Silicosis classification: Difference between revisions

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==Classification==
==Classification==
There are 5 subtypes of silicosis that are differentiated according to the duration of exposure, development of symptoms, pulmonary function, and findings on chest imaging.<ref name="pmid17400659">{{cite journal| author=Arakawa H, Johkoh T, Honma K, Saito Y, Fukushima Y, Shida H et al.| title=Chronic interstitial pneumonia in silicosis and mix-dust pneumoconiosis: its prevalence and comparison of CT findings with idiopathic pulmonary fibrosis. | journal=Chest | year= 2007 | volume= 131 | issue= 6 | pages= 1870-6 | pmid=17400659 | doi=10.1378/chest.06-2553 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=17400659 ; }} </ref><ref name="pmid11836467">{{cite journal| author=Park R, Rice F, Stayner L, Smith R, Gilbert S, Checkoway H| title=Exposure to crystalline silica, silicosis, and lung disease other than cancer in diatomaceous earth industry workers: a quantitative risk assessment. | journal=Occup Environ Med | year= 2002 | volume= 59 | issue= 1 | pages= 36-43 | pmid=11836467 | doi= | pmc=PMC1740205 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11836467 ; }} </ref>, <ref name="pmid17976433">{{cite journal| author=Greenberg MI, Waksman J, Curtis J| title=Silicosis: a review. | journal=Dis Mon | year= 2007 | volume= 53 | issue= 8 | pages= 394-416 | pmid=17976433 | doi=10.1016/j.disamonth.2007.09.020 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=17976433 ; }} </ref>
There are 5 subtypes of silicosis that are differentiated according to the duration of exposure, development of symptoms, pulmonary function, and findings on chest imaging.<ref name="pmid17400659">{{cite journal| author=Arakawa H, Johkoh T, Honma K, Saito Y, Fukushima Y, Shida H et al.| title=Chronic interstitial pneumonia in silicosis and mix-dust pneumoconiosis: its prevalence and comparison of CT findings with idiopathic pulmonary fibrosis. | journal=Chest | year= 2007 | volume= 131 | issue= 6 | pages= 1870-6 | pmid=17400659 | doi=10.1378/chest.06-2553 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=17400659 ; }} </ref><ref name="pmid11836467">{{cite journal| author=Park R, Rice F, Stayner L, Smith R, Gilbert S, Checkoway H| title=Exposure to crystalline silica, silicosis, and lung disease other than cancer in diatomaceous earth industry workers: a quantitative risk assessment. | journal=Occup Environ Med | year= 2002 | volume= 59 | issue= 1 | pages= 36-43 | pmid=11836467 | doi= | pmc=PMC1740205 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11836467 ; }} </ref><ref name="pmid17976433">{{cite journal| author=Greenberg MI, Waksman J, Curtis J| title=Silicosis: a review. | journal=Dis Mon | year= 2007 | volume= 53 | issue= 8 | pages= 394-416 | pmid=17976433 | doi=10.1016/j.disamonth.2007.09.020 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=17976433 ; }} </ref>


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Revision as of 15:51, 16 June 2015

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

There are 5 subtypes of silicosis that are differentiated according to the duration of exposure, development of symptoms, pulmonary function, and findings on chest imaging. Silicosis is classified as either simple chronic, complicated chronic, interstitial pulmonary fibrosis, accelerated silicosis, and acute silicosis.

Classification

There are 5 subtypes of silicosis that are differentiated according to the duration of exposure, development of symptoms, pulmonary function, and findings on chest imaging.[1][2][3]

Subtype Simple Chronic Complicated Chronic Interstitial Pulmonary Fibrosis Accelerated Silicosis Acute Silicosis
Duration of Exposure Disease develops > 10 years following exposure to low - moderate concentrations of silica dust Disease develops > 10 years following exposure to silica dust Disease develops > 10 years following exposure to silica dust. Disease develops 5 to 10 years following high exposure to silica dust Disease develops within 5 years of exposure to extremely high concentrations of silica dust
Symptoms Often asymptomatic Dyspnea and cough Dyspnea and cough Dyspnea, weakness, and weight loss Severe, disabling dyspnea, weakness, weight loss, and progressive respiratory failure
Pulmonary Function May be normal or reduced May be normal or reduced May be normal or reduced Reduced with rapid deterioration of FVC and FEV1 Reduced with restrictive changes and reduced diffusion capacity
Imaging Findings Nodules < 10 mm Nodules > 1 cm with either obstructive or restrictive changes of variable severity Diffuse reticulonodular pattern similar to idiopathic pulmonary fibrosis Rapidly progressing nodules and masses Bilateral perihilar acinar pattern consolidations with ground glass appearance

References

  1. Arakawa H, Johkoh T, Honma K, Saito Y, Fukushima Y, Shida H; et al. (2007). ; "Chronic interstitial pneumonia in silicosis and mix-dust pneumoconiosis: its prevalence and comparison of CT findings with idiopathic pulmonary fibrosis" Check |url= value (help). Chest. 131 (6): 1870–6. doi:10.1378/chest.06-2553. PMID 17400659.
  2. Park R, Rice F, Stayner L, Smith R, Gilbert S, Checkoway H (2002). ; "Exposure to crystalline silica, silicosis, and lung disease other than cancer in diatomaceous earth industry workers: a quantitative risk assessment" Check |url= value (help). Occup Environ Med. 59 (1): 36–43. PMC 1740205. PMID 11836467.
  3. Greenberg MI, Waksman J, Curtis J (2007). ; "Silicosis: a review" Check |url= value (help). Dis Mon. 53 (8): 394–416. doi:10.1016/j.disamonth.2007.09.020. PMID 17976433.

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