.M., Ed.; Doyma: Barcelona, Spain, 1987; pp. 74–91. [Google Scholar]
  16. Gremião, I.D.F.; Miranda, L.H.M.; Reis, E.G.; Rodrigues, A.M.; Pereira, S.A. Zoonotic Epidemic of Sporotrichosis: Cat to Human Transmission. PLoS Pathog. 2017, 13, e1006077. [Google Scholar] [CrossRef]
  17. Grisolia, J.C.; Santos, L.A.; Coelho, L.M.L.; Silva, R.R.; de Camargo, Z.P.; Velloso, T.R.G.; Coelho, L.F.; Chavasco, J.K.; Malaquias, L.C.C. Seroepidemiological survey on sporotrichosis-infection in rural areas of the south of Minas Gerais State, Brazil. Braz. J. Microbiol. 2020, 52, 41–47. [Google Scholar] [CrossRef]
  18. Lopes, L.; Schubach, A.; Costa, R. Sporothrix schenckii. An. Acad. Bras. Cienc. 2006, 78, 293–308. [Google Scholar] [CrossRef] [Green Version]
  19. CDC. Epidemiologic notes and reports multistate outbreak of sporotrichosis in seedling handlers. MMWR 1988, 37, 652–653. [Google Scholar]
  20. Dooley, D.; Bostic, P.; Beckius, M. Spook house sporotrichosis: A point-source outbreak of sporotrichosis associated with hay bale props in a Halloween haunted-house. Arch. Int. Med. 1997, 157, 1885–1887. [Google Scholar] [CrossRef]
  21. Rossow, J.A.; Queiroz-Telles, F.; Caceres, D.H.; Beer, K.D.; Jackson, B.R.; Pereira, J.G.; Ferreira Gremião, I.D.; Pereira, S.A. A One Health Approach to Combatting Sporothrix brasiliensis: Narrative Review of an Emerging Zoonotic Fungal Pathogen in South America. J. Fungi 2020, 6, 247. [Google Scholar] [CrossRef]
  22. Conti-Diaz, I.A. Sporotrichosis in Uruguay: Epidemiologic and Clinical Aspects; Pan American Health Organization Scientific Publication: Washington, DC, USA, 1980; pp. 312–321. [Google Scholar]
  23. Conti-Díaz, I. Esporotricosis. Rev. Méd. Uruguay 1987, 3, 135–147. [Google Scholar]
  24. Alves, S.H.; Boettcher, C.S.; de Oliveira, D.C.; Tronco-Alves, G.R.; Sgaria, M.A.; Thadeu, P.; Oliveira, L.T.; Santurio, J.M. Sporothrix schenckii associated with armadillo hunting in Southern Brazil: Epidemiological and antifungal susceptibility profiles. Rev. Soc. Bras. Med. Trop. 2010, 43, 523–525. [Google Scholar] [CrossRef] [Green Version]
  25. Rodrigues, A.; De Melo, M.; De Hoog, S.; Schubach, T.M.P.; Pereira, S.A.; Fernandes, G.F.; Bezerra, L.M.L.; Felipe, M.S.; de Camarago, Z.P. Phylogenetic analysis reveals a high prevalence of Sporothrix brasiliensis in feline sporotrichosis outbreaks. PLoS Negl. Trop. Dis. 2013, 7, e2281. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. Zhang, Y.; Hagen, F.; Stielow, B.; Rodrigues, A.M.; Samerpitak, K.; Zhou, X.; Feng, P.; Yang, L.; Chen, M.; Deng, S.; et al. Phylogeography and evolutionary patterns in Sporothrix spanning more than 14 000 human and animal case reports. Pers. Mol. Phylogeny Evol. Fungi 2015, 35, 1–20. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  27. Gremião, I.; Martins, E.; Montenegro, H.; Carneiro, A.J.B.; Xavier, M.O.; de Farias, M.R.; Monti, F.; Mansho, W.; Pereira, R.H.d.M.A.; Pereira, S.A.; et al. Guideline for the management of feline sporotrichosis caused by Sporothrix brasiliensis and literature revision. Braz. J. Microbiol. 2021, 52, 107–124. [Google Scholar] [CrossRef] [PubMed]
  28. Leme, L.R.P.; Schubach, T.M.P.; Santos, I.B.; Figueiredo, F.B.; Pereira, S.A.; Reis, R.S.; Mello, M.F.V.; Ferreira, A.M.R.; Quintella, L.P.; Schubach, A.O. Mycological evaluation of bronchoalveolar lavage in cats with respiratory signs from Rio de Janeiro, Brazil. Mycoses 2007, 50, 210–214. [Google Scholar] [CrossRef]
  29. De Miranda, L.H.; Silva, J.N.; Gremião, I.D.; Menezes, R.C.; Almeida-Paes, R.; Dos Reis, É.G.; De Oliveira, R.D.; De Araujo, D.S.; Ferreiro, L.; Pereira, S.A. Monitoring fungal burden and viability of Sporothrix spp. in skin lesions of cats for pre-dicting antifungal treatment response. J. Fungi 2018, 4, 92. [Google Scholar] [CrossRef] [Green Version]
  30. Bove, P.; Mayorga, J.; Herández, O. Sporotrichosis transmitted by a domestic cat. Case Report. Med. Cutan Iber. Lat. Am. 2008, 36, 33–35. [Google Scholar]
  31. Falcão, E.M.M.; Pires, M.C.D.S.; Andrade, H.B.; Gonçalves, M.L.C.; Almeida-Paes, R.; Valle, A.C.F.D.; Bastos, F.I.; Gutierrez-Galhardo, M.C.; Freitas, D.F.S. Zoonotic sporotrichosis with greater severity in Rio de Janeiro, Brazil: 118 hospitalizations and 11 deaths in the last 2 decades in a reference institution. Med. Mycol. 2019, 58, 141–143. [Google Scholar] [CrossRef] [PubMed]
  32. Barros, M.B.L.; Schubach, A.O.; Schubach, T.M.P.; Wanke, B.; Lambert-Passos, S.R. An epidemic of sporotrichosis in Rio de Janeiro, Brazil: Epidemiological aspects of a series of cases. Epidemiol. Infect. 2007, 136, 1192–1196. [Google Scholar] [CrossRef] [PubMed]
  33. Eudes, J.F.; dos Santos, I.B.; Reis, C.M.S.; Patané, J.S.L.; Paredes, V.; Benardes, J.P.R.A.; Poggiani, S.d.S.C.; Castrom, T.d.C.B.; Gomez, O.M.; Pereira, S.A.; et al. A novel Sporothrix brasiliensis genomic variant in Midwestern Brazil: Evidence for an older and wider sporotrichosis epidemic. Emerg. Microbes Infect. 2020, 9, 2515–2525. [Google Scholar] [CrossRef]
  34. Alba, C.; Pérez, A.; Toriello, C.; Romo-Lazano, Y.; López-Romero, E.; Ruiz-Baca, E. Molecular components of the Sporothrix schenckii complex that induce immune response. Curr. Microbiol. 2016, 73, 292–300. [Google Scholar] [CrossRef] [PubMed]
  35. Teixeira, M.; De Almeida, L.; Kubitschek, P.; Alves, F.L.; Kishima, É.S.; Abadio, A.K.R.; Fenandes, L.; Derengowski, L.S.; Ferreira, K.S.; Souza, R.C.; et al. Comparative genomics of the major fungal agents of human and animal Spo-rotrichosis: Sporothrix schenckii and Sporothrix brasiliensis. BMC Genom. 2014, 15, 943. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  36. Almeida-Paes, R.; de Oliveira, L.C.; Oliveira, M.M.E.; Gutierrez-Galhardo, M.C.; Nosanchuk, J.D.; Zancopé-Oliveira, R.M. Phenotypic Characteristics Associated with Virulence of Clinical Isolates from the Sporothrix Complex. BioMed. Res. Int. 2015, 2015, 212308. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  37. Pereira, M.; Freitas, R.; Nascimento, S.; Pantalaeão, L.; Vilar, E.G. Sporotrichosis: A Clinicopathologic Study of 89 Consecutive Cases, Literature Review, and New Insights About Their Differential Diagnosis. Am. J. Dermatopathol. 2020, 42, 751–755. [Google Scholar] [CrossRef] [PubMed]
  38. Gezuele, E.; Da Rosa, D. Relevancia del cuerpo asteroide esporotricósico en el diagnóstico rápido de la esporotricosis. Rev. Iberoam. Micol. 2005, 22, 147–150. [Google Scholar] [CrossRef]
  39. Da Rosa, D.; Gezuele, E.; Calegari, L.; Goñi, F. Asteroid body in sporotrichosis. Yeast viability and biological significance within the host immune response. Med. Mycol. 2008, 46, 443–448. [Google Scholar] [CrossRef] [Green Version]
  40. Civila, E.S.; Bonasse, J.; Conti-Diaz, I.A.; Vignale, R.A. Importance of the direct fresh examination in the diagnosis of cutaneous sporotrichosis. Int. J. Dermatol. 2004, 43, 808–810. [Google Scholar] [CrossRef]
  41. MacKinnon, J.; Conti-Diaz, I. The effect of temperature on sporotrichosis. Med. Mycol. 1963, 2, 56–59. [Google Scholar] [CrossRef]
  42. Diaz, I.A.C.; Civila, E.; Gezuele, E.; Lowinger, M.; Calegari, L.; Sanabria, D.; Fuentes, L.; Da Rosa, D.; Alzueta, G. Treatment of human cutaneous sporotrichosis with itraconazole. Mycoses 2009, 35, 153–156. [Google Scholar] [CrossRef]
  43. Giuffrida, R.; CaraDonna, E.; Borgia, F.; Bartolotta, A.; Cannavò, S.P. Pulse itraconazole in the treatment of lymphocutaneous sporotrichosis: A case report from Southern Italy and review of the literature. Dermatol. Ther. 2020, 33, e13716. [Google Scholar] [CrossRef]
Figure 1. Detailed distribution of cases according to age ranges. On the Y axis the number of cases is detailed, on the X axis the eta range is specified.
Figure 1. Detailed distribution of cases according to age ranges. On the Y axis the number of cases is detailed, on the X axis the eta range is specified.
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Figure 2. Distribution of cases of sporotrichosis in Uruguay. A color scale is used, blue corresponds to provinces with 5 cases or less, provinces in yellow between 6–10 cases, provinces in orange between 11–20 cases, red province with the highest number of cases (35 cases).
Figure 2. Distribution of cases of sporotrichosis in Uruguay. A color scale is used, blue corresponds to provinces with 5 cases or less, provinces in yellow between 6–10 cases, provinces in orange between 11–20 cases, red province with the highest number of cases (35 cases).
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Figure 3. Detailed distribution according to history of exposure. Yellow represents the percentage of total cases with a history of trauma from hunting armadillos. Green represents the percentage of total cases with a history of trauma with vegetables. In gray it is represented the percentage of total cases which does not have a traumatic antecedent or the patient does not know how to specify.
Figure 3. Detailed distribution according to history of exposure. Yellow represents the percentage of total cases with a history of trauma from hunting armadillos. Green represents the percentage of total cases with a history of trauma with vegetables. In gray it is represented the percentage of total cases which does not have a traumatic antecedent or the patient does not know how to specify.
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Figure 4. Detailed cases distribution in months of year. The X axis specifies the month of the year in which the diagnosis was made, and the Y axis details the number of cases of sporotrichosis diagnosed.
Figure 4. Detailed cases distribution in months of year. The X axis specifies the month of the year in which the diagnosis was made, and the Y axis details the number of cases of sporotrichosis diagnosed.
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Table 1. Demographic characteristics of 157 patients with sporotrichosis.
Table 1. Demographic characteristics of 157 patients with sporotrichosis.
Characteristicsn (%)
Sex
Male152 (97.0)
Female4 (2.5)
Occupation
Without occupational hazard (driver, dressmaker, housekeeper, teacher, student, administrative, employees, merchants) and retired85 (54.1)
Rural workers24 (15.3)
Gardeners6 (3.8)
Constructor4 (2.5)
Military officer and Police3 (1.9)
Non-registered35 (22.3)
Place of residence
Durazno34 (21.6)
Lavalleja18 (11.5)
Florida18 (11.5)
Treinta y Tres13 (8.3)
Tacuarembó10 (6.4)
Cerro Largo9 (5.7)
Canelones9 (5.7)
Montevideo5 (3.2)
Rocha4 (2.5)
Paysandú3 (1.9)
Flores3 (1.9)
Río Negro2 (1.3)
Colonia2 (1.3)
Artigas1 (0.64)
Rivera1 (0.64)
Maldonado1 (0.64)
Soriano1 (0.64)
Non-registered20 (12.7)
Table 2. Distribution according to lesion site, classification of sporotrichosis and direct mycology study results.
Table 2. Distribution according to lesion site, classification of sporotrichosis and direct mycology study results.
Characteristicsn (%)
Lesion site
Upper limbs115 (73.2)
lower limbs16 (10.2)
other locations (neck, chest and abdomen)6 (3.8)
Classification sporotrichosis
Nodular lymphatic120 (76.4)
Fixed cutaneous30 (19.1)
Non-registered7 (4.5)
Direct mycology study
Asteroid bodies82 (52.3)
Negative75 (47.7)
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MDPI and ACS Style

Cabeza, E.; Arrillaga, A.; Dalcín, L.; Carbia, M.; Arteta, Z.; Perera, P. Clinical and Epidemiological Characteristics of Sporotrichosis in a Reference Center of Uruguay. J. Fungi 2022, 8, 322. https://doi.org/10.3390/jof8030322

AMA Style

Cabeza E, Arrillaga A, Dalcín L, Carbia M, Arteta Z, Perera P. Clinical and Epidemiological Characteristics of Sporotrichosis in a Reference Center of Uruguay. Journal of Fungi. 2022; 8(3):322. https://doi.org/10.3390/jof8030322

Chicago/Turabian Style

Cabeza, Elisa, Annie Arrillaga, Lucía Dalcín, Mauricio Carbia, Zaida Arteta, and Patricia Perera. 2022. "Clinical and Epidemiological Characteristics of Sporotrichosis in a Reference Center of Uruguay" Journal of Fungi 8, no. 3: 322. https://doi.org/10.3390/jof8030322

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