Another interesting study is, -Mesothelioma: profile of keratin proteins and carcinoembryonic antigen: an immunoperoxidase study of 20 cases and comparison with pulmonary adenocarcinomas.- – Am J Pathol. 1982 July; 108(1): 80-87 by J. M. Corson and G. S. Pinkus. Here##Q##s an excerpt: -Abstract – The distribution of keratin proteins and carcinoembryonic antigen (CEA) in 20 diffuse pleural malignant mesotheliomas and 20 adenocarcinomas of your lung was determined using an indirect mmunoperoxidase method. Keratin proteins were identified in all of the mesotheliomas, with strong staining affecting 17 belonging to the cases. Tumor cells of diverse histologic types (tubular, papillary, solid, and spindle) revealed staining for keratin proteins. Many different staining patterns were observed, nevertheless the homogeneous pattern predominated, in a choice a diffuse (16 cases) or focal form (4 cases). CEA was usually absent (11 cases), but weak or equivocal staining had also been observed (8 cases), and 1 case uniquely exhibited moderate staining for CEA. On the other hand, adenocarcinomas belonging to the lung usually stained weakly or negatively (18 cases) for keratin proteins and exhibited a predominantly peripheral staining pattern. All cases, however, stained strongly or moderately for CEA. The profile of strong keratin staining and weak or absent CEA staining appears characteristic of mesotheliomas and could be diagnostically useful for defining the epithelial component these neoplasms also in distinguishing them from adenocarcinomas.-
Another interesting study is termed, -Distinction of mesothelioma from adenocarcinoma. An immunohistochemical approach- by Hector Battifora MD, Mary I. Kopinski BS – Cancer Volume 55, Issue 8, pages 1679-1685, 15 April 1985. Is an excerpt: -Abstract – The authors investigated the expression of keratin, carcinoembryonic antigen (CEA), plus an epithelial marker derived from milk fat globule membranes in 12 mesotheliomas and 100 diverse adenocarcinomas with immunohistochemical methods. The authors employed a monoclonal antibody to keratin designated as AE1, plus the following commercially available antisera: rabbit anti-whole human keratin, rabbit anti-CEA, in addition to a monoclonal antibody to a epithelial factor designated as MFG-2. Expression of keratin was discovered with the mesotheliomas and adenocarcinomas with antibody AE1 and with all the rabbit antiserum; CEA was detectable in 65% within the adenocarcinomas but two mesotheliomas also reacted weakly. With antibody MFG-2, great results were obtained in 85% belonging to the adenocarcinomas along with not one of the mesotheliomas. Every one of 64 (100%) breast-, lung- and ovary-derived adenocarcinomas immunostained positively with antibody MFG-2. This is often of particular significance because pulmonary and ovarian adenocarcinoma frequently can be indistinguishable clinically and histologically from epithelial mesothelioma. The authors conclude that antikeratin antibodies may not be useful for the difference of adenocarcinoma from mesothelioma. Because of its greater sensitivity and specificity, MFG-2 surpasses CEA within this differential diagnosis.-
Another interesting study is referred to as, -The Immunohistochemical Diagnosis of Mesothelioma: A Comparative Study of Epithelioid Mesothelioma and Lung Adenocarcinoma- by Ordez, Nelson G. M.D. – American Journal of Surgical Pathology: August 2003 – Volume 27 – Issue 8 – pp 1031-1051. Here is an excerpt: -Abstract – A multitude of immunohistochemical markers which may facilitate the excellence between epithelioid pleural mesotheliomas and pulmonary peripheral adenocarcinomas have recently become available. The aim of this research is to compare the power of these new markers with other sites which have been already popular for this reason as well as pick which are, presently, the most beneficial for discriminating between these malignancies. Sixty epithelioid mesotheliomas and 50 lung adenocarcinomas were investigated for expression in the following markers: Whilst you can find general agreement the fact that the immunohistochemical panels has to be made up of both positive and negative mesothelioma markers, a large amount of controversy exists regarding the value of a number of these markers, in addition to which combination is regarded as the valuable in assisting in distinguishing between epithelioid mesotheliomas and pulmonary adenocarcinomas (Table 1). One of the factors containing brought about the disparities within the conclusions reached in a great many belonging to the studies is always that different pools of markers were evaluated. Contributing to right here is the continual introduction of new markers that would potentially be of use inside the decides mesothelioma. With this study, we look into the worth of 19 markers in which there is certainly either evidence that they can might be beneficial in detecting mesothelioma or their value remains controversial, and discuss the causes of a few of the discrepancies. A comprehensive overview of the literature on these markers is additionally provided.-
All of us owe a debt of gratitude to these fine researchers. If you ever found one of these excerpts interesting, please look at the studies in their entirety.
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