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The Veterinary clinics of North America. Equine practice2008; 24(2); 261-v; doi: 10.1016/j.cveq.2008.04.001

Bone marrow and lymph node evaluation.

Abstract: Evaluation of equine bone marrow and lymph node samples can provide the definitive diagnosis in some cases, and may provide useful information in other cases. Some newer techniques, including immunophenotyping of cells and clonality assays, provide the capability to more precisely identify cells, both as to origin and malignancy. Use of these techniques on equine bone marrow and lymph node samples, and compiling of the data, will eventually provide invaluable information about equine neoplasia that will greatly improve the ability to predict tumor behavior and response to therapy.
Publication Date: 2008-07-26 PubMed ID: 18652955DOI: 10.1016/j.cveq.2008.04.001Google Scholar: Lookup
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Summary

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The research paper discusses the application of newer diagnostic techniques such as immunophenotyping and clonality assays on equine bone marrow and lymph node samples for better understanding and prediction of tumor behavior and response in horses.

Objective of the Research

The fundamental objective of the research conducted was to:

  • Enhance the diagnosis process of equine neoplasia (tumors in horses).
  • Evaluate the efficiency of newer techniques like immunophenotyping of cells and clonality assays on equine bone marrow and lymph node samples.
  • Understand/predict tumor development and therapy responses better.

New Techniques in Use

The researchers implemented new diagnostic techniques, immunophenotyping, and clonality assays in the study.

  • Immunophenotyping is a lab technique used to study the proteins (antigens) on the surface of cells. It helps in identifying and categorizing cells, based on their type and the origin of the cells.
  • Clonality assays, on the other hand, helps to determine whether a population of cells has arisen from a single cell (clone). They are tests that detect the clonal expansion of cells and are essential in diagnosing malignancies.

Using these techniques on equine bone marrow and lymph node samples provided more precise results in terms of identifying the origins of the cells and whether or not they are malignant.

Outcomes and Contributions

  • This study offers crucial data for the compilation and understanding of equine neoplasia (horse tumors), enabling better predictions of tumor behavior and response towards different treatments.
  • With the help of these advanced techniques, there can be definitive diagnoses in some cases, while in others, it provides valuable insights into the condition.
  • The prediction capability is quintessential for developing effective treatment strategies, improving the overall prognosis for horses affected by tumors.

The comprehensive evaluation of equine bone marrow and lymph node samples through these newer techniques enhances our understanding of equine neoplasia, propelling an improvement in diagnosis and treatment methods.

Cite This Article

APA
Tornquist SJ. (2008). Bone marrow and lymph node evaluation. Vet Clin North Am Equine Pract, 24(2), 261-v. https://doi.org/10.1016/j.cveq.2008.04.001

Publication

ISSN: 1558-4224
NlmUniqueID: 8511904
Country: United States
Language: English
Volume: 24
Issue: 2
Pages: 261-v

Researcher Affiliations

Tornquist, Susan J
  • Department of Biomedical Sciences, 200 Magruder Hall, College of Veterinary Medicine, Oregon State University, Corvallis, OR 97331, USA. susan.tornquist@oregonstate.edu

MeSH Terms

  • Animals
  • Bone Marrow / pathology
  • Horse Diseases / diagnosis
  • Horse Diseases / pathology
  • Horses
  • Immunophenotyping / veterinary
  • Lymph Nodes / pathology
  • Lymphatic Metastasis / diagnosis
  • Lymphatic Metastasis / pathology
  • Neoplasms / diagnosis
  • Neoplasms / pathology
  • Neoplasms / veterinary
  • Prognosis

Citations

This article has been cited 1 times.
  1. Miglio A, Morelli C, Gialletti R, Lauteri E, Sforna M, Marenzoni ML, Antognoni MT. Clinical and immunophenotypic findings in 4 forms of equine lymphoma.. Can Vet J 2019 Jan;60(1):33-40.
    pubmed: 30651648