Abstract
Objectives
This multicentre, retrospective observational study aimed to describe the clinical presentation, diagnostic methods, treatment and outcomes of cats with tracheal masses.
Methods
Eighteen cats from five academic or secondary/tertiary animal hospitals were included.
Results
The median age at diagnosis was 10.7 years (mean 9.5; range 1–17). There were nine castrated males, seven spayed females, one intact male and one intact female. Fourteen (78%) were domestic shorthairs, one (6%) was an Abyssinian, one (6%) was an American Shorthair, one (6%) was a Bengal and one (6%) was a Scottish Fold. The most common presenting complaints included chronic respiratory distress or dyspnoea (n = 14), followed by wheezing/gagging (n = 12), coughing (n = 5) and voice changes (n = 5). There was cervical tracheal involvement in 16/18, and two showed involvement of the intrathoracic trachea. The following methods were used for diagnosis: ultrasound-guided fine-needle biopsy (UG-FNB) and cytology (n = 8), bronchoscopic forceps biopsy and histopathology (n = 5), surgical resection and histopathology (n = 3), forceps biopsy via an endotracheal tube (n = 1) and histology of tissue sputtered from a cough (n = 1). Lymphoma was most often diagnosed (n = 15), followed by adenocarcinoma (n = 2) and squamous cell carcinoma (n = 1). Most lymphoma cases received chemotherapy with or without radiation according to various protocols, and partial (n = 5) or complete responses (n = 8) were noted. Kaplan–Meier survival data for cats with lymphoma revealed a median survival time of 214 days (95% confidence interval >149 days), which was significantly longer than that of other types of tumours (21 days).
Conclusions and relevance
Lymphoma was the most prevalent diagnosis, and showed a good response to chemotherapy with or without radiation therapy. Various diagnostic procedures were performed, and UG-FNB and cytology are good diagnostic procedures for cervical tracheal lesions. Owing to the variety of treatment protocols at different centres, it was impossible to compare outcomes.
Keywords: Tracheal mass, lymphoma, bronchoscopy, fine-needle biopsy
Introduction
Tracheobronchial mass lesions are occasionally encountered in cats and can cause airway obstruction and life-threatening respiratory distress. Although the true prevalence has not been determined, they have been reported sporadically and are diagnosed as lymphoma,1–7 epithelial and non-epithelial tumors1,8–16 and inflammatory lesions.1,17 There are several diagnostic methods, including thoracic and cervical radiographs, CT,3,4,7,12,14–16 bronchoscopy with brush cytology 2 or forceps biopsy,11,12 bronchoalveolar lavage fluid analysis, 4 cytology of materials obtained by fine-needle biopsy 3 and surgical excision with subsequent histopathology.12,14,16–18
Surgical debulking, 12 excision,7,14,16,19 stenting of the trachea, 15 chemotherapy2 –4 and radiation therapy2,3,14 have been reported for feline tracheal mass lesions. The prognosis varies among cases, and different survival times have been reported for the same histopathological diagnosis and treatment.
Therefore, we designed a multicentre retrospective observational study to look at the clinical presentations, diagnostic methods, treatments and outcomes of cats with tracheal masses.
Materials and methods
The present study was a retrospective multicentre cohort study. The primary investigator (HK) contacted five academic or secondary/tertiary animal hospitals (Japan Small Animal Cancer Center [Saitama, Japan], Nippon Veterinary and Life Science University Veterinary Medical Teaching Hospital [Tokyo, Japan], Veterinary Medical Center of the University of Tokyo [Tokyo, Japan], Hokkaido University Veterinary Teaching Hospital [Hokkaido, Japan] and DVMs Animal Medical Center Yokohama [Kanagawa, Japan]) to participate in this study and electronic medical records were collected, along with accompanying data, such as diagnostic images, imaging and histopathological reports.
Cats with tracheal mass lesions and a final diagnosis based on cytological and/or histopathological examination between 2010 and the end of June 2022 were included in the study. Data retrieved from medical records included breed, sex, age, weight, history/clinical signs, final diagnosis, diagnostic/surgical procedures and outcomes. Cases in which only a presumptive diagnosis was made using cytology or diagnostic treatment were excluded.
Survival analysis was performed using Kaplan–Meier curves and log-rank tests using R software.20,21 Statistical significance was set at P <0.05.
Results
Eighteen cats were included (Table 1): nine neutered males, seven neutered females, one intact male and one intact female. Fourteen (78%) were domestic shorthair, one (6%) was an Abyssinian, one (6%) was an American Shorthair, one (6%) was a Bengal and one (6%) was a Scottish Fold. The median age at diagnosis was 10.7 years (mean 9.5; range 1–17). Feline leukaemia virus (FeLV) antigen testing was positive in 1/11 cats tested, and feline immunodeficiency virus (FIV) antibody was positive in 1/11 cats.
Table 1.
Demographic data and summary of 18 cats with a tracheal mass included in the study
| Cat | Age (months) | Sex | Breed | Body weight (kg) | Diagnosis | Biopsy procedure | Location | Duration of clinical signs (days) | Metastasis | Treatment | Response to treatment | Survival time (days) | Outcome | PARR | IHC | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1 | 89 | MN | SF | 4.92 | Lymphoma | Bronchoscopic forceps biopsy | C7 | Ventral | 30 | None | Chemotherapy | CR | 85 | Survived | Negative | CD20 |
| 2 | 210 | MN | DSH | 5 | Lymphoma | Surgical biopsy | C2 | Ventral | 96 | None | Chemotherapy, surgery | CR | 884 | Died | Negative | CD20 |
| 3 | 151 | FI | Bengal | 4.6 | Lymphoma | UG-FNB | C2–4 | Ventral | 90 | None | Chemotherapy, radiation | CR | 140 | Died | Negative | ND |
| 4 | 177 | FN | DSH | 6.16 | Lymphoma | UG-FNB | C3–4 | Dorsal | 30 | Lung, suspected | Chemotherapy | CR | 784 | Survived | IgH | ND |
| 5 | 132 | FN | DSH | 4.4 | Lymphoma | Surgical biopsy | T3 | Filled | 20 | None | Surgery | ND | 6 | Died | ND | CD20 |
| 6 | 88 | FN | DSH | 4.1 | Lymphoma | Bronchoscopic forceps biopsy | T1 | Filled | 65 | Mediastinal lymph node | Chemotherapy, radiation | PR | 153 | Died | ND | ND |
| 7 | 125 | MN | Abyssinian | 4.35 | Lymphoma | Bronchoscopic forceps biopsy | C5–6 | Dorsal | 36 | None | Chemotherapy | PR | 149 | Died | ND | ND |
| 8 | 29 | FN | DSH | 4.54 | Lymphoma | UG-FNB | C6–7 | Filled | 14 | None | Chemotherapy | ND | 6 | Survived | ND | ND |
| 9 | 134 | FN | DSH | 3.26 | Lymphoma | UG-FNB | C2 | Ventral | 17 | None | Chemotherapy | CR | 785 | Died | ND | ND |
| 10 | 23 | MI | DSH | 5.5 | Lymphoma | UG-FNB | C2 | Filled | 11 | None | Chemotherapy | PR | 0 | Survived | IgH | ND |
| 11 | 54 | MN | DSH | 4.7 | Lymphoma | Bronchoscopic forceps biopsy | C5–6 | Ventral | 21 | None | Chemotherapy, radiation | CR | 168 | Survived | ND | CD20 |
| 12 | 135 | MN | DSH | 5 | Lymphoma | UG-FNB | C3–4 | Ventral and dorsal | 148 | Lung, suspected | Chemotherapy | CR | 136 | Survived | ND | ND |
| 13 | 132 | MN | DSH | 5.18 | Lymphoma | UG-FNB | C3–4 | Ventral | 9 | None | Chemotherapy, radiation | CR | 394 | Survived | ND | ND |
| 14 | 106 | FN | DSH | 2.73 | Lymphoma | UG-FNB | C2 | Ventral | 90 | Larynx | Chemotherapy, radiation | PR | 214 | Died | ND | ND |
| 15 | 55 | MN | DSH | 4 | Lymphoma | Bronchoscopic forceps biopsy | C2–4 | Ventral | 25 | None | Chemotherapy, radiation | PR | 93 | Died | IgH | ND |
| 16 | 163 | FN | DSH | 3.55 | Adenocarcinoma | Histopathology of the sample obtained by forceps biopsy via an endotracheal tube | C2–6 | Filled | 21 | Lung, suspected | Surgery | ND | 15 | Died | NA | NA |
| 17 | 102 | MN | ASH | 7 | Adenocarcinoma | Surgical biopsy | C7 | Dorsal | 46 | Lung, suspected | None | ND | 81 | Survived | NA | NA |
| 18 | 154 | MN | DSH | 3.95 | SCC | Surgical biopsy | C4–5 | Dorsal | ND | Lung, suspected | None | ND | 21 | Died | NA | NA |
PARR = PCR for antigen receptor rearrangement; IHC = immunohistochemistry; MN = male neutered; SF = Scottish Fold; CR = complete remission; DSH = domestic shorthair; FI = female intact; UG-FNB = ultrasound-guided fine-needle biopsy; ND = not determined; FN = female neutered; PR = partial response; MI = male intact; NA = not available; ASH = American Shorthair; SCC = squamous cell carcinoma
The most common presenting complaints were dyspnoea or respiratory distress (n = 14; 78%), followed by wheezing/gagging (n = 12; 67%), coughing (n = 5; 28%) and voice change (n = 2; 11%). The duration of these clinical signs was described in 17 cats as ranging from 9 to 148 days (median 30).
In all cases, the lesions were evaluated using cervical or thoracic radiography performed at the participating institutions or submitted by a referral veterinarian. Ultrasonography was performed on eight cats with cervical lesions, and CT was performed in 11 cases. Sixteen of 18 cats presented with involvement of the cervical trachea, and two with involvement of the intrathoracic trachea. Of the 16 cervical lesions, eight protruded from the ventral side of the trachea, four from the dorsal side and one from both sides. The lesion filled the lumen in the remaining three cats, and ventrodorsal localisation could not be determined. One thoracic lesion protruded from the ventral side and the other filled the lumen. In the craniocaudal direction, lesions were evenly distributed from the C2 to the T3 level (Figure 1). Ultrasonography of the cervical lesions showed a hypoechoic mass adjacent to the air in the trachea that narrowed the lumen and occasionally destroyed the wall of the trachea (Figure 2). CT confirmed the radiographic and ultrasonographic findings, and better visualised the extension of the lesion (Figure 3) or pulmonary metastasis in several cases.
Figure 1.

Representative lateral thoracic radiographic image in a lymphoma case. The trachea demonstrates narrowing by a dorsal soft tissue opacity at the level of the thoracic inlet (arrows)
Figure 2.

Transverse ultrasonographic image of a cervical lymphoma case showing a hypoechoic mass adjacent to the air in the lumen of the trachea (arrows). The line of the tracheal wall appears unclear on the right side due to the invasion of the lesion
Figure 3.
Lateral thoracic radiograph and transverse enhanced CT image of a thoracic lymphoma case. Radiography shows a ventral protrusion at the thoracic inlet (a, arrows), whereas CT imaging revealed the mass to be more extensively infiltrated, surrounding the trachea dorsally to the left and ventrally (b, arrows)
The following methods were used for diagnosis: ultrasound-guided fine-needle biopsy (UG-FNB) and cytology (n = 8), bronchoscopic forceps biopsy and histopathology (n = 5), surgical resection and histopathology (n = 3), forceps biopsy via an endotracheal tube (n = 1) and histology of tissue sputtered from a cough (n = 1). Lymphoma was diagnosed in 15 cases (eight by cytology and seven by histopathology). Other diagnoses included adenocarcinoma (n = 2) and squamous cell carcinoma (SCC; n = 1). PCR for antigen receptor rearrangements (PARR) analysis was performed on six lymphoma cases: three showed IgH clonal rearrangement, whereas three were negative for both T-cell receptor and IgH genes. Immunohistochemistry showed CD20 positivity in the four cats tested. In total, 7/15 lymphoma cases were determined to be of B-cell origin, and the T-cell/B-cell phenotype in the remaining cases was unknown.
Pulmonary involvement was suspected but not confirmed on either chest radiography or CT in two lymphoma cases. Sternal lymph node involvement was cytologically confirmed in another case of lymphoma. A laryngeal mass lesion was also noted in another lymphoma case but was not histologically or cytologically examined. Two carcinoma cases and one SCC case had single or multiple pulmonary nodules suggestive of metastasis.
A lymphoma patient underwent resection of the trachea and anastomosis but died 7 days after surgery. Although necropsy was not performed, tracheal dehiscence was suspected based on the findings of inflammatory pleural effusion. Resection of the tumour was performed in another cat with lymphoma after a partial response to two administrations of L-asparaginase followed by the finding of mediastinal emphysema, suggestive of tracheal perforation. The cat was discharged uneventfully, followed by multiagent chemotherapy. All other lymphoma cases received chemotherapy with (n = 6) or without (n = 7) radiation according to various protocols, including agents such as L-asparaginase, vincristine, cyclophosphamide, doxorubicin, cytarabine, nimustine, and bleomycin; partial (n = 5) or complete (n = 8) response was noted during the protocol in all 13 cases in which the outcome was followed.
In the case of adenocarcinoma, the cat became dyspnoeic upon awakening from anaesthesia for CT and underwent tracheal resection and anastomosis. The patient was discharged on postoperative day 10 but died at home on postoperative day 11. A patient with SCC was scheduled for radiotherapy but died of respiratory distress 21 days after the diagnosis.
Kaplan–Meier survival data for cats with lymphoma revealed a median survival time of 214 days (95% confidence interval >149, which was significantly longer than that of the other types of tumours (21 days; Figure 4).
Figure 4.

Kaplan–Meier survival curve showing lymphoma (solid line) vs other tumours (dotted line). X represents censored patients. The median survival time of 214 days (95% confidence interval >149) in lymphoma cases was significantly longer than that of other tumour types (21 days)
Discussion
In this retrospective study evaluating cases of feline tracheal masses, cats of various breeds had a chronic course of signs related to airway obstruction such as wheezing, gagging and dyspnoea. Most cats were relatively old, except for three with lymphoma, which were 1, 2 and 4 years old, respectively. The lesions were distributed from beneath the larynx to above the carina and were attached to either the ventral, dorsal or almost the entire lumen of the trachea. Therefore, tracheal masses should be included in the differential diagnosis of cats with chronic respiratory signs, and the neck and thorax should be carefully examined.
Most tracheal masses in the present study (n = 15/18) were lymphomas, which agrees with a previous report in which lymphoma was the most frequent diagnosis (n = 3/7). 1 Lymphoma cases were more likely to be included than other diagnoses in the present study, because lymphoma can be diagnosed cytologically more frequently than other types of lesions. It is possible that, in the case of lymphoma, a response to corticosteroids administered prior to diagnosis allows time for the owner and primary care veterinarian to consider referral, and more cases can be seen at a secondary care facility compared with non-lymphoma cases. For non-lymphoma tracheal masses, owners often give up further testing at the point of no response to experimental treatment. Moreover, it is possible that the percentage of lymphomas increased in this study because steroid treatment improved the condition of lymphoma cases and reduced the risk, allowing more cases to undergo diagnostic testing. Corticosteroids were administered before referral in 9/15 lymphoma cases. Although the exact proportion of lymphoma in the tracheal mass could not be determined due to the retrospective nature of the present study, it seems plausible that lymphoma is most frequently diagnosed in feline tracheal masses.
Tracheal lymphoma in this study occurred in young to older cats, mostly without FIV/FeLV infection. No breed or sex predisposition was identified. The lesion was located in both the neck and thorax but was predominant in the cervical trachea, and clinical signs included wheezing, gagging, respiratory distress, dyspnoea and coughing. This clinical picture follows those of previously reported cases. Cervical and thoracic radiography was the primary diagnostic modality for tracheal lesions, and ultrasonography, CT and bronchoscopy were the subsequent advanced imaging procedures that revealed details of the location, distribution and presence of metastasis. Lymphoma cases in the cervical trachea were diagnosed most frequently by UG-FNB and cytology, followed by endoscopic tissue biopsy. In a previous report, the diagnostic potential of ultrasonography and UG-FNB was not described in detail, and the results of this study emphasise the usefulness of this procedure for tracheal lesions. The high prevalence of lymphoma further supports the usefulness of UG-FNB, because there is a good chance of diagnosis by cytological examination. PARR analysis may support the diagnosis of lymphoma if cytology does not provide sufficient findings. Bronchoscopic forceps biopsy was performed on four cats without complications, and the samples obtained were sufficient for definitive diagnosis. The same method has also been reported,11,12 and other sampling methods using bronchoscopy include brush cytology2,9 and bronchoalveolar fluid analysis. 4 However, the number of cells obtained using brush cytology is not always sufficient for diagnosis. 7 Although severe complications such as massive haemorrhage and air leakage should always be considered, forceps biopsy under bronchoscopy is a valuable method for histological diagnosis of tracheal masses. No complication was noted with UG-FNB and endoscopy. However, cats with intratracheal mass lesions are at greater risk from general anaesthesia and bronchoscopic procedures. UG-FNB is preferable if the cat is not uncooperative and cervical ultrasonography can be safely performed without anaesthesia.
In this study, only 1/11 cases examined was positive for serum FIV antibody and FeLV antigen. This result was in agreement with the previous studies: none of the 13 cases examined were positive for FIV/FeLV.1 –5,7,18 However, FeLV antigen was immunohistochemically detected in 54% of the cases in a recent study of feline upper respiratory tract (namely nasal and nasopharyngeal) lymphoma, suggesting the role of FeLV at the genomic level. 22 The immunohistochemical investigation of FeLV antigen was not possible in this study due to the retrospective nature of the study and the small number of cases with histological investigation. Considering the similarities between nasopharyngeal and tracheal lymphomas, such as B-cell origin and diffuse large B-cell lymphoma (DLBCL) predominance, further studies on the relevance of FeLV in feline tracheal lymphoma are highly desirable.
PARR analysis or immunohistochemistry was performed in seven cases; six were of B-cell origin, whereas the immunophenotype of the remaining case could not be determined. B-cell origin has also been reported in feline tracheal lymphoma, 7 but the immunophenotype was not clarified in most previous reports.1,2,4,5,7 The results of the present study suggest that B-cell lymphoma is the predominant type of tracheal lymphoma in cats, in contrast to humans. In particular, a histological diagnosis of two cases specifically noted the histological type of DLBCL. This histological type is most frequently seen in feline lymphomas of other organs, such as lymphomas of the eye, 23 retina, 24 lung 25 and nose,22,26,27 except for gastrointestinal lymphomas, 28 where T-cell lymphomas predominate. Although anatomically different, the biological similarity of the same histological type in other organ lymphomas may help provide insight into the treatment and prognosis of tracheal lymphoma. However, further studies are needed to evaluate the true prevalence of each histological classification.
All lymphoma patients with a confirmed response to chemotherapy showed at least a partial response at any time point in the protocol, and 62% (n = 8/13) showed a complete response. This good response to chemotherapy has not been well described in the previous literature; however, long-term survival has been reported.1,2,4,7 Six cats received radiation and chemotherapy, whereas nine cats received only chemotherapy, and the survival time was not different between cats with and without radiation. However, because the protocols in each case were not standardised in this study, the appropriate chemotherapy with or without a radiation protocol was not determined.
Two adenocarcinomas and one SCC were included in the study. Although a small number of cases were included, signalment, clinical signs and imaging features were similar to those of lymphoma, and all cases had suspected pulmonary metastasis. Only one patient underwent aggressive surgical treatment, but the prognosis was poor, in contrast to the lymphoma cases. A high proportion of possible lung metastases differed from the previous study,6,8,9,12,14,19 which could be due to the difference in population.
Two patients that underwent resection and anastomosis died shortly after surgery. This procedure has been reported sporadically in the veterinary literature with occasional severe complications, such as cardiac arrest and laryngeal paralysis.7,12,14,16,18,19,29 Other reported surgical procedures include bronchoscopic debulking and stenting.12,15 Because of the small number of patients that underwent surgery, the feasibility of surgical procedures for tracheal masses in cats could not be determined. However, appropriate non-invasive diagnostic procedures should be pursued before invasive surgery for feline tracheal masses, as lymphoma is the most likely diagnosis and there are other reasonable treatment options for lymphoma, such as chemotherapy and radiation.
The limitations of this retrospective study include the bias of the case selection and the variation of the diagnostic tests, case management and treatment regimens. In particular, the lack of a complete histological report limited comprehensive histopathological subtyping in lymphoma cases that might potentially lead to the establishment of an ideal treatment protocol based on subtypes. Further study is recommended for this disease entity including prospectively collected cases with standardised diagnostics/treatment.
Conclusions
This study described a relatively large number of cats with tracheal masses. Lymphoma was the most prevalent diagnosis, with a good response to chemotherapy with or without radiation therapy. UG-FNB and cytology are reasonable diagnostic procedures for feline cervical tracheal masses.
Acknowledgments
We would like to thank Editage (www.editage.com) for English language editing.
Footnotes
The authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.
Funding: The authors received no financial support for the research, authorship, and/or publication of this article.
Ethical approval: The work described in this manuscript involved the use of non-experimental (owned or unowned) animals. Established internationally recognised high standards (‘best practice’) of veterinary clinical care for the individual patient were always followed and/or this work involved the use of cadavers. Ethical approval from a committee was therefore not specifically required for publication in JFMS. Although not required, where ethical approval was still obtained, it is stated in the manuscript.
Informed consent: Informed consent (verbal or written) was obtained from the owner or legal custodian of all animal(s) described in this work (experimental or non-experimental animals, including cadavers) for all procedure(s) undertaken (prospective or retrospective studies). No animals or people are identifiable within this publication, and therefore additional informed consent for publication was not required.
ORCID iD: Aki Fujiwara-Igarashi
https://orcid.org/0000-0003-0386-3728
Tetsuya Kobayashi
https://orcid.org/0000-0002-0100-8579
Aki Ohmi
https://orcid.org/0000-0001-7592-6391
Hajime Tsujimoto
https://orcid.org/0000-0002-3771-6235
References
- 1. Jakubiak MJ, Siedlecki CT, Zenger E, et al. Laryngeal, laryngotracheal, and tracheal masses in cats: 27 cases (1998–2003). J Am Anim Hosp Assoc 2005; 41: 310–316. [DOI] [PubMed] [Google Scholar]
- 2. Brown MR, Rogers KS, Mansell KJ, et al. Primary intratracheal lymphosarcoma in four cats. J Am Anim Hosp Assoc 2003; 39: 468–472. [DOI] [PubMed] [Google Scholar]
- 3. Brown EM, Rademacher N, Gieger TL, et al. What is your diagnosis? Tracheal lymphoma. J Am Vet Med Assoc 2010; 236: 953–954. [DOI] [PubMed] [Google Scholar]
- 4. Dugas B, Hoover J, Pechman R. Computed tomography of a cat with primary intratracheal lymphosarcoma before and after systemic chemotherapy. J Am Anim Hosp Assoc 2011; 47: e131–137. [DOI] [PubMed] [Google Scholar]
- 5. Kim D-Y, Kim J-R, Taylor HW, et al. Primary extranodal lymphosarcoma of the trachea in a cat. J Vet Med Sci 1996; 58: 703–706 [DOI] [PubMed] [Google Scholar]
- 6. Carlisle CH, Biery DN, Thrall DE. Tracheal and laryngeal tumors in the dog and cat: literature review and 13 additional patients. Vet Radiol Ultrasound 1991; 32: 229–235. [Google Scholar]
- 7. Bataller L, Tamborini A, L’Eplattenier H, et al. Successful treatment of tracheal lymphoma in a Siamese cat. JFMS Open Rep 2017; 3. DOI: 10.1177/2055116917742529. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8. Cain GR, Manley P. Tracheal adenocarcinoma in a cat. J Am Vet Med Assoc 1983; 182: 614–616. [PubMed] [Google Scholar]
- 9. Lobetti RG, Williams MC. Anaplastic tracheal squamous cell carcinoma in a cat. J S Afr Vet Assoc 1992; 63: 132–133. [PubMed] [Google Scholar]
- 10. Bell R, Philbey AW, Martineau H, et al. Dynamic tracheal collapse associated with disseminated histiocytic sarcoma in a cat. J Small Anim Pract 2006; 47: 461–464. [DOI] [PubMed] [Google Scholar]
- 11. Rossi G, Magi GE, Tarantino C, et al. Tracheobronchial neuroendocrine carcinoma in a cat. J Comp Pathol 2007; 137: 165–168. [DOI] [PubMed] [Google Scholar]
- 12. Queen EV, Vaughan MA, Johnson LR. Bronchoscopic debulking of tracheal carcinoma in 3 cats using a wire snare. J Vet Intern Med 2010; 24: 990–993. [DOI] [PubMed] [Google Scholar]
- 13. Jelinek F, Vozkova D. Carcinoma of the trachea in a cat. J Comp Pathol 2012; 147: 177–180. [DOI] [PubMed] [Google Scholar]
- 14. Green ML, Smith J, Fineman L, Proulx D. Diagnosis and treatment of tracheal basal cell carcinoma in a Maine coon and long-term outcome. J Am Anim Hosp Assoc 2012; 48: 273–277. [DOI] [PubMed] [Google Scholar]
- 15. Culp WTN, Weisse C, Cole SG, et al. Intraluminal tracheal stenting for treatment of tracheal narrowing in three cats. Vet Surg 2007; 36: 107–113. [DOI] [PubMed] [Google Scholar]
- 16. Drynan EA, Moles AD, Raisis AL. Anaesthetic and surgical management of an intra-tracheal mass in a cat. J Feline Med Surg 2011; 13: 460–462. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17. Sheaffer KA, Dillon AR. Obstructive tracheal mass due to an inflammatory polyp in a cat. J Am Anim Hosp Assoc 1996; 32: 431–434. [DOI] [PubMed] [Google Scholar]
- 18. Beaumont PR. Intratracheal neoplasia in two cats. J Small Anim Pract 1983; 23: 29–35. [DOI] [PubMed] [Google Scholar]
- 19. Miller ZA, Padgett S, Terreros A, et al. Tracheal squamous cell carcinoma treated with tracheal resection and anastomosis in a cat. Case Rep Vet Med 2020; 2020. DOI: 10.1155/2020/8818660. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20. R Team. R: a language and environment for statistical computing. Vienna: R Foundation for Statistical Computing, 2013. [Google Scholar]
- 21. Therneau T. A package for survival analysis in R_. R package version 3.2-13. https://CRAN.R-project.org/package=survival (2021, accessed 25 March 2023).
- 22. Santagostino SF, Mortellaro CM, Boracchi P, et al. Feline upper respiratory tract lymphoma: site, cyto-histology, phenotype, FeLV expression, and prognosis. Vet Pathol 2015; 52: 250–259. [DOI] [PubMed] [Google Scholar]
- 23. Musciano AR, Lanza MR, Dubielzig RR, et al. Clinical and histopathological classification of feline intraocular lymphoma. Vet Ophthalmol 2020; 23: 77–89. [DOI] [PubMed] [Google Scholar]
- 24. Malmberg JL, Garcia T, Dubielzig RR, et al. Canine and feline retinal lymphoma: a retrospective review of 12 cases. Vet Ophthalmol 2017; 20: 73–78. [DOI] [PubMed] [Google Scholar]
- 25. Leite-Filho RV, Panziera W, Bandinelli MB, et al. Pathological characterization of lymphoma with pulmonary involvement in cats. J Comp Pathol 2018; 165: 6–12. [DOI] [PubMed] [Google Scholar]
- 26. Day MJ, Henderson SM, Belshaw Z, et al. An immunohistochemical investigation of 18 cases of feline nasal lymphoma. J Comp Pathol 2004; 130: 152–161. [DOI] [PubMed] [Google Scholar]
- 27. Little L, Patel R, Goldschmidt M. Nasal and nasopharyngeal lymphoma in cats: 50 cases (1989–2005). Vet Pathol 2007; 44: 885–892. [DOI] [PubMed] [Google Scholar]
- 28. Wolfesberger B, Fuchs-Baumgartinger A, Greß V, et al. World Health Organisation classification of lymphoid tumours in veterinary and human medicine: a comparative evaluation of gastrointestinal lymphomas in 61 cats. J Comp Pathol 2018; 159: 1–10. [DOI] [PubMed] [Google Scholar]
- 29. Katayama M, Okamura Y, Katayama R, et al. Presumptive acute lung injury following multiple surgeries in a cat. Can Vet J 2013; 54: 381–386. [PMC free article] [PubMed] [Google Scholar]

