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Arch. Soc. Esp. Oftalmol ; 92(2): 82-85, feb. 2017. ilus
Article in Spanish | IBECS | ID: ibc-160377

ABSTRACT

CASO CLÍNICO: Presentamos un caso de linfoma linfocítico de células pequeñas primario de glándula lagrimal en un varón diagnosticado de síndrome antifosfolípido primario. Estos infrecuentes linfomas se presentan habitualmente en la clínica como diseminaciones secundarias a una leucemia linfocítica crónica, siendo rara su localización primaria en la órbita. DISCUSIÓN: Los linfomas no Hodgkin son un grupo muy heterogéneo de tumores. Aunque el tratamiento en su estadio IE suele ser radioterapia, debido a su asociación con un síndrome antifosfolípido, se realizó tratamiento sistémico con rituximab


CASER REPORT: We report a case of primary small-cell lymphocytic lacrimal gland lymphoma in a male diagnosed with primary antiphospholipid syndrome. These rare lymphomas are usually presented in the clinic as disseminations secondary to chronic lymphocytic leukaemia, and the primary site is rare in the orbit. DISCUSSION: Non-Hodgkin lymphomas are a heterogeneous group of tumours. Although treatment in the IE stage is usually radiotherapy, due to its association with antiphospholipid syndrome, systemic treatment with rituximab was administered


Subject(s)
Humans , Male , Middle Aged , Lymphoma, B-Cell/pathology , Lacrimal Apparatus/pathology , Eye Neoplasms/pathology , Rituximab/therapeutic use , Antiphospholipid Syndrome/complications , Immunophenotyping
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