Source:http://linkedlifedata.com/resource/pubmed/id/19132155
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2009-1-9
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pubmed:abstractText |
An overlap syndrome of dermatomyositis and scleroderma is reported. The case corresponded to a 27-year-old female with a clinical picture of 14 months evolution, characterized by proximal muscles weakness, erythematous rash in wrists, knees, ankles, Gottron sign, heliotrope periorbital rash and dysphagia. A muscle biopsy was compatible with dermatomyositis; meanwhile the skin biopsy was compatible with scleroderma. Muscle enzymes were increased. Interestingly, the antinuclear antibody determination in HEp-2 cells was positive with a remarkable titer of 81,920 exhibiting a nucleolar pattern. Anti-Jo1 antibody was negative, but anti-PM/Scl-100 positive. The patient received methylprednisolone and cyclophosphamide pulses, with gradual improvement. Present report constitutes a case of overlap dermatomyositis-scleroderma syndrome, with anti-PM/Scl autoantibodies (anti-exosome). The remarkable of this case was the exceptional high antinucleolar antibody titer.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:issn |
0048-7449
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
60
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
296-300
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pubmed:meshHeading |
pubmed-meshheading:19132155-Adult,
pubmed-meshheading:19132155-Autoantibodies,
pubmed-meshheading:19132155-Dermatomyositis,
pubmed-meshheading:19132155-Exosomes,
pubmed-meshheading:19132155-Female,
pubmed-meshheading:19132155-Humans,
pubmed-meshheading:19132155-Scleroderma, Systemic,
pubmed-meshheading:19132155-Syndrome
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pubmed:articleTitle |
A dermatomyositis and scleroderma overlap syndrome with a remarkable high titer of anti-exosome antibodies.
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pubmed:affiliation |
Department of Immunology, Centro de Biología Experimental, Universidad Autónoma de Zacatecas, Zac. 98040, México.
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pubmed:publicationType |
Journal Article,
Case Reports
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