IPLab:Lab 12:Acetaminophen Toxicity

Clinical Summary

This 77-year-old white male with a past medical history of severe osteo- and rheumatoid arthritis went to his internist for increasing joint pain and was started on a new medication containing a narcotic analgesic, acetaminophen, and a non-steroidal anti-inflammatory agent. The patient also self medicated with acetaminophen. Two days later he went back to his doctor complaining of nausea and vomiting, right upper quadrant pain, anorexia, and confusion. Lab evaluation revealed massively increased liver enzymes. The patient went into DIC and died in fulminant liver failure.

At autopsy the liver had large areas of pale softened tissue indicative of liver necrosis.

Images

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  This gross photograph of the liver from this patient demonstrates the pale areas of necrosis (arrows).

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  In this photomicrograph of the liver from this patient there are areas of hemorrhagic necrosis (arrows).

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  This is another example of the areas of hemorrhagic necrosis (arrows).

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  This is a medium-power photomicrograph of the areas of hemorrhagic necrosis. Note the coagulation necrosis and hemorrhage in this area. Viable hepatocytes can be seen along the edge of this lesion.

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  This is a high-power photomicrograph of the edge of the necrosis. Again, note the coagulation necrosis and hemorrhage in this area. The viable hepatocytes at the edge of this necrosis are vacuolated (arrows).

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  Photograph taken at autopsy demonstrating the severe necrosis of the skin of foot.

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  This low-power photomicrograph of the skin from this patient shows a blister and numerous thrombosed vessels (arrows) in the dermis.

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  This is a higher-power photomicrograph of the skin from this patient showing a blister and the thrombosed small vessels (arrows) in the dermis.

Study Questions

• What is the most likely cause for the liver necrosis seen in this patient?

The acetaminophen level on admission was not elevated; however, the patient had been in distress for some time and had not taken any acetaminophen within the previous 12 hours. Upon questioning, the patient admitted that he had continued to take his usual doses of acetaminophen even after his internist put him on new drugs. He was unaware that one of the new drugs he was taking had acetaminophen in it. Thus, he was taking an overdose of acetaminophen and this resulted in hepatic toxicity.

Adverse drug reactions can occur with therapeutic agents, but in this case the most probable cause for liver necrosis was the unintentional overdose of acetaminophen by this patient who was not aware that one of the new drugs he was taking already contained acetaminophen.

• Why did this patient develop DIC?

Liver necrosis releases thromboplastin and can initiate the coagulation cascade leading to intravascular coagulation.

Additional Resources

Reference

• eMedicine Medical Library: Acetaminophen Toxicity
• eMedicine Medical Library: Acute Liver Failure
• Merck Manual: Acetaminophen Poisoning

Journal Articles

• Schiødt FV, Lee WM, Bondesen S, Ott P, Christensen E. Influence of acute and chronic alcohol intake on the clinical course and outcome in acetaminophen overdose. Aliment Pharmacol Ther 2002 Apr;16(4):707-15.
• Yeates PJ, Thomas SH. Effectiveness of delayed activated charcoal administration in simulated paracetamol (acetaminophen) overdose. Br J Clin Pharmacol 2000 Jan;49(1):11-4.

Images

• PEIR Digital Library: Acetaminophen Toxicity Images
• WebPath: Hepatic Pathology