Literature DB >> 17613992

Characteristics of asbestos concentration in lung as compared to asbestos concentration in various levels of lymph nodes that collect drainage from the lung.

Ronald F Dodson1, Sara Shepherd, Jeffrey Levin, Samuel P Hammar.   

Abstract

Inhaled dust particulates are able to relocate to the extrapulmonary compartments, particularly the lymph nodes that drain the lung. There is little information about the concentration and type of asbestos in the lymphatics and lymph nodes. Quantitative analysis of asbestos lymph node burden conducted by light and analytical transmission electron microscopy has shown ferruginous bodies in lymph nodes that drain the lung and appreciable numbers of short asbestos fibers accumulate in lymph nodes in occupationally exposed individuals. The location of lymph nodes in the thoracic cavity was categorized according to the Naruke anatomical map. Tissue from eleven individuals with a history of asbestos exposure were selected for a comparative study of the asbestos content of lung with that found in the thoracic lymph nodes. The study used a digestion technique for tissue preparation and evaluated ferruginous body burden and concentration of asbestos fibers (> 0.5 microm in length). Comparison was made between sites and analysis was made as to the population of fibers detectable by light microscopy and defined as "Stanton fibers." The findings indicated the vast majority of all asbestos fiber types in all sites were shorter than 5 microm and would not have been counted in a light microscopy count scheme that included only those fibers > 5 microm. There were reproducible patterns of asbestos types of found in various lymph nodes, although there were variations in the amount of asbestos found in the sites sampled. In summary, asbestos fibers found in thoracic lymph nodes have predominately short fibers and, in this study group, consisted of a mixture of commercial and noncommercial amphiboles. When a long/thin fiber was found in the lung or lymph tissue, its detection required the use of analytical transmission electron microscopy for identification.

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Year:  2007        PMID: 17613992     DOI: 10.1080/01913120701423907

Source DB:  PubMed          Journal:  Ultrastruct Pathol        ISSN: 0191-3123            Impact factor:   1.094


  6 in total

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Journal:  J Cell Physiol       Date:  2012-01       Impact factor: 6.384

2.  Elemental and immunohistochemical analysis of the lungs and hilar lymph node in a patient with asbestos exposure, a pilot study.

Authors:  Yasuhiko Koga; Takahiro Satoh; Kyoichi Kaira; Masashi Koka; Takeshi Hisada; Junko Hirato; Bolag Altan; Masakiyo Yatomi; Akihiro Ono; Yosuke Kamide; Yasuo Shimizu; Haruka Aoki-Saito; Hiroaki Tsurumaki; Kimihiro Shimizu; Akira Mogi; Tamotsu Ishizuka; Masanobu Yamada; Kunio Dobashi
Journal:  Environ Health Prev Med       Date:  2016-10-03       Impact factor: 3.674

Review 3.  Non-neoplastic and neoplastic pleural endpoints following fiber exposure.

Authors:  V Courtney Broaddus; Jeffrey I Everitt; Brad Black; Agnes B Kane
Journal:  J Toxicol Environ Health B Crit Rev       Date:  2011       Impact factor: 6.393

Review 4.  Morphological and chemical mechanisms of elongated mineral particle toxicities.

Authors:  Ann E Aust; Philip M Cook; Ronald F Dodson
Journal:  J Toxicol Environ Health B Crit Rev       Date:  2011       Impact factor: 6.393

Review 5.  Nonpulmonary outcomes of asbestos exposure.

Authors:  Melisa Bunderson-Schelvan; Jean C Pfau; Robert Crouch; Andrij Holian
Journal:  J Toxicol Environ Health B Crit Rev       Date:  2011       Impact factor: 6.393

6.  Measurement of OH* Generation by Pulverized Minerals Using Electron Spin Resonance Spectroscopy and Implications for the Reactivity of Planetary Regolith.

Authors:  Donald A Hendrix; Sara T Port; Joel A Hurowitz; Martin A Schoonen
Journal:  Geohealth       Date:  2019-01-23
  6 in total

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