高度恶性的非霍奇金B型恶性淋巴瘤的突出眼和失明

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摘要

背景:非霍奇金淋巴瘤是一组异质性血液病,其特征是淋巴系统(B或T细胞)的恶性单克隆增殖。Orbicaly lolisa是罕见的,它主要出现在成年人身上。病例报告:我们报告了一例79岁的高级别NHML患者,其表现为失明和左眼突出持续3个月。眼科检查显示左盲伴眼腋突出1级。MRI颅眶客观化了左侧眶突圆锥内和圆锥外病变,该病变与左侧坏死的颈豆状腺病变的腔粘膜增厚有关。腔和ADP的活检对象为B型高恶性NHML。结果:患者在放疗前先进行诱导化疗。进化的标志是左侧突眼的消退。结论:NHML具有极端的临床多态性,尤其是在颈面部定位,使诊断困难并导致治疗延迟。
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Exophthalmos and Blindness Revealing a Non-Hodgkin’s Malignant Lymphoma Type B with High Grade of Malignancy
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.
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