| Literature DB >> 19267109 |
Alessandro Di Marzo1, Giampiero Parca, Gianluca Ingrosso, Cesare Giubilei, Michele Battista, Michaela Benassi, Rosaria Barbarino, Federica Proietti, Sara Costantini, Luana Di Murro, Rebeca Nicolais, Federico Santarelli, Riccardo Santoni.
Abstract
Granulocytic sarcomas (chloromas) are rare extra-medullary tumors arising from primitive granulocytic cells. The term "chloroma" is derived from the Greek word chloros (green), and it refers to the frequently greenish color of the tumor, which is due to the presence and oxidation of the myeloperoxidase enzyme. These tumors can arise de novo or can be associated with other myeloid disorders, such as acute or chronic myeloid leukemia, myeloproliferative or myelodysplastic conditions. Presentation can occur prior to, in association with the underlying myeloid disorder, or upon relapse. The location of the tumor can vary: sub-periosteal bone, skull, pelvis, ribs, sternum or lymph nodes. We report the case of a 58-year-old man who presented right exophthalmos and ophthalmoplegy with computerized tomography (CT) evidence of a retro-orbital mass, which histology confirmed to be a granulocytic sarcoma.Entities:
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Year: 2008 PMID: 19267109 DOI: 10.1177/030089160809400618
Source DB: PubMed Journal: Tumori ISSN: 0300-8916