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										<responseDate>2026-05-20T09:04:08Z</responseDate>
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									<identifier>oai:www.peertechzpublications.org:10.17352/ac.000026</identifier>
									<datestamp>2025-11-12</datestamp>
									<setSpec>PTZ.AC:VOL10</setSpec>
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									<oai_dc:dc xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:mml="http://www.w3.org/1998/Math/MathML" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
										<dc:title>
										Acquired Hemophilia-A Mimicking Trauma-induced Coagulopathy in a Young Polytrauma Patient
										</dc:title><dc:creator>Andrea Capponi</dc:creator><dc:description>&lt;p&gt;Trauma-induced coagulopathy (TIC) is a common early complication in major trauma, typically presented with prolonged PT and aPTT. However, isolated or disproportionate aPTT prolongation warrants consideration of alternative diagnoses, such as acquired hemophilia A, a rare autoimmune disorder marked by factor VIII inhibitors and severe bleeding. This case describes a young, previously healthy trauma patient whose presentation mimicked TIC but was ultimately diagnosed with acquired hemophilia A, requiring immunosuppressive therapy and bypassing agents. The case underscores the importance of maintaining a broad differential diagnosis for coagulopathy in trauma settings to ensure timely recognition and appropriate management of rare but life-threatening conditions.&lt;/p&gt;</dc:description>
										<dc:publisher>Annals of Circulation - Peertechz Publications</dc:publisher>
										<dc:date>2025-11-12</dc:date>
										<dc:type>Case Report</dc:type>
										<dc:identifier>https://doi.org/10.17352/ac.000026</dc:identifier>
										<dc:language>en</dc:language>
										<dc:rights>Copyright © Andrea Capponi et al.</dc:rights>
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