By Anita R. Kiehl, Maron Brown Calderwood Mays
Atlas for the analysis of Tumors within the puppy and Cat is a diagnostic software for opting for if samples are irregular and defining the reason for the abnormality, with 386 medical photos depicting common and irregular results.
- Offers a quick assessment of the equipment used to supply a analysis and diagnosis from a biopsy tissue sample
- Pairs images of biopsy samples with photomicrographs of cells received through high quality needle aspirate
- Includes an invaluable bankruptcy masking pattern dealing with, staining, and shipping
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Extra resources for Atlas for the diagnosis of tumors in the dog and cat
There are areas of collagen necrosis with dense infiltrates of eosinophils. Identification of mitotic figures is difficult in these areas, and they should be avoided because the irregular appearance of eosinophil nuclei could cause a spurious elevation in the mitotic count. 56 Canine cutaneous mast cell tumor grade 1 biopsy. 5x. 57 Canine cutaneous mast cell tumor grade 2 biopsy. 10x. 58 Canine cutaneous mast cell tumor grade 2 biopsy. 10x. 59 Canine mast cell tumor FNA. 50x. 60 Canine cutaneous mast cell tumor grade 3.
There are variably granulated mast cells with small but slightly pleomorphic nuclei, 0–1 mitotic figures/HPF with an MI of 2/10 HPF, and the tumor extends to the deep dermis. 2). 58 shows a canine cutaneous mast cell tumor grade 2 Patnaik scale. This grade 2 (Patnaik), low‐grade (two‐ tier) cutaneous mast cell tumor has small, variably granulated mast cells with small nuclei with mild a nisokaryosis, and is confined to the dermis. There are areas of collagen necrosis with dense infiltrates of eosinophils.
This lesion may be exacerbated by solar exposure and may prove multiple and recurrent with continued solar exposure. Bacteria may grow in the ulcerated surface (arrowheads). 16 shows a biopsy of a feline squamous cell carcinoma. An adult male neutered cat had ulcerated bleeding lesions on the ear tips, which were biopsied, revealing a disorganized proliferation of squamous epithelial cells with moderate to marked nuclear pleomorphism, nuclear and cytoplasmic dysmaturation, 0–5 mitotic figures/ HPF, and stromal invasion that extended to the margins of the tissue submitted.