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Anais Brasileiros de Dermatologia

On-line version ISSN 1806-4841

An. Bras. Dermatol. vol.84 no.3 Rio de Janeiro July 2009

http://dx.doi.org/10.1590/S0365-05962009000300017 

CORRESPONDENCE

 

Exposure to metallic mercury and contact dermatitis*

 

 

Paolo D. PigattoI; Chiara MarsiliII; Gianpaolo GuzziIII

IDepartment of Technology for Health, Dermatological Clinic, IRCCS Galeazzi Hospital, University of Milan - Milan, Italy
IIDepartment of Technology for Health, Dermatological Clinic, IRCCS Galeazzi Hospital, University of Milan - Milan, Italy
IIIItalian Association for Metals and Biocompatibility Research – A.I.R.M.E.B. - Milan, Italy

Mailing Address

 

 

To the Editor:

In their interesting Case Report about a single and unintentional exposure of leg skin to metallic mercury in an 18-year-old man, De Capitani et al. 1 state – in the Abstract section - that "Urinary mercury 36h after contact was 5.9 μg/L, and one week later 19.6 μg/L, indicating dermal absorption. " We think that their case report deserves comment on several points.

First, the authors argue that the slight elevated urinary mercury concentration is due to transdermal absorption of metallic mercury through his leg skin. Although metallic mercury absorption through the skin can occur in humans, the rates of elemental mercury dermal absorption is approximately 2.2 percent of the uptake quantity in the lungs. 2

Given that the lungs may have been the relevant entry route of elemental mercury emitted from liquid metallic mercury contained in a glass jar and the absorption through the respiratory tract is about 80 percent, we believe that this should have been added to their interpretation of case results.

Thus, it is unlikely that the increased levels of mercury in urine – which were observed in their patient – were due to the sole skin absorption of elemental metallic mercury leaked from glass bottle.

Second, in the Introduction section, they state that elemental mercury is "a non-liposoluble substance". 1 Instead, to our knowledge, elemental mercury is a highly lipid-soluble metal.3

Third, even if patch tests for screening of contact allergy to mercury antigens were not performed after exposure to metallic mercury, as the authors noted, the hypothesis of systemic absorption of metallic mercury through lungs as well as his leg skin is likely to explain erythematous dermatitis spreading to at sites distant from the initial site of mercury exposure.

Finally, De Capitani et al. 1 have prescribed systemic corticosteroid to their patient. In our experience, we found that systemic as well as topical steroid are not the optimal management strategy in individuals with mercury overexposure 4 due to their lack of specificity and physicians should carefully consider adverse health effects of treatment with steroid for mercury intoxication before starting any course of action.

 

REFERENCES

1. De Capitani EM, Souza EM, Vieria RJ, Madureira PR. Contact dermatitis to elemental mercury with distant lesion. An Bras Dermatol. 2009;84:75-7         [ Links ]

2. Hursh JB, Clarkson TW, Miles EF, Goldsmith LA. Percutaneous absorption of mercury vapour by man. Arch Environ Health. 1989;44:120-7         [ Links ]

3. Goyer RA, Clarkson TW. Toxic effects of metals. In: Klaassen CD. Casarett & Doull’s Toxicology: The basic science of poisons. 6th ed. New York: McGraw Hill; 2001. p. 811-7         [ Links ]

4. Pigatto PD, Guzzi G. Systemic Allergic Dermatitis Syndrome caused by Mercury. Contact Dermatitis. 2008;59:66        [ Links ]

 

 

Mailing Address:
Gianpaolo Guzzi, D.D.S.
President
Italian Association for Metals and
Biocompatibility Research, A.I.R.M.E.B.
Via A. Banfi, 4
20122 Milan – Italy
Tel./Fax: 55 +39-02-782 561 55 +39-02-919 758 53
e-mail: gianpaolo_guzzi@fastwebnet.it

 

 

Conflict of interest: None
Financial funding: None
How to cite this article: Pigatto PD, Marsili C, Guzzi G. Exposure to metalic mercury and contact dermatitis. An Bras Dermatol. 2009;84(3):303.