Elsevier

Human Pathology

Volume 35, Issue 12, December 2004, Pages 1515-1523
Human Pathology

Original contributions
Proposed criteria for mixed-dust pneumoconiosis: Definition, descriptions, and guidelines for pathologic diagnosis and clinical correlation1

An outline of this consensus was presented at the 6th International Conference on Environmental & Occupational Lung Disease at Vancouver, British Columbia, Canada (February 11–14, 1999).
https://doi.org/10.1016/j.humpath.2004.09.008Get rights and content

Abstract

We defined mixed-dust pneumoconiosis (MDP) pathologically as a pneumoconiosis showing dust macules or mixed-dust fibrotic nodules (MDF), with or without silicotic nodules (SN), in an individual with a history of exposure to mixed dust. We defined the latter arbitrarily as a mixture of crystalline silica and nonfibrous silicates. According to our definition of MDP, therefore, MDF should outnumber SN in the lung to make a pathologic diagnosis of MDP. In the absence of confirmation of exposure, mineralogic analyses can be used to support the pathologic diagnosis. The clinical diagnosis of MDP requires the exclusion of other well-defined pneumoconioses, including asbestosis, coal workers’ pneumoconiosis, silicosis, hematite miners’ pneumoconiosis, welders’ pneumoconiosis, berylliosis, hard metal disease, silicate pneumoconiosis, diatomaceous earth pneumoconiosis, carborundum pneumoconiosis, and corundum pneumoconiosis. Typical occupations associated with the diagnosis of MDP include metal miners, quarry workers, foundry workers, pottery and ceramics workers, and stonemasons. Irregular opacities are the major radiographic findings in MDP (ILO 1980), in contrast to silicosis, in which small rounded opacities predominate. Clinical symptoms of MDP are nonspecific. MDP must be distinguished from a variety of nonoccupational interstitial pulmonary disorders.

Section snippets

Historical remarks and experimental backgrounds

In 1934, Stewart and Faulds6 reported the clinicopathologic and mineralogic features of lung changes in 15 hematite miners; these features closely resemble those of mixed-dust fibrosis. Stewart and Faulds6 categorized it as “sidero-silicosis” at that time. The term mixed-dust pneumoconiosis (Mischstaubpneumokoniose) was first introduced by Uehlinger in 1946.1 According to his clinicopathologic descriptions of MDP, “mixed dust granulomas” are softer than those of the silicotic lesion, and the

Pathologic features

Three types of lesions are typically seen in individuals who are exposed to dusts containing a mixture of crystalline silica and silicates. These include macules, mixed-dust fibrotic lesions (MDF), and silicotic nodules.23 Macules are nonpalpable lesions consisting of interstitial accumulations of dust-laden macrophages. These typically show a peribronchiolar or perivascular distribution and are associated with a delicate meshwork of reticulin fibers without obvious collagenization (Fig 1).

Mineralogic analysis

Mineralogic analysis of tissue specimens may be performed in a number of different ways. One approach is the ashing of the tissue and analysis of recovered dust gravimetrically and by x-ray diffraction.25, 26 To obtain accurate identification of the mineral species, the x-ray diffraction analysis is required, employing the x-ray absorption correction.27, 28 Unfortunately, this approach requires a large sample of lung tissue. Another approach involves in situ analysis of tissue sections by

Clinical diagnosis

The diagnosis is aided by a well-documented occupational history of concomitant exposure to mixed dust as defined above. Typical occupations associated with a diagnosis of MDP include metal miners, quarry workers, foundry workers, pottery and ceramics workers, and stonemasons. Lesions found in coal workers’ pneumoconiosis and hematite miners’ pneumoconiosis are very similar to those observed in MDP.4 However, we are arbitrarily restricting the definition of MDP to exclude these and other

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