- Case Report
- Open Access
Two cases of hard metal lung disease showing gradual improvement in pulmonary function after avoiding dust exposure
Journal of Occupational Medicine and Toxicology volume 10, Article number: 29 (2015)
We present herein two cases of hard metal lung disease (HMLD) with distinct pathological findings. Both cases showed gradual improvements in pulmonary function over a period of a few years (Case 1: 30 months; Case 2: 12 months) after the avoidance of dust exposure, while improvements on high-resolution computed tomography were modest. The increased lymphocytes and decreased CD4/CD8 ratio in BALF observed at initial diagnosis normalized after the avoidance of dust exposure in one case. To the best of our knowledge, this is the first report demonstrating continual follow-up of pulmonary function and radiographic findings, and a comparison of BALF findings before and after avoidance of hard metal dust exposure.
Hard metal lung disease (HMLD) is a rare occupational lung disease that can occur in workers engaged in the manufacture, utilization, or maintenance of tools composed of hard metal, a synthetic compound composed of tungsten carbide and cobalt [1, 2]. Although giant cell interstitial pneumonitis (GIP) is known as a typical pathological finding for this disease [3–5], some cases without GIP have also been reported [6, 7]. The clinical course of this disease varies, with some cases requiring corticosteroid treatment and others showing spontaneous improvement simply by avoiding exposure to hard metal [5, 8–12]. We report two cases of HMLD with distinct pathological findings: one as typical GIP; and the other characterized by peribronchial fibrosis without typical features of GIP. Continual follow-up of pulmonary function and radiological findings as well as comparisons of bronchoalveolar lavage fluid (BALF) findings before and after dust exposure were obtained.
A 50-year-old non-smoking woman presented with a 6-month history of nonproductive cough, which had started 8 years after she began working with a hard metal grinder without using a dust protective mask. High-resolution computed tomography (HRCT) of the chest showed diffuse centrilobular micronodular opacities and curved linear shadows in the dorsum (Fig. 1a). Pulmonary function test results were almost within normal levels for vital capacity (VC) (2.20 L; percentage predicted VC (%VC), 86.6 %), forced expiratory volume in 1 s (FEV1) (2.07 L; percentage predicted FEV1 (%FEV1), 95.4 %), total lung capacity (TLC) (3.33 L; percent predicted TLC (%TLC), 87.2 %), and diffusing capacity of the lung for carbon monoxide (%DLCO; 77.8 %). BALF obtained from the right middle lobe (S5) showed an increased percentage of lymphocytes (55.0 %) and a decreased CD4/CD8 ratio (0.40) (Table 1). Multinucleated giant cells were not observed in BALF. Thoracoscopic lung biopsy (video-assisted thoracoscopic surgery (VATS)) of the right upper and lower lobes was performed, and microscopic examination revealed peribronchiolar fibrosis with lymphocytic infiltration. Although a few multinucleated giant cells were observed, no features diagnostic of GIP were evident (Fig. 2). Elemental analysis of the lung tissue using an electron probe microanalyzer with a wavelength-dispersive spectrometer (EPMA-1610; Shimadzu Ltd, Kyoto, Japan) revealed the presence of tungsten and cobalt in the peribronchial fibrotic region (Fig. 3). Furthermore, X-ray absorption fine structure (XAFS) analysis confirmed that the tungsten present in the samples was in the form of tungsten carbide (data not shown). These results clearly indicated that the subject had inhaled hard metal, leading to the diagnosis of HMLD.
After reaching this diagnosis, we recommended the patient quit her job or transfer to a different workplace to completely avoid exposure to hard metal dust. However, she continued working at the same place without using a dust protective mask for financial reasons, and nonproductive cough continued. In addition, pulmonary function continued to worsen. Finally, 18 months after diagnosis, she obtained a transfer to a different department where she was completely isolated from exposure to hard metal dust. Her cough improved and had completely disappeared by 2 months after ending exposure to hard metal dust. A series of pulmonary function tests revealed continuous improvements over the course of 30 months without exposure to hard metal dust (Fig. 4), although improvements in HRCT findings were modest (Fig. 1b). BALF findings obtained at 21 months after ceasing hard metal dust exposure showed a decreased percentage of lymphocytes (26.3 %) and an increase in the CD4/CD8 ratio (1.72) compared to the initial findings (Table 1). She did not take any corticosteroids or other immunosuppressive drugs during this follow-up period.
A 45-year-old non-smoking man presented with a 2-year history of dyspnea, which had started 11 years after he began a job mixing raw materials for manufacturing hard metal tools without using a dust protective mask. Chest HRCT showed diffuse centrilobular micronodular and reticular shadows (Fig. 5a). Pulmonary function testing showed a low VC (2.10 L; %VC, 46.0 %), FEV1 (1.61 L; %FEV1, 41.9 %), TLC (3.32 L; %TLC, 55.9 %), and DLCO (%DLCO, 65.0 %). Although BALF obtained from the right middle lobe (S5) demonstrated normal cell counts, multinucleated giant cells were observed (Table 2). VATS of the left upper and lower lobes were performed, and histopathological examination revealed interstitial fibrosis accompanied by multinucleated giant cell infiltration into peribronchiolar and alveolar tissues, leading to a diagnosis of GIP (Fig. 6). Elemental analysis of the lung tissue revealed the presence of tungsten in the bronchioles and alveoli (Fig. 7), and XAFS analysis confirmed the presence of tungsten carbide (data not shown), thus leading to the clinical diagnosis of HMLD.
Three weeks after his first visit, the patient obtained a transfer to a different department with reduced (but not eliminated) exposure to dust. Dyspnea gradually improved after reducing the dust exposure. Although a series of pulmonary function tests revealed improvements over the course of a year (Fig. 8), improvements in HRCT findings were modest (Fig. 5b). Multinucleated giant cells remained observable in BALF a year after reducing dust exposure, and cell differentiation was similar to that before the avoidance of dust exposure (Table 2). The patient did not take any corticosteroids or other immunosuppressive drugs during this follow-up period.
The clinical features of HMLD are known to be heterogeneous in several respects, such as pathological findings, BALF findings, and clinical course. In the two cases we encountered, thoracoscopic lung biopsy revealed distinct pathological findings, with one case characterized by typical GIP, and the other by diffuse centrilobular fibrosis around the respiratory bronchioles without GIP. In a study of 100 cases of HMLD, Asghar et al.  described 41 cases not showing GIP findings, and some cases only showed infiltration of lymphocytes and fibrosis in peribronchial lesions similar to that noted in our Case 1. Tanaka et al.  recently examined 19 cases of HMLD diagnosed in Japan and described various pathological findings, including typical GIP, centrilobular fibrosis, and usual interstitial pneumonia (UIP) pattern. In the present cases, differences in the type of job (Case 1: grinder of hard metal; Case 2: mixer of raw materials) and/or genetic backgrounds of the two patients may have been involved in the different pathological findings observed.
Avoidance of exposure to hard metal dust is central to preventing deterioration of this disease in any case, and improvements of the symptoms and/or radiological findings after avoiding exposure have been reported in several previous studies [5, 8–10]. However, to the best of our knowledge, no previous reports have provided continuous follow-up information on pulmonary function and radiological findings after reducing exposure to hard metal dust exposure. Of note, pulmonary function displayed gradual improvement after reducing dust exposure in both cases, while improvements in HRCT findings were more modest. As shown in Case 1, the improvement in pulmonary function was continuing even 2 years after starting avoidance of hard metal dust. Clinicians should thus keep in mind that gradual improvement of pulmonary function can be expected over the course of years, despite the lowered pulmonary function before the avoidance of dust exposure. Immunological responses to hard metal ingredients trapped in the bronchioles and/or to cobalt dissolved in the lungs might gradually diminish after marked reductions in exposure. We therefore speculate that the persistence of hard metal in the lung may determine the clinical course of the disease after the avoidance of dust exposure.
In some previously reported cases, respiratory failure progressed to death despite suspending exposure to the dust [11, 12], while in others, the symptoms and/or radiological findings improved with the avoidance of exposure [8–10]. The pathogenesis of HMLD is thus considered to encompass a wide spectrum of cases, from mimicking hypersensitivity pneumonitis to those similar to typical pneumoconiosis generally caused by silica and asbestos, progressing even after the avoidance of dust exposure.
Although previous studies have suggested that increased lymphocytes and decreased CD4/CD8 ratio are characteristic BALF findings in subjects with HMLD [7, 9, 12, 13], this does not always seem to be the case. In fact, in the present study, BALF findings from Case 2 showed normal cell differentiation and CD4/CD8 ratio. To date, no reports have compared BALF findings of subjects with HMLD before and after the avoidance of dust exposure similar to that encountered in the present study. The increased lymphocytes and decreased CD4/CD8 ratio observed at initial diagnosis in our Case 1 normalized by 9 months after reducing dust exposure, indicating altered immune cellular responses to hard metal in the pathogenesis of this case.
We have presented two cases of HMLD with continuous follow-up of pulmonary function and radiological findings before and after avoidance of hard metal dust exposure. The clinical courses of the two cases were presented, together with a comparison of BALF findings before and after avoidance of dust exposures.
Written informed consent was obtained from both patients for the publication of this case report and the accompanying images.
Coates EO, Watson JHL. Diffuse interstitial lung disease in tungsten carbide workers. Ann Intern Med. 1971;75:709–16.
Nemery B. Metal toxicity and the respiratory tract. Eur Respir J. 1990;3:202–19.
Cugell DW. The hard metal disease. Clin Chest Med. 1992;13:269–79.
Ohori NP, Sciurba FC, Owens GR, et al. Giant-cell interstitial pneumonia and hard-metal pneumoconiosis. Am J Surg Pathol. 1989;13:581–7.
Nemery B, Verbeken EK, Demedts M. Giant cell interstitial pneumonia (hard metal lung disease, cobalt lung). Semin Respir Crit Care Med. 2001;22:435–48.
Asghar H, Hunt A, Bryan R, Abraham JL. Pathologic spectrum and lung dust burden in giant cell interstitial pneumonia (Hard metal disease/cobalt pneumonitis): Review of 100 cases. Arch Environ Occup Health. 2008;63:51–70.
Tanaka J, Moriyama H, Terada M, et al. An observational study of giant cell interstitial pneumonia and fibrosis in hard metal lung disease. BMJ Open. 2014;4:e004407.
Okuno K, Kobayashi K, Kotani Y, Ohnishi H, Ohbayashi C, Nishimura Y. A case of hard metal lung disease resembling a hypersensitive pneumonia in radiological images. Intern Med. 2010;49:1185–9.
Kinoshita M, Sueyasu Y, Watanabe H, Tanoue S, Okubo Y, Koga T, et al. Giant cell interstitial pneumonia in two hard metal workers: the role of bronchoalveolar lavage in diagnosis. Respirology. 1999;4:263–6.
Demedts M, Gheysens B, Nagels J, Verbeken E, Lauweryns J, van den Eeckhout A, et al. Cobalt lung in diamond polishers. Am Rev Respir Dis. 1984;130:130–5.
Seike M, Usuki J, Uematsu K, Enomoto T, Shinoda K, Yoshimori K, et al. Giant cell interstitial pneumonia in a metal grinder with an abnormally high level of serum CA19-9. Nihon Kyobu Shikkan Gakkai Zasshi (Article in Japanese). 1995;33:894–9.
Nemery B, Nagels J, Verbeken E, Dinsdale D, Demedts M. Rapidly fatal progression of cobalt lung in a diamond polisher. Am Rev Respir Dis. 1990;141:1373–8.
Forni A. Bronchoalveolar lavage in the diagnosis of hard metal disease. Sci Total Environ. 1994;150:69–76.
We would like to express our sincere gratitude to Dr. Takeshi Hosokawa, former Assistant Professor of the First Department of Medicine, Hokkaido University School of Medicine, who passed away on January 17th, 2013. We are also thankful to Dr. Yasuhiro Hida (Cardiovascular and Thoracic Surgery, Hokkaido University Hospital) for performing thoracoscopic lung biopsy, and to Drs. Akira Isada, Takashi Inomata (First Department of Medicine, Hokkaido University School of Medicine), Kenzo Okamoto, and Kiyonobu Kimura (Hokkaido Chuo Rosai Hospital) for their valuable discussions.
The authors declare that they have no competing interests.
HT, SK, and MN wrote the manuscript. HT and SK contributed to the treatment of both patients. KK was involved in performing the thoracoscopic lung biopsy. YM, KH, and HK performed pathological diagnosis. HM and MU were involved in performing the elemental analysis. All authors have read and approved the final manuscript.
About this article
Cite this article
Terui, H., Konno, S., Kaga, K. et al. Two cases of hard metal lung disease showing gradual improvement in pulmonary function after avoiding dust exposure. J Occup Med Toxicol 10, 29 (2015). https://doi.org/10.1186/s12995-015-0070-9
- Hard metal lung disease
- Pulmonary function
- Dust exposure