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MERCURY 272<br />

2. HEALTH EFFECTS<br />

Tunnessen et al. 1987; Veien 1990; Warkany <strong>and</strong> Hubbard 1953). In many of the dermal cases, a contact<br />

dermatitis type of response was observed. However, a nonallergic pruritus is characteristic of acrodynia, a<br />

hypersensitive reaction to mercury exposure observed primarily in children, <strong>and</strong> several of the above cases<br />

may have been attributable to this syndrome (Aronow et al. 1990; Engleson <strong>and</strong> Herner 1952; Foulds et al.<br />

1987; Jalili <strong>and</strong> Abbasi 1961; Karpathios et al. 1991; Tunnessen et al. 1987; Warkany <strong>and</strong> Hubbard 1953).<br />

Other dermal reactions characteristic of acrodynia include heavy perspiration (Aronow et al. 1990; Fagala <strong>and</strong><br />

Wigg 1992; Karpathios et al. 1991; Sexton et al. 1976; Warkany <strong>and</strong> Hubbard 1953) <strong>and</strong> itching, reddened,<br />

swollen <strong>and</strong>/or peeling skin on the palms of the h<strong>and</strong>s <strong>and</strong> soles of the feet (Aronow et al. 1990; Fagala <strong>and</strong><br />

Wigg 1992; Jalili <strong>and</strong> Abbasi 1961; Karpathios et al. 1991; Tunnessen et al. 1987; Warkany <strong>and</strong> Hubbard<br />

1953). No animal studies were located to support these findings. However, these results demonstrate that<br />

two populations may experience dermal effects as a result of mercury exposure. One is those persons who<br />

develop an allergic reaction to mercury. The other is those who are hypersensitive to mercury <strong>and</strong> who<br />

develop acrodynia upon exposure. It is unknown whether sufficiently high concentrations of inorganic<br />

mercury in soil or methylmercury in fish may exist at hazardous waste sites to trigger allergic dermatitis in<br />

sensitive persons or acrodynia in those predisposed to develop this syndrome.<br />

Ocular Effects. Ocular effects have been observed in persons exposed to high concentrations of metallic<br />

mercury vapors. These effects are probably due to direct contact of the mercury vapor with the eyes. The<br />

observed effects include red <strong>and</strong> burning eyes, conjunctivitis (Bluhm et al. 1992a; Foulds et al. 1987;<br />

Karpathios et al. 1991; Schwartz et al. 1992; Sexton et al. 1976), <strong>and</strong> a yellow haze on the lenses of the eye<br />

(Atkinson 1943; Bidstrup et al. 1951; Locket <strong>and</strong> Nazroo 1952). The yellow haze was associated with longterm<br />

occupational exposures. Animal studies were not available to support these findings. However, the<br />

evidence suggests that exposure to high levels of mercury vapor may result in ocular irritation.<br />

Other Systemic Effects. Studies of workers exposed to mercury vapor found no effect on serum levels of<br />

thyroid-stimulating hormone (Erfurth et al. 1990; McGregor <strong>and</strong> Mason 1991). However, an enlarged<br />

thyroid, with elevated triiodothyronine <strong>and</strong> thyroxine, as well as reduced thyroid-stimulating hormone<br />

developed in a 13-year-old boy exposed to mercury vapor <strong>for</strong> 2 weeks (Karpathios et al. 1991). Animal<br />

studies generally support an effect of acute-duration high-level exposure on the thyroid, although the results<br />

have been somewhat variable (Goldman <strong>and</strong> Blackburn 1979; Sin <strong>and</strong> The 1992; Sin et al. 1990). A single<br />

intramuscular injection of 14.8 mg Hg/kg in rabbits resulted in increased thyroid peroxidase <strong>and</strong> triiodo­<br />

thyronine <strong>and</strong> decreased thyroxine (Ghosh <strong>and</strong> Bhattacharya 1992). A study in which rats received three

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