Incidencia 2011-2022
Incidencia 2011-2022
Incidencia 2011-2022
In support of improving patient care, this activity has been planned and implemented by Medscape, LLC and Emerging Infectious Diseases.
Medscape, LLC is jointly accredited with commendation by the Accreditation Council for Continuing Medical Education (ACCME), the
Accreditation Council for Pharmacy Education (ACPE), and the American Nurses Credentialing Center (ANCC), to provide continuing education
for the healthcare team.
Medscape, LLC designates this Journal-based CME activity for a maximum of 1.00 AMA PRA Category 1 Credit(s)™. Physicians should
claim only the credit commensurate with the extent of their participation in the activity.
Successful completion of this CME activity, which includes participation in the evaluation component, enables the participant to earn up to
1.0 MOC points in the American Board of Internal Medicine's (ABIM) Maintenance of Certification (MOC) program. Participants will earn MOC
points equivalent to the amount of CME credits claimed for the activity. It is the CME activity provider's responsibility to submit participant
completion information to ACCME for the purpose of granting ABIM MOC credit.
All other clinicians completing this activity will be issued a certificate of participation. To participate in this journal CME activity: (1) review the
learning objectives and author disclosures; (2) study the education content; (3) take the post-test with a 75% minimum passing score and
complete the evaluation at http://www.medscape.org/journal/eid; and (4) view/print certificate. For CME questions, see page XXX.
NOTE: It is Medscape's policy to avoid the use of Brand names in accredited activities. However, in an effort to be as clear as possible, the
use of brand names should not be viewed as a promotion of any brand or as an endorsement by Medscape of specific products.
Release date: June 16, 2023; Expiration date: June 16, 2024
Learning Objectives
Upon completion of this activity, participants will be able to:
• Assess cat-transmitted sporotrichosis disease incidence, demographics, and clinical and laboratory findings,
based on a medical record review of 216 sporotrichosis cases diagnosed during 2011 to 2022 in Curitiba, Brazil
• Evaluate cat-transmitted sporotrichosis geographic distribution and incidence trends, based on a medical
record review of 216 sporotrichosis cases diagnosed during 2011 to 2022 in Curitiba, Brazil
• Determine the clinical and public health implications of cat-transmitted sporotrichosis disease incidence, clinical
syndromes, and geographic distribution, based on a medical record review of 216 sporotrichosis cases diagnosed during 2011 to 2022
in Curitiba, Brazil
CME Editor
Tony Pearson-Clarke, MS, Technical Writer/Editor, Emerging Infectious Diseases. Disclosure: Tony Pearson-Clarke, MS, has no relevant
financial relationships.
CME Author
Laurie Barclay, MD, freelance writer and reviewer, Medscape, LLC. Disclosure: Laurie Barclay, MD, has no relevant financial relationships.
Authors
Regielly C.R. Cognialli, MS; Diego H. Cáceres, MS; Fernanda de A.G.D. Bastos, MS; Francelise B. Cavassin, PhD; Bruno P.R. Lustosa,
MS; Vânia A. Vicente, PhD; Giovanni L. Breda, MS; Izabella Santos-Weiss, PhD; and Flávio Queiroz-Telles, PhD.
Author affiliations: Federal University of Paraná Program in Internal Medicine and Health Science, Curitiba, Brazil (R.C.R. Cognialli,
F. de A.G.D. Bastos); Federal University of Paraná Hospital de Clínicas, Curitiba (R.C.R. Cognialli, G.L. Breda); Center of Expertise in
Mycology Radboudumc/CWZ, Nijmegen, the Netherlands (D.H. Cáceres); Universidad del Rosario Studies in Translational
Microbiology and Faculty of Medical Sciences, Emerging Diseases Research Group, Bogota, Colombia (D.H. Cáceres); Faculdades
Pequeno Príncipe, Curitiba (F.B. Cavassin); Federal University of Paraná Basic Pathology Department, Curitiba (B.P.R. Lustosa,
V.A. Vicente); Federal University of Paraná Department of Clinical Analysis, Curitiba (I. Santos-Weiss); Federal University of Paraná
Department of Public Health, Curitiba (F Queiroz-Telles)
DOI: https://doi.org/10.3201/eid2907.230155
1330 Emerging Infectious Diseases • www.cdc.gov/eid • Vol. 29, No. 7, July 2023
Sporothrix brasiliensis, Brazil, 2011–2022
Zoonotic outbreaks of sporotrichosis are increasing in institution, the Hospital de Clínicas of the Federal
Brazil. We examined and described the emergence of University of Paraná (HC/UFPR), a tertiary referral
cat-transmitted sporotrichosis (CTS) caused by the fun- hospital in Curitiba, Paraná’s largest city. Our study
gal pathogen Sporothrix brasiliensis. We calculated in- was approved by the HC/UFPR ethical committee
cidence and mapped geographic distribution of cases (registration no. 12379819.4.0000.0096).
in Curitiba, Brazil, by reviewing medical records from
216 sporotrichosis cases diagnosed during 2011–May Methods
2022. Proven sporotrichosis was established in 84 (39%)
patients and probable sporotrichosis in 132 (61%). In- Study Design
cidence increased from 0.3 cases/100,000 outpatient
We identified cases from the hospital database by
visit-years in 2011 to 21.4 cases/100,000 outpatient visit-
using code B42 from the International Classification
years in 2021; of the 216 cases, 58% (n = 126) were
diagnosed during 2019–2021. The main clinical form of of Diseases, 10th Revision. Our study analyzed data
sporotrichosis was lymphocutaneous (63%), followed by from all proven and probable CTS cases from HC/
localized cutaneous (24%), ocular (10%), multisite infec- UFPR during January 2011–May 2022.
tions (3%), and cutaneous disseminated (<0.5%). Since
the first report of CTS in Curitiba in 2011, sporotrichosis Case Definition
has increased substantially, indicating continuous dis- We used case definitions approved by the Brazilian
ease transmission. Clinician and public awareness of Ministry of Health (23–25). Proven human CTS was
CTS and efforts to prevent transmission are needed. defined as microbiologic evidence (positive culture or
histopathology) of sporotrichosis, presence of lesions
Emerging Infectious Diseases • www.cdc.gov/eid • Vol. 29, No. 7, July 2023 1331
RESEARCH
Results
We included 216 CTS cases in this analysis. Case-pa-
tients were more frequently female than male (ratio
1.8:1) except in the 11–17 year age group (Figure 2).
Median age among CTS case-patients was 40 years
(interquartile range 22.5–56.0 years) (Table 2); 29
(13%) patients were <18 years of age. Overall, 11%
of patients had occupations with disease-related risk
factors, including 9 veterinarians, 5 veterinary stu-
dents, 3 pet sitters, and 2 gardeners. The most fre-
quent clinical form of sporotrichosis was lymphocu-
taneous (n = 136, 63%), followed by fixed cutaneous
(n = 53, 25%), ocular (n = 21, 10%), mixed forms (n = 5,
2%), and cutaneous disseminated (n = 1, <0.5%). We
observed that some CTS case-patients had unusual
clinical manifestations (Figure 3).
Overall, 84 (39%) patients had proven CTS and
132 (61%) had probable CTS. Among probable CTS
cases, we tested 18 patients by microscopy and cul-
ture, and all tested negative. Laboratory testing was
Figure 1. Burden of sporotrichosis in South America and distribution not requested for the 14 remaining probable CTS
of cat-transmitted sporotrichosis in humans caused by Sporothrix
case-patients; the main causes for not testing were
brasiliensis, 2022. Cat icons indicate countries where cases of
cat-transmitted sporotrichosis caused by S. brasiliensis have been specimen unavailability for microbiology testing and
reported; arrows indicate transmission from cats to cats, humans, previous initiation of antifungal treatment. Among
and dogs. the proven CTS cases, Sporothrix isolates were collect-
ed from direct swabbing of lesion secretions for 50 pa-
calculated descriptive statistics to record the character- tients, skin biopsy for 29, and aspirate from abscesses
istics of the cases. We also calculated the incidence rate for 5. Average times for positive Sporothrix culture
per 100,000 outpatient all-reason visits per year (outpa- results varied by specimen type: specimens collected
tient visit-years [OPVY]). We performed analyses using using the swab method averaged 6 days (range 3–17
Medcalc version 19.0 statistical software and used Qgis days), compared with 13 days (range 4–30 days) for
Table 1. Cat-transmitted sporotrichosis case definitions used in study of human cases in Curitiba, Brazil, 2011–2021*
Definition Epidemiology Clinical Laboratory
Proven History of trauma or contact Lesions compatible Positive culture and/or histopathology (microbiological
with a cat with sporotrichosis with sporotrichosis evidence)
Probable History of trauma or contact Lesions compatible Human: Negative culture and/or histopathology.†
with a cat with sporotrichosis with sporotrichosis Sick cat: A) sporotrichosis diagnosed by culture and/or
histopathology in a veterinarian laboratory; B) cat resident in a
region with confirmed presence of cats with sporotrichosis
(data verified by public health authorities)
Possible History of trauma or contact Lesions compatible Absent
with a cat with sporotrichosis with sporotrichosis
Non-CTS History of trauma or contact with Lesions compatible Negative culture and/or histopathology for Sporothrix spp.†
a cat with sporotrichosis with sporotrichosis Definition of other case of disease (infectious or noninfectious)
*Adapted from Guide to Health Surveillance, 5th ed (23–25). CTS, cat-transmitted sporotrichosis.
†Negative culture for Sporothrix spp. alone does not rule out diagnosis (limitation of the culture).
1332 Emerging Infectious Diseases • www.cdc.gov/eid • Vol. 29, No. 7, July 2023
Sporothrix brasiliensis, Brazil, 2011–2022
Emerging Infectious Diseases • www.cdc.gov/eid • Vol. 29, No. 7, July 2023 1333
RESEARCH
1334 Emerging Infectious Diseases • www.cdc.gov/eid • Vol. 29, No. 7, July 2023
Sporothrix brasiliensis, Brazil, 2011–2022
Emerging Infectious Diseases • www.cdc.gov/eid • Vol. 29, No. 7, July 2023 1335
RESEARCH
Figure 6. Locations of human cat-transmitted sporotrichosis cases (red dots) treated at Hospital de Clínicas, Federal University of
Paraná, Curitiba, Brazil, during 2011–May 2022, and evolution of spatial distribution of cases in the city of Curitiba. A–D) Locations of
all human cases in Brazil (A), Paraná state (B), Metropolitan Region of Curitiba (C), and Curitiba (D). E–H) Distribution of new human
cases in Curitiba during 2011–2013 (E), 2014–2016 (F), 2017–2019 (G), and 2020–May 2022 (H).
1336 Emerging Infectious Diseases • www.cdc.gov/eid • Vol. 29, No. 7, July 2023
Sporothrix brasiliensis, Brazil, 2011–2022
Emerging Infectious Diseases • www.cdc.gov/eid • Vol. 29, No. 7, July 2023 1337
RESEARCH
those and other prevention and control measures 10. Pereira SA, Gremião ID, Kitada AA, Boechat JS, Viana PG,
in a timely manner is urgently needed to repress Schubach TM. The epidemiological scenario of feline
sporotrichosis in Rio de Janeiro, state of Rio de Janeiro,
the increased incidence and spread of this serious Brazil. Rev Soc Bras Med Trop. 2014;47:392–3.
health condition. https://doi.org/10.1590/0037-8682-0092-2013
11. Rodrigues AM, Della Terra PP, Gremião ID, Pereira SA,
Orofino-Costa R, de Camargo ZP. The threat of emerging and
Acknowledgments re-emerging pathogenic Sporothrix species. 2020;185:813–42.
We thank Lili Volochen Lopuch and Adriana de Fátima 12. Rossow JA, Queiroz-Telles F, Caceres DH, Beer KD,
Gabriel for all support with collecting and preparing Jackson BR, Pereira JG, et al. A One Health approach to
combatting Sporothrix brasiliensis: narrative review of an
samples and Regiane Cognialli Born for the map design. emerging zoonotic fungal pathogen in South America.
We also thank We also thank Jeremy Gold for reviewing J Fungi (Basel). 2020;6:247. https://doi.org/10.3390/
the manuscript. jof6040247
13. Rodrigues AM, Gonçalves SS, de Carvalho JA,
Borba-Santos LP, Rozental S, Camargo ZP. Current progress
on epidemiology, diagnosis, and treatment of sporotrichosis
About the Author and their future trends. J Fungi (Basel). 2022;8:776.
Ms. Cognialli is a mycologist at Hospital de Clínicas of https://doi.org/10.3390/jof8080776
14. Brandolt TM, Madrid IM, Poester VR, Sanchotene KO,
Federal University of Paraná and a PhD student at Federal
Basso RP, Klafke GB, et al. Human sporotrichosis: a
University of Paraná, Curitiba, Paraná, Brazil. Her primary zoonotic outbreak in southern Brazil, 2012–2017. Med
interest is in neglected endemic mycosis. Mycol. 2018;57:myy082. https://doi.org/10.1093/mmy/
myy082
15. Poester VR, Mattei AS, Madrid IM, Pereira JTB, Klafke GB,
References Sanchotene KO, et al. Sporotrichosis in southern Brazil,
1. Orofino-Costa R, Macedo PM, Rodrigues AM, towards an epidemic? Zoonoses Public Health. 2018;65:815–
Bernardes-Engemann AR. Sporotrichosis: an update on 21. https://doi.org/10.1111/zph.12504
epidemiology, etiopathogenesis, laboratory and clinical 16. Etchecopaz AN, Lanza N, Toscanini MA, Devoto TB,
therapeutics. An Bras Dermatol. 2017;92:606–20. Pola SJ, Daneri GL, et al. Sporotrichosis caused by Sporothrix
https://doi.org/10.1590/abd1806-4841.2017279 brasiliensis in Argentina: case report, molecular identification
2. Queiroz-Telles F, Bonifaz A, Rossow J, Chindamporn A. and in vitro susceptibility pattern to antifungal drugs.
Sporothrix and sporotrichosis. In: Encyclopedia of infection J Mycol Med. 2020;30:100908. https://doi.org/10.1016/
and immunity. New York: Elsevier Science; 2021. j.mycmed.2019.100908
3. Queiroz-Telles F, Fahal AH, Falci DR, Caceres DH, 17. Etchecopaz A, Toscanini MA, Gisbert A, Mas J, Scarpa M,
Chiller T, Pasqualotto AC. Neglected endemic mycoses. Iovannitti CA, et al. Sporothrix brasiliensis: a review of an
Lancet Infect Dis. 2017;17:e367–77. https://doi.org/10.1016/ emerging South American fungal pathogen, its related
S1473-3099(17)30306-7 disease, presentation and spread in Argentina. J Fungi
4. Chakrabarti A, Bonifaz A, Gutierrez-Galhardo MC, (Basel). 2021;7:170. https://doi.org/10.3390/jof7030170
Mochizuki T, Li S. Global epidemiology of sporotrichosis. 18. Thomson P, González C, Blank O, Ramírez V, Río Cd,
Med Mycol. 2015;53:3–14. https://doi.org/10.1093/mmy/ Santibáñez S, et al. Sporotrichosis outbreak due to Sporothrix
myu062 brasiliensis in domestic cats in Magallanes, Chile: a
5. Gremião ID, Miranda LH, Reis EG, Rodrigues AM, One-Health-approach study. J Fungi (Basel). 2023;9:226.
Pereira SA. Zoonotic epidemic of sporotrichosis: cat to https://doi.org/10.3390/jof9020226
human transmission. PLoS Pathog. 2017;13:e1006077. 19. Rachman R, Ligaj M, Chinthapalli S, Serafino Wani R.
https://doi.org/10.1371/journal.ppat.1006077 Zoonotic acquisition of cutaneous Sporothrix braziliensis
6. Schechtman RC, Falcão EMM, Carard M, García MSC, infection in the UK. BMJ Case Rep. 2022;15:e248418.
Mercado DS, Hay RJ. Sporotrichosis: hyperendemic by zoo- https://doi.org/10.1136/bcr-2021-248418
notic transmission, with atypical presentations, 20. Barnacle JR, Chow YJ, Borman AM, Wyllie S, Dominguez V,
hypersensitivity reactions and greater severity. An Bras Russell K, et al. The first three reported cases of Sporothrix
Dermatol. 2022;97:1–13. https://doi.org/10.1016/j.abd. brasiliensis cat-transmitted sporotrichosis outside South
2021.07.003 America. Med Mycol Case Rep. 2022;39:14–7. https://doi.org/
7. Barros MB, Schubach AO, do Valle AC, Gutierrez 10.1016/j.mmcr.2022.12.004
Galhardo MC, Conceição-Silva F, Schubach TM, et al. 21. Marinho Falcão EMM, Rocha Romão A, de Avelar
Cat-transmitted sporotrichosis epidemic in Rio de Janeiro, Figueiredo Mafra Magalhães M, de Lima Filho JB,
Brazil: description of a series of cases. Clin Infect Dis. Francesconi do Valle AC, Bastos FI, et al. A spatial analysis
2004;38:529–35. https://doi.org/10.1086/381200 of the spread of hyperendemic sporotrichosis in the state
8. de Lima Barros MB, Schubach TM, Galhardo MC, of Rio de Janeiro, Brazil. J Fungi (Basel). 2022;8:434.
de Oliviera Schubach A, Monteiro PC, Reis RS, et al. https://doi.org/10.3390/jof8050434
Sporotrichosis: an emergent zoonosis in Rio de Janeiro. Mem 22. Rabello VBS, Almeida MA, Bernardes-Engemann AR,
Inst Oswaldo Cruz. 2001;96:777–9. https://doi.org/10.1590/ Almeida-Paes R, de Macedo PM, Zancopé-Oliveira RM.
S0074-02762001000600006 The historical burden of sporotrichosis in Brazil: a systematic
9. Gremião IDF, Oliveira MME, Monteiro de Miranda LH, review of cases reported from 1907 to 2020. Braz J Microbiol.
Saraiva Freitas DF, Pereira SA. Geographic expansion of 2022;53:231–44. https://doi.org/10.1007/s42770-021-00658-1
sporotrichosis, Brazil. Emerg Infect Dis. 2020;26:621–4. 23. Queiroz-Telles F, Bonifaz A, Cognialli R, Lustosa BPR,
https://doi.org/10.3201/eid2603.190803 Aparecida Vicente V, Ramírez-Marín HA. Sporotrichosis in
1338 Emerging Infectious Diseases • www.cdc.gov/eid • Vol. 29, No. 7, July 2023
Sporothrix brasiliensis, Brazil, 2011–2022
children: case series and narrative review. Curr Fungal Infec 38. Arinelli A, Aleixo A, Freitas DFS, do Valle ACF, Almeida-
Rep. 2022;33–46. Paes R, Gutierrez-Galhardo MC, et al. Ocular sporotrichosis:
24. Ministry of Health of Brazil. Guide to health surveillance [in 26 cases with bulbar involvement in a hyperendemic area of
Portuguese]. 5th ed. Brasilia (Brazil): Ministry of Health of zoonotic transmission. Ocul Immunol Inflamm. 2019;28:764–71.
Brazil; 2022. 39. Ferreira TA, Sodré CT, Costa JM, Setta CRP,
25. Cognialli R, Bloss K, Weiss I, Caceres DH, Davis R, Ramos-E-Silva M. Primary conjunctival sporotrichosis:
Queiroz-Telles F. A lateral flow assay for the immunodiagnosis an atypical presentation of the disease. JAAD Case Rep.
of human cat-transmitted sporotrichosis. Mycoses. 2022;65:926– 2018;4:497–9. https://doi.org/10.1016/j.jdcr.2018.01.022
34. https://doi.org/10.1111/myc.13516 40. Lacerda Filho AM, Cavalcante CM, Da Silva AB, Inácio CP,
26. de Andrade Galliano Daros Bastos F, Raimundo Cognialli RC, de Lima-Neto RG, Liete de Andrade MC, et al. High-virulence
Rodrigues de Farias M, Dos Santos Monti F, Wu K, cat-transmitted ocular sporotrichosis. Mycopathologia.
Queiroz-Telles F. Spread of Sporothrix spp. through 2019;184:547–9. https://doi.org/10.1007/s11046-019-00347-6
respiratory droplets from infected cats: a potential route of 41. Aidar MN, Rebeschini BM, Salgado Silveira da Mata CT,
transmission. Med Mycol. 2022;60:myac079. Borges TC, Dos Santos Araújo MEX. The importance of
27. Viezzer J, Moraes E, Biondi D, Martini A, Scarano F. considering the possibility of ocular sporotrichosis in areas
Green areas, population and income in Curitiba, PR, Brasil with high incidence rates of sporotrichosis. Arq Bras
[in Portuguese]. Rev Soc Bras Arb Urb. 2022;17:37–49. Oftalmol. 2022: S0004-27492022005006208.
https://doi.org/10.5380/revsbau.v17i2.85848 42. Marimon R, Cano J, Gené J, Sutton DA, Kawasaki M,
28. Queiroz-Telles F, Buccheri R, Benard G. Sporotrichosis in Guarro J. Sporothrix brasiliensis, S. globosa, and S. mexicana, three
immunocompromised hosts. J Fungi (Basel). 2019;5:8. new Sporothrix species of clinical interest. J Clin Microbiol.
https://doi.org/10.3390/jof5010008 2007;45:3198–206. https://doi.org/10.1128/JCM.00808-07
29. Munhoz LS, Poester VR, Severo CB, Trápaga MR, Madrid IM, 43. Della Terra PP, Rodrigues AM, Fernandes GF, Nishikaku AS,
Benelli JL, et al. Update of the epidemiology of the Burger E, Pires de Camargo Z. Exploring virulence and
sporotrichosis epidemic in the state of Rio Grande do Sul, immunogenicity in the emerging pathogen Sporothrix
Brazil. Mycoses. 2022;65:1112–8. https://doi.org/10.1111/ brasiliensis. PLoS Negl Trop Dis. 2017;11:e0005903.
myc.13497 https://doi.org/10.1371/journal.pntd.0005903
30. Alzuguir CLC, Pereira SA, de Avelar Figueiredo Mafra 44. Almeida-Paes R, de Oliveira MM, Freitas DF, do Valle AC,
Magalhães, Almeida-Paes R, Freitas DFS, Oliveira LFA, Zancopé-Oliveira RM, Gutierrez-Galhardo MC. Sporotricho-
et al. Geo-epidemiology and socioeconomic aspects of sis in Rio de Janeiro, Brazil: Sporothrix brasiliensis is associ-
human sporotrichosis in the municipality of Duque ated with atypical clinical presentations. PLoS Negl Trop Dis.
de Caxias, Rio de Janeiro, Brazil, between 2007 and 2016. 2014;8:e3094. https://doi.org/10.1371/journal.pntd.0003094
Trans R Soc Trop Med Hyg. 2020;114:99–106. 45. de Carvalho JA, Hagen F, Fisher MC, de Camargo ZP,
31. Barros MB, de Almeida Paes R, Schubach AO. Sporothrix Rodrigues AM. Genome-wide mapping using new AFLP
schenckii and sporotrichosis. Clin Microbiol Rev. 2011;24:633– markers to explore intraspecific variation among pathogenic
54. https://doi.org/10.1128/CMR.00007-11 Sporothrix species. PLoS Negl Trop Dis. 2020;14:e0008330.
32. de Oliveira Bento A, de Sena Costa AS, Lima SL, do Monte https://doi.org/10.1371/journal.pntd.0008330
Alves M, de Azevedo Melo AS, Rodrigues AM, et al. 46. Teixeira MM, Almeida-Paes R, Bernardes-Engemann AR,
The spread of cat-transmitted sporotrichosis due to Nicola AM, de Macedo PM, Valle ACF, et al. Single
Sporothrix brasiliensis in Brazil towards the northeast nucleotide polymorphisms and chromosomal copy number
region. PLoS Negl Trop Dis. 2021;15:e0009693. variation may impact the Sporothrix brasiliensis antifungal
https://doi.org/10.1371/journal.pntd.0009693 susceptibility and sporotrichosis clinical outcomes. Fung Gen
33. Barros MB, Schubach AO, Schubach TM, Wanke B, Biol 2022;163:103743.
Lambert-Passos SR. An epidemic of sporotrichosis in Rio de 47. Huang M, Ma Z, Zhou X. Comparative genomic data
Janeiro, Brazil: epidemiological aspects of a series of cases. provide new insight on the evolution of pathogenicity in
Epidemiol Infect. 2008;136:1192–6. https://doi.org/10.1017/ Sporothrix species. Front Microbiol. 2020;11:565439.
S0950268807009727 https://doi.org/10.3389/fmicb.2020.565439
34. Mialski R, de Almeida JN Jr, da Silva LH, Kono A, 48. Sanchotene KO, Madrid IM, Klafke GB, Bergamashi M,
Pinheiro RL, Teixeira MJ, et al. Chronic meningitis and hy- Della Terra PP, Rodrigues AM, et al. Sporothrix brasiliensis
drocephalus due to Sporothrix brasiliensis in outbreaks and the rapid emergence of feline sporotrichosis.
immunocompetent adults: a challenging entity. Open Forum Mycoses. 2015;58:652–8. https://doi.org/10.1111/myc.12414
Infect Dis. 2018;5:ofy081. https://doi.org/10.1093/ofid/ofy081 49. Valeriano CAT, Ferraz CE, Marques Evangelista Oliveira M,
35. Bonifaz A, Tirado-Sánchez A. Cutaneous disseminated and Inácio CP, de Oliveira EP, Lacerda AM, et al. Cat-transmitted
extracutaneous sporotrichosis: current status of a complex disseminated cutaneous sporotrichosis caused by Sporothrix
disease. J Fungi (Basel). 2017;3:6. https://doi.org/10.3390/ brasiliensis in a new endemic area: case series in the
jof3010006 northeast of Brazil. JAAD Case Rep. 2020;6:988–92.
36. Orofino-Costa R, Freitas DFS, Bernardes-Engemann AR, https://doi.org/10.1016/j.jdcr.2020.07.047
Rodrigues AM, Talhari C, Ferraz CE, et al. Human 50. Andrade EHP, Bastos CV, Silva AVD, Moreira SM,
sporotrichosis: recommendations from the Brazilian Society Costa TGA, Salvato LA, et al. Household outbreak of
of Dermatology for the clinical, diagnostic and therapeutic sporotrichosis: towards the One Health approach. Rev Soc
management. An Bras Dermatol. 2022;97:757–77. Bras Med Trop. 2022;55:e0021. https://doi.org/
https://doi.org/10.1016/j.abd.2022.07.001 10.1590/0037-8682-0021-2022
37. Queiroz-Telles F, Cognialli RC, Salvador GL, Moreira GA,
Herkert PF, Hagen F. Cutaneous disseminated Address for correspondence: Flávio Queiroz-Telles, Federal
sporotrichosis in immunocompetent patient: case report
University of Paraná, 280 Padre Camargo, Curitiba, Paraná, Brazil;
and literature review. Med Mycol Case Rep. 2022;36:31–4.
https://doi.org/10.1016/j.mmcr.2022.05.003 email: queiroz.telles@uol.com.br
Emerging Infectious Diseases • www.cdc.gov/eid • Vol. 29, No. 7, July 2023 1339