Abstract

Synthetic cannabinoids (SCs) abuse is on the rise because they are easily obtained over the counter; they are potent psychoactive compounds and routine drug testing does not detect them. As their abuse is on the rise, so are their detrimental side effects; however, the occurrence of acute hepatitis due to SCs abuse has been reported only once before. In this case, testing revealed that the patient was also heterozygous for alpha-1-antitrypsin (A-1-AT) with the phenotype of PI⁎EM. This mutant phenotype has never been reported as a cause of A-1-AT disease and the abuse of SCs in a patient with this phenotype has also never been reported. This case illustrates the possible need to expand routine drug testing for SCs and consider A-1-AT phenotyping in certain clinical scenarios.

Highlights

  • SCs are known as spice or K2, and their abuse has increased over the past few decades; they are associated with severe toxicity including seizures, cardiac arrhythmias, acute kidney injury, extreme agitation, and shortness of breath [1], but acute liver failure has only been reported once before [2]

  • A patient with a history of synthetic marijuana abuse was admitted for hepatitis and jaundice

  • SCs, known as spice or K2, are a diverse group of chemicals that act on the central nervous system’s cannabinoid receptors but are significantly more potent than naturally occurring delta-9-tetrahydrocannabinol. Their abuse has increased over the past few decades in part because in some states they can be obtained over the counter and routine drug testing does not detect them

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Summary

Introduction

SCs are known as spice or K2, and their abuse has increased over the past few decades; they are associated with severe toxicity including seizures, cardiac arrhythmias, acute kidney injury, extreme agitation, and shortness of breath [1], but acute liver failure has only been reported once before [2]. The association with mutant phenotypes of alpha-1-antitrypsin has never been reported before and the phenotype Pi∗EM has never been associated with disease of any type. This case report describes the clinical and pathologic consequences of using SCs in a patient with Pi∗EM phenotype

Case Report
23.2 Negative
Discussion
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