| Literature DB >> 24899008 |
Kosar Hussain1, Jawed Abubaker2, Javeed Ahmad Dar3, Raees Ahmed2.
Abstract
We describe the case of a young man who presented with abdominal pain, vomiting and acute symmetric peripheral polyneuropathy. He was noted to have high anion gap metabolic acidosis with high lactate levels and persistently high arterial and venous pO2 values. The cerebrospinal fluid was acellular with a high protein and the nerve conduction study was consistent with axonal sensorimotor neuropathy. His clinical condition deteriorated rapidly despite full supportive care and he subsequently died of multiorgan failure. An extensive workup for various infectious, autoimmune and other possible aetiologies was carried out to identify the underlying cause for his fulminant illness. All diagnostic workup was non-conclusive except for a significantly elevated serum aluminium level. We have discussed the possibility of aluminium phosphide poisoning in view of the clinical presentation. 2014 BMJ Publishing Group Ltd.Entities:
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Year: 2014 PMID: 24899008 PMCID: PMC4054481 DOI: 10.1136/bcr-2014-203989
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X