IPLab:Lab 13:Meningococcemia

Clinical Summary

This 20-month-old black female was active and without complaint until 4 p.m. on the evening prior to her death, when according to her mother she acted as if she did not feel well. The mother reported that the child had felt warm at bedtime (8 p.m.) so she had given her some acetaminophen. At midnight, the child was given another dose of acetaminophen. The child slept with her mother that night who reported last hearing her daughter make a sound at approximately 7:30 a.m. The mother checked in on her daughter at 8:45 a.m. and found her to be unresponsive. The girl was dead when paramedics arrived. Her past medical history was unremarkable and there had been no recent illness among other family members.

Images

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  In this gross photograph from the autopsy, note the areas of hemorrhage in the inguinal region.
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  This is a closer view of the inguinal region taken at autopsy. The areas of hemorrhage include purpura and petechiae (arrows).
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  In this gross photograph of the abdomen taken at the autopsy, there are petechial hemorrhages on the viscera (arrows).
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  This photomicrograph of the skin shows thrombi and fibrin clots in small vessels in the dermis. This is indicative of the endothelial damage caused by the Neisseria meningitidis endotoxin. This endotoxin-induced damage to the endothelium of small blood vessels throughout the body results in widespread petechiae and purpura.
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  This is a gross photograph of cross sections through the adrenal glands from this case. Both adrenal glands are markedly hemorrhagic.
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  This is a low-power photomicrograph of the adrenal gland from this case. Note that the entire gland is hemorrhagic.
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  This higher-power photomicrograph of the adrenal gland from this case provides an example of hemorrhagic necrosis.
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  This is a higher-power photomicrograph of a smear of cerebrospinal fluid taken at autopsy. Note the Gram-negative cocci in this smear, indicative of N. meningitidis.

Study Questions

• What is the Waterhouse-Friderichsen syndrome?

This is a syndrome consisting of the sudden onset of rapidly progressing illness with shock, cyanosis, hemorrhagic skin lesions, bilateral adrenal cortical hemorrhage, and usually death within 24 hours. It is the result of fulminant bacterial sepsis, often due to Neisseria meningitides, although many other organisms can be involved. N. meningitides releases a toxin that damages endothelial cells in small vessels all over the body. In the adrenal, this vascular damage and subsequent thrombosis leads to hemorrhagic necrosis.

• What is the source of Neisseria meningitides?

Man is the only host. The organism lives in the nasopharynges of apparently unaffected individuals.

• What is the favorite site of growth of Neisseria meningitides during clinical illness?

Cerebrospinal fluid is the favorite site of growth for the bacteria and meningitis is the most common illness. Other sites include heart valves, pericardium, joints, and the lungs.

Additional Resources

Reference

• eMedicine Medical Library: Meningococcemia
• Merck Manual: Acute Bacterial Meningitis

Journal Articles

• Leclerc F, Leteurtre S, Cremer R, Fourier C, Sadik A. Do new strategies in meningococcemia produce better outcomes? Crit Care Med 2000 Sep;28(9 Suppl):S60-3.

Images

• PEIR Digital Library: Meningococcemia Images
• PEIR Digital Library: Adrenal Hemorrhage Images

Cyanosis is a bluish discoloration of the skin and mucous membranes resulting from increased concentrations of reduced hemoglobin in the blood. Cyanosis occurs when the blood oxygen saturation falls below 85%.