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Logo of mjafiGuide for AuthorsAbout this journalExplore this journalMedical Journal, Armed Forces India
 
Med J Armed Forces India. 2005 January; 61(1): 76–78.
Published online 2011 July 21. doi:  10.1016/S0377-1237(05)80127-3
PMCID: PMC4923352

Mercury Toxicity - A Case Report

Introduction

Throughout the centuries, there have been several incidents of mercury toxicity. As early as 1500 B.C we know that the Egyptians used mercury, as it was found in their tombs [1]. Men may encounter mercury in an inorganic (elemental or mercuric salt) or an organic form. All three are toxic. Elemental mercury is used in Dental amalgams, thermometers and sphygmomanometers [2]. We report one such case in a dental hygienist.

Case Report

Twenty-six year old dental hygienist with five years of service who was making dental amalgams for three and a half years without taking universal precautions was hospitalised with 02 days history of irregular, low grade fever and left sided pleuritic chest pain. He had no other complaints and denied history of any major illness in the past. Clinical examination did not reveal any abnormality. Haemogram, urine analysis and metabolic profile were normal. Chest radiograph revealed distinct metallic density opacities in all zones bilaterally (Fig 1). CT scan thorax revealed additional mediastinal metallic opacities (Fig 2). A week after admission he developed an abscess over the right forearm that did not respond to antibiotics, and hence incision and drainage was done which drained pus mixed with metallic mercury globules (1.5 ml weighing 20 g). This clinched the diagnosis of chronic elemental mercury poisoning due to inhalation of elemental mercury vapours during preparation of dental amalgams. Retrospectively the patient was evaluated. He denied any history suggestive of CNS involvement (hyperactivity, insomnia, tremors, loss of memory, abnormal behaviour, ataxia), GI involvement (anorexia, weight loss, diarrhoea, vomiting), ocular or auditory involvement. Radiographs of the right arm (AP and lateral view) (Fig 3), left thigh and abdomen (Fig 4) revealed soft tissue metallic deposits. Peripheral visual field charting, slit lamp examination and pure tone audiometry were normal. He was offered chelation therapy with Capsule D-penicillamine, to begin with 250 mg b.i.d. an hour after meals, which was increased to 1 gm/day in divided doses for 2 weeks. The course was repeated and post treatment radiographs revealed scattering of metallic deposits.

Fig. 1
Chest radiograph showing distinct metallic density opacities bilaterally
Fig. 2
CT scan thorax revealing pulmonary parenchymal and mediastinal metallic opacities
Fig. 3
Radiograph right arm (AP and lateral view) showing soft tissue metallic deposits
Fig. 4
Abdominal radiograph revealing pelvic metallic deposits

Discussion

For centuries several incidents of mercury toxicity have been reported. Some recent exposures include Minamata Bay in Japan (1960), mercury contaminated fish in Canada and methylmercury treated grain in Iraq (1960 and 1970). Mercury is the only metal that is liquid at room temperature & weighs 13.55g per ml. It is found in both organic and inorganic forms. The inorganic form can be further divided into elemental mercury and mercuric salts. All forms are toxic and manifestations depend on the nature of exposure, the intensity of exposure and the chemical form [3, 4]. Mercury poisoning can result from vapour inhalation, ingestion, injection and absorption through the skin.

Our case had mercury toxicity due to inhalation of elemental mercury vapours. It is found in liquid form and easily vaporises at room temperature and is well absorbed (80%) through inhalation. Sources of toxicity include barometers, batteries, bronzing, calibration instruments, dental amalgams, electro-plating, finger printing products, mercury lamps, and jewellary industry, paints, silver and gold production and thermometers. Its lipid soluble property allows for easy passage through alveoli into the blood stream and red blood cells. Once inhaled, elemental mercury is mostly converted to an inorganic divalent or mercuric form by catalase in the erythrocytes. This inorganic component has poor lipid solubility, limited permeability to the blood brain barrier and is excreted in faeces. But the nonoxidised component accounts for CNS toxicity, where it is ionized and trapped. Elemental mercury is not well absorbed by GI tract and therefore, when ingested, is only mildly toxic. Acute exposure to inhaled elemental mercury can lead to fever chills, dyspnea, metallic taste, pleuritic chest pain, stomatitis and lethargy. Recovery is usually without sequelae but pulmonary complications like pneumatocoele, interstitial fibrosis, pneumothorax, pneumomediastinum and fatal ARDS has been reported [5]. Chronic exposure leads to renal failure dementia and acrodynia, tremors, gingivitis and erythrism, tunnel vision and ataxia.

Management

Supportive care begins with ABCs (airway, breathing and circulation), especially when dealing with inhalation of elemental mercury and ingestion of caustic inorganic mercury. The next step is to remove the contaminated clothing and copious irrigation of the exposed skin. Emesis is not induced for the caustic inorganic form, but for the organic ingestion gastric lavage with protein containing solutions (e.g. milk, egg whites) is recommended especially when mercury is visible in the abdominal radiographs. Activated charcoal is indicated for GI decontamination, as it will bind to both organic and inorganic mercury to some extent. Use chelating agents if the patient is symptomatic, if systemic absorption is anticipated or if increased blood or urine levels are present. British Anti Lewisite (BAL) is used only in acute inorganic ingestion. D-penicillamine forms a complex with mercury and is excreted in urine and can be used if there is no renal failure. A safer drug 2,3 - dimercaptosuccinic acid (DMSA) is useful in both inorganic and organic mercurials.

Our case had chronic elemental mercury vapour exposure related to his profession. In all probability mercury got disseminated to subcutaneous tissue/skin, and abdomen after getting absorbed from the alveoli. Formation of abscesses and mercury gradually ulcerating out from the epidermis has been reported in the past [6]. In view of objective evidence of systemic mercurial deposits, nonavailability of blood and urine mercury levels, he was offered chelation therapy with D-penicillamine, which is known to give variable results [4]. He is under regular follow-up and till now has no toxic manifestations [6].

References

1. Graeme KA, Pollack CV., Jr. Heavy metal toxicity, Part I: arsenic and mercury. J Emeg Med. 1998;16(1):45–56. [PubMed]
2. Graef JW. Heavy metal poisoning. In: Isselbacher KJ, Braunwald E, Wilson JD, Martin JB, Fauci AS, Kasper DL, editors. Harrison's principle of internal medicine. 13th ed. McGraw-Hill Inc; 1994. pp. 2464–2465.
3. Young J. Mercury. In: Goldfrank LR, editor. Vol 74. McGraw-Hill; New York: 1994. pp. 1051–1062. (Goldfrank's toxicology emergencies).
4. Aggarwal P, Wali JP, editors. Diagnosis and management of common poisoning. Oxford University Press; Delhi: 1997. Mercury; pp. 244–252.
5. Taueg C, Sanfillipo DJ, Rowens B. Acute and chronic poisoning from residential exposures to elemtental mercury-Michigan 1989–1990. J Toxicol Clin Toxicol. 1992;30(1):63–67. [PubMed]
6. Reynolds JEF. Metals and some metallic salts. In: Wade A, Reynolds JEF, editors. Martindale: The extra pharmacopia. 27th ed. The Pharmaceutical press; London: 1977. pp. 888–910.

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