Premium
Cytochemical Staining Characteristics of Lymph Nodes From Normal and Lymphoma‐Affected Dogs
Author(s) -
Raskin Rose E.,
Nipper Marlin N.
Publication year - 1992
Publication title -
veterinary clinical pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.537
H-Index - 51
eISSN - 1939-165X
pISSN - 0275-6382
DOI - 10.1111/j.1939-165x.1992.tb00585.x
Subject(s) - pathology , lymph , staining , germinal center , mantle zone , lymphoma , follicular hyperplasia , cytochemistry , canine lymphoma , lymphocyte , chemistry , biology , b cell , medicine , immunology , antibody , ultrastructure
Summary Frozen sections and imprint smears were used to evaluate the presence and pattern of cytochemical staining reactions in the B‐ and T‐cell regions of lymph nodes from normal dogs and dogs with lymphoma. Staining procedures evaluated included peroxidase (PER), Sudan black B (SBB), naphthol AS‐D chloroacetate esterase (CAE), α‐naphthyl butyrate esterase (NBE), acid phosphatase (ACP), and leukocyte alkaline phosphatase (LAP). In normal lymph nodes, macrophages and some lymphocytes within the interfollicular (T‐cell) region and medulla stained positive with ACP and NBE. Smaller numbers of macrophages also occurred sporadically within the germinal follicles. Cells positive for PER, SBB, and CAE were scattered infrequently throughout all regions of the normal lymph node, consistent with granulocytes and mast cells. The LAP stained cells were predominantly and prominently located within the mantle zone of secondary follicles and to a much lesser extent within the germinal centers, compatible with B‐cell lymphocytes derived from follicular center cells. Of the 12 dogs with lymphoma, 7 cases (4 immunoblastic, 2 large noncleaved, 1 small noncleaved) stained diffusely positive with LAP; 4 cases (all lymphoblastic) had numerous focally positive lymphocytes using ACP and NBE; and 1 case (immunoblastic) did not stain positive with any of the cytochemical reactions. Cytochemical staining of canine lymph nodes with NBE, ACP, and LAP proved useful in distinguishing between B‐ or T‐cell regions and detecting different cell types of canine lymphoma.