Practical pathology for thermal tissue applications

The development of minimally invasive medical devices, which employ hyperthermic and/or cryothermic modalities to treat a variety of organ system diseases, is a rapidly expanding field. Consultation with a knowledgeable pathologist during the development of these devices is crucial, as characterization of the treated tissues can support the device’s safety and future efficacy. The properties of thermally treated tissues often share a set of overlapping histopathologic characteristics, regardless of organ system. Several methods for optimally evaluating these thermal changes have been developed that depend on the tissue’s post-treatment time interval. For devices associated with hyperthermic collagen denaturation, bright field or polarized light microscopy of hematoxylin and eosin stained sections can be utilized to assess thermal spread within the tissue. For applications resulting in collagen denaturation with associated desiccation, trichrome staining may provide additional information. For cryothermic devices, these collagen-based methods are generally less informative. Tetrazolium-based tissue viability staining (triphenyltetrazolium chloride, TTC; nitroblue tetrazolium, NBT; NADH/NADPH staining) can be used to assess for the presence of associated tissue necrosis within either hyperthermically or cryothermically treated tissues. The advantages and limitations of several of these methods will be discussed.

[1]  J D Humphrey,et al.  Time-temperature equivalence of heat-induced changes in cells and proteins. , 1998, Journal of biomechanical engineering.

[2]  James E. Coad,et al.  Evolution of pathology techniques for evaluating energy-based tissue effects , 2013, Photonics West - Biomedical Optics.

[3]  James E. Coad,et al.  Thermotolerance of human myometrium: implications for minimally invasive uterine therapies , 2013, Photonics West - Biomedical Optics.

[4]  James E. Coad Practical pathology perspectives for minimally invasive hyperthermic medical devices , 2011, BiOS.

[5]  S. Thomsen,et al.  Changes in birefringence as markers of thermal damage in tissues , 1989, IEEE Transactions on Biomedical Engineering.

[6]  James E. Coad,et al.  Healing responses following cryothermic and hyperthermic tissue ablation , 2009, BiOS.

[7]  J. Chan,et al.  The Wonderful Colors of the Hematoxylin–Eosin Stain in Diagnostic Surgical Pathology , 2014, International journal of surgical pathology.

[8]  James E. Coad,et al.  Non-ablative hyperthermic mesenchymal regeneration: a proposed mechanism of action based on the Vivev model , 2011, BiOS.

[9]  James E. Coad,et al.  Developing clinically successful biomedical devices by understanding the pathophysiology of the target tissue: insights from over 25 years at the microscope , 2007, SPIE BiOS.

[10]  James E. Coad,et al.  Histologic differences between cryothermic and hyperthermic therapies , 2003, SPIE BiOS.

[11]  J. Jakobsen,et al.  Radiofrequency (thermal) ablation versus no intervention or other interventions for hepatocellular carcinoma. , 2013, The Cochrane database of systematic reviews.

[12]  M. Hickey,et al.  Endometrial resection and ablation techniques for heavy menstrual bleeding. , 2013, The Cochrane database of systematic reviews.

[13]  J. Hinshaw,et al.  Thermal ablation. , 2011, Seminars in roentgenology.

[14]  M. Beland,et al.  Thermal ablation in interventional oncology. , 2007, Seminars in roentgenology.

[15]  James E. Coad Thermal fixation: a central outcome of hyperthermic therapies (Invited Paper) , 2005, SPIE BiOS.

[16]  Rebecca Radabaugh,et al.  Arrhenius parameters for primary thermal injury in human tonsillar tissue , 2011, BiOS.

[17]  James E. Coad,et al.  Tissue sealing device associated thermal spread: a comparison of histologic methods for detecting adventitial collagen denaturation , 2013, Photonics West - Biomedical Optics.

[18]  L Solbiati,et al.  Percutaneous radiofrequency tissue ablation: does perfusion-mediated tissue cooling limit coagulation necrosis? , 1998, Journal of vascular and interventional radiology : JVIR.