Literature DB >> 19669671

Stereologic analysis of tissue compartments of gunshot-injured and blunt-injured spleen.

Novica M Milićević1, Jasna B Trbojević-Stanković, Cinthia B Drachenberg, Zivana Milićević.   

Abstract

The spleen is composed of several tissue compartments and the respective histoquantitative data are essential for complete understanding of immune or pathological processes in this organ. The aim of our study was to determine and compare the stereologic parameters of all tissue compartments of the gunshot-injured and blunt-injured human spleen. The model-based stereology with point-counting method was utilized to study the volume densities of red pulp, perifollicular zone, marginal zone, white pulp (follicles and periarteriolar lymphoid sheath), and connective tissue. The areal numerical density (the number of follicles per mm(2) of tissue section), the numerical density (the number of follicles per mm(3) of tissue) of lymphoid follicles and the mean follicle diameter were also determined. Our study provides stereological parameters for all tissue compartments of the human spleen. No morphometric differences were registered between tissue compartments of the blunt-injured and gunshot-injured spleen. As the gunshot-injured spleen was taken as presumably unstimulated in immunological regard, our results suggest that both gunshot-injured and blunt-injured organs may be used as models of the normal human spleen.

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Year:  2009        PMID: 19669671     DOI: 10.1007/s12253-009-9189-2

Source DB:  PubMed          Journal:  Pathol Oncol Res        ISSN: 1219-4956            Impact factor:   3.201


  17 in total

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Review 4.  Germinal centre cell kinetics.

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5.  Stereological study of tissue compartments of the human spleen.

Authors:  Z Milićević; A Cuschieri; A Xuereb; N M Milićević
Journal:  Histol Histopathol       Date:  1996-10       Impact factor: 2.303

6.  Early tumor effect on splenic Th lymphocytes in mice.

Authors:  J A Segura; L G Barbero; J Márquez
Journal:  FEBS Lett       Date:  1997-09-01       Impact factor: 4.124

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8.  Splenic pathology after traumatic injury.

Authors:  D C Farhi; R Ashfaq
Journal:  Am J Clin Pathol       Date:  1996-04       Impact factor: 2.493

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Authors:  N M Milićević; A Cuschieri; A Xuereb; Z Milićević
Journal:  Gen Diagn Pathol       Date:  1996-06

10.  Regulation of the immune response. 3. Kinetic differences between thymus- and bone marrow- derived lymphocytes in the proliferative response to heterologous erythrocytes.

Authors:  J W Kappler; M Hoffmann
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  1 in total

1.  Effects of early and late adverse experiences on morpho-quantitative characteristics of Sprague-Dawley rat spleen subjected to stress during adulthood.

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  1 in total

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