Bilateral Exophtalmy, Revealing a Lymphoma not Hodgkinien of the Coat Type

Y. Mouzari, Ould Hamed Ma, R. Zerrouk, F. Elasri, K. Reda, A. Oubaaz
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Abstract

Introduction: The Non hodgkinien lymphma (NHL) orbital location is a rare tumor, difficult to diagnose. The mantle cell lymphoma represents 6% of cases of LNH B. We report a patient of 60 years with bilateral exophthalmia revealing a mantle cell lymphoma. Clinical Observation: A man of 60 years ran for ophthalmological emergencies in an array of orbital cellulitis of the right eye. This swelling was that day, painful, inflammatory, axile, irreducible, and non-pulsatile, with limited horizontal movement of the eyeball. In general terms, the patient has axillary lymph nodes and supraclavicular without splenomegaly. A biopsy of the orbital mass produced by trans-conjunctival, concluded in a non-Hodgkin lymphoma B type mantle (CD20 +, CD5 +, cyclin D1 +). The assessment of extension realized in the Hematology Clinic department shows that this is a mantle cell lymphoma NHL B stage (nodes above and below the diaphragm, bilateral eyelid damage, spinal cord and location). After 3 treatments Rituximab-CHOP and DHAP-Rituximab treatments 3, obtaining a complete remission. Discussion: The mantle cell lymphoma represents about 6% of NHL. Its incidence is estimated between 0.07 and three cases per 100 000 population per year. The geographical area and ethnicity shows a higher frequency in Caucasians than in African Americans. Ocular involvement in the NHL is a rare event, as evidenced by the limited number of cases reported in the literature. It may be opening that is the case of our patient, or alter the course of lymphoma known. Conclusion: The eye location of mantle cell lymphoma is a rare entity. The clinical picture of this location can be misleading, particularly that of orbital cellulitis. The tumor biopsy confirms the diagnosis. Despite the treatment regimens, the prognosis of this type of lymphoma is reserved.
双侧眼外肿大,显示非霍奇金淋巴瘤
非霍奇金淋巴瘤(NHL)是一种罕见的肿瘤,诊断困难。套细胞淋巴瘤占LNH b病例的6%。我们报告一位60岁的患者,双侧突出眼显示套细胞淋巴瘤。临床观察:一名60岁男子因右眼眼窝蜂窝织炎就诊。这天,这种肿胀是疼痛的、炎性的、轴状的、不可消除的、无搏动性的,眼球的水平运动受限。一般来说,患者有腋窝淋巴结和锁骨上淋巴结,但没有脾肿大。经结膜眶肿块活检,结论为非霍奇金淋巴瘤B型套膜(CD20 +, CD5 +, cyclin D1 +)。在血液科完成的延伸评估显示,这是一个套细胞淋巴瘤NHL B期(横膈膜上下淋巴结,双侧眼睑损伤,脊髓及位置)。经3次利妥昔单抗- chop和dhap -利妥昔单抗治疗,获得完全缓解。讨论:套细胞淋巴瘤约占NHL的6%。其发病率估计为每年每10万人0.07至3例。从地理区域和种族来看,白种人的发病率高于非裔美国人。NHL的眼部受累是一种罕见的事件,文献中报道的病例数量有限。它可能是开放的,这是我们的病例,或改变淋巴瘤的进程已知。结论:眼内发生套细胞淋巴瘤是一种罕见的疾病。这一部位的临床表现容易引起误解,尤其是眼眶蜂窝织炎。肿瘤活检证实了诊断。尽管治疗方案,这种类型的淋巴瘤的预后是保留的。
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