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		<swivt:creationDate rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2026-07-31T11:51:06+00:00</swivt:creationDate>
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		<rdfs:label>WBR0750</rdfs:label>
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		<property:AnswerA rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Endomysial inflammation</property:AnswerA>
		<property:AnswerAExp rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Endomysial inflammation is characteristic of polymyositis.</property:AnswerAExp>
		<property:AnswerB rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Perimysial inflammation</property:AnswerB>
		<property:AnswerBExp rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Perimysial inflammation is characteristic of dermatomyositis.</property:AnswerBExp>
		<property:AnswerC rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Non-caseating granulomas</property:AnswerC>
		<property:AnswerCExp rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Non-caseating granulomas are commonly observed in sarcoidosis.</property:AnswerCExp>
		<property:AnswerD rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Precipitation of monosodium urate crystals</property:AnswerD>
		<property:AnswerDExp rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Precipitation of monosodium urate crystals is characteristic of gout.</property:AnswerDExp>
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		<property:Explanation rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Dermatomyositis is an inflammatory myopathy characterized by symmetric proximal and truncal weakness with or without associated pain. Physical examination is typically remarkable for Gottron papules (violaceous flat-topped papules and plaques in the dorsal aspect of the hand) and characteristic heliotrope rash (periorbital violaceous erythema with periorbital edema). Work-up often demonstrates elevation of muscle biomarkers, such as creatine kinase. Pathologically, dermatomyositis is considered a perimysial inflammation with lymphocytic infiltration that is generally confined to the septa. Dermatomyositis has a bi-modal peak incidence. In adult patients &gt; 50 years of age, the diagnosis of dermatomyositis prompts the investigation of a malignancy due to frequent association. This is not true, however, for those diagnosed at young age.&lt;br/&gt;
'''Educational Objective:''' Dermatomyositis is characterized by perimysial inflammation.&lt;br/&gt;
'''References:''' Khan S, Christopher-Stine L. Polymyositis, dermatomyositis, and autoimmune necrotizing myopathy: clinical features. Rheum Dis Clin N Am. 2011; 37:143-158.&lt;br
Dalakas M. Polymyositis, dermatomyositis, and inclusion-body myositis. N Engl J Med. 1991; 325:1487-1498.&lt;br&gt;
First Aid 2014 page 429.</property:Explanation>
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