Skip to main content

Ulceroglandular form of tularemia after squirrel bite: a case report



The diagnosis of tularemia is not often considered in Germany as the disease is still rare in this country. Nonetheless, Francisella tularensis, the causative agent of tularemia, can infect numerous animal species and should, therefore, not be neglected as a dangerous pathogen. Tularemia can lead to massively swollen lymph nodes and might even be fatal without antibiotic treatment. To our knowledge, the case described here is the first report of the disease caused by a squirrel bite in Germany.

Case presentation

A 59-year-old German woman with a past medical history of hypothyroidism and cutaneous lupus erythematosus presented at the emergency room at St. Katharinen Hospital with ongoing symptoms and a swollen right elbow persisting despite antibiotic therapy with cefuroxime for 7 days after she had been bitten (right hand) by a wild squirrel (Eurasian red squirrel). After another 7 days of therapy with piperacillin/tazobactam, laboratory analysis using real-time polymerase chain reaction (PCR) confirmed the suspected diagnosis of tularemia on day 14. After starting the recommended antibiotic treatment with ciprofloxacin, the patient recovered rapidly.


This is the first report of a case of tularemia caused by a squirrel bite in Germany. A naturally infected squirrel has recently been reported in Switzerland for the first time. The number of human cases of tularemia has been increasing over the last years and, therefore, tularemia should be taken into consideration as a diagnosis, especially in a patient bitten by an animal who also presents with headache, increasing pain, lymphadenitis, and fever, as well as impaired wound healing. The pathogen can easily be identified by a specific real-time PCR assay of wound swabs and/or by antibody detection, for example by enzyme-linked immunosorbent assay (ELISA), if the incident dates back longer than 2 weeks.

Peer Review reports


Here, we present the case of a 59-year-old German woman who was admitted to our hospital after a squirrel bite with an ulcerative lesion at digit IV of the right hand and a lymphadenitis at the right elbow combined with persistent fever, myalgia, and headache. The diagnosis of tularemia was based on the results of a specific real-time polymerase chain reaction (PCR) assay that showed positivity for Francisella tularensis, and on culture of the material on agar plates showing growth typical of Francisella.

Tularemia, also called “rabbit fever,” is a rare, but potentially severe zoonosis caused by F. tularensis. The disease has been described in more than 250 animal species, including mammals, birds, amphibians, fish, and invertebrates, all of which potentially transmit the bacterium to humans. Transmission of F. tularensis to humans may also occur through mosquito or tick bites and through the consumption of contaminated water or food [1,2,3,4,5]. Human-to-human transmission has not yet been reported [6]. Four F. tularensis subspecies (tularensis, holarctica, mediasiatica and novicida) care known to cause tularemia, but only two, F. tularensis ssp. tularensis and F. tularensis ssp. holarctica (Fth), are of clinical relevance. To our knowledge, however, the only F. tularensis subspecies identified in Germany so far is Fth [7]. In endemic regions, especially, hunters and forest workers are at an increased risk for tularemia. Because of the low prevalence of the disease in Germany [8], physicians might be unaware or underestimate the disease, which leads to delayed adequate diagnoses and specific treatment [9,10,11,12].

Only rarely can the sources of human infections be verified. For example, during a recent outbreak that was linked to freshly pressed grape must, a wood mouse was identified as a potential source of contamination [9, 11, 13]. To our knowledge, the case described here is the first report in Germany of a human infection caused by a squirrel bite occurring, although a naturally infected squirrel has also been reported from Switzerland recently [14].

Case presentation

A 59-year-old German woman with a past medical history of hypothyroidism and cutaneous lupus erythematosus presented at the hospital´s emergency room 7 days after having been bitten by a wild Eurasian red squirrel (Sciurus vulgaris).

The patient reported having noticed a squirrel lying motionless on the ground when she took a walk. As soon as she tried to examine the animal, it started biting her, biting digit IV of the right hand and digit II of the left hand. After the wounds had been cleaned and dressed, she was started the same day on antibiotic therapy consisting of cefuroxime 500 mg orally twice a day. Tetanus vaccination status was also checked. On day 6 after the bite, the patient presented at the hospital’s emergency room showing the following symptoms: general malaise, aching head and body, fever, chill, and a swollen right elbow. She did not report having suffered from nausea, vomiting, or sensitivity to light or noise.

The clinical examination showed a minor bite on digit IV of the right hand, located near the middle phalanx, slightly reddened, yet without clear inflammatory signs. There was no pain to pressure, no movement restriction, nor any sensory deficit. There were also visible signs of lymphadenitis at the ulnar side of the right elbow. The peripheral sensitivity as well as movement skills and blood flow were intact. At the index finger of the left hand, another minor bite without any local or proximal signs of inflammation was recorded. The physical examination did not reveal anything unusual. The vital parameters were stable, with the exception of a negligible sinus tachycardia. No signs of meningism were found.

Laboratory tests showed an increase in the C-reactive protein (CRP) up to 28.6 mg/L (reference < 5 mg/L), but no leukocytosis. The test for procalcitonin (indicating bacterial inflammation) was negative. Sampled cerebrospinal fluid and urine were also negative in standard laboratory tests. X-rays of the thorax and of digit IV of the right hand and a native computed tomography (CT) brain scan did not show any pathological outcomes. Real-time PCR assays for severe acute respiratory syndrome Coronavirus 2 (SARS-CoV-2), respiratory syncytial virus, and influenza A and B were negative. Starting on day 7, the medical treatment also comprised combination therapy with intravenous antibiotics (ampicillin/sulbactam, 2 g/1 g) 3 times a day. However, the patient’s condition did not improve and fever rose up to 39.2 °C and persisted until day 12. Blood culture remained negative, even at 14 days after inoculation. CRP increased up to 185 mg/L on day 12. As a consequence, treatment was intensified by commencing combination antibiotic therapy with piperacillin/tazobactam (4 g/0.5 g) on day 11. Followin initiation of therapy with piperacillin/tazobactam, the CRP fell to 74 mg/L (day 14) and there was a mild persisting leukocytosis (12.14 × 103).

In parallel, the wound on the patient’s right hand developed an ulcer-like lesion showing swollen reddened edges and a central incrustation (Fig. 1). The lymphadenitis of the right elbow persisted. It was at this stage that tularemia was suspected as a possible diagnosis for the first time. Following a phone call with the reference laboratory for human tularemia at the Robert Koch Institute (RKI) on day 14, the decision was made to send a wound swab sample from digit IV of the patient’s right hand (A-1825/1) to the Robert Koch Institute (RKI) for microbiological examination. In addition, a serum sample (A-1825/2) was taken for antibody detection (day 14). An enzyme-linked immunosorbent assay (ELISA) showed that antibodies against the lipopolysaccharide of F. tularensis Igpoly, immunoglobulin (Ig)G and IgM were borderline.

Fig. 1
figure 1

Picture of the right hand of the patient at day 14 after the squirrel bite on the digit IV. After presentation of the ulcerous lesion and the local lymphadenitis of the right elbow in combination with the non-effective antibiotic treatment using three different antibiotics over 2 weeks, the suspicion of an ulcero-glandular tularemia was expressed

To isolate living bacteria and extract DNA, the wound swab was suspended in 900 µL double-distilled water, and a 450-µL of the suspension was centrifuged. The resulting pellet was used for genomic desoxyribonucleic acid (DNA) extraction (DNeasy Blood and Tissue kit; Qiagen, Hilden, Germany). A real-time PCR based on F. tularensis-specific primers (for genes fopA and tul4) confirmed the presence of F. tularensis DNA in the wound swab sample. Subspecies Fth was identified by block PCR targeting the region of difference 1 (RD1) according to protocols described by Broekhuijsen et al. [15]. For culture, 50 µL of the swab suspension was inoculated in 10 mL medium T [16] and streaked onto MTKH [17], as well as onto chocolate agar plates and Neisseria selective medium plus (both Oxoid Germany GmbH, Wesel, Germany). The liquid medium and the agar plates were incubated at 37 °C with 5% CO2. Bacterial growth typical for F. tularensis could be observed on MTKH on day 3 of culture and on the chocolate and Neisseria agar plates on day 4. The patient’s cerebrospinal fluid did not test positive for F. tularensis.

Minimal inhibitory concentration testing according to the Clinical and Laboratory Standards Institute (CLSI; guidelines for F. tularensis demonstrated an in vitro sensitivity to all antibiotics recommended for treatment of tularemia (for example, ciprofloxacin, gentamycin, levofloxacin) [6, 18]. The patient’s antibiotic treatment applied until that stage turned out to be inadequate (resistance against ampicillin/sulbactam, and cefuroxime, piperacillin/tazobactam are ineffective in the treatment for tularemia). In a sequencing study (MiSeq sequencer [Illumina Inc., San Diego, CA, USA], see [13] for details) and the phylogenetic analysis (Geneious prime [Biomatters, Auckland, New Zealand], Mauve alignment, followed by neighbor-joining clustering, see [19] for details), the DNA from Fth strain A-1825/1, isolated from the patient’s wound swab, was shown to belong to biovar I, clade B.6 and subclade B.49 (Fig. 2).

Fig. 2
figure 2

Phylogenetic relationship of Francisella tularensis ssp. holarctica (Fth) in a wound swab sample from digit IV of the patient’s right hand (A-1825/1) (red, in bold) to Fth isolates from North Rhine-Westphalia (NW), Rhineland-Palatinate (RP), and Hesse (He). Strains belonging to the erythromycin-sensitive major clade B.6 are indicated in blue. For each genome sequence, the year of sampling, the host organism, sampling spot (German federal states), and the known final subclade are given. Host organisms: Be beaver, Br brock, H human, Le Lepus, Sc Sciurus, Wb wild boar. Germany’s federal states: BB Brandenburg, HE Hesse, NI Lower Saxony, NW North Rhine-Westphalia, RP Rhineland-Palatinate. Countries: D Germany, FR France. Asterisk indicates no bacterial isolate, genomic DNA only; for further details, see [13]. The analysis was based on a Mauve alignment for colinear genomes. Genomes were generated by DNA sequencing and mapping of DNA reads to the genome of F. tularensis ssp. holarctica (Fth) strain LVS (for details, see [19]). For the clustering, the neighbor-joining bootstrap method was used, with F. tularensis ssp. holarctica (Fth) strain OSU18 as an outgroup

When the reference laboratory for human tularemia underpinned the suspected diagnosis on day 14, the treatment was immediately adjusted, and 500 mg of ciprofloxacin was administered twice a day for 14 days. Under the adjusted treatment, the patient recovered immediately (the CRP dropped to 15 mg/L) and she could be discharged fever-free with a negligible headache on day 17.

Discussion and conclusions

We report here the case of an ulcero-glandular tularemia after a squirrel bite. Healthcare staff treat persons with animal bites, mainly by dogs, cats, and snakes [20], on a daily basis. In such cases, the risk of a systemic infection depends on a number of different parameters, such as the type of injury, the animal involved, and the patient’s own immune defense. The treatment should include immediate irrigation and debridement of the wound, a prophylaxis against tetanus, and possibly against rabies, and an antibiotic treatment (depending on the risk for a systemic infection) [21]. Although the risk of being bitten and/or infected by a wild Eurasian red squirrel (Sciurus vulgaris) is low [22], Europe has seen an increase in the number of tularemia cases in both humans and animals during the past decades [2, 7, 8]. While only one report of a natural infection with Fth in a wild Eurasian red squirrel, in Switzerland, has been published [14], it is known that squirrels, although being herbivores, may be a reservoir of F. tularensis, as are many other rodents. The human case of tularemia reported here from Germany also confirms the possibility of a European squirrel infected by Fth. After contact with squirrels, tularemia should, therefore, be considered as a differential diagnosis to prevent a delay of specific treatment [9, 10, 13].

Studies on Francisella isolates from humans and wild animals in Germany have revealed an unexpected genetic diversity of Fth [19, 23,24,25] that is not only of academic interest: the phylogenetic analysis showed that Fth isolates of biovar I are erythromycin-susceptible and mainly occur in western Europe, whereas isolates of biovar II are erythromycin-resistant and mainly occur in northern and eastern Europe. A similar north-west divide has been observed in Germany [7, 19, 26,27,28,29,30,31,32]. The phylogenetic analysis of the draft genome sequence of strain A-1825 reported here, isolated from the patient in the Rhein-Erft region (Rhein-Erft-Kreis) in North Rhine-Westphalia, revealed that it belongs to erythromycin-sensitive biovar I (major clade B.6), subclade B.49 (Fig. 2). As mentioned, this is not surprising as Fth isolates of biovar I appear more often in the south-west of Germany. The same applies to B.6 strains being more often detected in Rhineland-Palatinate and Hesse, near the Rhein-Erft region [7, 19, 28].

The clinical manifestation of tularemia depends on the portal of entry of the bacteria into the organism. Consequently, the disease is defined by the following different forms: ulcero-glandular or glandular, oropharyngeal, ocular-glandular, and respiratory [1, 3, 6]. The ulcero-glandular form of tularemia mostly occurs after direct skin contact with an infected animal or by percutaneous penetration of the pathogen after a bite by a wild or domestic animal (cats, dogs) or by a tick [2, 33,34,35,36,37]. The following primary clinical symptoms may occur 1–14 days (mainly 3–5 days) after penetration of the pathogen: fever, malaise, headache, melalgia, and swollen lymph nodes [6, 8, 18]). Subsequently, an ulcerous lesion at the portal of entry and swollen lymph nodes may appear. The ocular-glandular form can be caused by eye contact with contaminated materials and may result in a conjunctivitis. The oropharyngeal form is characterized by a mostly unilateral cervical lymph node swelling, stomatitis, tonsillitis, and pharyngitis after ingestion of contaminated food or water. The respiratory form of tularemia after inhalation of the pathogen may cause cough, chest pain, dyspnea, and pneumonia [6]. For diagnosis, serological methods, antigen detection, or molecular methods are used [38]. Specific real-time PCR assays and bacterial growth on suitable agar plates (for example, chocolate, Neisseria selective medium plus) allow the pathogen to be identified in clinical material, such as wound swabs or blood cultures [38]. If an isolate is available, mass-assisted laser desorption/ionization time-of-flight spectrometry can be used for identification of F. tularensis. Whole-genome sequencing and PCR targeting the RD1 for subspecies differentiation [15] are methods which enable further characterization of the pathogen [3]. Serological methods, for example ELISA or western blot, can be used for antibody detection against the lipopolysaccharide of F. tularensis to confirm tularemia retrospectively, but only if the incident occurred more than 2–3 weeks prior to the tests or assays.

The clinical presentation of this case in combination with the ineffective antibiotic treatment, namely, three different antibiotics in 2 weeks, underpinned the suspected diagnosis of an ulcero-glandular form of tularemia proposed by clinicians and specialists from the reference laboratory. After the appropriate antibiotic treatment with ciprofloxacin, the patient recovered immediately and could be discharged from hospital on day 3 after treatment adaptation (aminoglycosides, quinolones, tetracyclines, and chloramphenicol) [37].

Availability of data and materials

Not applicable.


  1. Ellis J, Oyston PC, Green M, Titball RW. Tularemia. Clin Microbiol Rev. 2002;15(4):631–46.

    Article  Google Scholar 

  2. Hestvik G, Warns-Petit E, Smith LA, Fox NJ, Uhlhorn H, Artois M, et al. The status of tularemia in Europe in a one-health context: a review. Epidemiol Infect. 2015;143(10):2137–60.

    Article  CAS  Google Scholar 

  3. Maurin M, Gyuranecz M. Tularaemia: clinical aspects in Europe. Lancet Infect Dis. 2016;16(1):113–24.

    Article  Google Scholar 

  4. Sjostedt A. Special topic on Francisella tularensis and tularemia. Front Microbiol. 2011;2:86.

    Article  Google Scholar 

  5. Telford SR 3rd, Goethert HK. Ecology of Francisella tularensis. Annu Rev Entomol. 2020;65:351–72.

    Article  CAS  Google Scholar 

  6. World Health Organization. WHO guidlines on tularemia. 2007. Accessed 14 Jan 2022.

    Google Scholar 

  7. Appelt S, Faber M, Koppen K, Jacob D, Grunow R, Heuner K. Francisella tularensis subspecies holarctica and tularemia in Germany. Microorganisms. 2020;8(9):1448.

    Article  CAS  Google Scholar 

  8. Faber M, Heuner K, Jacob D, Grunow R. Tularemia in Germany—a re-emerging zoonosis. Front Cell Infect Microbiol. 2018;8:40.

    Article  Google Scholar 

  9. Burckhardt F, Hoffmann D, Jahn K, Heuner K, Jacob D, Vogt M, et al. Oropharyngeal tularemia from freshly pressed grape must. N Engl J Med. 2018;379(2):197–9.

    Article  Google Scholar 

  10. Hauri AM, Hofstetter I, Seibold E, Kaysser P, Eckert J, Neubauer H, et al. Investigating an airborne tularemia outbreak, Germany. Emerg Infect Dis. 2010;16(2):238–43.

    Article  Google Scholar 

  11. Wetzstein N, Karcher I, Kupper-Tetzel CP, Kann G, Hogardt M, Jozsa K, et al. Clinical characteristics in a sentinel case as well as in a cluster of tularemia patients associated with grape harvest. Int J Infect Dis. 2019;84:116–20.

    Article  Google Scholar 

  12. Jacob D, Barduhn A, Tappe D, Rauch J, Heuner K, Hierhammer D, et al. Outbreak of tularemia in a group of hunters in Germany in 2018—kinetics of antibody and cytokine responses. Microorganisms. 2020;8(11):1645.

    Article  CAS  Google Scholar 

  13. Jacob D, Koppen K, Radonic A, Haldemann B, Zanger P, Heuner K, et al. Molecular identification of the source of an uncommon tularaemia outbreak, Germany, autumn 2016. Euro Surveill. 2019.

    Article  PubMed  PubMed Central  Google Scholar 

  14. Pisano SRR, Kittl S, Eulenberger U, Jores J, Origgi FC. Natural infection of a European red squirrel (Sciurus vulgaris) with Francisella tularensis subsp. holarctica. J Wildl Dis. 2021;57(4):970–3.

    Article  Google Scholar 

  15. Broekhuijsen M, Larsson P, Johansson A, Bystrom M, Eriksson U, Larsson E, et al. Genome-wide DNA microarray analysis of Francisella tularensis strains demonstrates extensive genetic conservation within the species but identifies regions that are unique to the highly virulent F. tularensis subsp. tularensis. J Clin Microbiol. 2003;41(7):2924–31.

    Article  CAS  Google Scholar 

  16. Becker S, Lochau P, Jacob D, Heuner K, Grunow R. Successful re-evaluation of broth medium T for the growth of Francisella tularensis ssp. and other highly pathogenic bacteria. J Microbiol Methods. 2016;121:5–7.

    Article  Google Scholar 

  17. Tlapak H, Koppen K, Rydzewski K, Grunow R, Heuner K. Construction of a new phage integration vector pFIV-Val for use in different Francisella species. Front Cell Infect Microbiol. 2018;8:75.

    Article  Google Scholar 

  18. RKI: RKI Ratgeber für Ärzte. 2016.;jsessionid=F5417746F9D2FDD7B9D541C944F9EBAC.internet101. Accessed 21 Jan 2022.

  19. Appelt S, Koppen K, Radonic A, Drechsel O, Jacob D, Grunow R, et al. Genetic diversity and spatial segregation of Francisella tularensis subspecies holarctica in Germany. Front Cell Infect Microbiol. 2019;9:376.

    Article  CAS  Google Scholar 

  20. World Health Organization. Fact sheets: animal bites. 2018. Accessed 29 Nov 2021.

  21. Aziz H, Rhee P, Pandit V, Tang A, Gries L, Joseph B. The current concepts in management of animal (dog, cat, snake, scorpion) and human bite wounds. J Trauma Acute Care Surg. 2015;78(3):641–8.

    Article  Google Scholar 

  22. Wyatt JP. Squirrel bites. BMJ. 1994;309(6970):1694.

    Article  CAS  Google Scholar 

  23. Gehringer H, Schacht E, Maylaender N, Zeman E, Kaysser P, Oehme R, et al. Presence of an emerging subclone of Francisella tularensis holarctica in Ixodes ricinus ticks from south-western Germany. Ticks Tick Borne Dis. 2013;4(1–2):93–100.

    Article  Google Scholar 

  24. Muller W, Hotzel H, Otto P, Karger A, Bettin B, Bocklisch H, et al. German Francisella tularensis isolates from European brown hares (Lepus europaeus) reveal genetic and phenotypic diversity. BMC Microbiol. 2013;13:61.

    Article  Google Scholar 

  25. Schulze C, Heuner K, Myrtennas K, Karlsson E, Jacob D, Kutzer P, et al. High and novel genetic diversity of Francisella tularensis in Germany and indication of environmental persistence. Epidemiol Infect. 2016;144(14):3025–36.

  26. Karlsson E, Golovliov I, Larkeryd A, Granberg M, Larsson E, Ohrman C, et al. Clonality of erythromycin resistance in Francisella tularensis. J Antimicrob Chemother. 2016;71(10):2815–23.

    Article  CAS  Google Scholar 

  27. Kudelina RI. Change in the properties of the causative agent of tularemia due to erythromycin. Zh Mikrobiol Epidemiol Immunobiol. 1973;50(12):98–101.

    CAS  PubMed  Google Scholar 

  28. Linde J, Homeier-Bachmann T, Dangel A, Riehm JM, Sundell D, Ohrman C, et al. Genotyping of Francisella tularensis subsp. holarctica from Hares in Germany. Microorganisms. 2020;8(12):1932.

    Article  Google Scholar 

  29. Svensson K, Granberg M, Karlsson L, Neubauerova V, Forsman M, Johansson A. A real-time PCR array for hierarchical identification of Francisella isolates. PLoS ONE. 2009;4(12): e8360.

    Article  Google Scholar 

  30. Vogler AJ, Birdsell D, Price LB, Bowers JR, Beckstrom-Sternberg SM, Auerbach RK, et al. Phylogeography of Francisella tularensis: global expansion of a highly fit clone. J Bacteriol. 2009;191(8):2474–84.

    Article  CAS  Google Scholar 

  31. Tomaso H, Hotzel H, Otto P, Myrtennas K, Forsman M. Antibiotic susceptibility in vitro of Francisella tularensis subsp. holarctica isolates from Germany. J Antimicrob Chemother. 2017;72(9):2539–43.

    Article  CAS  Google Scholar 

  32. Wittwer M, Altpeter E, Pilo P, Gygli SM, Beuret C, Foucault F, et al. Population genomics of Francisella tularensis subsp. holarctica and its implication on the eco-epidemiology of tularemia in Switzerland. Front Cell Infect Microbiol. 2018;8:89.

    Article  Google Scholar 

  33. Boone I, Hassler D, Nguyen T, Splettstoesser WD, Wagner-Wiening C, Pfaff G. Tularaemia in southwest Germany: three cases of tick-borne transmission. Ticks Tick Borne Dis. 2015;6(5):611–4.

    Article  CAS  Google Scholar 

  34. Borde JP, Zange S, Antwerpen MH, Georgi E, von Buttlar H, Kern WV, et al. Five cases of vector-borne Francisella tularensis holarctica infections in south-western Germany and genetic diversity. Ticks Tick Borne Dis. 2017;8(5):808–12.

    Article  Google Scholar 

  35. Kittl S, Francey T, Brodard I, Origgi FC, Borel S, Ryser-Degiorgis MP, et al;. First European report of Francisella tularensis subsp. holarctica isolation from a domestic cat. Vet Res. 2020;51(1):109.

    Article  CAS  Google Scholar 

  36. Kwit NA, Schwartz A, Kugeler KJ, Mead PS, Nelson CA. Human tularaemia associated with exposure to domestic dogs—United States, 2006–2016. Zoonoses Public Health. 2019;66(4):417–21.

    Article  Google Scholar 

  37. Fohle E, Smith BA, Guerrero DM. A rare case of spontaneous splenic rupture secondary to tularemia following a cat bite. Cureus. 2021;13(2): e13218.

    PubMed  PubMed Central  Google Scholar 

  38. Wawszczak M, Banaszczak B, Rastawicki W. Tularemia—a diagnostic challenge. Ann Agric Environ Med. 2022;29(1):12–21.

    Article  Google Scholar 

Download references


The authors would like to thank the technical assistants Iris Klein, Anne Barduhn, Silke Becker, and Petra Lochau for microbiological, immunological, and molecular analyses of the samples, and Anna-Maria Rohleder at ZBS2/RKI for proofreading.


Open Access funding enabled and organized by Projekt DEAL. The article processing charge was funded by the Robert Koch Institute.

Author information

Authors and Affiliations



HB, DJ, and KH wrote the manuscript. HB and JZ were primary clinicians involved in the management of the patient. JZ and HS edited the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Klaus Heuner.

Ethics declarations

Ethics approval and consent to participate

No ethics approval was required.

Consent for publication

Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.

Competing interest

The authors declare that they have no competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Borgschulte, H.S., Jacob, D., Zeeh, J. et al. Ulceroglandular form of tularemia after squirrel bite: a case report. J Med Case Reports 16, 309 (2022).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: