CASE REPORT
Intra-abdominal transmissible venereal tumor
in a dog: a case report
Tumor venéreo transmissível intra-abdominal em cadela: relato
de caso p-ISSN 0100-2430
e-ISSN 2527-2179
Alexandre José Rodrigues Bendas1* , Pablo Luiz das Neves Moreto2 , Adriano Baldaia Coxo2 ,
Paula Gazé Holguin2 & Denise do Vale Soares2
1
Veterinarian, DSc. Departamento de medicina e cirurgia veterinária (DMCV), Instituto de Veterinária (IV), Universidade Federal
Rural do Rio de Janeiro (UFRRJ). Campus Seropédica, RJ, Brazil.
2
Veterinarian, Autonomus, Rio de Janeiro, RJ, Brazil
How to cite: Bendas, A. J. R., Moreto, P. L. N.,
Abstract Coxo, A. B., Holguin, P. G., & Soares, D. V. (2022).
Transmissible venereal tumor (TVT) is a malignant round cell neoplasm that primarily affects the Intra-abdominal transmissible venereal tumor
genital region of dogs. Despite being sexually transmitted, transmission can occur through contact with in a dog: a case report. Brazilian Journal of
Veterinary Medicine, 44, e001422. [Link]
mucous membranes and cutaneous tissue. Although less routine, TVT has been described in several org/10.29374/2527-2179.bjvm001422
extragenital regions, such as the nasal plane, oral cavity, eyeball, eyelid, and anus. Although metastases
are infrequent, they can occur in the skin, inguinal lymph nodes, liver, kidneys, spleen, intestine, heart, Received: April 18, 2022.
Accepted: July 13, 2022.
brain, lungs, and other organs. The clinical signs of TVT are usually related to serosanguineous secretion,
intense odor, deformity, ulceration, and possibly areas of necrosis. In cases of metastases, clinical signs *Correspondence
will depend on the affected organ. The treatment of choice for TVT is chemotherapy with vincristine. Alexandre José Rodrigues Bendas
The present study aimed to report the case of a 2-year-old mixed-breed canine with intra-abdominal Departamento de Medicina e Cirurgia
Veterinária (DMCV), Instituto de Veterinária
nodules detected by ultrasound examination, which were later diagnosed as a TVT by histopathology (IV), Universidade Federal Rural do Rio de
and immunohistochemistry. Janeiro – UFRRJ
Keywords: abdominal neoplasm, immunohistochemistry, round cell neoplasm. Rodovia BR 465, Km 7, Campus Universitário,
Bairro Zona Rural
CEP 23897-000 - Seropédica (RJ), Brasil
Resumo E-mail: alexandrebendas@[Link]
O tumor venéreo transmissível (TVT) é uma neoplasia maligna de células redondas que acomete
principalmente a região genital de cães. Apesar de ser sexualmente transmissível, a transmissão pode
ocorrer através do contato com mucosas e tecidos da pele. Embora menos rotineiro, o TVT tem sido
descrito em diversas regiões extragenitais, como plano nasal, cavidade oral, globo ocular, pálpebra e ânus.
Embora as metástases sejam infrequentes, elas podem ocorrer na pele, linfonodos inguinais, fígado, rins,
baço, intestino, coração, cérebro, pulmão e outros órgãos. Os sinais clínicos do TVT geralmente estão
relacionados à secreção serossanguinolenta, odor intenso, deformidade, ulceração, podendo ou não
haver áreas de necrose e, nos casos de metástases, os sinais clínicos vão depender do órgão acometido.
O tratamento de escolha para TVT é a quimioterapia, com uso de vincristina. O presente trabalho tem
como objetivo relatar o caso de um canino de dois anos de idade, sem raça definida, com nódulos intra-
abdominais detectados ao exame ultrassonográfico, que posteriormente foram diagnosticados como
tumor venéreo transmissível por meio de histopatologia e imunohistoquímica.
Palavras-chave: neoplasia abdominal, imuno-histoquímica, neoplasia de células redondas.
Introduction
Canine transmissible venereal tumor (TVT), also known as canine condyloma, granuloma
venereum, infectious sarcoma, or venereal lymphosarcoma, is the oldest known tumor and is
among the main neoplasms affecting dogs (Dagli, 2019; Daleck & Denardi, 2016).
Currently, TVT is classified as a round cell neoplasm (Hedlund, 2005), in the same group as
mast cell tumors, basal cell carcinomas, histiocytomas, and lymphomas (Vermooten, 1987). Copyright Bendas et al. This is an Open
This neoplasm is naturally contagious and sexually transmitted among dogs, especially those of Access article distributed under the terms
of the Creative Commons Attribution
straying life and of reproductive age (Tinucci-Costa & Castro, 2009), and possibility of experimental Non-Commercial License which permits
transplantation has also been demonstrated (Silveira et al., 2009). Although sexual acts are the unrestricted non-commercial use,
distribution, and reproduction in any
most frequent means of transmission of TVT, other means exist, such as the habit of licking and medium provided the original work is
sniffing other dogs (Oliveira, 2019; Park et al., 2006; Strakova & Murchison, 2014) that can lead properly cited.
Bendas et al. 2022. Brazilian Journal of Veterinary Medicine, 44, e001422. DOI: 10.29374/2527-2179.bjvm001422 1/6
Intra-abdominal transmissible venereal tumor in a dog: a case report
to tumor cell implantation in the nasal and oral cavities. Additionally, direct contact between
sites with skin lesions can cause eye and skin lesions (Lapa, 2009; Tinucci-Costa & Castro, 2009).
Although metastases are not frequent and are rarer than those to extracutaneous locations,
which affect approximately 1% of dogs (Tinucci-Costa & Castro, 2009), they can occur in the
skin, inguinal lymph nodes, liver, kidneys, spleen, intestine, heart, brain, lungs, and other organs
(Brandão et al., 2002; Chikweto et al., 2013; Tinucci-Costa & Castro, 2009).
The clinical signs reported in dogs with TVT and those with genital lesions range from the
presence of a mass, which can be single or multiple, usually friable on the foreskin or vulva
(Brandão et al., 2002; Oliveira, 2019), serosanguineous secretion, odor intensity, deformity,
ulceration, and areas with or without necrosis. When tumors and/or their metastases occur in
extragenital regions, other clinical signs may be present depending on the location of the affected
organ (Oliveira, 2019), which may manifest in the form of respiratory disorders, such as dyspnea,
abdominal pain, and dysphagia (Huppes et al., 2014; Lapa, 2009; Tinucci-Costa & Castro, 2009).
TVT diagnosis in the extragenital regions can be more difficult depending on the anatomical
location of the tumors (Oliveira, 2019). However, in both cases, an accurate diagnosis of primary
or metastatic TVT can only be established with the aid of cytological or histopathological
examination (Oliveira, 2019; Tinucci-Costa & Castro, 2009).
The treatment of choice for this type of neoplasm is chemotherapy (Rogers et al., 1998).
Vincristine sulfate is the first-choice drug for the antineoplastic chemotherapy of TVTs, which can
be administered at a dose of 0.025 mg/kg up to 1 mg/kg or 0.5 mg/m2 IV, weekly, for 3–6 weeks,
with an interval of 7 days between the doses (Fossum, 2005; Ramadinha et al., 2016; Tinucci-
Costa & Castro, 2009). The prognosis is generally considered favorable, with a good response
to chemotherapy, total tumor remission, and clinical improvement in the animal. However, in
cases exhibiting resistance to chemotherapy or metastases in the central nervous system and
eyes, the prognosis is limited (Ganguly et al., 2016; Tinucci-Costa & Castro, 2009).
The present study aimed to report the case of a 2-year-old mixed-breed canine, with intra-
abdominal TVT.
Case description
A mixed-breed female canine with an estimated age of 2 years, weighing 8 kg, was brought
for care after being found on the street. She was underweight, with pale mucous membranes,
fleas, ticks, and other parameters that were within the normal range. A vermifuge was prescribed,
ectoparasiticide was administered, blood was collected for blood count, and ultrasound was
requested. The hemogram revealed normocytic normochromic nonregenerative anemia
(hematocrit 23%; reference value: 37–55%), leukocytosis without left shift (36,100; reference value:
6,000–17,000 n/μL), thrombocytopenia (22,000/μL; reference value: 150,000 – 500,000/μL), and
antibodies against Ehrlichia spp., Anaplasma spp., Borrelia burgdorferi, and Dirofilaria immitis
antigens (SNAP test 4Dx® Idexx). The sample was positive for Anaplasma spp. and Ehrlichia spp.
Based on this result, doxycycline (5 mg/kg/BID for 28 days) and prednisone (0.5 mg/kg/SID/5 days)
were prescribed. The owner chose to not perform the ultrasound. A return visit was requested
within 7 days to reassess the condition and perform a new blood count, but the patient was not
brought back to the clinic.
Two months after the first consultation, the patient returned with a complaint of non-specific
vomiting, which had started 2 days before the patient’s presentation to the clinic. Maropitant
(1 mg/kg/SID/SC) was administered, omeprazole (1 mg/kg/SID/5 days) and a homemade diet
were prescribed, the ultrasound request was reinforced, and blood analysis was requested,
but they were not performed. After the initial improvement, vomiting was noted again at the
end of treatment, which was associated with inappetence, anorexia, and prostration. The dog
was hospitalized, and the previously requested examinations were performed. Hematological
analyses revealed polycythemia (hematocrit 58%; reference value: 37–55%), thrombocytosis
(848,000; reference value: 150,000–500,000 n/μL), and leukocytosis (18,500; reference value:
6,000–17,000 n/μL) with a left shift. Biochemical tests revealed an increase in the levels of alkaline
phosphatase (116.10; reference value: 8 to 88 mU/mL), urea (146; reference value: 11 to 60 mg/
dL), cholesterol (260; reference value: 140 to 210 mg/dL), and decreased levels of potassium
(3.10; reference value: 4.37 to 5.65 mEq/L) and sodium (138; reference value: 141.10 to 152.3); the
Bendas et al. 2022. Brazilian Journal of Veterinary Medicine, 44, e001422. DOI: 10.29374/2527-2179.bjvm001422 2/6
Intra-abdominal transmissible venereal tumor in a dog: a case report
other indexes were within the normal range. Abdominal ultrasonography revealed numerous
heterogeneous oval structures, predominantly hypoechoic, with some present in the central
region filled with cloudy liquid, measuring from 0.80 x 1.23 cm to 1.47 x 4.81 cm, presence of
free fluid with cloudy appearance, rich in debris, a diffuse increase in abdominal echogenicity
compatible with peritonitis (Figure 1A and 1B), and an absence of uterus and ovaries.
Figure 1A and 1B. Abdominal ultrasound revealing numerous heterogeneous oval structures, predominantly
hypoechoic (structures between markers [+]).
An abdominal fluid sample was collected for analysis, in addition to a guided puncture of
the nodules for cytology. Fluid analysis revealed several red blood cells, frequent segmented
neutrophils, foamy macrophages, and frequent degenerated cells, and the material was classified
as pyogranulomatous inflammatory exudate. Cytological examination of the nodules revealed
several erythrocytes, frequent neutrophils, and several epithelioid cells with an eccentric nucleus
and basophilic and vacuolated cytoplasm, rendering diagnosis unattainable.
The patient remained hospitalized and was administered meropenem (24 mg/kg/SID/IV),
scopolamine with dipyrone (25 mg/kg/TID/IV), ondansetron (1 mg/kg/BID/IV), omeprazole
(1 mg/kg/IV), and tramadol (4 mg/kg/BID/IV). Exploratory laparotomy and biopsy for histopathological
analysis were chosen owing to the inconclusive fluid and cytology analysis results; additionally,
there was no improvement in the clinical picture with the instituted therapy. During laparotomy,
diffuse peritonitis, abscess points, and the presence of purulent secretions were observed in the
cavity, in addition to several reddish nodules of varying sizes implanted throughout the abdominal
cavity (mesentery, omentum, liver, and spleen) (Figure 2A and 2B).
Figure 2A and 2B. Exploratory laparotomy revealing multiple reddish nodular formations of varying sizes,
implanted throughout the abdominal cavity.
Bendas et al. 2022. Brazilian Journal of Veterinary Medicine, 44, e001422. DOI: 10.29374/2527-2179.bjvm001422 3/6
Intra-abdominal transmissible venereal tumor in a dog: a case report
Ten intracavitary nodules were removed for biopsy, and purulent material was collected for
culture and antibiogram. The animal stayed in the clinic for 5 days after receiving supportive
treatment. During hospitalization, a total of three abdominocenteses were performed, with
removal of the purulent fluid (average 400–600 mL). Since no improvement was noted, those
responsible decided to request the animal’s discharge and returned 2 days later for euthanasia.
Culture and antibiogram revealed the presence of Proteus spp., which was sensitive to only two
antibiotics tested (neomycin and meropenem) and resistant to all other antibiotics (ampicillin,
amoxicillin + clavulanic acid, cefoxitin, ceftazidime, cephalexin, ceftriaxone, cefovecin, ciprofloxacin,
cotrimoxazole (sulfamethoxazole + trimethoprim), enrofloxacin, gentamicin, tetracycline,
marbofloxacin, and norfloxacin). Histopathological analysis of the abdominal nodules revealed a
round cell neoplasm, morphologically compatible with a TVT or large cell lymphoma (Figure 3).
Based on these findings, we decided to perform immunohistochemical analysis of the neoplasm,
which confirmed the presence of TVT.
Figure 3. Presence of numerous round to oval cells with multivacuolated cytoplasm. Many cells have more
than one nucleolus. Other cytological features of TVT are the granular appearance of karyoplasm owing to
chromatin agglomeration and an increased nucleus:cytoplasm ratio.
Discussion
Since the patient was found on the street, it was not possible to determine her reproductive
status from the history/anamnesis. Hemoparasites were initially suspected owing to the
presence of ectoparasites (mainly ticks) and pale mucous membranes, and was later confirmed
by changes in blood count (regenerative normochromic normocytic anemia, leukocytosis, and
thrombocytopenia) and antibody research (Mylonakis et al., 2019). Based on these results, treatment
with doxycycline (the antibiotic of choice for the treatment of rickettsiosis) and prednisone (to
reduce the immune-mediated reaction) were chosen (Mylonakis et al., 2019). The spay suture
wound could not be identified in the linea alba during the abdominal examination; therefore,
abdominal ultrasonography was requested to determine whether the patient was spayed, but
it was not authorized, and there was no return for a new blood count.
After the onset of vomiting, a new blood count revealed thrombocytosis and polycythemia
that could be related to dehydration and the loss of electrolytes through vomiting (hyponatremia
and hypokalemia). However, an infectious condition was suspected owing to leukocytosis, with
the main suspicion of uterine infection. (Tello & Perez-Freytes, 2017). Ultrasound examination
revealed absence of the uterus and ovaries, which may indicate that the patient was spayed.
Assessing the etiology of intra-abdominal nodular structures using ultrasound was not possible;
hence, ultrasound-guided cytology and analysis of abdominal free fluid were requested.
The fluid was classified as a pyogranulomatous inflammatory exudate, which may explain
the leukocytosis revealed in the blood count report. Therefore, antibiotic therapy was added to
the protocol established on admission. The cytology of the nodules was inconclusive and may
Bendas et al. 2022. Brazilian Journal of Veterinary Medicine, 44, e001422. DOI: 10.29374/2527-2179.bjvm001422 4/6
Intra-abdominal transmissible venereal tumor in a dog: a case report
be related to the limitations of the technique or failures when obtaining the material guided
by ultrasound (Magalhães et al., 2001). Owing to the impossibility of concluding the diagnosis,
laparotomy and material collection for histopathological evaluation were chosen as the techniques
of choice (Magalhães et al., 2001).
During exploratory laparotomy, the absence of the uterus and ovaries was confirmed; however,
tissue reactions were noted in the topography of the ovaries and cervix, indicating that the animal
had possibly undergone ovariohysterectomy (OVH). The diagnosis of intra-abdominal TVT by
histopathology associated with the probable OVH may indicate that the animal, when undergoing
the surgical procedure, already had the neoplasm, and that the tumor cells were implanted in
the abdomen during the procedure (Bhutani et al., 2016; Ganguly et al., 2016).
Despite the antibiotic (meropenem) treatment, no improvement was observed in the production
of purulent abdominal fluid, which eventually led to the decision of euthanasia.
Differential diagnosis for TVT and large cell lymphoma using histopathological analysis was
recommended; hence, immunohistochemical analysis, considered the “gold standard” for neoplastic
differentiation, was performed (Ganguly et al., 2016), confirming the neoplasm to be a TVT.
Conclusion
The present study reports a rare case of TVT and demonstrates the importance of laparotomy
as an auxiliary method in the diagnosis of neoplasms in the cases where traditional imaging
methods have limitations.
Ethics statement
All procediments were consented by the animal owner.
Financial support
None.
Conflict of interests
There is no conflicts of interest.
Authors’ contributions
AJRB - Writing, Review and Editing manuscript. PLNM - The clinical veterinarian responsible
for conducting the case and review the manuscript. ABC - The veterinary surgeon responsible
for the surgery and review the manuscript. PGH - The veterinary oncologist responsible for
monitoring the case and review the manuscript. DVS - The ultrasound veterinary responsible
for the ultrasound exams and review the manuscript.
Availability of complementary results
The manuscript refers to a case report, with no research data available online.
The study was carried ou at the Institute of Specialties in Veterinary Medicine (IEMEV)
Botafogo, Rio de Janeiro, RJ, Brazil.
References
Bhutani, M. S., Uthamanthil, R., Suzuki, R., Shetty, A., Klumpp, S. A., Nau, W., & Stafford, R. J. (2016). Endoscopic
ultrasound-guided inoculation of transmissible venereal tumor in the colon: A large animal model for colon
neoplasia. Endoscopic Ultrasound, 5(2), 85-93. [Link] PMid:27080606.
Brandão, C. V., Borges, A. G., Ranzani, J. J. T., Rahal, S. C., Teixeira, C. R., & Rocha, N. S. (2002). Tumor venéreo
transmissível: Estudo retrospectivo de 127 casos (1998-2000). Revista de Educação Continuada em Medicina
Veterinária e Zootecnia do CRMV-SP, 5(1), 25-31. [Link]
Chikweto, A., Kumthekar, S., Larkin, H., Deallie, C., Tiwari, K. P., Sharma, R. N., & Bhaiyat, M. I. (2013). Genital and
extragenital canine transmissible venereal tumor in dogs in Grenada, West Indies. Open Journal of Veterinary
Medicine, 3(2), 111-114. [Link]
Bendas et al. 2022. Brazilian Journal of Veterinary Medicine, 44, e001422. DOI: 10.29374/2527-2179.bjvm001422 5/6
Intra-abdominal transmissible venereal tumor in a dog: a case report
Dagli, M. L. Z. (2019). Oncologia veterinária. In M. M. Jericó, J. P. Andrade Neto & M. M. Kogika (Eds.), Tratado de
Medicina Interna de Cães e Gatos (1. ed.). Roca.
Daleck, C. R., & Denardi, A. B. (2016). Oncologia em Cães e Gatos (2. ed.). Roca.
Fossum, T. W. (2005). Cirurgia de Pequenos Animais (4. ed.). Elsevier.
Ganguly, B., Das, U., & Das, A. K. (2016). Canine transmissible venereal tumour: A review. Veterinary and Comparative
Oncology, 14(1), 1-12. [Link] PMid:23981098.
Hedlund, C. S. (2005). Cirurgia dos sistemas reprodutivo e genital. In T. Fossum (Eds.), Cirurgia de Pequenos
Animais (2. ed.). Roca.
Huppes, R. R., Silva, C. G., Uscategui, R. A. R., De Nardi, A. B., Souza, F. W., Tinucci-Costa, M., Amorim, R. L.,
Pazzini, J. M., & Faria, J. L. M. (2014). Tumor Venéro Transmissível (TVT): Estudo retrospectivo de 144 casos.
Ars Veterinária, 30(1), 13-18. [Link]
Lapa, F. A. S. (2009). Comparative study of the effectiveness of two protocols of treatment of the transmissible
venereal tumor in dogs [Dissertação de Mestrado]. Universidade do Oeste Paulista.
Magalhães, A. M., Ramadinha, R. R., Barros, C. S. L., & Peixoto, P. V. (2001). Comparative study between cytology
and histopathology for the diagnosis of canine neoplasms. Pesquisa Veterinária Brasileira, 21(1), 23-32.
Mylonakis, M. E., Harrus, S., & Breitschwerdt, E. B. (2019). An update on the treatment of canine monocytic
ehrlichiosis (Ehrlichia canis). Veterinary Journal (London, England), 246(April), 45-53. [Link]
tvjl.2019.01.015. PMid:30902188.
Oliveira, C. M. (2019). Doenças do sistema genital e reprodutor. In M. M. Jericó, J. P. Andrade Neto & M. M. Kogika
(Eds.), Tratado de Medicina Interna de Cães e Gatos (1. ed.). Roca.
Park, M. S., Kim, Y., Kang, M. S., Oh, S. Y., Cho, D. Y., Shin, N. S., & Kim, D. Y. (2006). Disseminated transmissible
venereal tumor in a dog. Journal of Veterinary Diagnostic Investigation, 18(1), 130-133. [Link]
7/104063870601800123. PMid:16566273.
Ramadinha, R. R., Teixeira, R. S., Bomfim, P. C., Mascarenhas, M. B., França, T. N., Peixoto, T. C., Costa, S. Z. R.,
& Peixoto, P. V. (2016). Resposta do tumor venéreo transmissível canino à quimioterapia com sulfato de
vincristina e vimblastina. Revista Brasileira de Medicina Veterinária, 38(Supl. 1), 65-69.
Rogers, K. S., Walker, M. A., & Dillon, H. B. (1998). Transmissible venereal tumor: A retrospective study of 29
cases. Journal of the American Animal Hospital Association, 34(6), 463-470. [Link]
34-6-463. PMid:9826280.
Silveira, A. C. T., Gerardi, D., Mouro, J. V., Costa, M. T., & Alessi, A. C. (2009). Expressão imunoistoquímica de
linfócitos T e B e do TGF- β no tumor venéreo transmissível canino experimentalmente transplantado.
Ciência Rural, 39(4), 1148. [Link]
Strakova, A., & Murchison, E. P. (2014). The changing global distribution and prevalence of canine transmissible
venereal tumour. BMC Veterinary Research, 10, 168. [Link] PMid:25186078.
Tello, L., & Perez-Freytes, R. (2017). Fluid and electrolyte therapy during vomiting and diarrhea. The Veterinary
Clinics of North America. Small Animal Practice, 47(2), 505-519. [Link]
PMid:27939861.
Tinucci-Costa, M., & Castro, K. F. (2009). Tumor venéreo transmissível canino. In C. R. Daleck & A. B. Denardi
(Eds.), Oncologia em Cães e Gatos (2. ed., pp. 991-1013). Roca.
Vermooten, M. I. (1987). Canine transmissible venereal tumour (TVT): A review. Journal of the South African
Veterinary Association, 58(3), 147-150. PMid:3334057.
Bendas et al. 2022. Brazilian Journal of Veterinary Medicine, 44, e001422. DOI: 10.29374/2527-2179.bjvm001422 6/6