What histologic finding best differentiates inflammatory bowel disease from small cell lymphoma in feline intestinal tissue?

Study for the ACVIM Small Animal Internal Medicine Exam to enhance your veterinary knowledge. Prepare with flashcards and multiple-choice questions, featuring hints and explanations. Ensure success in your exam journey!

Multiple Choice

What histologic finding best differentiates inflammatory bowel disease from small cell lymphoma in feline intestinal tissue?

Explanation:
Distinguishing IBD from small cell lymphoma in feline intestine relies on both the cellular makeup of the infiltrate and the immunophenotype of the cells. Inflammatory bowel disease is a chronic inflammatory process that characteristically shows a lymphoplasmacytic infiltrate, meaning a mix of T cells, B cells, and plasma cells. Immunostaining reflects this diversity, with a combination of CD3-positive T cells and B-cell markers (such as CD79a) present in the infiltrate. The tissue architecture can be relatively preserved apart from inflammatory changes, and you don’t see a uniform population of small, mature lymphocytes. In contrast, small cell lymphoma is a neoplastic process with a monomorphic population of small, mature lymphocytes that are predominantly T cells. Immunohistochemistry typically shows strong CD3 positivity with a homogeneous infiltrate, and the lymphoma can cause mucosal architectural disruption, including increased intraepithelial lymphocytes and villous blunting due to lymphomatous invasion of the mucosa. The presence of a heavy monomorphous CD3+ infiltrate, rather than a mixed inflammatory infiltrate, is the key differentiator. So the best differentiating finding is the combination of a lymphoplasmacytic infiltrate with mixed T and B cell immunophenotypes in IBD versus a dense, monomorphic CD3+ T-cell population with mucosal architectural changes in small cell lymphoma.

Distinguishing IBD from small cell lymphoma in feline intestine relies on both the cellular makeup of the infiltrate and the immunophenotype of the cells. Inflammatory bowel disease is a chronic inflammatory process that characteristically shows a lymphoplasmacytic infiltrate, meaning a mix of T cells, B cells, and plasma cells. Immunostaining reflects this diversity, with a combination of CD3-positive T cells and B-cell markers (such as CD79a) present in the infiltrate. The tissue architecture can be relatively preserved apart from inflammatory changes, and you don’t see a uniform population of small, mature lymphocytes.

In contrast, small cell lymphoma is a neoplastic process with a monomorphic population of small, mature lymphocytes that are predominantly T cells. Immunohistochemistry typically shows strong CD3 positivity with a homogeneous infiltrate, and the lymphoma can cause mucosal architectural disruption, including increased intraepithelial lymphocytes and villous blunting due to lymphomatous invasion of the mucosa. The presence of a heavy monomorphous CD3+ infiltrate, rather than a mixed inflammatory infiltrate, is the key differentiator.

So the best differentiating finding is the combination of a lymphoplasmacytic infiltrate with mixed T and B cell immunophenotypes in IBD versus a dense, monomorphic CD3+ T-cell population with mucosal architectural changes in small cell lymphoma.

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