Canine Melanoma Diagnosis in Dogs By Student Name Institute Name Course Name
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Canine Melanoma Diagnosis in Dogs By Student Name Institute Name Course Name Date Introduction
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Melanoma is a common form of cancer in dogs, and its medical diagnosis is a complicated process. Dogs possessing this cancer may have one of two types of melanoma. There is a malignant form and a benign form. Both of these forms can be related to stress, trauma, or excessive licking in an area where cells start to multiply resulting in this disease. The malignant form of melanoma is a metastatic disease meaning that it is rapid and aggressive, with essentially no cure. This can be compared to the benign form that is less invasive and is usually restricted to one area on the skin distinguishing challenges between the two types of melanomas. There is an array of preliminary tests done in modern veterinarian medicine to detect malignant and benign melanoma. These include fine needle aspirates, radiograph/ultrasound imaging, microscopic imaging, and histopathologic analyzation. The problem with these methods is that they can deliver conflicting results, making it hard to diagnose melanoma (Ballegeer, Hollinger & Kunst, 2013). Canine melanoma is mostly considered as canine oral malignancy. Causes of this condition are associated with local invasiveness or lung and metastasis to the lymph nodes representing between 80% to 100%. Research conducted on this condition found a more favorable prognosis. Histomorphology report showed 92% of tumors in canine melanocytic were diagnosed as malignant while 59% of these tumors presented features of a malignant. Another study revealed that only 5% (3/64) of dogs who were well-differentiated and had a heavily pigmented canine melanomas died of tumor-related causes. A subsequent study that was cited revealed a one-year survival rate for affected dogs and had results at the rate of 45.2% (19/42) for cases of canine melanomas. According to the above data, it reveals that diagnosis of canine melanoma may result to different data according to the method that was used to detect the condition calling for the most accurate methods for diagnosing this condition (Brockley, Cooper, & Bennett, 2013). The most diagnosed canine melanoma are accounting to 7% of all malignant tumors cases that have been reported in dogs and about 160,000 cases malignant tumors reported worldwide each yearmostfrequentlyat(62%)amongreported1652melanomascasescomparedtothe aggressive median survival rate of 200 days. The most metastasizing tumors are Non-UV- dependent canine melanoma malignancies with a post-surgery rate of 173 days of survival. According to support evidence on this research, pre-clinical trial and medical monitoring appears to be a reliable method for diagnosis canine melanoma and also in testing human cancers caused by this infection as well as the disease in dogs (Campbell, Farmery, George, & Farrant, 2013). To add to that, researchers from the Veterinary Medical Diagnostic Laboratory in Missouri studied 338 different cases of canine melanoma. Though they found significant trends in Melan A reactivity (a protein found on melanomas), the prognosis for canine melanomas is unrelated to sex, the location of a tumor, amount of pigment, and microscopic appearance. Further evidence shows that traditional veterinarian practices such as the ones discussed above are not effective ways to diagnose melanoma. Histopathologic examination and fine needle aspirates performed on tumors cannot be substituted with one another. They can deliver conflicting results, making it hard to confidently diagnose melanoma (Gillard et al., 2014). Statement of Purpose Melanoma has been associated with most malignancies in the dog. Both mucosal and oral melanoma is considered an extremely malignant tumor that is associated with a high degree of high metastatic propensity and local invasiveness. Studies on this condition have revealed that this condition is extremely prognostic. WHO states that the staging process for dogs associated with canine melanoma depends on the size of the lymph node or tumor. Negative diagnosis of
the condition is associated with size, stage, evidence of metastasis, and histologic criteria (Chapman, & Hostutler, 2013). Melanoma is an aggressive tumor whose species may rise at the different anatomical site when it affects dogs. Development of canine melanoma my subsequently cause infections to other anatomical sites with different frequencies for every site that is affected. As stated above, there is a big challenge and gap in the diagnosis of canine melanoma. The variations in diagnosis are as a result of factors such as; inability to categorize melanoma as skin cancer,the degree of skin pigmentation and other tumors are unpigmented. Melanomas viewed microscopically may present features of other types of tumors thereby making a poor diagnosis melanoma. A study conducted on Hovawart dog that was treated for melanoma malignant showed a dog's spine had a haired tumor which had physical characteristics that resembled benign tumor but the fact it was malignant. According to diagnosis done through ultrasound and radiograph, the findings did not show any sign of melanoma making it impossible to diagnose for cancer before the surgical procedure (Chow, Stent, & Milne, 2014). This study aims to determine gaps and variations among different diagnostic methods for canine melanoma.This study will focus on specificdiagnosis methods such as; histopathologic analyzation, microscopic imaging, radiograph ultrasound imaging, and fine needle aspirate. CHAPTER 2 LITERATURE REVIEW
Introduction Diagnosis of canine melanoma in dogs can be challenging because of the variety of histological appearances of canine melanocytic neoplasms. This chapter aims at discussing the literature review on major methodological flow or gaps in research for canine melanoma diagnosis. This chapter will also review other literature on inconsistencies in theories and findings related to canine melanoma diagnosis as well as establishing important areas that can be useful for future studies. Histopathologic analyzation Melanomas comprise about 6% of tumors in the skin in heavily pigmented dogs but commonly in neoplasm of the canine oral cavity. There is a description of the histologic classification of melanomas as malignant and benign. According to findings from other researchers, cutaneous melanomas are benign while the majority of canine melanomas are behaviorally malignant. Other researches found that behavior of canine melanoma is not correlated with a histologic appearance at the rate of 10 to 40% of histologically benign oral compared to canine cutaneous melanoma.Thismakestherapeuticprotocolsthatfocusonthehistologicappearanceof melanoma to be inappropriate. Similarly, single parameter flow cytometry can detect changes associated with malignancy, provide quantitative measurements of DNA and increase proliferation rate (Paoloni et al., 2015). Cytometry has also been used in some cases to demonstrate small numbers of malignant cells among targeted species, even after determining histologic diagnosis was equivocal (Ottnod et al., 2013). Individual cells are used to determine the DNA of the specifies through measuring DNA specific dye and fluorescence emitted after stoichiometric nucleotide. This technique has been used in the diagnosis of canine melanoma in dogs through a retrospective analysis of formalin fixed in the cytometric analysis. This method of diagnosis is used to determine behavioral characteristics of canine melanoma to evaluate the flow of cytometry within the species (Rossi et al., 2015). Correct histopathological analyzation helps in predicting the biological behaviors of melanomas. Accordingtoanotherstudythatwasconductedtodeterminetheeffectivenessof histopathological analyzation, eight of behaviors that were detected were associated with benign melanoma while fourteen behaviors were associated with histologically benign as well as having more histological criteria or malignancy. This study helps to understand how histopathological analysis can be used to determine the presence of canine melanoma in dogs. It also establishes its unique technique of determining this malignant thus proving the importance of histopathological
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analyzation(Shafieeetal.,2013). Radiograph and Ultrasound Imaging According to a study on a 6-year-old male boxer dog which was referred at Western College of Veterinary Medicine, the dog had a history of unilateral nasal discharge through its right nostril, and blindness over two days and progressive lethargy. On palpation, no pain was detected at retropulsion of the eyes. The submandibular lymph nodes were also observed to be in normal in size and texture. According to examination, there was a bilateral absence of menace response as well as poor direct consensual pupillary light reflexes and bilateral mydriasis. According to this study, nasal cavity was observed to be destroyed and extended into the cranium. Imaging report found a focal round the spleen. There was also expanding and infiltrating the submucosa which was destroying the nasal bone and ulcerating the nasal mucosa causing a poorly demarcated and densely cellular neoplastic mass which composed of cells arranged that were in an interlacing bundles. Radiograph imaging also revealed polygonal to spindloid with distinct cell borders which contained eosinophilic cytoplasm that is mostly associated with dark brown melanin pigment (Oblak, Boston, Woods, & Nykamp, 2015). Radiograph report also showed oval to spindloid that was associated with stippled chromatin that had at least one or three distinct nucleoli. Areas of necrosis and nasal bone invasion were observed. Neoplastic cells were seen effacing the brain and infiltrating. According to the study, there was no evidence of metastasis within any other organs examined including the spleen and draining lymph nodes. According to evidenceofcaninemelanomadiagnosis,malignantmelanomawasconfirmedby immunohistochemistry hence resulting in a positive melan A (Cabon et al., 2016). The study was evident that melanocytes were not present in nasal mucosa; hence malignant canine cases were high among dogs. The clinical presentation of this tumor showed the development of neurological signs that had a larger mass around the canine area of nasal origin on the dog subjected to the study. There are insufficient studies to confirm melanocytes from the dogs hence limiting clinical presentation of these cases as well as the existence of canine melanoma within nasal mucosa in the dog (Iida et al., 2013). Fine needle aspirate A fine needle aspirate is not a biopsy, but it's a diagnosis technique where a sample of the mass is taken by the use of a skinny little needle.On the use of this technique, the vet disinfects the surface of the site to be aspirated, often after clipping the hair, to prevent infection.Next, a needle is introduced into the area of interest, and the plunger is drawn back, creating a vacuum
imaging revealed that the most common area that was affected by this condition was the mandibular labial mucosa at 53%. Imaging report also showed that other sites that other anatomical sites affected by this condition were the tongue, but it was a rare observation. The most breeds of dogs at high risks of being affected by canine oral malignant melanoma were dogs with pigmented oral mucosa and small breeds of dogs (Teixeira et al., 2014). Other scientific studies revealed that most dogs that were affected with canine melanoma were of ages between 10.5 to 12years of age, but an average age for canine melanoma condition in dogs was 11.4years, but male dogs were more susceptible to the condition compared to female dogs. In a microscopic imaging study that was done among 70 dogs with canine melanoma, 11.4% of the dogs had mandibular lymph node while 1.4 had lung metastasis as other organs affected by themalignant.Canineswithmelanomaswerealsoobservedwithmetastasiswhen lymphadenomegaly was confirmed to be present resulting to median survival time for dogs with untreated melanoma (Tuohy, Selmic, Worley, Ehrhart, & Withrow, 2014). Conclusion In conclusion, canine melanomas is a very aggressive tumor affecting a large number of dogs. There is a wide scientific effort in finding the best technological methods of detecting canine melanomas in dogs and address gaps in other researches on this malignancy. Consequently, there is a need for more studies to be conducted for assessment of appropriate diagnosis method for canine melanoma to avoid limiting assessment to a single lymph node. Lastly, the study also proved existence of gaps in research about diagnosis of canine melanoma in dogs. This was evident in explanation above since every method has its own findig on possible diagnosis methods of this condition hence need for an extensive research to find the most appropriate diagnostic method for this condition in dogs.
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Oblak, M. L., Boston, S. E., Woods, J. P., & Nykamp, S. (2015). Comparison of concurrent imaging modalities for the staging of dogs with appendicular primary bone tumors. Veterinary and comparative oncology, 13(1), 28-39. Ottnod, J. M., Smedley, R. C., Walshaw, R., Hauptman, J. G., Kiupel, M., & Obradovich, J. E. (2013). A retrospective analysis of the efficacy of Oncept vaccine for the adjunct treatment of canine oral malignant melanoma. Veterinary and Comparative Oncology, 11(3), 219-229. Paoloni, M., Mazcko, C., Selting, K., Lana, S., Barber, L., Phillips, J., & Avery, A. (2015). DefiningthepharmacodynamicprofileandtherapeuticindexofNHS-IL12 immunocytokine in dogs with malignant melanoma. PLoS One, 10(6), e0129954. Pierezan, F., Mansell, J., Ambrus, A., & Hoffmann, A. R. (2014). Immunohistochemical expression of ionized calcium binding adapter molecule 1 in cutaneous histiocytic proliferative,neoplasticandinflammatorydisordersofdogsandcats.Journalof comparative pathology, 151(4), 347-351. Rossi, F., Aresu, L., Vignoli, M., Buracco, P., Bettini, G., Ferro, S., ... & Bellei, E. (2015). Metastatic cancer of unknown primary in 21 dogs. Veterinary and comparative oncology, 13(1), 11-19. Shafiee, R., Javanbakht, J., Atyabi, N., Kheradmand, P., Kheradmand, D., Bahrami, A., ... & Khadivar, F. (2013). Diagnosis, classification, and grading of canine mammary tumors as a model to study dog cancer: an Clinico-Cytohistopathological study with environmental factors influencing public health and medicine. Cancer cell international, 13, 79-79. Simpson, R. M., Bastian, B. C., Michael, H. T., & Smedley, R. C. (2014). Sporadic naturally occurring melanoma in dogs as a preclinical model for human melanoma. Pigment cell & melanoma research, 27(1), 37-47. Teixeira, T. F., Gentile, L. B., Da Silva, T. C., Mennecier, G., Chaible, L. M., Cogliati, B., ... & Dagli, M. L. Z. (2014). Cell proliferation and expression of connexins differ in melanotic and amelanotic canine oral melanomas. Veterinary research communications, 38(1), 29- 38. Tuohy, J. L., Selmic, L. E., Worley, D. R., Ehrhart, N. P., & Withrow, S. J. (2014). Outcome following curative-intent surgery for oral melanoma in dogs: 70 cases (1998â2011). Journal of the American Veterinary Medical Association, 245(11), 1266-1273. Wall, C. R., Cook, C. R., & Cook, J. L. (2015). Diagnostic sensitivity of radiography, ultrasonography,andmagneticresonanceimagingfordetectingshoulder osteochondrosis/osteochondritis dissecans in dogs. Veterinary Radiology & Ultrasound, 56(1), 3-11.