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7.
Arch Soc Esp Oftalmol ; 92(2): 82-85, 2017 Feb.
Article in English, Spanish | MEDLINE | ID: mdl-27268701

ABSTRACT

CASE 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)
Eye Neoplasms/pathology , Lacrimal Apparatus/pathology , Leukemia, Lymphocytic, Chronic, B-Cell/pathology , Antiphospholipid Syndrome/complications , Biopsy , Eye Neoplasms/complications , Eye Neoplasms/diagnostic imaging , Eye Neoplasms/drug therapy , Humans , Immunoglobulin kappa-Chains/analysis , Immunophenotyping , Immunotherapy , Lacrimal Apparatus/diagnostic imaging , Leukemia, Lymphocytic, Chronic, B-Cell/complications , Leukemia, Lymphocytic, Chronic, B-Cell/diagnostic imaging , Leukemia, Lymphocytic, Chronic, B-Cell/drug therapy , Male , Middle Aged , Neoplasm Proteins/analysis , Rituximab/therapeutic use , Tomography, X-Ray Computed
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