Diffuse large B-cell lymphoma with DNA copy number changes in a Japanese black calf.
Masaki MaezawaKen-Ichi WatanabeYoshiyasu KobayashiKio YoshidaJames K ChambersKazuyuki UchidaReo MaruyamaHisashi InokumaPublished in: Veterinary research communications (2024)
A 2-month-old Japanese Black calf exhibited mandibular and superficial cervical lymph node swelling. Fine needle aspiration cytology of the superficial cervical lymph node revealed large lymphoblast-like cells with mitoses. Hematological examination revealed remarkable lymphocytosis with atypical lymphocytes. Increased activities of serum total lactate dehydrogenase and thymidine kinase were detected. At necropsy, generalized swelling of lymph nodes was observed. Histopathological analysis revealed diffuse proliferation of medium-sized round centroblastic neoplastic cells that were positive for CD20, CD79α, PAX5, and BLA-36, and negative for CD3, CD5, CD10, and CD34. The calf was diagnosed with centroblastic diffuse large B-cell lymphoma (DLBCL) based on these findings. Analysis of DNA copy number variation revealed an increased copy number for the GIMAP family relative to that in healthy cattle. Moreover, decreases in copy numbers of GBP-1, MIR3141, OR5P1E, and PTPRG relative to those in healthy cattle were also observed. Because DNA copy number variation represent a major contribution to the somatic mutation landscapes in human tumors, these findings suggest that DNA copy number changes might have contributed to the onset of DLBCL in the present case.
Keyphrases
- copy number
- diffuse large b cell lymphoma
- lymph node
- mitochondrial dna
- circulating tumor
- fine needle aspiration
- epstein barr virus
- cell free
- genome wide
- single molecule
- single cell
- neoadjuvant chemotherapy
- sentinel lymph node
- dna methylation
- ultrasound guided
- induced apoptosis
- endothelial cells
- cell proliferation
- nucleic acid
- signaling pathway
- high grade
- low grade
- long non coding rna
- squamous cell carcinoma
- circulating tumor cells
- early stage
- nk cells
- oxidative stress
- induced pluripotent stem cells
- cell cycle arrest