Skip to main content
Log in

Does the intensity of the inflammatory reaction in a bruise depend on its proximity to the site of trauma?

  • Original Article
  • Published:
Forensic Science, Medicine, and Pathology Aims and scope Submit manuscript

Abstract

Whole blood was withdrawn by tail vessel puncture from anesthetized adult male Sprague–Dawley rats and 0.1 ml was re-injected subcutaneously at each of two sites on their abdominal wall. In addition, two adjacent sites were injected with 0.1 ml of sterile saline, and two more sites were only punctured using an injecting needle. In the second part of the study anesthetized adult male Sprague–Dawley rats had two sites on the abdominal wall pinched using a small pair of forceps, two adjacent sites received an injection of 0.1 ml of whole blood obtained by tail vessel puncture, and two more sites were both pinched and injected with 0.1 ml of whole blood. At intervals of 3, 6, 12 h, 1, 2, 3, 5, and 7 days the animals were euthanized and the skin of the abdomen was processed for histological assessment. Hemosiderin staining in tissues from the first part of the study was assessed qualitatively by scoring sections as 0, 1, 2, or 3 (representing no staining, mild staining, moderate staining, and intense staining) and semi quantitatively using a Nanozoomer Digital Pathology Scanner (NDP Scan U10074-01, Hamamatsu Photonics K.K., Japan). No inflammatory reaction was observed at the sites subjected to needle puncture only. At the sites of saline injection a mild reaction occurred. At the sites where the blood had been injected an intense inflammatory cell response occurred centrally, but not toward the periphery where blood had tracked. In the second experiment the most intense inflammation was also observed in the sites where there had been a pinch and injection of blood. Again, this was maximal centrally with reduced inflammation peripherally. Perls’ staining of hemosiderin was comparable in both models, with iron first observed at day 1 at the region of the injection site. At the sites of injection only, and the sites of injection plus pinch, blood had spread laterally. Hemosiderin staining appeared first and more intensely at the site of injection/trauma. The intensity of the inflammatory response in this animal model of bruising was, therefore, directly related to the proximity to the site of trauma; the appearance and intensity of hemosiderin staining was also influenced by the location within the bruises. This study has shown that histological changes that may be utilized to date bruises may be significantly influenced by the site of the biopsy.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

References

  1. King BR. Aging bruises an inexact science. Emerg Med News. 2004;26:10.

    Google Scholar 

  2. Langlois NEI. The science behind the quest to determine the age of bruises—a review of the English language literature. Forensic Sci Med Pathol. 2007;3(4):241–51.

    Article  Google Scholar 

  3. Nash KR, Sheridan DJ. Can one accurately date a bruise? State of the science. J Forensic Nurs. 2009;5:31–7.

    Article  PubMed  Google Scholar 

  4. Grossman SE, Johnston A, Vanezis P, Perrett D. Can we assess the age of bruises? An attempt to develop an objective technique. Med Sci Law. 2011;51:170–6.

    Article  PubMed  Google Scholar 

  5. Byard RW, Wick R, Gilbert JD, Donald T. Histologic dating of bruises in moribund infants and young children. Forensic Sci Med Pathol. 2008;4:187–92.

    Article  PubMed  Google Scholar 

  6. Sheridan DJ, Nash KR. Acute injury patterns of intimate partner violence victims. Trauma Violence Abus. 2007;8:281–9.

    Article  Google Scholar 

  7. Randeberg LL, Haugen OA, Haaverstad R, Svaasand LO. A novel approach to age determination of traumatic injuries by reflectance spectroscopy. Lasers Surg Med. 2006;38:277–89.

    Article  PubMed  Google Scholar 

  8. Bancroft JD, Cook HC. Manual of histological techniques and their diagnostic application. 1st ed. Singapore: Churchill Livingstone; 1994.

    Google Scholar 

  9. Helps SC, Thornton E, Kleinig TJ, Manavis J, Vink R. Automatic nonsubjective estimation of antigen content visualized by immunohistochemistry using color deconvolution. Appl Immunohistochem Mol Morphol. 2012;20:82–90.

    Article  PubMed  CAS  Google Scholar 

  10. Ruifrock AC, Johnston DA. Quantification of histochemical staining by color deconvolution. Anal Quant Cytol Histol. 2001;23:291–9.

    Google Scholar 

  11. Landini G. Colour Deconvolution V 1.5. 2010. http://www.dentistry.bham.ac.uk/landinig/software/cdeconv/cdeconv.html. Accessed June 2012.

  12. Castle M, Keller J. Rolling Ball. 2007. http://rsbweb.nih.gov/ij/plugins/rolling-ball.html. Accessed June 2012.

  13. Esmon CT. Role of coagulation inhibitors in inflammation. Thromb Haemost. 2001;86:51–6.

    PubMed  CAS  Google Scholar 

  14. Cirino G, Cicala C, Bucci M, Sorrentino L, Ambrosini G, DeDominicis G, et al. Factor Xa as an interface between coagulation and inflammation. Molecular mimicry of factor Xa association with effector cell protease receptor-1 induces acute inflammation in vivo. J Clin Invest. 1997;99:2446–51.

    Article  PubMed  CAS  Google Scholar 

  15. Cicala C, Cirino G. Linkage between inflammation and coagulation: an update on the molecular basis of the crosstalk. Life Sci. 1998;62:1817–24.

    Article  PubMed  CAS  Google Scholar 

  16. Muir R, Niven JSF. The local formation of blood pigments. J Pathol. 1935;41:183–97.

    Article  CAS  Google Scholar 

  17. Laiho K. Time dependence of hemoglobin degradation. In: Oehmichen M, Kirchner H, editors. The wound healing process—forensic pathological aspects. Lübeck: Schmidt-Römhild; 1995.

    Google Scholar 

  18. Kleinig TJ, Helps SC, Ghabriel MN, Manavis J, Leigh C, Blumbergs PC, et al. Hemoglobin crystals: a pro-inflammatory potential confounder of rat experimental intracerebral hemorrhage. Brain Res. 2009;1287:164–72.

    Article  PubMed  CAS  Google Scholar 

  19. Gensa D, Woo CH, Fudenberg HH, Schmid R. Erythrocyte catabolism by macrophages in vitro. The effect of hydrocortisone on erythrophagocytosis and on the induction of heme oxygenase. J Clin Invest. 1973;52:812–22.

    Article  Google Scholar 

Download references

Acknowledgments

The authors acknowledge the work and support of Ms Maria Bellis, Ms Jayne Skinner, Ms Tasma How and Ms Melissa Walker.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Neil E. I. Langlois.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ross, C., Byard, R.W. & Langlois, N.E.I. Does the intensity of the inflammatory reaction in a bruise depend on its proximity to the site of trauma?. Forensic Sci Med Pathol 9, 358–362 (2013). https://doi.org/10.1007/s12024-013-9466-y

Download citation

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12024-013-9466-y

Keywords

Navigation