{"title":"Exophthalmos and Blindness Revealing a Non-Hodgkin’s Malignant Lymphoma\nType B with High Grade of Malignancy","authors":"","doi":"10.33140/jocr/02/04/00001","DOIUrl":null,"url":null,"abstract":"Background: Non-Hodgkin’s lymphomas represent a heterogeneous group of haematological disorders characterized\nby a malignant monoclonal proliferation of the lymphoid system (B or T cells). Orbicatory lolisation is rare, it is seen\nmainly in adults.\nCase Report: We report the case of a 79-year-old patient with a high-grade NHML, revealed by blindness and left\nexophthalmos evolving for 3 months. Ophthalmological examination revealed left blindness with axil exophthalmos\ngrade 1. MRI cranio-orbital objectified a left orbital processe lesion intra and extra conical associated with a mucosal\nthickening of the cavum with left necrotic jugulocarotidian adenopathies. A biopsy of the cavum and ADP objectified\na NHML of type B with high grade of malignancy.\nResult: The patient was put on induction chemotherapy first before being placed on radiotherapy. The evolution was\nmarked by the regression of the left exophthalmia.\nConclusion: The NHML is characterized by an extreme clinical polymorphism, especially in the cervicofacial\nlocalizations, make the diagnosis difficult and lead to a delay in management.","PeriodicalId":91268,"journal":{"name":"HSOA journal of ophthalmology & clinical research","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-11-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"HSOA journal of ophthalmology & clinical research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.33140/jocr/02/04/00001","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Non-Hodgkin’s lymphomas represent a heterogeneous group of haematological disorders characterized
by a malignant monoclonal proliferation of the lymphoid system (B or T cells). Orbicatory lolisation is rare, it is seen
mainly in adults.
Case Report: We report the case of a 79-year-old patient with a high-grade NHML, revealed by blindness and left
exophthalmos evolving for 3 months. Ophthalmological examination revealed left blindness with axil exophthalmos
grade 1. MRI cranio-orbital objectified a left orbital processe lesion intra and extra conical associated with a mucosal
thickening of the cavum with left necrotic jugulocarotidian adenopathies. A biopsy of the cavum and ADP objectified
a NHML of type B with high grade of malignancy.
Result: The patient was put on induction chemotherapy first before being placed on radiotherapy. The evolution was
marked by the regression of the left exophthalmia.
Conclusion: The NHML is characterized by an extreme clinical polymorphism, especially in the cervicofacial
localizations, make the diagnosis difficult and lead to a delay in management.