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Systemic Mastocytosis - a Diagnostic Challenge

dc.contributor.authorLladó, AC
dc.contributor.authorMihon, C
dc.contributor.authorSilva, M
dc.contributor.authorGalzerano, A
dc.date.accessioned2015-04-17T15:54:57Z
dc.date.available2015-04-17T15:54:57Z
dc.date.issued2014
dc.description.abstractMastocytosis refers to a group of disorders characterized by the infiltration of clonally derived mast cells to the skin or extracutaneous tissues resulting in a heterogeneous clinical picture. It is a rare hematologic disorder in all its forms. The exact incidence is unknown; it affects patients of any age and males and females equally. Its molecular pathogenesis is incompletely understood. The clinical features of mastocytosis result from both chronic and episodic mast cell mediator release, signs and symptoms arising from diffuse or focal tissue infiltration, and, occasionally, the presence of an associated non-mast cell clonal hematologic disease. The histopathologic analysis is essential for definitive diagnosis but there is no curative treatment. The authors report a clinical case of a 72-year-old woman with no history of allergies, with bicytopenia, weight loss, and diffuse axial osteolytic lesions. This is a rare clinical case of aggressive systemic mastocytosis for which palliative treatment can improve survival and quality of life. A brief review of the literature about this pathology is also included.por
dc.identifier.citationRev Bras Hematol Hemoter. 2014 May-Jun;36(3):226-9por
dc.identifier.urihttp://hdl.handle.net/10400.17/2108
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherAssociação Brasileira de Hematologia, Hemoterapia e Terapia Celularpor
dc.subjectHSAC MEDpor
dc.subjectBiopsypor
dc.subjectAllergy and Immunologypor
dc.subjectBone Marrow Cellspor
dc.titleSystemic Mastocytosis - a Diagnostic Challengepor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage229por
oaire.citation.startPage226por
oaire.citation.titleRevista Brasileira de Hematologia e Hemoterapiapor
rcaap.rightsopenAccesspor
rcaap.typearticlepor

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