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dc.creatorHorta H,Pabla
dc.creatorQuevedo L,Iván
dc.date2004-04-01
dc.date.accessioned2020-02-17T15:33:44Z
dc.date.available2020-02-17T15:33:44Z
dc.identifierhttps://scielo.conicyt.cl/scielo.php?script=sci_arttext&pid=S0034-98872004000400011
dc.identifier.urihttps://revistaschilenas.uchile.cl/handle/2250/130922
dc.descriptionPoems syndrome (polyneuropathy, organomegaly, endocrine abnormality, M-protein, plasma cell dyscrasia, and skin lesions) is a plasma cell dyscrasia whose pathogenesis is unknown. We report a 60 years old woman that presented a tetraparesis caused by a sensitive motor polyneuropathy. The subsequent work up revealed an IgA type monoclonal gammopathy, hepatomegaly, hyperestrogenism, primary adrenal failure, hypothyroidism, hyperpigmentation and erythematous lesions in the skin and ankle edema. The patient is being treated with prednisone 0.5 mg/kg and levothyroxine 100 µg/day, with partial remission of her symptoms (Rev Méd Chile 2004; 132: 485-8)
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dc.languagees
dc.publisherSociedad Médica de Santiago
dc.relation10.4067/S0034-98872004000400011
dc.rightsinfo:eu-repo/semantics/openAccess
dc.sourceRevista médica de Chile v.132 n.4 2004
dc.subjectIgA
dc.subjectParaproteinemias
dc.subjectPoems syndrome
dc.titleSíndrome de Poems: Caso clínico


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