Title: Sickle Cell Disease- Acute Presentations, Deadly Effects<br/>Author: Jon Mark Hirshon<br/><a href='http://umem.org/profiles/faculty/96/'>[Click to email author]</a><hr/><p>
Sickle Cell Disease (SCD) is a hemoglobinopathy that is considered a relatively rare disease in the United States, affecting about 90,000-100,000 individuals.</p>
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Globally, SCD affects millions, primarily in West and Central Africa.</p>
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Acute presentations of SCD include:</p>
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Acute Pain (Sickle Cell or Vaso-occlusive) Crisis
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Most common presentation in emergency departments</li>
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Severe Anemia
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Splenic sequestration crisis</li>
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Aplastic crisis</li>
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Hemolytic crisis</li>
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Infections
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Particularly from encapsulated organisms because of a damaged spleen (functional asplenia)</li>
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Acute Chest Syndrome
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From damaged lung tissues leading to hypoxia</li>
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A leading cause of death for patients SCD</li>
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Stroke</li>
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Priapism</li>
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Other organ dysfunction including kidney failure and eye problems (retinopathy)</li>
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The bottom line: </p>
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<strong>Sickle Cell Disease is a serious, painful and potentially life threatening disease that can cause major damage to multiple organ systems.</strong></li>
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<fieldset><legend>References</legend>
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<a href="http://www.cdc.gov/ncbddd/sicklecell/data.html">http://www.cdc.gov/ncbddd/sicklecell/data.html</a></p>
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<a href="http://www.nhlbi.nih.gov/health/health-topics/topics/sca/signs">http://www.nhlbi.nih.gov/health/health-topics/topics/sca/signs</a></p>
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http://emedicine.medscape.com/article/205926-clinical</p>
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