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Indeterminate cell histiocytosis in association with acute myeloid leukemia

dc.contributor.authorVentura, F
dc.contributor.authorPereira, T
dc.contributor.authorDuarte, ML
dc.contributor.authorMarques, H
dc.contributor.authorPardal, F
dc.contributor.authorBrito, C
dc.date.accessioned2012-01-13T14:15:28Z
dc.date.available2012-01-13T14:15:28Z
dc.date.issued2010
dc.description.abstractIndeterminate cell histiocytosis (ICH) is a rare proliferative disorder, in which the predominant cells share morphologic and immunophenotypic features from both Langerhans and non-Langerhans cell histiocytosis. We describe a 62-year-old man presenting a 2-month history of firm nodular lesions on the upper lip. Histopathology, immunohistochemical, and ultrastructural analysis showed typical findings of ICH. The patient was treated with thalidomide and almost complete regression of the lesions was reached within 7 months. Nevertheless, one month after remission, he developed an acute myeloid leukemia of the subtype monocytic leukemia (M5). The patient's condition rapidly worsened and he died due to a respiratory failure four weeks later. We present this case because apart of being rare it joins the effectiveness of thalidomide and the association with an acute monocytic leukemia. A review of the literature is made.por
dc.identifier.citationDermatol Res Pract. 2010:569345por
dc.identifier.urihttp://hdl.handle.net/10400.23/103
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherHindawipor
dc.subjectHistiocitosepor
dc.subjectLeucemia Mielóide Agudapor
dc.titleIndeterminate cell histiocytosis in association with acute myeloid leukemiapor
dc.typejournal article
dspace.entity.typePublication
rcaap.rightsopenAccesspor
rcaap.typearticlepor

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