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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/64244
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dc.contributor.authorde Campos, E. P.-
dc.contributor.authorBertoli, C. J.-
dc.contributor.authorBarbosa, K. S.-
dc.date.accessioned2014-05-27T11:17:28Z-
dc.date.accessioned2016-10-25T18:12:56Z-
dc.date.available2014-05-27T11:17:28Z-
dc.date.available2016-10-25T18:12:56Z-
dc.date.issued1992-07-01-
dc.identifierhttp://dx.doi.org/10.1590/S0037-86821992000300008-
dc.identifier.citationRevista da Sociedade Brasileira de Medicina Tropical, v. 25, n. 3, p. 195-200, 1992.-
dc.identifier.issn0037-8682-
dc.identifier.urihttp://hdl.handle.net/11449/64244-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/64244-
dc.description.abstractThe primary complex like Ghon was observed in a child's clinical roentgenographic study. C.S., white, male, 6 years old, was born in Curitiba (PR), Brazil and living in Guaratingueta (SP), Brazil, developed common cold, bimodal diary fever, chills, shake and sweats. Dyspnea, cough with general lymphadenopathy. Foot and right shoulder arthralgias. Six months ago visited a cave, equitation practice, dog and cat contacts and no transfusion, frontal sweats, fever (38.4 degrees C). T.A. was 8/6, tachycardia in generalized lymphadenopathy. Cardiopulmonary system was normal, mesogastric tumoral mass, hepatosplenomegaly and no ascites. Bone marrow with eosinophilia; nodule demonstrated presence of P. brasiliensis, hypoalbuminemia; hyperglobulinemia; anemia; leukocytosis with eosinophilia. Immunodiffusion with exoantigen 43 kd of P. brasiliensis was 1/32. Primary complex like Ghon was observed in interstitial pneumonia followed by mediastinal and mesogastric mass (35 to 40 days). Clavicular osteolytic lesions (45 to 60 days) appeared during paracoccidioidomycosis therapy. Recovery was observed 2 months after treatment of acute infantile paracoccidioidomycosis.en
dc.format.extent195-200-
dc.language.isopor-
dc.sourceScopus-
dc.subjectcotrimoxazole-
dc.subjectTrimethoprim Sulfamethoxazole Combination-
dc.subjectacute disease-
dc.subjectbiopsy-
dc.subjectcase report-
dc.subjectchild-
dc.subjectdifferential diagnosis-
dc.subjectfever-
dc.subjecthuman-
dc.subjectisolation and purification-
dc.subjectlung-
dc.subjectlung mycosis-
dc.subjectlymph node-
dc.subjectmale-
dc.subjectmicrobiology-
dc.subjectParacoccidioides-
dc.subjectpathology-
dc.subjectremission-
dc.subjectreview-
dc.subjectSouth American blastomycosis-
dc.subjectAcute Disease-
dc.subjectBiopsy-
dc.subjectCase Report-
dc.subjectChild-
dc.subjectDiagnosis, Differential-
dc.subjectEnglish Abstract-
dc.subjectFever-
dc.subjectHuman-
dc.subjectLung-
dc.subjectLung Diseases, Fungal-
dc.subjectLymph Nodes-
dc.subjectMale-
dc.subjectParacoccidioidomycosis-
dc.subjectRemission Induction-
dc.subjectTrimethoprim-Sulfamethoxazole Combination-
dc.titleLinfonodo pulmonar na paracoccidioidomicose aguda infantil (relato de um caso).pt
dc.title.alternativePulmonary lymph node in acute juvenile paracoccidioidomycosis (a case report)en
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.identifier.doi10.1590/S0037-86821992000300008-
dc.identifier.scieloS0037-86821992000300008-
dc.rights.accessRightsAcesso aberto-
dc.identifier.file2-s2.0-0026894953.pdf-
dc.relation.ispartofRevista da Sociedade Brasileira de Medicina Tropical-
dc.identifier.scopus2-s2.0-0026894953-
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