dc.creatorCampos, Fernando Peixoto Ferraz de
dc.creatorSilva, Aloísio Souza Felipe da
dc.creatorZerbini, Maria Claudia Nogueira
dc.creatorMartines, João Augusto dos Santos
dc.date.accessioned2014-01-29T18:00:04Z
dc.date.accessioned2018-07-04T16:42:58Z
dc.date.available2014-01-29T18:00:04Z
dc.date.available2018-07-04T16:42:58Z
dc.date.created2014-01-29T18:00:04Z
dc.date.issued2013
dc.identifierAutopsy and Case Reports, v.3, n.4, p.29-36, 2013
dc.identifierhttp://www.producao.usp.br/handle/BDPI/43900
dc.identifier10.4322/acr.2013.036
dc.identifierhttp://www.autopsyandcasereports.org/ojs/index.php/autopsy/article/view/203/374
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1639376
dc.description.abstractPrimary lung lymphoma is a rare entity accounting for approximately 0.3% of all primary neoplasia of the lung and includes diffuse large B-cell lymphoma (DLBL) and lymphomatoid granulomatosis (LYG). Considering that clinical features may be similar, whereas epidemiology, morphology, and radiological features are different, the authors report a case of a middle-aged man who presented multiple pulmonary nodules in the lower lobes and groundglass opacities scattered bilaterally on computed tomography. Clinically, he presented a consumptive syndrome with respiratory failure and pleurisy, which progressed until death. The autopsy findings were consistent with lymphomatoid granulomatosis (LYG) grade 3/ diffuse large B-cell lymphoma (DLBL). The authors call attention to the difficulty of establishing an accurate diagnosis, mainly when the demonstration of EBV-infected atypical B-cells fails.
dc.languageeng
dc.publisherHospital Universitário da USP
dc.publisherSão Paulo
dc.relationAutopsy and Case Reports
dc.rightsopenAccess
dc.subjectLung
dc.subjectLymphoproliferative Disorders
dc.subjectRespiratory Insufficiency
dc.subjectAutopsy
dc.titlePrimary diffuse large B-cell lymphoma or lymphomatoid granulomatosis grade 3: a still-puzzling diagnosis in autopsy
dc.typeArtículos de revistas


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